Ursenbach Axel, Sireyjol Antoine, Delpierre Cyrille, Duvivier Claudine, Hocqueloux Laurent, Rey David
Le Trait d'Union, HIV-Infection Care Center, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Statoscop, Toulouse, France.
HIV Med. 2025 Jan;26(1):166-172. doi: 10.1111/hiv.13698. Epub 2024 Aug 28.
Prevention of cardiovascular disease is a major issue in the current management of people living with HIV. Concern is growing about the metabolic impact of integrase strand transfer inhibitors (INSTIs), which could lead to an increased risk of diabetes, but the data are conflicting. This is an updated version of our previous analysis, with longer follow-up and new molecules.
We retrospectively evaluated the incidence of new-onset diabetes in people living with HIV starting combined antiretroviral therapy with an INSTI compared with non-nucleoside reverse transcriptase inhibitors and protease inhibitors. Data were collected from the Dat'AIDS cohort study, a collaboration of 30 HIV treatment centres in France. We used a propensity score-based inverse probability of treatment weighting approach to adjust for baseline characteristics between the two groups (INSTI and non-INSTI).
Between 2009 and 2021, a total of 12 150 people living with HIV were included. The incidence of diabetes was higher in the INSTI group than in the non-INSTI group (hazard ratio 1.38; 95% confidence interval 1.07-1.77; p = 0.012). Regardless of the third drug, but to a greater extent for INSTIs, we observed a peak of new-onset diabetes in the year following initiation of combined antiretroviral therapy.
The incidence of diabetes was higher in people treated with integrase inhibitors than in those receiving other third agents. This increased risk occurred both during the first year of treatment and in the longer term.
预防心血管疾病是当前HIV感染者管理中的一个主要问题。人们越来越关注整合酶链转移抑制剂(INSTIs)对代谢的影响,这可能会增加患糖尿病的风险,但数据存在矛盾。这是我们之前分析的更新版本,随访时间更长且纳入了新分子。
我们回顾性评估了开始接受含INSTI的联合抗逆转录病毒治疗的HIV感染者与接受非核苷类逆转录酶抑制剂和蛋白酶抑制剂的患者中新发糖尿病的发生率。数据来自法国30个HIV治疗中心合作开展的Dat'AIDS队列研究。我们采用基于倾向评分的治疗权重逆概率方法来调整两组(INSTI组和非INSTI组)之间的基线特征。
2009年至2021年期间,共纳入了12150名HIV感染者。INSTI组的糖尿病发生率高于非INSTI组(风险比1.38;95%置信区间1.07 - 1.77;p = 0.012)。无论第三种药物是什么,但在更大程度上对于INSTIs,我们观察到在开始联合抗逆转录病毒治疗后的第一年新发糖尿病出现了峰值。
接受整合酶抑制剂治疗的患者糖尿病发生率高于接受其他第三种药物治疗的患者。这种增加的风险在治疗的第一年及长期均存在。