933 
ART Exposure and Insulin Resistance in the Women’s Interagency HIV Study
Phyllis Tien*1, M Schneider2, S Cole2, A Levine3, M Cohen4, J DeHovitz5, M Young6, and J Justman7
1VAMC and Univ of California, San Francisco, US; 2Johns Hopkins Univ Bloomberg Sch of Publ Hlth, Baltimore, MD, US; 3Univ of Southern California, Los Angeles, US; 4CORE Ctr and Storger Hosp, Chicago, IL, US; 5State Univ of NewYork Downstate Med Ctr, Brooklyn, US; 6Georgetown Univ Med Ctr, Washington, DC, US; and 7Columbia Univ, New York, NY, US
Background: Insulin
resistance (IR) has been of increased concern since the introduction of
effective ART, but the associated factors remain ill-defined. We determine the
relationship of the type and duration of ART exposure with IR in a nationally
representative sample of HIV+ and at-risk HIV– women.
Methods: Prospective
cohort study between October 2000 and March 2007 of 1614 HIV+ and
604 HIV– participants from the Women’s Interagency HIV Study. The homeostasis model assessment (HOMA) defined
as [fasting insulin (µIU/mL) x fasting glucose (FG) (mg/dL)]/405 estimated
IR at 11,019 semiannual visits. The first visit with both FG and insulin data
available was considered the index visit.
Results: HIV+
women had higher median HOMA (2.19 vs 1.83, p <0.001) at index. After
adjustment, HIV+ women had larger median HOMA than HIV– women:
1.20 (95%CI 1.11 to 1.30) times larger for those reporting protease inhibitor
(PI) -containing HAART since the prior visit; 1.10 (95%CI 1.01 to 1.20) times
larger for those reporting non-PI-containing HAART since the prior visit. Those
reporting mono/combination ART and no ART since the prior visit had larger HOMA
than HIV– women, but the association did not reach statistical
significance: 1.05 (95%CI 0.93 to 1.19 and 1.05 (95%CI 0.96 to 1.15),
respectively. Other factors associated with larger HOMA in multivariable
analysis included body mass index (per 5 unit increase: 1.18; 95%CI 1.16 to 1.20),
hepatitis C virus (HCV) seropositivity (1.17; 95%CI 1.09 to 1.24), Hispanic
ethnicity compared to African American (1.13; 95%CI 1.06 to 1.19), menopause (1.11;
95%CI 1.02 to 1.21), family history of diabetes mellitus (1.05; 95%CI 1.00 to 1.11),
and CD4 count (per 100 cell increase) (1.01; 95%CI 1.00 to 1.02). Among HIV+
women, cumulative exposure to nucleoside reverse transcriptase inhibitors
(NRTI) of >0 to 3 years or >3 years was associated with median HOMA 1.06 (95%CI
0.98 to 1.16) and 1.13 (95%CI 1.02 to 1.25) times larger, respectively, than
the HOMA without any cumulative NRTI exposure. Cumulative exposure to stavudine
of >0 to 1 year or >1 year was associated with HOMA 1.07 (95%CI 0.98 to 1.16)
and 1.15 (95%CI 1.05 to 1.27) times larger, respectively, than the HOMA without
any cumulative stavudine use.
Conclusions: Longer
cumulative exposure to NRTI; in particular stavudine was associated with
greater insulin resistance in HIV+ women. The role of insulin
resistance and cardiovascular disease in HIV+ individuals remains a
paramount clinical concern.
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