Department of Epidemiology, Columbia University Mailman School of Public Health, New York, NY.
Center for Biostatistics in AIDS Research, Harvard T.H. Chan School of Public Health, Boston, MA.
AIDS. 2024 Jul 1;38(8):1111-1119. doi: 10.1097/QAD.0000000000003877. Epub 2024 Mar 19.
HIV treatment regimen during pregnancy was associated with preterm delivery (PTD) in the PROMISE 1077 BF trial. Systemic inflammation among pregnant women with HIV could help explain differences in PTD by treatment regimen. We assessed associations between inflammation, treatment regimen, and PTD.
DESIGN/METHODS: A nested 1 : 1 case-control study ( N = 362) was conducted within a multicountry randomized trial comparing three HIV regimens in pregnant women: zidovudine alone, or combination antiretroviral therapy (ART) with lopinavir/ritonavir and either zidovudine or tenofovir. Cases were women with PTD (<37 weeks of gestational age). The following inflammatory biomarkers were measured in plasma samples using immunoassays: soluble CD14 (sCD14) and sCD163, intestinal fatty acid-binding protein, interleukin (IL)-6, interferon γ, and tumor necrosis factor α. We fit regression models to assess associations between second trimester biomarkers (measured before ART initiation at 13-23 weeks of gestational age and 4 weeks later), treatment regimen, and PTD. We also assessed whether inflammation was a mediator in the relationship between ART regimen and PTD.
Persistently high interleukin-6 was associated with increased PTD. Compared with zidovudine alone, the difference in biomarker concentration between week 0 and week 4 was significantly higher ( P < 0.05) for both protease inhibitor-based regimens. However, the estimated proportion of the ART effect on increased PTD mediated by persistently high biomarker levels was 5% or less for all biomarkers.
Persistently high IL-6 during pregnancy was associated with PTD. Although protease inhibitor-based ART was associated with increases in inflammation, factors other than inflammation likely explain the increased PTD in ART-based regimens compared with zidovudine alone.
在 PROMISE 1077 BF 试验中,HIV 治疗方案与早产(PTD)有关。HIV 孕妇的全身炎症可能有助于解释不同治疗方案之间 PTD 的差异。我们评估了炎症、治疗方案和 PTD 之间的关系。
在一项多国家随机试验中,进行了一项嵌套的 1:1 病例对照研究(N=362),该试验比较了三种 HIV 治疗方案在孕妇中的应用:齐多夫定单药治疗或联合洛匹那韦/利托那韦与齐多夫定或替诺福韦联合的抗逆转录病毒治疗(ART)。病例为 PTD(<37 周妊娠龄)的妇女。使用免疫测定法在血浆样本中测量以下炎症生物标志物:可溶性 CD14(sCD14)和 sCD163、肠脂肪酸结合蛋白、白细胞介素(IL)-6、干扰素γ和肿瘤坏死因子α。我们拟合回归模型来评估妊娠中期生物标志物(在妊娠 13-23 周和 4 周后开始 ART 前测量)与治疗方案和 PTD 之间的关系。我们还评估了炎症是否是 ART 方案与 PTD 之间关系的中介。
持续高 IL-6 与 PTD 增加有关。与齐多夫定单药治疗相比,两种蛋白酶抑制剂方案的周 0 和周 4 之间生物标志物浓度的差异显著更高(P<0.05)。然而,所有生物标志物中,持续高水平生物标志物对增加的 PTD 的 ART 效应的估计比例均为 5%或更小。
妊娠期间持续高 IL-6 与 PTD 有关。虽然基于蛋白酶抑制剂的 ART 与炎症增加有关,但与齐多夫定单药治疗相比,ART 方案中 PTD 增加的原因可能不仅仅是炎症。