Department of Pediatrics, Division of Pediatric Infectious Diseases, Northwestern University Feinberg School of Medicine, Chicago, Illinois, USA.
Department of Pediatrics, Ann and Robert H. Lurie Children's Hospital of Chicago, Chicago, Illinois, USA.
Clin Infect Dis. 2024 Sep 26;79(3):727-733. doi: 10.1093/cid/ciae088.
There are little data on changes in insulin sensitivity during the first few years of life following in utero human immunodeficiency virus (HIV) and antiretroviral (ARV) exposure.
The Tshilo Dikotla study enrolled pregnant persons with HIV (PWH) (receiving tenofovir/emtricitabine or lamivudine plus dolutegravir or efavirenz) and pregnant individuals without HIV, as well as their liveborn children. Newborns were randomized to receive either zidovudine (AZT) or nevirapine (NVP) postnatal prophylaxis. Homeostasis Model Assessment for Insulin Resistance (HOMA-IR) was assessed at birth and 1, 18, 24, and 36 months of life. We fit linear mixed-effects models to evaluate the association between in utero HIV/ARV exposure and average HOMA-IR from birth through 36 months of life, adjusting for confounders.
A total of 419 children were included (287 with in utero HIV/ARV exposure and uninfected [CHEU] and 132 without in utero HIV/ARV exposure [CHUU]). CHEU were born to older women (29.6 vs 25.3 years of age) with higher gravidity (3 vs 1). HOMA-IR was persistently higher in CHEU versus CHUU in adjusted analyses (mean difference of 0.07 in log10 HOMA-IR, P = .02) from birth through 36 months of life. Among CHEU, no differences in HOMA-IR were observed from birth through 36 months by in utero ARV exposure status or between AZT and NVP infant prophylaxis arms.
In utero HIV/ARV exposure was associated with lower insulin sensitivity throughout the first 36 months of life, indicating persistent early life metabolic disturbances which may raise concern for poorer metabolic health later in life.
在子宫内暴露于人类免疫缺陷病毒 (HIV) 和抗逆转录病毒 (ARV) 后,生命的最初几年中胰岛素敏感性的变化数据很少。
Tshilo Dikotla 研究纳入了 HIV 阳性孕妇 (PWH)(接受替诺福韦/恩曲他滨或拉米夫定加多替拉韦或依非韦伦)和未感染 HIV 的孕妇,以及她们的活产婴儿。新生儿随机接受齐多夫定 (AZT) 或奈韦拉平 (NVP) 产后预防。在出生时以及 1、18、24 和 36 个月时评估稳态模型评估的胰岛素抵抗 (HOMA-IR)。我们拟合线性混合效应模型,以评估子宫内 HIV/ARV 暴露与出生至 36 个月期间平均 HOMA-IR 之间的关联,同时调整混杂因素。
共纳入 419 名儿童(287 名有子宫内 HIV/ARV 暴露和未感染 [CHEU],132 名无子宫内 HIV/ARV 暴露 [CHUU])。CHEU 的母亲年龄较大(29.6 岁比 25.3 岁),孕次较多(3 次比 1 次)。在调整后的分析中,CHEU 的 HOMA-IR 始终高于 CHUU(出生至 36 个月时对数 10 HOMA-IR 的平均差异为 0.07,P =.02)。在 CHEU 中,从出生到 36 个月,无论子宫内 ARV 暴露状况如何,或 AZT 和 NVP 婴儿预防手臂之间,HOMA-IR 均无差异。
子宫内 HIV/ARV 暴露与生命最初 36 个月的胰岛素敏感性降低相关,表明早期存在持续的代谢紊乱,这可能会引起对以后生命代谢健康较差的担忧。