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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" dtd-version="1.3" xml:lang="en" article-type="research-article"><?properties manuscript?><processing-meta base-tagset="archiving" mathml-version="3.0" table-model="xhtml" tagset-family="jats"><restricted-by>pmc</restricted-by></processing-meta><front><journal-meta><journal-id journal-id-type="nlm-journal-id">101618821</journal-id><journal-id journal-id-type="pubmed-jr-id">41837</journal-id><journal-id journal-id-type="nlm-ta">Lancet Diabetes Endocrinol</journal-id><journal-id journal-id-type="iso-abbrev">Lancet Diabetes Endocrinol</journal-id><journal-title-group><journal-title>The lancet. Diabetes &#x00026; endocrinology</journal-title></journal-title-group><issn pub-type="ppub">2213-8587</issn><issn pub-type="epub">2213-8595</issn></journal-meta><article-meta><article-id pub-id-type="pmid">37356445</article-id><article-id pub-id-type="pmc">11070656</article-id><article-id pub-id-type="doi">10.1016/S2213-8587(23)00129-8</article-id><article-id pub-id-type="manuscript">NIHMS1977150</article-id><article-categories><subj-group subj-group-type="heading"><subject>Article</subject></subj-group></article-categories><title-group><article-title>Global Inequity in Diabetes 3</article-title><subtitle>Disparities in diabetes prevalence and management by race and ethnicity in the USA: defining a path forward</subtitle></title-group><contrib-group><contrib contrib-type="author"><name><surname>Hassan</surname><given-names>Saria</given-names></name><degrees>MD</degrees><aff id="A1">Department of Medicine, Emory Global Diabetes Research Center, Emory University, Atlanta, GA, USA; Hubert Department of Global Health, Rollins School of Public Health, Atlanta, GA, USA</aff></contrib><contrib contrib-type="author"><name><surname>Gujral</surname><given-names>Unjali P</given-names></name><degrees>PhD</degrees><aff id="A2">Emory Global Diabetes Research Center, Emory University, Atlanta, GA, USA; Hubert Department of Global Health, Rollins School of Public Health, Atlanta, GA, USA</aff></contrib><contrib contrib-type="author"><name><surname>Quarells</surname><given-names>Rakale C</given-names><prefix>Prof</prefix></name><degrees>PhD</degrees><aff id="A3">Emory Global Diabetes Research Center, Emory University, Atlanta, GA, USA; Department of Community Health and Preventive Medicine, Morehouse School of Medicine, Atlanta, GA, USA</aff></contrib><contrib contrib-type="author"><name><surname>Rhodes</surname><given-names>Elizabeth C</given-names></name><degrees>PhD</degrees><aff id="A4">Emory Global Diabetes Research Center, Emory University, Atlanta, GA, USA; Hubert Department of Global Health, Rollins School of Public Health, Atlanta, GA, USA</aff></contrib><contrib contrib-type="author"><name><surname>Shah</surname><given-names>Megha K</given-names></name><degrees>MD</degrees><aff id="A5">Department of Family and Preventive Medicine, Emory Global Diabetes Research Center, Emory University, Atlanta, GA, USA</aff></contrib><contrib contrib-type="author"><name><surname>Obi</surname><given-names>Jane</given-names></name><degrees>MPH</degrees><aff id="A6">Emory School of Medicine, and the Nutrition and Health Sciences Doctoral Program, Laney Graduate School, Emory Global Diabetes Research Center, Emory University, Atlanta, GA, USA</aff></contrib><contrib contrib-type="author"><name><surname>Lee</surname><given-names>Wei-Hsuan</given-names></name><degrees>MPhil</degrees><aff id="A7">Department of Medicine, Emory University, Atlanta, GA, USA</aff></contrib><contrib contrib-type="author"><name><surname>Shamambo</surname><given-names>Luwi</given-names></name><degrees>BSc</degrees><aff id="A8">Department of Medicine, Emory University, Atlanta, GA, USA</aff></contrib><contrib contrib-type="author"><name><surname>Weber</surname><given-names>Mary Beth</given-names></name><degrees>PhD</degrees><aff id="A9">Emory School of Medicine, and the Nutrition and Health Sciences Doctoral Program, Laney Graduate School, Emory Global Diabetes Research Center, Emory University, Atlanta, GA, USA; Hubert Department of Global Health, Rollins School of Public Health, Atlanta, GA, USA</aff></contrib><contrib contrib-type="author"><name><surname>Venkat Narayan</surname><given-names>K M</given-names><prefix>Prof</prefix></name><degrees>MD</degrees><aff id="A10">Department of Medicine, Emory School of Medicine, and the Nutrition and Health Sciences Doctoral Program, Laney Graduate School, Emory Global Diabetes Research Center, Emory University, Atlanta, GA, USA; Hubert Department of Global Health, Rollins School of Public Health, Atlanta, GA, USA</aff></contrib></contrib-group><author-notes><fn fn-type="con" id="FN1"><p id="P1">Contributors</p><p id="P2">All authors conceptualised the outline for the paper. RCQ and W-HL wrote the first draft of the section on differences in diabetes burden within racial and ethnic groups. MBW and JO wrote the first draft of the section on differences in diabetes burden and diabetes-related complications by race or ethnicity in young people. UPG wrote the first draft of the section on the pathophysiology of diabetes and diabetes disparities. SH, ECR, MKS, and LS wrote the first draft of the section on contributors to diabetes disparities in the USA. SH revised drafts and wrote the introduction and recommendation sections. KMVN reviewed all drafts and made edits.</p></fn><corresp id="CR1">Correspondence to: Dr Saria Hassan, Department of Medicine, Emory School of Medicine, Emory University, Atlanta, GA 30322, USA, <email>saria.hassan@emory.edu</email></corresp></author-notes><pub-date pub-type="nihms-submitted"><day>21</day><month>4</month><year>2024</year></pub-date><pub-date pub-type="ppub"><month>7</month><year>2023</year></pub-date><pub-date pub-type="epub"><day>22</day><month>6</month><year>2023</year></pub-date><pub-date pub-type="pmc-release"><day>06</day><month>5</month><year>2024</year></pub-date><volume>11</volume><issue>7</issue><fpage>509</fpage><lpage>524</lpage><abstract id="ABS1"><p id="P3">Type 2 diabetes disparities in the USA persist in both the prevalence of disease and diabetes-related complications. We conducted a literature review related to diabetes prevention, management, and complications across racial and ethnic groups in the USA. The objective of this review is to summarise the current understanding of diabetes disparities by examining differences between and within racial and ethnic groups and among young people (aged &#x0003c;18 years). We also examine the pathophysiology of diabetes as it relates to race and ethnic differences. We use a conceptual framework built on the socioecological model to categorise the causes of diabetes disparities across the lifespan looking at factors in five domains of health behaviours and social norms, public awareness, structural racism, economic development, and access to high-quality care. The range of disparities in diabetes prevalence and management in the USA calls for a community-engaged and multidisciplinary approach that must involve community partners, researchers, practitioners, health system administrators, and policy makers. We offer recommendations for each of these groups to help to promote equity in diabetes prevention and care in the USA.</p></abstract></article-meta></front><body><sec id="S1"><title>Introduction</title><p id="P4">Type 2 diabetes is a highly prevalent, costly, chronic disease that poses a serious threat to both domestic and global health. The International Diabetes Federation reports that 10% of adults (aged 20&#x02013;79 years) have type 2 diabetes worldwide, with North America reporting 51 million adults living with this disease.<sup><xref rid="R1" ref-type="bibr">1</xref></sup> In the USA specifically, an estimated 37&#x000b7;3 million (11&#x000b7;1% of the population) had type 2 diabetes in 2020.<sup><xref rid="R2" ref-type="bibr">2</xref></sup> Type 2 diabetes is currently one of the leading causes of death in the USA with a crude death rate of 26&#x000b7;7 per 100 000 people.<sup><xref rid="R2" ref-type="bibr">2</xref></sup> Type 2 diabetes prevalence varies between states in the USA, ranging from 3&#x000b7;3% (95% CI 2&#x000b7;2&#x02013;4&#x000b7;5) in Teton County, WY, to 19&#x000b7;5% (17&#x000b7;2&#x02013;22&#x000b7;0) in Oglala Lakota County, SD, in 2017.<sup><xref rid="R3" ref-type="bibr">3</xref></sup> There is also 7-fold to 8-fold variation in incidence of age-standardised diagnosed diabetes across US counties.<sup><xref rid="R4" ref-type="bibr">4</xref></sup> A common and potentially preventable disease, type 2 diabetes imposes substantial health and economic burdens in the USA, where the medical costs and lost work wages of people diagnosed with the disease total an estimated US$327 billion annually.<sup><xref rid="R5" ref-type="bibr">5</xref></sup></p><p id="P5">The burden of type 2 diabetes in the USA is not shared equally between different racial and ethnic groups. Several reviews from the past 5 years have discussed disparities in the prevalence of diabetes and diabetes-related complications by racial and ethnic groups in the USA. For example, Cheng and colleagues&#x02019; 2019 review<sup><xref rid="R6" ref-type="bibr">6</xref></sup> of the literature showed persistent disparity in the prevalence of diabetes in the USA with Hispanic American adults (aged &#x02265;20 years) having the highest prevalence (22&#x000b7;1%) followed by non-Hispanic Black adults (20&#x000b7;4%), and non-Hispanic Asian American adults (19&#x000b7;1%) compared with the non-Hispanic White American adult population (12&#x000b7;1%). In their 2021 study, Wang and colleagues<sup><xref rid="R7" ref-type="bibr">7</xref></sup> showed that there continues to be poor control of risk factors such as blood sugar levels, blood pressure, cholesterol concentrations, and smoking among individuals with type 2 diabetes. Moreover, non-Hispanic Black individuals were significantly less likely than non-Hispanic White adults to have these risk factors controlled.<sup><xref rid="R7" ref-type="bibr">7</xref></sup> In 2021, Ezzatvar and colleagues<sup><xref rid="R8" ref-type="bibr">8</xref></sup> described the persistent disparities in diabetes-related complications and all-cause mortality that are in part a consequence of poorly controlled risk factors. In 2022, El Hussein and colleagues<sup><xref rid="R9" ref-type="bibr">9</xref></sup> described disparities in the prescribing of new diabetes medication (eg, GLP-1 receptor agonists, DPP-4 inhibitors, and SGLT2 inhibitors), with Black (hazard ratio 0&#x000b7;81, 95% CI 0&#x000b7;71&#x02013;0&#x000b7;94) and American Indian and Native American individuals (0&#x000b7;51, 0&#x000b7;26&#x02013;0&#x000b7;99) less likely to be prescribed these medications than White individuals.