Department of Hygiene, Epidemiology and Medical Statistics, Medical School, National and Kapodistrian University of Athens, 11527 Athens, Greece.
5th Department of Internal Medicine-Division of Infectious Diseases, Evangelismos General Hospital of Athens, 10676 Athens, Greece.
Viruses. 2022 Jul 29;14(8):1677. doi: 10.3390/v14081677.
Recent research on antiretroviral treatment (ART) for HIV suggests that integrase strand transfer inhibitors (INSTIs) cause faster weight gain compared to other drug classes. Here, we investigated changes in body mass index (BMI) and obesity prevalence after treatment initiation and corresponding differences between drug classes. Data were derived from a large collaborative cohort in Greece. Included individuals were adults who started ART, in or after 2010, while previously ART naïve and achieved virologic response within the first year of ART. Data were analysed using mixed fractional polynomial models. INSTI regimens led to the more pronounced BMI increases, followed by boosted PI and NNRTI based regimens. Individuals with normal initial BMI are expected to gain 6 kg with an INSTI regimen compared to 4 kg with a boosted PI and less than 3 kg with a NNRTI regimen after four years of treatment. Prevalence of obesity was 5.7% at ART initiation and 12.2%, 14.2% and 18.1% after four years of treatment with NNRTIs, PIs, and INSTIs, respectively. Dolutegravir or Raltegravir were associated with marginally faster BMI increase compared to Elvitegravir. INSTIs are associated with faster weight gain. INSTIs' increased risk of treatment emergent obesity and, possibly, weight-related co-morbidities should be judged against their improved efficacy and tolerability but increased clinical attention is required.
最近的抗逆转录病毒治疗(ART)研究表明,与其他药物类别相比,整合酶链转移抑制剂(INSTIs)会导致更快的体重增加。在这里,我们研究了治疗开始后体重指数(BMI)和肥胖患病率的变化,以及药物类别之间的相应差异。数据来自希腊的一个大型合作队列。纳入的个体为成年人,他们在 2010 年或之后开始接受 ART,并且在接受 ART 之前没有接受过治疗,并且在 ART 的第一年就实现了病毒学反应。使用混合分数多项式模型分析数据。INSTI 方案导致 BMI 增加更为明显,其次是增效 PI 和 NNRTI 方案。与接受增效 PI 和 NNRTI 方案治疗的个体相比,初始 BMI 正常的个体在接受 INSTI 方案治疗四年后预计会增加 6 公斤体重,而接受增效 PI 方案和接受 NNRTI 方案治疗的个体预计会增加 4 公斤体重和不到 3 公斤体重。在开始 ART 时肥胖的患病率为 5.7%,而在接受 NNRTIs、PIs 和 INSTIs 治疗四年后,肥胖的患病率分别为 12.2%、14.2%和 18.1%。与 Elvitegravir 相比,Dolutegravir 或 Raltegravir 与 BMI 增加速度稍快相关。INSTIs 与体重增加更快相关。应该根据 INSTIs 改善的疗效和耐受性来判断它们增加治疗后出现肥胖和可能与体重相关的合并症的风险,但需要增加临床关注。