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Weight gain and metabolic effects in persons with HIV who switch to ART regimens containing integrase inhibitors or tenofovir alafenamide

Supporting Files
File Language:
English


Details

  • Alternative Title:
    J Acquir Immune Defic Syndr
  • Personal Author:
  • Description:
    Background:

    The timing and magnitude of antiretroviral therapy-associated weight change attributions are unclear.

    Setting:

    HIV Outpatient Study participants.

    Methods:

    We analyzed 2007-2018 records of virally suppressed (VS) persons without integrase inhibitor (INSTI) experience who switched to either INSTI- or another non-INSTI-based ART, and remained VS. We analyzed BMI changes using linear mixed models (LMM), INSTI-and tenofovir alafenamide (TAF) contributions to BMI change by LMM-estimated slopes, and BMI inflection points.

    Results:

    Among 736 participants (5,316 person-years), 441 (60%) switched to INSTI-based ART; the remainder to non-INSTI-based ART. Mean follow-up was 7.15 years for INSTI recipients, 7.35 years for non-INSTI. Pre-switch, INSTI and non-INSTI groups had similar median BMI (26.3 versus 25.9 kg/m2, p=0.41). INSTI regimens included raltegravir (178), elvitegravir (112) and dolutegravir (143). Monthly BMI increases post-switch were greater with INSTI than non-INSTI (0.0525 versus 0.006, p<0.001). A BMI inflection point occurred eight months after switch among INSTI users; slopes were similar regardless of TAF use immediately post-switch. Among INSTI+TAF users, during eight months post-switch, 87% of BMI slope change was associated with INSTI use, 13% with TAF use; after eight months, estimated contributions were 27% and 73%, respectively. For non-INSTI+TAF, 84% of BMI gain was TAF-associated consistently post switch. Persons switching from TDF to TAF had greater BMI increases than others (p<0.001).

    Conclusion:

    Among VS persons who switched ART, INSTI and TAF use were independently associated with BMI increases. During eight months post-switch, BMI changes were greatest and most associated with INSTI use; afterward, gradual BMI gain was largely TAF-associated.

  • Subjects:
  • Keywords:
  • Source:
    J Acquir Immune Defic Syndr. 92(1):67-75
  • Pubmed ID:
    36150045
  • Pubmed Central ID:
    PMC11706360
  • Document Type:
  • Funding:
  • Volume:
    92
  • Issue:
    1
  • Collection(s):
  • Main Document Checksum:
    urn:sha-512:69927ec586ce68a3338aed565d68ed8e2b12122267f25778c26deb2c228af8950c8438a3eb5227c0f13ed3b2a0d334acbbfd0ad7180d8b0783ddd3d2aae58b88
  • Download URL:
  • File Type:
    Filetype[PDF - 384.81 KB ]
File Language:
English
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