</p><p id="P6">The limitation of many of these reviews is that they analyse racial and ethnic groups as one homogeneous entity. However, there is growing realisation of the importance of examining within-group differences to address diabetes disparities.<sup><xref rid="R10" ref-type="bibr">10</xref>,<xref rid="R11" ref-type="bibr">11</xref></sup> Furthermore, focusing solely on adults with diabetes overlooks the degree to which child and adolescent onset type 2 diabetes is contributing to the growing burden of disease and worsening disparities. Not only has the prevalence of type 2 diabetes among young people (aged 10&#x02013;19 years) nearly doubled in the past two decades (from 34 per 100 000 in 2001 to 67 per 100 000 in 2017), but the highest number of young people living with type 2 diabetes per 1000 individuals is seen among Black or American Indian populations.<sup><xref rid="R12" ref-type="bibr">12</xref></sup> The story of disparities in diabetes in the USA is, therefore, incomplete if not considering the whole lifespan.</p><p id="P7">Our objective in this Series paper is to compile and summarise key literature examining diabetes disparities across the lifespan and within racial and ethnic groups. We then provide a summary of more recent literature looking at the role of genetics and emerging views on pathophysiological basis of different diabetes phenotypes. Finally, we provide a framework to summarise the multilevel contributors to diabetes disparities in the USA. Leveraging this more informative view of disparities, we recommend a path forward to address knowledge gaps and an implementation and policy agenda to promote diabetes health equity.</p><sec id="S2"><title>Definition of racial and ethnic groups</title><p id="P8">We define racial and ethnic groups in this Series paper using the Office of Management and Budget Standards (OMB) definition.<sup><xref rid="R13" ref-type="bibr">13</xref></sup> The racial groups are American Indian or Alaska Native, Asian, Black or African American, Native Hawaiian or other Pacific Islander, and White. The ethnic groups are Hispanic and non-Hispanic. From here on, we will refer to non-Hispanic Black as Black, and non-Hispanic White as White. American Indian or Alaska Native might also be referred to as Native American on the basis of study descriptions.</p></sec></sec><sec id="S3"><title>Conceptual framework</title><p id="P9">We consider the contributors to diabetes disparities across the lifespan, within, and between racial and ethnic groups using a modified version of the conceptual framework proposed by Agarwal and colleagues in this Series paper.<sup><xref rid="R14" ref-type="bibr">14</xref></sup> We consider the domains of health behaviours and social norms, structural racism, access to high-quality care, economic development, and public awareness. We discuss how these domains differentially exert their influence at the individual, interpersonal, community, and societal levels across the lifespan (<xref rid="F1" ref-type="fig">figure 1</xref>).</p></sec><sec id="S4"><title>The burden of diabetes-related disparities in the USA</title><sec id="S5"><title>Differences in diabetes burden and diabetes-related complications by race or ethnicity in young people</title><p id="P10">Parallel to the growing epidemic of childhood obesity, prevalence and incidence of type 2 diabetes in children and adolescents has increased since the turn of the 21st century, with continued and persistent earlier onset of diagnosis, which has been exacerbated by the COVID-19 pandemic.<sup><xref rid="R15" ref-type="bibr">15</xref></sup> The burden of type 1 and type 2 diabetes varies by race and ethnicity, as reported in the SEARCH for Diabetes in Youth Study (SEARCH; <xref rid="F1" ref-type="fig">figure 1</xref>). Although this Series paper is focused on type 2 diabetes, type 1 diabetes continues to play an important role in diabetes in young people. We note here that data in young people are limited by racial and ethnic group differences and not within racial and ethnic groups; therefore, this topic will not be discussed in the young people section (<xref rid="F2" ref-type="fig">figure 2</xref>).</p><p id="P11">SEARCH has conducted diabetes surveillance in young people in the USA for nearly two decades. In 2001, 6379 individuals aged 0&#x02013;19 years were identified with diabetes within a population of approximately 3&#x000b7;5 million, with Native American young people having the largest proportion (76%) of type 2 diabetes.<sup><xref rid="R17" ref-type="bibr">17</xref></sup> Population projections from this study estimated roughly 154 000 young people aged 0&#x02013;19 years were living with diabetes in the USA in 2001. Since 2001, diabetes prevalence in young people has increased among all racial and ethnic groups, with the largest increases among Asian and Pacific Islander (these groups were not separated in SEARCH), Black, and Hispanic children. Between 2009 and 2017, the estimated prevalence of diabetes in Black children increased by 7&#x000b7;1% (95% CI 4&#x000b7;8 to 9&#x000b7;4), compared with 7&#x000b7;3% (2&#x000b7;7 to 12&#x000b7;1) in Asian and Pacific Islander children, 4&#x000b7;8% (0&#x000b7;7 to 9&#x000b7;0) in American Indian children, 3&#x000b7;2% (1&#x000b7;4 to 5&#x000b7;0) in Hispanic children, and 1&#x000b7;4% (&#x02013;1&#x000b7;2 to 4&#x000b7;1) in White children.<sup><xref rid="R12" ref-type="bibr">12</xref>,<xref rid="R16" ref-type="bibr">16</xref></sup> A separate study showed a pronounced increase in diabetes among American Indian and Alaska Native young people (aged 15&#x02013;19 years), with a 68% increase in cases of diagnosed type 2 diabetes from 1994 to 2004.<sup><xref rid="R12" ref-type="bibr">12</xref>,<xref rid="R18" ref-type="bibr">18</xref></sup> The COVID-19 pandemic has been associated with a rise of incident paediatric diabetes cases, with one study finding incident type 2 diabetes cases decreasing moderately by 7&#x000b7;4% in the 2 years before the pandemic and increasing 182% during the pandemic (n=141; 1&#x000b7;45 cases per month; p&#x0003c;0&#x000b7;001). Type 2 diabetes cases increased by more in Black children (76&#x000b7;6%) than in White children (56&#x000b7;7%; p=0&#x000b7;001) and more in boys (58&#x000b7;9%) than in girls (40&#x000b7;4%; p=0&#x000b7;005).<sup><xref rid="R19" ref-type="bibr">19</xref></sup> Among American Indian children and adolescents, metabolic abnormalities led to greater relative risk of diabetes in children (aged 5&#x02013;11 years) compared with adolescents (aged 12&#x02013;19 years).<sup><xref rid="R20" ref-type="bibr">20</xref>,<xref rid="R21" ref-type="bibr">21</xref></sup> With one in five adolescents in the USA having prediabetes, the problem of diabetes among young people will probably continue to grow.<sup><xref rid="R22" ref-type="bibr">22</xref></sup></p><p id="P12">Overall, adolescents have more rapid and complete onset of &#x003b2;-cell failure compared with adults, increasing urgency for the few available treatment options.<sup><xref rid="R23" ref-type="bibr">23</xref></sup> Furthermore, the onset of diabetes-related complications in specific racial and ethnic groups is accelerated in young people. The Pediatric Diabetes Consortium Registry reported significant race and ethnic differences in HbA<sub>1c</sub> and C-peptide levels, with Black young people (aged &#x0003c;18 years) having higher HbA<sub>1c</sub> and lower C-peptide than White young people. Black children are significantly more likely than White children (odds ratio [OR] 4&#x000b7;85, 95% CI 1&#x000b7;49&#x02013;15&#x000b7;77) to have poor glycaemic control (HbA<sub>1c</sub> &#x0003e;9&#x000b7;5%) at 1 year from time of diagnosis.<sup><xref rid="R24" ref-type="bibr">24</xref></sup> Non-alcoholic fatty liver disease was diagnosed in 9% of Hispanic children and 11% of White children, compared with 2% of Black children.<sup><xref rid="R25" ref-type="bibr">25</xref></sup> Similarly, Hispanic children have significantly elevated liver aminotransferases compared with Black children.<sup><xref rid="R26" ref-type="bibr">26</xref></sup></p></sec><sec id="S6"><title>Differences in diabetes burden within racial and ethnic groups</title><p id="P13">Here, we describe within-group differences in diabetes prevalence, burden, and management among Hispanic, Black, and Asian individuals. Data on differences within White, American Indian, and Pacific Islander populations are scarce. White people are often viewed as one large, homogeneous group; however, many people who identify as White in the USA might represent different and culturally distinct subgroups, such as people born within the USA and those born overseas (eg, Europe or the Middle East), or religious subgroups. Although studies exploring these subgroups are scarce, differences in diabetes prevalence by rural versus urban residency have been found.<sup><xref rid="R27" ref-type="bibr">27</xref>,<xref rid="R28" ref-type="bibr">28</xref></sup> Additionally, demographic-adjusted models have shown increased diabetes risk among White populations based on residency in the so-called stroke belt of the southeastern USA (OR 1&#x000b7;22, 95% CI 1&#x000b7;09&#x02013;1&#x000b7;36) and buckle of eastern North Carolina, South Carolina, and Georgia (1&#x000b7;26, 1&#x000b7;10&#x02013;1&#x000b7;44), compared with residency in other parts of the USA.<sup><xref rid="R29" ref-type="bibr">29</xref></sup></p><p id="P14">Within the Hispanic population, the national diabetes statistic report of 2020 highlights differences in age-adjusted prevalence of diagnosed diabetes among Hispanic Americans, with Cuban Americans having the lowest prevalence at 6&#x000b7;5%, compared with 12&#x000b7;4% in Puerto Rican American and 13&#x000b7;4% in Mexican American adults.<sup><xref rid="R2" ref-type="bibr">2</xref></sup> These differences have been shown using different datasets as well, including the nationally representative NESARC-III study.<sup><xref rid="R22" ref-type="bibr">22</xref></sup> The Hispanic Community Health Study/Study of Latinos (HCHS/SOL) corroborates these findings with a population-based cohort. A longitudinal analysis from HCHS/SOL showed persistent differences in diabetes incidence within the Hispanic population with higher incidence among those with Puerto Rican and Mexican backgrounds.