Metabolic Changes Associated With the Use of Integrase Strand Transfer Inhibitors Among Virally Controlled Women

被引:51
作者
Summers, Nathan A. [1 ,2 ]
Lahiri, Cecile D. [1 ]
Angert, Christine D. [3 ]
Aldredge, Amalia [4 ]
Mehta, C. Christina [3 ]
Ofotokun, Ighovwerha [1 ]
Kerchberger, Anne M. [4 ]
Gustafson, Deborah [5 ]
Weiser, Sheri D. [6 ]
Kassaye, Seble [7 ]
Konkle-Parker, Deborah [8 ]
Sharma, Anjali [9 ]
Adimora, Adaora A. [10 ]
Bolivar, Hector [11 ]
Cocohoba, Jennifer [12 ]
French, Audrey L. [13 ]
Golub, Elizabeth T. [14 ]
Sheth, Anandi N. [1 ]
机构
[1] Emory Univ, Dept Med, Div Infect Dis, Sch Med, 341 Ponce de Leon Ave, Atlanta, GA 30308 USA
[2] Univ Tennessee, Ctr Hlth Sci, Dept Med, Div Infect Dis, Memphis, TN 38163 USA
[3] Emory Univ, Rollins Sch Publ Hlth, Dept Biostat & Bioinformat, Atlanta, GA 30322 USA
[4] Emory Univ, Sch Med, Atlanta, GA USA
[5] State Univ New York Downstate Hlth Sci Univ, Dept Neurol, Brooklyn, NY USA
[6] Univ Calif San Francisco, Sch Med, Dept Med, Div HIV Infect Dis & Global Med, San Francisco, CA 94143 USA
[7] Georgetown Univ, Dept Med, Div Infect Dis, Med Ctr, Washington, DC USA
[8] Univ Mississippi, Dept Med, Div Infect Dis, Med Ctr, Jackson, MS USA
[9] Albert Einstein Coll Med, Dept Med, Bronx, NY 10467 USA
[10] Univ N Carolina, Dept Med, Div Infect Dis, Sch Med, Chapel Hill, NC 27515 USA
[11] Univ Miami Hlth Syst, Dept Med, Div Infect Dis, Miami, FL USA
[12] Univ Calif San Francisco, Dept Clin Pharm, Sch Pharm, San Francisco, CA 94143 USA
[13] CORE Ctr Stroger Cook Cty Hosp, Div Infect Dis, Chicago, IL USA
[14] Johns Hopkins Bloomberg Sch Publ Hlth, Dept Epidmiol, Baltimore, MD USA
关键词
HIV; INSTI; ART; diabetes mellitus; BP; hypertension; BETA-CELL FUNCTION; INSULIN-RESISTANCE; WEIGHT-GAIN; ANTIRETROVIRAL THERAPY; PROTEASE INHIBITOR; BLOOD-PRESSURE; DIABETES-MELLITUS; UNITED-STATES; HIV; DOLUTEGRAVIR;
D O I
10.1097/QAI.0000000000002447
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background: Integrase strand transfer inhibitors (INSTIs) have been associated with weight gain among women living with HIV. We aimed to investigate the association between INSTIs and change in cardiometabolic risk indicators. Setting: Retrospective cohort. Methods: Data from 2006 to 2017 were analyzed from women living with HIV enrolled in the longitudinal Women's Interagency HIV Study who were virally controlled on antiretroviral therapy (ART) for >= 5 consecutive semiannual visits. Women who switched/added an INSTI to ART (INSTI group) were compared with women who remained on non-INSTI ART (non-INSTI group). Outcomes included changes in fasting lipids and glucose, hemoglobin A1c (HbA1c), blood pressure (BP), and incident diabetes, hypertension, and insulin resistance. Outcomes were measured 6-12 months before and 6-18 months after INSTI switch/add in the INSTI group with comparable visits in the non-INSTI group. Longitudinal linear regression models compared change over time in each outcome by the study group. Results: One thousand one hundred eighteen participants (234 INSTI, 884 non-INSTI) were followed for a median 2.0 (Q1 1.9, Q3 2.0) years. Participants were median age 49 years, 61% Black, and 73% overweight or obese (body mass index >= 25 kg/m(2)). Compared with non-INSTI, the INSTI group experienced greater increases in HbA1c (+0.05 vs. -0.06 mg/dL, P = 0.0318), systolic BP (+3.84 vs. +0.84 mm Hg, P = 0.0191), and diastolic BP (+1.62 vs. -0.14 mm Hg, P = 0.0121), with greatest change in HbA1c among women on INSTIs with >= 5% weight gain. Conclusions: INSTI use was associated with unfavorable changes in HbA1c and systolic and diastolic BP during short-term follow-up. Further research is needed to understand long-term cardiometabolic effects of INSTI use.
引用
收藏
页码:355 / 362
页数:8
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