Mounzer Karam, Brunet Laurence, Sension Michael, Hsu Ricky K, Osterman Michael D, Fusco Jennifer S, Whiteside Yohance O, Fusco Gregory P
Philadelphia FIGHT Community Health Centers, Philadelphia, LA, USA.
Epividian, Inc, 150 Fayetteville Street Suite 2300, Raleigh, NC, 27601, USA.
AIDS Res Ther. 2025 Jun 21;22(1):64. doi: 10.1186/s12981-025-00761-5.
Weight gain has been associated with the use of antiretrovirals in people with HIV, especially with integrase inhibitors or tenofovir alafenamide, and among women. In 2018, doravirine became the latest non-nucleoside reverse transcriptase inhibitor to be approved in the US. We assessed changes in weight over time among virologically suppressed individuals who switched to a regimen containing doravirine (DOR).
From the US-based OPERA cohort, treatment-experienced adults with HIV who switched to a DOR-containing regimen between 30AUG2018-30NOV2022 with a viral load < 50 copies/mL were included (followed through 31MAY2023). The study population was characterized and a linear mixed model was used to estimate rates of weight change on DOR. Results were stratified by sex, by patterns of efavirenz (EFV) and/or tenofovir disoproxil fumarate (TDF) use before/after switch to DOR, and by integrase inhibitor (INSTI) & tenofovir alafenamide (TAF) use combination (restricted to individuals who maintained the same combination before/after switch).
Of 388 included individuals, 21% were women, 33% were Black, and 78% were obese or overweight at DOR switch. Overall, people who switched to DOR lost an average of 0.80 kg/year (95% CI: -1.32, -0.28). Both women and men experienced statistically significant weight loss; women (70% Black, 70% aged ≥ 40 years) lost weight at a rate of -1.67 kg/year (95% CI: -3.32, -0.02) and men at a rate of -0.60 kg/year (95% CI: -1.12, -0.08). When EFV and TDF were absent before and after switch to DOR, statistically significant weight loss was observed. Among those who had the same INSTI and TAF combination throughout and had any INSTI or TAF use, a statistically non-significant trend toward weight loss was observed.
In one of the first real-world analyses of weight changes among virologically suppressed individuals who switched to a DOR-containing regimen in the US, DOR was associated with statistically significant weight loss. Patterns of use of other antiretrovirals did not fully explain the observed weight loss. These findings are clinically meaningful given that most individuals included were overweight or obese at switch to DOR and that women were predominantly of perimenopausal or menopausal age.
体重增加与艾滋病毒感染者使用抗逆转录病毒药物有关,尤其是与整合酶抑制剂或替诺福韦艾拉酚胺有关,在女性中也是如此。2018年,多拉韦林成为美国最新获批的非核苷类逆转录酶抑制剂。我们评估了转换至含多拉韦林(DOR)方案的病毒学抑制个体随时间的体重变化。
从美国的OPERA队列中,纳入2018年8月30日至2022年11月30日期间转换至含DOR方案且病毒载量<50拷贝/mL的有治疗经验的成年艾滋病毒感染者(随访至2023年5月31日)。对研究人群进行特征描述,并使用线性混合模型估计DOR治疗时的体重变化率。结果按性别、转换至DOR前后依非韦伦(EFV)和/或富马酸替诺福韦二吡呋酯(TDF)的使用模式,以及整合酶抑制剂(INSTI)和替诺福韦艾拉酚胺(TAF)的联合使用情况进行分层(仅限于转换前后维持相同联合用药的个体)。
在纳入的388名个体中,21%为女性,33%为黑人,在转换至DOR时78%肥胖或超重。总体而言,转换至DOR的人平均每年体重减轻0.80千克(95%置信区间:-1.32,-0.28)。女性和男性均经历了具有统计学意义的体重减轻;女性(70%为黑人,70%年龄≥40岁)体重减轻率为每年-1.67千克(95%置信区间:-3.32,-0.02),男性为每年-0.60千克(95%置信区间:-1.12,-0.08)。转换至DOR前后若不存在EFV和TDF,则观察到具有统计学意义的体重减轻。在整个过程中使用相同INSTI和TAF联合用药且使用过任何INSTI或TAF的个体中,观察到体重减轻的统计学意义不显著的趋势。
在美国对转换至含DOR方案的病毒学抑制个体的体重变化进行的首批真实世界分析之一中,DOR与具有统计学意义的体重减轻相关。其他抗逆转录病毒药物的使用模式不能完全解释观察到的体重减轻。鉴于纳入的大多数个体在转换至DOR时超重或肥胖,且女性主要处于围绝经期或绝经年龄,这些发现具有临床意义。