<sup><xref rid="R30" ref-type="bibr">30</xref>,<xref rid="R31" ref-type="bibr">31</xref></sup></p><p id="P15">US-born Black individuals and non-US born Black individuals of sub-Saharan African or Caribbean descent are often analysed as one racial group (Black) in the literature, although research disaggregating these groups has shown important differences in diabetes prevalence.<sup><xref rid="R32" ref-type="bibr">32</xref></sup> Several studies have indicated the higher prevalence of diabetes among US-born versus African-born or Caribbean-born Black adults.<sup><xref rid="R33" ref-type="bibr">33</xref>,<xref rid="R34" ref-type="bibr">34</xref></sup> Ford and colleagues<sup><xref rid="R10" ref-type="bibr">10</xref></sup> used National Health Interview Survey data to show that Black individuals born in Africa or the Caribbean had significantly lower odds of having diabetes (OR 0&#x000b7;75, 95% CI 0&#x000b7;62&#x02013;0&#x000b7;89) compared with US-born Black individuals. Within the population of Black individuals born in Africa or the Caribbean, studies have shown little to no difference between those born in the Caribbean and those born in sub-Saharan Africa. Nevertheless, increasing time in the USA and higher levels of acculturation were associated with increased odds of diabetes diagnosis among foreign-born Black individuals.<sup><xref rid="R33" ref-type="bibr">33</xref></sup> This increase has highlighted the importance of furthering our understanding of the differences between Black people born within and outside of the USA, as a unique opportunity to examine genetic differences, sociocultural contexts, migration experience, and population characteristics.<sup><xref rid="R35" ref-type="bibr">35</xref></sup></p><p id="P16">Asian Americans are a large and diverse population, although they are often grouped into one large racial and ethnic group.<sup><xref rid="R36" ref-type="bibr">36</xref></sup> South Asian Americans have higher age-adjusted prevalence of diabetes and gestational diabetes than other Asian American subgroups.<sup><xref rid="R37" ref-type="bibr">37</xref></sup> Filipino American and Korean American adults have the next highest prevalence of diabetes among Asian Americans;<sup><xref rid="R38" ref-type="bibr">38</xref>,<xref rid="R39" ref-type="bibr">39</xref></sup> prevalence of diabetes among Korean Americans was 10% in New York City and 11&#x000b7;9% in California,<sup><xref rid="R40" ref-type="bibr">40</xref>,<xref rid="R41" ref-type="bibr">41</xref></sup> with Korean Americans having very low rates of physical activity compared with other Asian subgroups.<sup><xref rid="R42" ref-type="bibr">42</xref>,<xref rid="R43" ref-type="bibr">43</xref></sup> Of all Asian American subgroups, Chinese Americans continue to have the lowest rates of diabetes.<sup><xref rid="R44" ref-type="bibr">44</xref></sup></p><p id="P17">Factoring in within-group differences will allow us to better understand trends in diabetes prevalence epidemiologically. We can better target resources and interventions if we look at subgroups within racial and ethnic groups whose rising rates might be otherwise masked. These described differences within racial and ethnic groups are crucial considerations when designing interventions for diabetes prevention or management.</p><sec id="S7"><title>Disparities in diabetes complications</title><p id="P18">Disparities in diabetes prevalence are compounded by disparities in diabetes-related complications. Although disparities in diabetes-related complications in young people have been described, there are scarce data on differences in complications within racial and ethnic groups. Diabetes-related microvascular complications include chronic kidney disease, retinopathy, and amputations. Among US adults with diabetes, 39&#x000b7;2% were reported to have chronic kidney disease (stages 1&#x02013;4). This prevalence was higher among Black adults, with 23&#x000b7;1% having chronic kidney disease stage 3&#x02013;4, compared with 17&#x000b7;2% of White adults and 8&#x000b7;9% of Hispanic adults with diabetes.<sup><xref rid="R45" ref-type="bibr">45</xref></sup> Diabetes is now the leading cause of new cases of blindness among adults in the USA.<sup><xref rid="R46" ref-type="bibr">46</xref></sup> Diabetic retinopathy is more prevalent in Black individuals (38&#x000b7;8%) than in Hispanic individuals (31&#x000b7;0%) and White individuals (26&#x000b7;4%). Black and Hispanic individuals with diabetic retinopathy are much more likely to progress to visual impairment and blindness than White individuals.<sup><xref rid="R46" ref-type="bibr">46</xref>&#x02013;<xref rid="R48" ref-type="bibr">48</xref></sup> Odds for major amputation were significantly greater in Black (OR 1&#x000b7;44, 95% CI 1&#x000b7;36&#x02013;1&#x000b7;53), Hispanic (1&#x000b7;33, 1&#x000b7;25&#x02013;1&#x000b7;41), and Native American (1&#x000b7;47, 1&#x000b7;2&#x02013;1&#x000b7;8) patients with diabetic foot infections than in White patients.<sup><xref rid="R49" ref-type="bibr">49</xref></sup> Asian patients had a 64% lower rate of major amputation in cases of diabetic foot infections compared with White patients.<sup><xref rid="R50" ref-type="bibr">50</xref></sup></p><p id="P19">Cardiovascular and cerebrovascular disease are the major macrovascular complications of diabetes. To prevent these complications, individuals with diabetes should meet the recommended ABC metrics for cardiovascular disease risk reduction&#x02014;ie, HbA<sub>1c</sub> &#x0003c;7%, blood pressure &#x0003c;130/80 mm Hg, LDL cholesterol &#x0003c;100 mg/dL. Multiple studies have shown that Black Americans and Mexican Americans are less likely to meet all three ABC goals than White individuals.<sup><xref rid="R51" ref-type="bibr">51</xref></sup> Cardiovascular disease is the leading cause of mortality among people with diabetes in the USA.<sup><xref rid="R52" ref-type="bibr">52</xref></sup> Although overall cardiovascular death in the USA decreased significantly between 1988 and 2015, gaps in mortality between racial and ethnic groups have persisted.<sup><xref rid="R52" ref-type="bibr">52</xref></sup></p></sec><sec id="S8"><title>Disparities in diabetes management</title><p id="P20">Disparities between racial and ethnic groups for diabetes management have received little attention in the past; however, there are important differences between these groups&#x02014;eg, geographical location (ie, rural and urban), income, and insurance status. Disparities can be seen at the level of diabetes screening as well as management. Large disparities exist in the diagnosis of diabetes with all racial and minority ethnic populations (eg, Black, Hispanic, and Asian) being more likely to have undiagnosed diabetes than White individuals in the USA.<sup><xref rid="R53" ref-type="bibr">53</xref></sup> For screening of diabetes-related complications in the USA, only 33&#x02013;68% of adults with diabetes obtain an annual dilated eye exam; however, these screening rates are even lower in Black individuals and Latino individuals.<sup><xref rid="R48" ref-type="bibr">48</xref></sup> A 2008 qualitative review of various minority groups, including Black, American Indian, and Latino, reported substantially decreased rates of eye examinations in these populations.<sup><xref rid="R54" ref-type="bibr">54</xref></sup> New modalities for efficient screening using artificial intelligence, machine learning, and telehealth have the potential to increase access to retinopathy screening for minority populations; however, data on their reach and uptake are not yet available. Similarly, data on reach and uptake of new modalities to treat diabetic retinopathy including intravitreal anti-VEGF injections, which present opportunities to prevent blindness, are not yet available.</p><p id="P21">Diabetes management also refers to medication and equipment that is prescribed. A 2021 review looked at access to GLP-1 receptor agonists and found that Asian, Black, and Hispanic individuals and those with low incomes were less likely to receive treatment with GLP-1 receptor agonists than White individuals and those with better incomes.<sup><xref rid="R55" ref-type="bibr">55</xref></sup> This disparity is important to recognise given the known cardiovascular benefits of GLP-1 receptor agonists. Further disparity can be seen in access to new technology. Data show that for continuous glucose monitoring (CGM), for example, Black individuals have the lowest rates of access across age groups, health insurance coverage, and location.<sup><xref rid="R56" ref-type="bibr">56</xref>,<xref rid="R57" ref-type="bibr">57</xref></sup></p></sec></sec><sec id="S9"><title>Pathophysiology of diabetes and diabetes disparities</title><sec id="S10"><title>Increased diabetes risk at low BMI in minority race and ethnic populations</title><p id="P22">Overweight and obesity are well established risk factors for diabetes. However, evidence suggests that the relationship between bodyweight and diabetes is not linear, and that diabetes at low BMI is considerably more prevalent in minority race and ethnic populations.<sup><xref rid="R58" ref-type="bibr">58</xref></sup> A study from 2022 of diabetes prevalence in US Asian adults by weight found an increased burden of diabetes risk among south Asian Americans and Filipino Americans who had a BMI within a healthy range compared with White Americans and Chinese Americans.<sup><xref rid="R59" ref-type="bibr">59</xref></sup> Additionally, a study examining the prevalence of diabetes by BMI status and place of birth found that the prevalence of diabetes in immigrants with a healthy weight from India and Africa was higher than the prevalence of diabetes in immigrants with obesity from Europe.<sup><xref rid="R60" ref-type="bibr">60</xref></sup> A 2019 study examining racial and ethnic disparities in the prevalence of diabetes by BMI category in six racial and ethnic groups in the USA found that in those with a healthy weight, the prevalence of diabetes was 5&#x000b7;0% in White participants, 10&#x000b7;1% in Asian participants, 9.6% in American Indian and Alaskan Native participants, 13&#x000b7;0% in Hispanic participants, 13&#x000b7;5% in Black participants, and 18&#x000b7;0% in Hawaiian and Pacific Islander participants.<sup><xref rid="R61" ref-type="bibr">61</xref></sup> Furthermore, when examining the relative risks for diabetes for each BMI category across all racial and ethnic groups, White participants showed the greatest sensitivity to changes in BMI followed by Asian, American Indian and Alaskan Native, Hispanic, Hawaiian and Pacific Islander, and Black participants.