Greater Cognitive Deficits with Sleep-Disordered Breathing Among Individuals with Genetic Susceptibility to Alzheimer Disease: The Multi-Ethnic Study of Atherosclerosis
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2017/11/01
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Details
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Personal Author:Charles LE ; Djonlagic I ; Fitzpatrick AL ; Johnson DA ; Lane J ; O'Hara R ; Rapp SR ; Redline S ; Reid M ; Saxena R ; Wang R
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Description:Rationale: There are conflicting findings regarding the link between sleep apnea and cognitive dysfunction. Objective: Investigate associations between indicators of sleep-disordered breathing (SDB) and cognitive function in the Multi-Ethnic Study of Atherosclerosis and assess effect modification by the apolipoprotein epsilon-4 (APOE-epsilon4) allele. Methods: A diverse population (N=1,752) underwent Type 2 in-home polysomnography, which included measurement of % sleep time <90% oxyhemoglobin saturation (%Sat<90%) and apnea-hypopnea index (AHI). Epworth Sleepiness Scale score (ESS) and sleep apnea syndrome (SAS; AHI > 5 and ESS> 10) were also analyzed. Cognitive outcomes included the Cognitive Abilities Screening Instrument (CASI); Digit Symbol Coding Test (DSC); and Digit Span Tests (DST) Forward and Backward. Results: Participants were 45.4% male, age 68.1(standard deviation: 9.1) years with a median AHI=9.0 and mean ESS=6.0. Approximately, 9.7% had SAS and 26.8% had at least one copy of the APOepsilon-4 allele. In adjusted analyses, a one standard deviation increase in %Sat<90% and ESS score were associated with a poorer attention and memory assessed by the DST Forward score (β=-0.12 (standard error: 0.06) and β=-0.13 (0.06), respectively; P<0.05). SAS and higher ESS scores were also associated with poorer attention and processing speed as measured by the DSC, β=-0.69 (0.35) and β=-1.42 (0.35), respectively (P<0.05). The presence of APOE-epsilon4 allele modified the associations of %Sat<90% with DST forward and of ESS with DSCT, Pinteraction<0.05. Conclusions: Overnight hypoxemia and sleepiness were associated with cognition. The average effect estimates were small, similar to effects estimated for several other individual dementia risk factors. Associations were strongest in APOE-epsilon4 risk allele carriers. Our results: 1) suggest that SDB be considered among a group of modifiable dementia risk factors; and 2) highlight the potential vulnerability of APOE-epsilon4 risk allele carriers with SDB. [Description provided by NIOSH]
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ISSN:2329-6933
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Volume:14
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Issue:11
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NIOSHTIC Number:nn:20050114
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Citation:Ann Am Thorac Soc 2017 Nov; 14(11):1697-1705
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Contact Point Address:Dayna A Johnson, Harvard Medical School, Sleep Medicine, 221 Longwood Ave. BLI 225, Boston, Massachusetts, 02115 United States
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Email:djohnson@research.bwh.harvard.edu
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Federal Fiscal Year:2018
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Peer Reviewed:True
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Source Full Name:Annals of the American Thoracic Society
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Main Document Checksum:urn:sha-512:ed77b46991b0c409dc6c34df5361ab300fd4ef507a86eee6eb2e76559ddc750e81c962dc39d961e8215832882555fb8066a1ef3143cc98c1a0bac2ddfe91b9ef
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