Department of Medicine, Division of Infectious Diseases, Emory University School of Medicine, Atlanta, GA.
Department of Medicine, Division of Infectious Diseases, University of Tennessee Health Science Center, Memphis, TN.
J Acquir Immune Defic Syndr. 2020 Nov 1;85(3):355-362. doi: 10.1097/QAI.0000000000002447.
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.
Retrospective cohort.
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.
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). 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.
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.
整合酶链转移抑制剂(INSTIs)与 HIV 感染者的体重增加有关。我们旨在研究 INSTIs 与心血管代谢风险指标变化之间的关系。
回顾性队列。
对 2006 年至 2017 年期间参加纵向妇女机构 HIV 研究(Women's Interagency HIV Study)的 HIV 感染者的数据进行了分析,这些感染者在接受抗逆转录病毒治疗(ART)时连续 5 个半年访视时病毒得到了控制。将接受 INSTI 转换/添加 ART(INSTI 组)的女性与仍接受非 INSTI ART 的女性(非 INSTI 组)进行比较。结果包括空腹血脂和血糖、糖化血红蛋白(HbA1c)、血压(BP)以及糖尿病、高血压和胰岛素抵抗的发生率。INSTI 组在 INSTI 转换/添加前 6-12 个月和转换/添加后 6-18 个月进行测量,并在非 INSTI 组进行了可比的访视。通过研究组比较了每个结果在时间上的变化。
1118 名参与者(234 名 INSTI,884 名非 INSTI)随访中位数为 2.0 年(Q1 1.9,Q3 2.0)。参与者的中位年龄为 49 岁,61%为黑人,73%超重或肥胖(体重指数≥25kg/m2)。与非 INSTI 相比,INSTI 组的 HbA1c 增加更多(+0.05 对-0.06mg/dL,P=0.0318),收缩压增加更多(+3.84 对+0.84mmHg,P=0.0191),舒张压增加更多(+1.62 对-0.14mmHg,P=0.0121),在 INSTI 体重增加≥5%的女性中,HbA1c 的变化最大。
在短期随访期间,INSTI 的使用与 HbA1c 以及收缩压和舒张压的不利变化有关。需要进一步研究以了解 INSTI 使用的长期心血管代谢影响。