<sup><xref rid="R61" ref-type="bibr">61</xref></sup> These results do not indicate greater sensitivity to excess adiposity in non-White populations, rather they suggest that factors other than BMI are driving the disproportionate burden of diabetes in non-White populations, both in the USA and globally. Additionally, these data have implications for screening and prevention. Elevated BMI should not necessarily be the first criterion to consider when screening for diabetes in minority race and ethnic populations as it could result in a substantial number of at-risk individuals being missed. Furthermore, prevention strategies that target weight loss could be less effective in minority racial and ethnic groups when diabetes in individuals with a healthy weight is prevalent.</p></sec><sec id="S11"><title>Differences in the contributions of insulin secretion by racial and ethnic group</title><p id="P23">Traditionally, diabetes pathogenesis has been described as obesity-driven insulin resistance followed by a subsequent decline in insulin secretion, eventually leading to overt type 2 diabetes.<sup><xref rid="R62" ref-type="bibr">62</xref></sup> However, evidence suggests that some racial and ethnic groups might also exhibit early declines in insulin secretion, which can contribute to excess diabetes risk in the absence of obesity. A study comparing the prevalence and associated risk factors of diabetes in four racial and ethnic groups in the USA found that south Asian Americans, Black Americans, Hispanic Americans, and Chinese Americans all had a diabetes prevalence that was at least two-times, if not three-times, higher than that of White Americans.<sup><xref rid="R37" ref-type="bibr">37</xref></sup> Furthermore, these same groups all had worse insulin secretion than the White Americans. Additionally, a 2004 study by Torr&#x000e9;ns and colleagues<sup><xref rid="R63" ref-type="bibr">63</xref></sup> assessed differences in insulin sensitivity and &#x003b2;-cell function between non-diabetic premenopausal or early perimenopausal non-Hispanic White women and African American, Chinese American, Japanese American, and non-Mexican-American Latino women. Torr&#x000e9;ns and colleagues found that Japanese American and Chinese American women had worse insulin secretion than non-Hispanic White women, whereas African American women had higher insulin secretion than non-Hispanic White women, and insulin secretion was similar between non-Mexican-American Latino women and non-Hispanic White women, after correcting for confounders.<sup><xref rid="R63" ref-type="bibr">63</xref></sup></p></sec><sec id="S12"><title>The role of ectopic fat in diabetes development</title><p id="P24">Although obesity is a well known risk factor in diabetes pathogenesis, the pattern and placement of fat deposition is also important as several organs including the muscle, liver, and pancreas are all highly involved in glucose metabolism.<sup><xref rid="R62" ref-type="bibr">62</xref></sup> Notably, hepatic fat content, independent of BMI has been associated with metabolic disturbances even in individuals with a healthy weight and normoglycaemia.<sup><xref rid="R64" ref-type="bibr">64</xref>,<xref rid="R65" ref-type="bibr">65</xref></sup> Furthermore, pancreatic fat content has been associated with poor insulin secretion in individuals without diabetes.<sup><xref rid="R66" ref-type="bibr">66</xref>,<xref rid="R67" ref-type="bibr">67</xref></sup> Therefore, increased fat deposition in the liver and pancreas could lead to early metabolic disturbances and subsequent diabetes risk. Studies have pointed to large differences in ectopic fat deposition by racial and ethnic group.<sup><xref rid="R68" ref-type="bibr">68</xref>,<xref rid="R69" ref-type="bibr">69</xref></sup> There has not been an exploration of how these differences change across the lifespan and if there are any differences within racial and ethnic groups.</p><p id="P25">The aforementioned studies related to ectopic fat suggest that increased susceptibility to diabetes in some racial and ethnic groups such as Asian American individuals could be associated with ectopic fat deposition contributing to increased insulin resistance and worse insulin secretion. However, in other groups such as Black Americans, the increased risk of diabetes persists despite normal rates of ectopic, particularly hepatic, fat deposition. The combined contributions of hepatic and pancreatic fat to insulin resistance and insulin secretion in various ethnic groups has not been well studied, and could provide target mechanisms for treatment and prevention across populations.</p></sec><sec id="S13"><title>Diabetes subgroups and race and ethnic risk factor burden</title><p id="P26">Type 2 diabetes risk is multifaceted and there is a need to better classify the heterogeneity in diabetes development as there might be differences in underlying disease aetiology and progression, particularly among different race and ethnic populations. Studies categorising diabetes subgroups have found variations in the distribution of cohort membership by racial and ethnic group. For example, a study seeking to characterise potential diabetes subgroups among race and ethnic populations in the USA identified five distinct subgroups&#x02014;ie, older age at diabetes onset (mean age 66&#x000b7;8 years [SD 8&#x000b7;3]), severe hyperglycaemia (mean HbA<sub>1c</sub> 8&#x000b7;3% [1&#x000b7;8]), severe obesity (mean BMI 35&#x000b7;4 kg/m&#x000b2; [6&#x000b7;2]), younger age (mean age 23&#x000b7;8 years [7&#x000b7;7]) at diabetes onset, and insulin use.<sup><xref rid="R70" ref-type="bibr">70</xref></sup> In 2022, a systematic review of 18 studies characterising novel diabetes clusters based on clinical variables found that in Asian populations, the cluster of severe insulin deficiency was more common than severe insulin resistance whereas the cluster of severe insulin resistance was more common in populations with European ancestry.<sup><xref rid="R71" ref-type="bibr">71</xref></sup> Given the differences in diabetes pathophysiology among ethnic groups, there is a need for more targeted diagnosis, prevention, and treatment, as methods traditionally applied to one population might not be applicable to all.</p></sec></sec><sec id="S14"><title>The role of polygenic scores</title><p id="P27">During the past decade, there have been substantial advances in our understanding of the genetic basis for type 2 diabetes.<sup><xref rid="R72" ref-type="bibr">72</xref></sup> Identified individual genetic variants can only provide a modest effect on risk, but when combined into a polygenic risk score, they provide information on disease predisposition and could be useful for guiding clinical management. These polygenic risk scores are determined using ever-growing genome-wide association studies. Polygenic risk scores have been used to identify subtypes of diabetes, predict risk for type 2 diabetes, and predict effectiveness of interventions. In a diabetes prevention programme post-hoc analysis, polygenic risk scores identified subgroups at high risk for whom successful lifestyle modification was associated with an improved absolute reduction in the risk of incident diabetes.<sup><xref rid="R73" ref-type="bibr">73</xref></sup> As polygenic risk scores become more widely available, it is important to remember that genetics represent only one contributor to individual disease risk and profile.73 Additionally, there is a need to ensure that the benefits of these risk scores are equitably available to all. Equitable access to polygenic risk scores is especially important as much of the genome-wide association studies and sequence data are derived from individuals of European descent. As such, there is an urgency to build a repository for other ethnic groups as well.</p></sec></sec><sec id="S15"><title>Contributors to diabetes disparities in the USA</title><p id="P28">The factors within domains and across levels of influence that could contribute to diabetes disparities are summarised in the table.</p><sec id="S16"><title>Contributors to diabetes disparities between racial and ethnic groups</title><p id="P29">The complex interplay of factors across all five domains and all levels of influence contribute to disparities between racial and ethnic groups. Structural racism play a prominent role at all levels. Past policies, laws, and economies contribute to where people live, their access to sufficient and healthy food, and their access to health-care services.<sup><xref rid="R106" ref-type="bibr">106</xref>,<xref rid="R110" ref-type="bibr">110</xref>,<xref rid="R111" ref-type="bibr">111</xref>,<xref rid="R113" ref-type="bibr">113</xref>,<xref rid="R115" ref-type="bibr">115</xref></sup> For example, redlining and predatory lending affected where and what type of housing was available to Black individuals, forcing them to live in less healthy and worse resourced neighbourhoods compared with other racial and ethnic groups. Furthermore, these same areas received fewer government and private sector investments, leading to fewer facilities, such as health facilities and food access points.<sup><xref rid="R161" ref-type="bibr">161</xref>,<xref rid="R162" ref-type="bibr">162</xref></sup> These factors, stemming largely from structural racism and discrimination, play an important role in driving racial and ethnic inequities in diabetes and diabetes-related complications.<sup><xref rid="R163" ref-type="bibr">163</xref></sup> At the community level, neighbourhoods with primarily Black and Hispanic individuals tend to have little space for physical activity, more food deserts (ie, neighbourhoods of 5000&#x02013;15 000 people served by two or fewer big supermarkets), and restricted access to health care compared with other neighbourhoods. These factors have been linked to physical inactivity, poor diet quality, and reduced use of health-care services, which in turn have been found to contribute to the development of diabetes and poor diabetes management.<sup><xref rid="R112" ref-type="bibr">112</xref></sup> Additionally, neighbourhoods with Black and Hispanic individuals have higher levels of toxic environmental exposures than other neighbourhoods, and a growing body of evidence indicates that these exposures are associated with the development of diabetes.<sup><xref rid="R112" ref-type="bibr">112</xref></sup> The interpersonal level reflects relationships between individuals in a family, within a social network, or with health-care professionals. The many forms of interpersonal racism and discrimination can play an important role in health disparities including in those with diabetes. For example, perceived racism has been associated with increased incidence of diabetes in Black women.