Division of Maternal-Fetal Medicine, Department of Obstetrics & Gynecology, Beth Israel Deaconess Medical Center, Harvard Medical School.
Boston University, Chobanian & Avedisian School of Medicine, Department of Pediatrics, Boston Medical Center, Boston, MA, USA.
AIDS. 2024 Oct 1;38(12):1749-1757. doi: 10.1097/QAD.0000000000003979. Epub 2024 Jul 17.
To examine the risk of preterm birth (PTB) and small for gestational age (SGA) among women with HIV compared to women without HIV. Secondary objectives were to explore the role of maternal immune activation (IA) and effect of cART timing on these outcomes.
Prospective observational cohort.
Urban government-run clinic at Chawama Hospital in Lusaka, Zambia.
A total of 1481 women with and without HIV with singleton pregnancies enrolled before 26 weeks' gestation by ultrasound dating.
From August 2019 to November 2022, pregnant women were enrolled in a 1 : 1 ratio of HIV infection. Maternal baseline clinical factors were collected, as well as CD4 + , viral load and CD8 + T-cell IA in women with HIV. Birth outcomes were also collected. The association of HIV-exposure and cART timing on outcomes was assessed by multivariable logistic regression. The independent role of IA was determined by mediation analysis.
PTB (<37 weeks) and SGA.
There were 38 fetal deaths and 1230 singleton live births. Maternal HIV infection was associated with PTB [adjusted odds ratio (AOR) 1.60, 95% confidence interval (CI) 1.11-2.32] and to a lesser extent SGA (AOR 1.29, 95% CI 0.98-1.70). Maternal cART timing impacted these associations, with highest risk in women who started cART after conception (PTB AOR 1.77, 95% CI 1.09-2.87, SGA AOR 1.52, 95% CI 1.04-2.22). Maternal IA was not associated with PTB independent of HIV infection.
HIV is associated with PTB. Risk of PTB and SGA was highest in women with HIV who started cART in pregnancy, a modifiable risk factor.
研究与未感染 HIV 的女性相比,感染 HIV 的女性发生早产(PTB)和胎儿生长受限(SGA)的风险。次要目标是探讨母婴免疫激活(IA)的作用以及 cART 时机对这些结局的影响。
前瞻性观察队列。
赞比亚卢萨卡 Chawama 医院的城市政府运营诊所。
共有 1481 名感染 HIV 和未感染 HIV 的单胎妊娠妇女在超声妊娠 26 周前被纳入研究。
2019 年 8 月至 2022 年 11 月,按照 1:1 的比例纳入感染 HIV 的孕妇。收集孕妇的基线临床因素,以及 HIV 感染孕妇的 CD4+、病毒载量和 CD8+T 细胞 IA。还收集了出生结局。通过多变量逻辑回归评估 HIV 暴露和 cART 时机对结局的影响。通过中介分析确定 IA 的独立作用。
PTB(<37 周)和 SGA。
有 38 例胎儿死亡和 1230 例单胎活产。母婴 HIV 感染与 PTB 相关(调整后的优势比(AOR)为 1.60,95%置信区间(CI)为 1.11-2.32),与 SGA 的关联较小(AOR 为 1.29,95%CI 为 0.98-1.70)。孕产妇 cART 时机影响这些关联,在妊娠后开始 cART 的妇女中风险最高(PTB AOR 为 1.77,95%CI 为 1.09-2.87,SGA AOR 为 1.52,95%CI 为 1.04-2.22)。独立于 HIV 感染,母婴 IA 与 PTB 无关。
HIV 与 PTB 相关。HIV 感染妇女妊娠后开始 cART 的风险最高,这是一个可改变的危险因素。