<sup><xref rid="R152" ref-type="bibr">152</xref></sup> This association is hypothesised to be through biological mechanisms including increase in chronic stress. These interpersonal relationships in turn affect the gut microbiome, lifestyle behaviours, mental health, and access to care.<sup><xref rid="R156" ref-type="bibr">156</xref></sup> The determinants are all inter-related and overlapping. The factors within the structural racism domain overlap with the economic development domain and the access to high-quality care domain as outlined.</p><p id="P30">Native Americans have the highest age-adjusted prevalence of diabetes compared with all other racial and ethnic groups in the USA. Native Americans have 2&#x000b7;0 times higher diabetes prevalence and 1&#x000b7;9 times higher diabetes-related mortality than White Americans.<sup><xref rid="R164" ref-type="bibr">164</xref></sup> The disproportionate prevalence and disease burden of diabetes has been associated with factors in the economic development domain with social disadvantages faced by American Indian and other Native American communities, including high rates of neighbourhood poverty, inadequate access to health services, and long-standing economic adversity. These factors in turn are related to the health behaviours and social norms domain, where they facilitate unhealthy day-to-day living practices that ultimately contribute to disease, and subsequently hinder optimal management of chronic illnesses. The structural racism domain is also relevant in this case as discrimination has been associated with increased prevalence of diabetes among American Indians and other Native Americans. Some findings have shown that microaggressions experienced by American Indians and other Native Americans with diabetes in health-care settings were associated with greater reports of worse physical and mental health, including increased hospitalisations and depressive symptoms within the previous year.<sup><xref rid="R156" ref-type="bibr">156</xref></sup></p><p id="P31">Although pathophysiology of diabetes is important to consider, and there might be a role of genome-wide association studies, it is important to recognise that biological factors are not a cause of disparities. There is a growing body of evidence on biological and epigenetic differences that contribute to the risk of developing diabetes.<sup><xref rid="R165" ref-type="bibr">165</xref></sup> However, race is a socially constructed variable, not a biologically constructed one.<sup><xref rid="R166" ref-type="bibr">166</xref></sup> Existing literature suggests that acknowledging the admixture of multiple ethnic groups is crucial in efforts to further define any genetic predisposition to diabetes.<sup><xref rid="R167" ref-type="bibr">167</xref></sup> Admixture is also an important consideration when looking at the performance of diagnostic tests such as HbA<sub>1c</sub> in different racial and ethnic groups.<sup><xref rid="R168" ref-type="bibr">168</xref>,<xref rid="R169" ref-type="bibr">169</xref></sup></p></sec><sec id="S17"><title>Contributors to diabetes disparities within racial and ethnic groups</title><p id="P32">Using the modified framework proposed by Agarwal and colleagues,<sup><xref rid="R14" ref-type="bibr">14</xref></sup> we can see that factors at the individual, interpersonal, community, and societal levels together contribute to differences within racial and ethnic groups (<xref rid="T1" ref-type="table">table</xref>). The health behaviours and social norms domain plays an important role as a contributor to diabetes disparities. Diversity within racial and ethnic groups in cultural practices, knowledge, and beliefs can contribute to differences in dietary and lifestyle habits that in turn can drive within racial and ethnic group differences.<sup><xref rid="R170" ref-type="bibr">170</xref></sup> Cultural practices, knowledge, and beliefs can also contribute to different relationships with the health-care profession, which might lead to different levels of trust and adherence to medical advice.<sup><xref rid="R132" ref-type="bibr">132</xref>&#x02013;<xref rid="R135" ref-type="bibr">135</xref></sup> Economic development is also important. Previous studies have consistently found that people with lower socioeconomic status are more likely to develop diabetes and experience more diabetes-related complications compared with those with higher socioeconomic status.<sup><xref rid="R98" ref-type="bibr">98</xref></sup> There is also a rural and urban divide that can help explain disparities within groups given rural counties have the highest diabetes-related mortality.<sup><xref rid="R171" ref-type="bibr">171</xref></sup> Examining trends in diabetes-related mortality in urban and rural areas in the USA between 1999 and 2018, Kobo and colleagues found that diabetes-related age-adjusted mortality rates of both Black and White adults decreased in urban but not rural areas.<sup><xref rid="R172" ref-type="bibr">172</xref></sup> The socioeconomic and built environment can also contribute to disparities within racial and ethnic groups. In 2014, Gaskin and colleagues described the &#x0201c;nexus of race, poverty, and place&#x0201d; and showed that both individual poverty and living in a poor neighbourhood increased the odds of having diabetes for Black and White adults.<sup><xref rid="R173" ref-type="bibr">173</xref></sup> In 2019, a systematic review and meta-analysis of longitudinal studies found strong evidence for relationships between neighbourhood walkability and diabetes outcomes.<sup><xref rid="R174" ref-type="bibr">174</xref></sup> Results from an analysis of nationally representative county-level data showed that counties with higher rates of unemployment and poverty had higher incidence rates of diabetes compared with counties with lower levels of unemployment and poverty, whereas counties with greater access to healthy food and more opportunities for exercise had fewer cases of diabetes.<sup><xref rid="R4" ref-type="bibr">4</xref></sup></p><p id="P33">The association between social determinants of health and diabetes differs by ethnicity within the Black population. For example, the association of health insurance, income, and education with diabetes was different among African Americans, African immigrants, and African Caribbeans.<sup><xref rid="R34" ref-type="bibr">34</xref></sup> The differences described within the Hispanic population are most likely multifactorial but are still not fully understood.<sup><xref rid="R30" ref-type="bibr">30</xref></sup> Finally, within the Asian American population, we described how south Asians have the highest prevalence of diabetes. The causes of this are multifactorial and are likely due to not only patterns of immigration and sociodemographic characteristics, but also might be related to distinct cardiometabolic phenotypes that increase the risk of diabetes among south Asians.<sup><xref rid="R175" ref-type="bibr">175</xref></sup></p></sec><sec id="S18"><title>Contributors to diabetes disparities among children and adolescents</title><p id="P34">Risk factors for type 2 diabetes in children and adolescents (aged &#x0003c;18 years) are similar to those of adults. Studies have found that intergenerational factors, malnutrition, little physical exercise, obesity, family history, and low or very high birthweight elevate diabetes risk in children.<sup><xref rid="R176" ref-type="bibr">176</xref></sup> Poor sleep has also been linked to diabetes risk among both adults and children, with one multiethnic study in the UK finding that children aged 9&#x02013;10 years had reduced risk of type 2 diabetes for every additional hour of sleep duration.<sup><xref rid="R177" ref-type="bibr">177</xref></sup></p><p id="P35">Obesity and insulin resistance in children portends an increased risk of developing diabetes. There is now good evidence to show that stress, obesity, and hyperglycaemia in lactating mothers is associated with increased rates of obesity and insulin resistance in their offspring.<sup><xref rid="R178" ref-type="bibr">178</xref></sup> Additionally, overnutrition as a consequence of an infant being born small for gestational age, as well as early weaning from breastmilk are associated with obesity and insulin resistance.<sup><xref rid="R178" ref-type="bibr">178</xref></sup> Lastly, on the other end of the spectrum, a combination of early-life undernutrition and later development of obesity is associated with increased risk of type 2 diabetes in adulthood.<sup><xref rid="R179" ref-type="bibr">179</xref></sup></p><p id="P36">Economic development also has a role for racial and ethnic disparities in young people. For example, lower socioeconomic status and living in poor areas are associated with higher diabetes risk, a 34% increased likelihood of developing obesity, and a 60% increased likelihood of developing diabetes, when compared with living in high income areas.<sup><xref rid="R180" ref-type="bibr">180</xref>,<xref rid="R181" ref-type="bibr">181</xref></sup> Additionally, compared with White women, Asian and Hispanic women have a higher prevalence of gestational diabetes, which has been associated with increased risk in offspring of developing type 2 diabetes later in life.<sup><xref rid="R182" ref-type="bibr">182</xref>,<xref rid="R183" ref-type="bibr">183</xref></sup></p><p id="P37">Diabetes disparities are now evident across the lifespan with the emerging concept of intergenerational risk of developing diabetes.<sup><xref rid="R184" ref-type="bibr">184</xref></sup> Young people who identify as Native American, American Indian, or Alaska Native; Black; and Hispanic have an increased burden of diabetes and obesity. This burden is in part due to social determinants of health within the structural racism domain that are &#x0201c;systemic, population-based, cyclical, and intergenerational.&#x0201d;<sup><xref rid="R185" ref-type="bibr">185</xref></sup> These same social determinants of health are rooted in racism that is internalised, or at the interpersonal, institutional, and societal levels. These factors are experienced by the family (including children) and not only the adult. Additionally, intergenerational poverty makes it harder for children to find a way out of the cycle of intergenerational risk. Although socioeconomic status is complex and multidimensional, all indicators are strongly patterned by racial and ethnic group: &#x0201c;for every dollar of wealth that Whites have, Asian households have 83 cents, Black households have 6 cents, and Hispanic households have 7 cents&#x0201d;.<sup><xref rid="R186" ref-type="bibr">186</xref></sup></p></sec></sec><sec id="S19"><title>Recommendations and future directions</title><p id="P38">We have provided an overview of the literature from the past decade on disparities in diabetes between and within racial and ethnic groups in the USA across the lifespan. This overview provides a US-focused framing that adds to the other two papers in this Series<sup><xref rid="R14" ref-type="bibr">14</xref>,<xref rid="R187" ref-type="bibr">187</xref></sup> and The Lancet <italic toggle="yes">Commission on Diabetes</italic>.<sup><xref rid="R188" ref-type="bibr">188</xref></sup> This Series paper highlights the importance of considering the complexity of disparities in diabetes and diabetes-related complications beyond racial and ethnic groups to consider within-group differences, how disparities differ in children and adolescents, and the complex pathophysiology. Using a comprehensive framework, this Series paper also emphasises that these disparities arise from many multilevel factors. With these key points in mind, we propose a path forward for providers, researchers, funders, and policy makers to address diabetes disparities (<xref rid="F2" ref-type="fig">figure 2</xref>, panel).</p><sec id="S20"><title>Generate a community-engaged and multidisciplinary research agenda that adopts a life course approach and addresses pathophysiological and multilevel causes of diabetes disparities</title><p id="P39">This Series paper has thus far highlighted the complexity and multifaceted nature of diabetes disparities. Solutions must, therefore, meet this complexity by ensuring a multidisciplinary approach that carefully engages affected communities in an equitable manner. Increased attention to more detailed diabetes phenotypic structures (see previous sections) is important to guide tailored prevention and management strategies. Understanding diabetes phenotypes and the resulting tailored management strategies can provide the health-care community with the needed information to move towards effective and equitable precision medicine in diabetes care. As we give the pathophysiology of diabetes more attention, researchers should be sure not to confuse social constructs such as race with biological factors such as genetics.<sup><xref rid="R189" ref-type="bibr">189</xref></sup> As we promote ideas around precision medicine for diabetes care, it is crucial to curb any misconceptions of this idea and ensure emergent technologies and advancements overcome current inequities in access. Community-engaged and community-based participatory research is essential for designing acceptable and feasible strategies of promoting uptake of diabetes treatment interventions among disadvantaged groups. These strategies will need to be tailored to groups across the lifespan (strategies related to young people [aged &#x0003c;18 years] will differ from those targeting older people [aged &#x0003e;65 years]). These strategies will also need to be tailored across and within racial and ethnic groups given much of the social and behavioural norms that differ between these groups. To do this well, research needs to continue to disaggregate the large groupings of Black, Asian, and Hispanic individuals.</p><p id="P40">As we see the growth of the fields of environmental justice, climate, and health, we must pay attention to their effects on diabetes prevalence, management, and thereby disparities. We need more community-engaged research to document the attribution of environmental factors on diabetes risk and management. Moreover, we need community-engaged research to co-design strategies with communities to mitigate the effects of environmental hazardous exposures and climate change on health. Researchers need to apply a health equity lens to ensure that novel therapeutics and diagnostics are implemented without worsening disparities.</p><p id="P41">The field of implementation science increasingly offers approaches to integrating health equity into intervention design and implementation and should be embraced along with equitable partner and community engagement as the field moves to develop, implement, and scale evidence-based interventions to reduce diabetes disparities.<sup><xref rid="R190" ref-type="bibr">190</xref>,<xref rid="R191" ref-type="bibr">191</xref></sup></p></sec><sec id="S21"><title>Principles of equitable, sustainable, and cost-effective research that addresses the multilevel and multidisciplinary behavioural, social, and structural determinants of diabetes disparities must be embraced by the funding community</title><p id="P42">Funders of community or clinic-based diabetes research should require a health equity plan for all phases of diabetes research&#x02014;ie, a statement on how the research will promote health equity or at the very least not increase disparities. To achieve this goal, principles of implementation science should be considered even at the effectiveness and clinical trial stages of research to ensure an understanding of how to promote equity as the research progresses. Practically speaking this means evaluating key implementation outcomes such as reach, acceptability, appropriateness, feasibility, and adoption early on. Studying implementation outcomes enables investigators to start to identify early on potential barriers for equitable implementation in the real world. Defining implementation outcomes also provides an opportunity to tailor implementation strategies to age groups and differences within racial and ethnic groups.</p><p id="P43">Upon review of the multilevel causes of diabetes disparities across the lifespan, it becomes apparent that multilevel and multidisciplinary approaches are crucial to solving the problem of diabetes disparities. Funders should recognise this importance and provide opportunities for multidisciplinary teams to address this need in collaboration with communities. To promote community-based participatory research that addresses these multilevel factors, funders should invest in strengthening capacity among early stage investigators in the intersection of diabetes and health equity with a focus on trainees from under-represented groups. Moreover, given the value of implementation science in improving equity in health service delivery, training, and funding for early-stage investigators to conduct health-equity focused implementation science research could accelerate the implementation and dissemination of evidence-based interventions in routine practice.<sup><xref rid="R189" ref-type="bibr">189</xref></sup> Furthermore, there is a need to provide training opportunities for more experienced scientists to embrace and incorporate principles of community engagement and health equity into existing research programmes.</p></sec><sec id="S22"><title>Practitioners on the front lines of diabetes prevention and management need to know and understand the multilevel factors contributing to diabetes disparities including those at the provider, community, and health-system levels</title><p id="P44">Front-line providers play an important role in addressing disparities through their one-on-one interaction with patients, through institutional change, and through community engagement. At an individual level, the role of health-care providers&#x02019; implicit bias has long been studied and the effect of training on reducing disparities examined.<sup><xref rid="R192" ref-type="bibr">192</xref></sup> Continued attention to implicit bias with focus on understanding gaps in translational effectiveness is important.<sup><xref rid="R193" ref-type="bibr">193</xref></sup> At an institutional level, front-line practitioners have a role in addressing structural barriers to access to care for their patients. It is crucial to develop evidence-based approaches to address structural barriers to health-care access such as inadequacies of language services, variable dependence on technology, transportation challenges, and financial constraints. Lastly, engaging with community members to actively understand the challenges faced by patients and develop equitable solutions is essential.<sup><xref rid="R194" ref-type="bibr">194</xref>&#x02013;<xref rid="R196" ref-type="bibr">196</xref></sup> We need participatory action research engaging community partners in prioritising and developing approaches for overcoming these health system barriers. This participatory action research provides an opportunity for health providers to understand differences across the lifespan as well as tailoring approaches to within group differences.</p><p id="P45">In their approach to counselling and management of patients, health providers must learn to recognise differences in phenotypic presentation of diabetes to tailor therapy. Recognising the structural and environmental factors that contribute to diabetes and poor management of diabetes in some communities is imperative as we design therapies, set policy, and provide advice. Training providers on the role of social and environmental determinants of health is crucial to ensuring future practitioners overcome their own and their institution&#x02019;s contribution to health disparities.</p></sec><sec id="S23"><title>Policy makers must recognise their role in health disparities both based on historical policy decisions as well as current ones to make necessary policy changes to reduce disparities</title><p id="P46">In this Series paper, we summarised the various ways in which policy decisions now (eg, scarcity of policies to drive investment in disadvantaged neighbourhoods) and in the past (eg, redlining), differentially affect the health of minority race and ethnic communities and, therefore, drive health disparities. Addressing social determinants of health holds great potential for progress towards reducing diabetes disparities.<sup><xref rid="R98" ref-type="bibr">98</xref>,<xref rid="R197" ref-type="bibr">197</xref></sup> As health-care quality improvement efforts to address diabetes care advance, there is a need for rigorous studies to design and test delivery models that integrate social care into medical care; for example, through screening of individuals&#x02019; social risks and assets and strategies to address or mitigate the adverse effects of social adversity on diabetes management.<sup><xref rid="R198" ref-type="bibr">198</xref></sup> In addition to addressing social determinants of diabetes within the health-care system, there are opportunities to fill gaps in evidence on the effectiveness of large-scale policies and programmes such as food and agricultural policies and programmes in promoting healthy eating and physical activity and thereby contributing to the prevention of diabetes and diabetes-related complications, including their effect on diabetes disparities.<sup><xref rid="R199" ref-type="bibr">199</xref></sup></p><p id="P47">Recognising the role of institutional racism on existing policies is crucial to revising and developing evidence-based solutions to policy change that can overcome these barriers to care. Further research is needed to inform policies that can address some of the structural and social determinants of health that are the root causes of health disparities, both between and within racial and ethnic groups.<sup><xref rid="R200" ref-type="bibr">200</xref></sup> To achieve this goal, policy and programme monitoring should integrate health equity indicators so that the differential effect of policies can be documented and thus the impact of policy change reported on health disparities. This type of attention would help promote accountability and generate data needed to inform change.</p></sec></sec><sec id="S24"><title>Conclusions</title><p id="P48">Disparities in the prevalence and management of diabetes in the USA persist today due to multilevel and multidisciplinary factors from the individual level to the systems level. Disparities should be examined beyond differences between racial and ethnic groups to include differences within race and ethnic groups and across the lifespan. Our Review systematically outlines those differences and their drivers and offers actionable recommendations at the researcher, practitioner and health-system, and policy levels to promote health equity in diabetes moving forward.</p></sec><sec sec-type="supplementary-material" id="SM1"><title>Supplementary Material</title><supplementary-material id="SD1" position="float" content-type="local-data"><label>Supplementary Material</label><media xlink:href="NIHMS1977150-supplement-Supplementary_Material.pdf" id="d66e868" position="anchor"/></supplementary-material></sec></body><back><ack id="S25"><title>Acknowledgments</title><p id="P49">We would like to thank Sara Hendrix and Samaia Hill for their assistance with the literature search. We would like to acknowledge the following funders: SH was supported by a grant from National Institutes of Health (NIH) and National Heart, Lung, and Blood Institute (K23HL152368). RCQ was supported by grants from NIH (1U01DK132737, P30DK111024-06W2, and P30DK111024). KMVN was also supported by a grant from NIH (P30DK111024). MKS is supported in part by the National Institute on Minority Health and Health Disparities (K23 MD015088-04), the Emory School of Medicine Doris Duke Charitable Foundation COVID-19 Fund to Retain Clinical Scientists, and the Georgia Clinical &#x00026; Translational Science Alliance (UL1-TR002378).</p></ack><fn-group><fn id="FN2"><p id="P50">This is the third in a <bold>Series</bold> of three papers about Global Inequity in Diabetes (papers 1 and 2 appear in <italic toggle="yes">The Lancet</italic>). 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</mixed-citation></ref></ref-list></back><floats-group><fig position="float" id="F1"><label>Figure 1:</label><caption><title>Conceptual framework for diabetes disparities in the USA (adapted from Agarwal et al<sup><xref rid="R14" ref-type="bibr">14</xref></sup>)</title></caption><graphic xlink:href="nihms-1977150-f0001" position="float"/></fig><fig position="float" id="F2"><label>Figure 2:</label><caption><title>Type 1 and type 2 diabetes incidence per 100 000 person-years (2014&#x02013;15) and prevalence per 100 000 individuals (2017): results from the SEARCH for Diabetes in Youth Study<xref rid="R12" ref-type="bibr">12</xref>,<xref rid="R16" ref-type="bibr">16</xref></title></caption><graphic xlink:href="nihms-1977150-f0002" position="float"/></fig><table-wrap position="float" id="T1" orientation="landscape"><label>Table:</label><caption><title>Contributors (ie, levels of influence and domains of influence over the life course) to diabetes using Agarwal and colleagues&#x02019; framework<xref rid="R14" ref-type="bibr">14</xref></title></caption><table frame="void" rules="groups"><colgroup span="1"><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/><col align="left" valign="middle" span="1"/></colgroup><thead><tr><th align="left" valign="middle" rowspan="1" colspan="1"/><th align="left" valign="middle" rowspan="1" colspan="1">Individual</th><th align="left" valign="middle" rowspan="1" colspan="1">Interpersonal</th><th align="left" valign="middle" rowspan="1" colspan="1">Community</th><th align="left" valign="middle" rowspan="1" colspan="1">Societal</th></tr></thead><tbody><tr><td align="left" valign="top" rowspan="1" colspan="1">Health behaviours and social norms</td><td align="left" valign="top" rowspan="1" colspan="1">Health behaviours and coping strategies: smoking and sedentary lifestyle; sociodemographic; cultural identity; response to discrimination; cultural beliefs;<xref rid="TFN1" ref-type="table-fn">*</xref> stigma;<xref rid="TFN1" ref-type="table-fn">*</xref> acculturation; body image perceptions;<xref rid="TFN1" ref-type="table-fn">*</xref> poor English proficiency;<xref rid="TFN1" ref-type="table-fn">*</xref> and comorbid health conditions:<sup><xref rid="R74" ref-type="bibr">74</xref></sup> depression,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R75" ref-type="bibr">75</xref></sup> hypertension,<xref rid="TFN1" ref-type="table-fn">*</xref> heart disease,<xref rid="TFN1" ref-type="table-fn">*</xref> and autoimmune conditions<xref rid="TFN1" ref-type="table-fn">*</xref></td><td align="left" valign="top" rowspan="1" colspan="1">Family functioning: parental modelling;<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref> and caregiver&#x02013;child interaction: gestational diabetes,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R76" ref-type="bibr">76</xref>&#x02013;<xref rid="R78" ref-type="bibr">78</xref></sup> intrauterine exposure to diabetes,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R21" ref-type="bibr">21</xref>,<xref rid="R79" ref-type="bibr">79</xref></sup> and preterm birth<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R80" ref-type="bibr">80</xref>,<xref rid="R81" ref-type="bibr">81</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Community functioning: food eating practices of a community (eg, type of food and communal eating),<sup><xref rid="R82" ref-type="bibr">82</xref>,<xref rid="R83" ref-type="bibr">83</xref></sup> acculturation,<sup><xref rid="R84" ref-type="bibr">84</xref></sup> fear of Western medical practices, scarcity of preventive health seeking behaviour,<sup><xref rid="R85" ref-type="bibr">85</xref></sup> social dietary temptations and overcoming temptations,<sup><xref rid="R84" ref-type="bibr">84</xref></sup> apathy (ie, the inevitability of diabetes in the community),<sup><xref rid="R86" ref-type="bibr">86</xref>,<xref rid="R87" ref-type="bibr">87</xref></sup> and weight perception<sup><xref rid="R88" ref-type="bibr">88</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Policies and laws: reducing stress exposure via policy,<sup><xref rid="R89" ref-type="bibr">89</xref></sup> association between food prices and insulin resistance,<sup><xref rid="R90" ref-type="bibr">90</xref></sup> mandating diabetes education through policy,<sup><xref rid="R91" ref-type="bibr">91</xref></sup> social norms, societal structural discrimination, smoking as a norm in American Indian and other Native American communities,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R92" ref-type="bibr">92</xref></sup> machismo (ie, masculine ideologies) as driver of health neglect in Mexican men,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R93" ref-type="bibr">93</xref></sup> cultural traditions as a challenge to immigrants managing chronic illness,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R94" ref-type="bibr">94</xref></sup> effect of colonisation on diabetes risk factors in Indigenous communities,<sup><xref rid="R95" ref-type="bibr">95</xref></sup> and education discrimination<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R96" ref-type="bibr">96</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Economic development</td><td align="left" valign="top" rowspan="1" colspan="1">Personal environment:<sup><xref rid="R97" ref-type="bibr">97</xref></sup> income, employment status and job stability, and education level</td><td align="left" valign="top" rowspan="1" colspan="1">Household environment: household food insecurity,<sup><xref rid="R98" ref-type="bibr">98</xref></sup> homelessness,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R99" ref-type="bibr">99</xref></sup> housing instability,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R100" ref-type="bibr">100</xref></sup> and energy insecurity;<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R101" ref-type="bibr">101</xref></sup> school or work environment; and stress at work<sup><xref rid="R102" ref-type="bibr">102</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Community environment,<sup><xref rid="R98" ref-type="bibr">98</xref></sup> neighbourhood walkability,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R103" ref-type="bibr">103</xref></sup> exposure to greenspace,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R104" ref-type="bibr">104</xref></sup> community resources, poor access to affordable diabetes-friendly food compared with relatively easy access to unhealthy food,<sup><xref rid="R105" ref-type="bibr">105</xref>&#x02013;<xref rid="R107" ref-type="bibr">107</xref></sup> and area deprivation index (housing, income, employment, education)<sup><xref rid="R108" ref-type="bibr">108</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Societal structure: neighbourhood discrimination,<sup><xref rid="R106" ref-type="bibr">106</xref>,<xref rid="R109" ref-type="bibr">109</xref></sup> neighbourhood disadvantage contributes to disproportionate diabetes burden,<sup><xref rid="R110" ref-type="bibr">110</xref>&#x02013;<xref rid="R112" ref-type="bibr">112</xref></sup> and food insecurity<sup><xref rid="R113" ref-type="bibr">113</xref>&#x02013;<xref rid="R115" ref-type="bibr">115</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Public awareness</td><td align="left" valign="top" rowspan="1" colspan="1">Diabetes knowledge and distress,<sup><xref rid="R116" ref-type="bibr">116</xref></sup> diabetes-related knowledge,<xref rid="TFN1" ref-type="table-fn">*</xref> and diabetes self-management knowledge<xref rid="TFN1" ref-type="table-fn">*</xref></td><td align="left" valign="top" rowspan="1" colspan="1">Social networks, parental and familial modelling,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R117" ref-type="bibr">117</xref></sup> social support;<sup><xref rid="R118" ref-type="bibr">118</xref></sup> family and peer norms and traditional gender roles:<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R118" ref-type="bibr">118</xref></sup> familial social interactions;<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R118" ref-type="bibr">118</xref></sup> and social norms<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R119" ref-type="bibr">119</xref>,<xref rid="R120" ref-type="bibr">120</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Community norms; local structural discrimination; diabetes-related social stigma;<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R121" ref-type="bibr">121</xref>,<xref rid="R122" ref-type="bibr">122</xref></sup> and young adults: community expectations of self-independence, employment, and care of siblings<sup><xref rid="R123" ref-type="bibr">123</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">..</td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Access to high-quality care</td><td align="left" valign="top" rowspan="1" colspan="1">Insurance coverage, health literacy, and treatment preferences; regional variation;<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R124" ref-type="bibr">124</xref></sup> health literacy and numeracy;<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R125" ref-type="bibr">125</xref>,<xref rid="R126" ref-type="bibr">126</xref></sup> fear of medications and insulin medication adherence;<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R127" ref-type="bibr">127</xref></sup> and cost<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R128" ref-type="bibr">128</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Patient&#x02013;clinician relationship: perceived discrimination,<sup><xref rid="R129" ref-type="bibr">129</xref></sup> communication,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R130" ref-type="bibr">130</xref>&#x02013;<xref rid="R133" ref-type="bibr">133</xref></sup> lack of trust,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R132" ref-type="bibr">132</xref>,<xref rid="R134" ref-type="bibr">134</xref>,<xref rid="R135" ref-type="bibr">135</xref></sup> physicians&#x02019; empathy,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R136" ref-type="bibr">136</xref></sup> medical decision-making, not enough shared decision-making,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R132" ref-type="bibr">132</xref>,<xref rid="R137" ref-type="bibr">137</xref></sup> non-adherence labelling,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R138" ref-type="bibr">138</xref>,<xref rid="R139" ref-type="bibr">139</xref></sup> discriminatory health-care practices,<sup><xref rid="R140" ref-type="bibr">140</xref>,<xref rid="R141" ref-type="bibr">141</xref></sup> and variations in phenotypes not targeted<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R70" ref-type="bibr">70</xref>,<xref rid="R142" ref-type="bibr">142</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Health-care access, subspecialty care (endocrinologist),<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R143" ref-type="bibr">143</xref></sup> safetynet clinics and hospitals,<xref rid="TFN1" ref-type="table-fn">*</xref> mental health services,<xref rid="TFN1" ref-type="table-fn">*</xref> diabetes self-management education,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R144" ref-type="bibr">144</xref></sup> and transition services for young adults from the paediatrician to adult provider<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R123" ref-type="bibr">123</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Health-care affordability and quality, differential access to technology for diabetes management (including telehealth and continous glucose monitoring),<sup><xref rid="R145" ref-type="bibr">145</xref></sup> differential access to new anti-diabetic medication,<sup><xref rid="R146" ref-type="bibr">146</xref></sup> and differential access to subspecialty care<sup><xref rid="R147" ref-type="bibr">147</xref></sup></td></tr><tr><td align="left" valign="top" rowspan="1" colspan="1">Structural racism</td><td align="left" valign="top" rowspan="1" colspan="1">Sociodemographic, cultural identity, response to discrimination, stigma,<xref rid="TFN1" ref-type="table-fn">*</xref> acculturation, poor English proficiency,<xref rid="TFN1" ref-type="table-fn">*</xref> chronic stress,<sup><xref rid="R148" ref-type="bibr">148</xref></sup> poor sleep, and obesity<sup><xref rid="R149" ref-type="bibr">149</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Interpersonal discrimination, major experiences of discrimination,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R150" ref-type="bibr">150</xref>,<xref rid="R151" ref-type="bibr">151</xref></sup> perceived everyday racism,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R152" ref-type="bibr">152</xref></sup> lifetime racism,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R152" ref-type="bibr">152</xref></sup> racial discrimination,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R153" ref-type="bibr">153</xref>&#x02013;<xref rid="R155" ref-type="bibr">155</xref></sup> and microaggressions<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R156" ref-type="bibr">156</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Community environment,<sup><xref rid="R98" ref-type="bibr">98</xref></sup> neighbourhood walkability,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R103" ref-type="bibr">103</xref></sup> exposure to greenspace,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R104" ref-type="bibr">104</xref></sup> community resources, restricted access to affordable diabetes-friendly food compared with relatively easy access to unhealthy food,<sup><xref rid="R105" ref-type="bibr">105</xref>&#x02013;<xref rid="R107" ref-type="bibr">107</xref></sup> area deprivation index (housing, income, employment, education),<sup><xref rid="R108" ref-type="bibr">108</xref></sup> and environmental exposures: air pollution,<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R157" ref-type="bibr">157</xref></sup> heat exposure,<xref rid="TFN1" ref-type="table-fn">*</xref><sup><xref rid="R158" ref-type="bibr">158</xref></sup> and endocrine-disrupting chemicals<xref rid="TFN2" ref-type="table-fn">&#x02020;</xref><sup><xref rid="R159" ref-type="bibr">159</xref></sup></td><td align="left" valign="top" rowspan="1" colspan="1">Societal structure: neighbourhood discrimination,<sup><xref rid="R106" ref-type="bibr">106</xref>,<xref rid="R109" ref-type="bibr">109</xref></sup> neighbourhood disadvantage contributes to disproportionate diabetes burden,<sup><xref rid="R110" ref-type="bibr">110</xref>&#x02013;<xref rid="R112" ref-type="bibr">112</xref></sup> and food insecurity;<sup><xref rid="R113" ref-type="bibr">113</xref>&#x02013;<xref rid="R115" ref-type="bibr">115</xref></sup> and exposure: climate-induced extreme weather events (heat, cold, natural disasters);<sup><xref rid="R160" ref-type="bibr">160</xref></sup> and sanitation</td></tr></tbody></table><table-wrap-foot><fn id="TFN1"><label>*</label><p id="P53">Disparities in diabetes management and control only.</p></fn><fn id="TFN2"><label>&#x02020;</label><p id="P54">Disparities in diabetes incidence only.</p></fn></table-wrap-foot></table-wrap><boxed-text id="BX1" position="float"><caption><title><italic toggle="yes">Panel:</italic> Recommendations for addressing disparities in diabetes</title></caption><p id="P55">Generate a community-engaged and multidisciplinary research agenda that adopts a life course approach and addresses pathophysiological and multilevel causes of diabetes disparities</p><list list-type="bullet" id="L1"><list-item><p id="P56">Community-based participatory research to guide precision medicine approaches</p></list-item><list-item><p id="P57">Incorporation of environmental and climate justice principles</p></list-item><list-item><p id="P58">Equitable partnerships</p></list-item></list><p id="P59">Principles of equitable, sustainable, and cost-effective research that addresses the multilevel and multidisciplinary behavioural, social, and structural determinants of diabetes disparities must be embraced by the funding community</p><list list-type="bullet" id="L2"><list-item><p id="P60">Funders should require a health equity plan</p></list-item><list-item><p id="P61">Multilevel and multidisciplinary approaches</p></list-item><list-item><p id="P62">Strengthening capacity among diverse early-stage investigators</p></list-item></list><p id="P63">Practitioners on the front lines of diabetes prevention and management need to know and understand the multilevel factors contributing to diabetes disparities including those at the provider, community, and health-system levels</p><list list-type="bullet" id="L3"><list-item><p id="P64">Awareness of implicit bias</p></list-item><list-item><p id="P65">Addressing barriers to accessing quality health care</p></list-item><list-item><p id="P66">Tailoring therapy to diabetes phenotypes</p></list-item></list><p id="P67">Policy makers must recognise their role in health disparities both based on historical policy decisions and current ones to make necessary policy changes to reduce disparities</p><list list-type="bullet" id="L4"><list-item><p id="P68">Models of care that integrate social care into medical care</p></list-item><list-item><p id="P69">Policies to address social determinants of health within the health-care system</p></list-item><list-item><p id="P70">Addressing institutional racism</p></list-item></list></boxed-text><boxed-text id="BX2" position="float"><caption><title>Search strategy and selection criteria</title></caption><p id="P71">We identified references for this Series paper through searches of PubMed for articles published between Jan 1, 2012, and Jan 31, 2022, to reflect the past decade of innovation and discovery in the diabetes disparities literature. Additional articles published before Jan 1, 2012, and after Jan 31, 2022, were included when relevant and important to this Series paper. Our search was designed to identify relevant literature across three main themes: diabetes disparities across the lifespan, diabetes disparities within racial and ethnic groups, and diabetes phenotypes. As this is a narrative review, our objective was to use this search to provide key articles that together could yield a more nuanced understanding of diabetes disparities. A full description of our methods can be found in the <xref rid="SD1" ref-type="supplementary-material">appendix</xref>.</p></boxed-text></floats-group></article>