Section of Infectious Diseases, Department of Pediatrics, Tulane University School of Medicine, New Orleans, LA.
Department of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, MA.
J Acquir Immune Defic Syndr. 2020 Nov 1;85(3):346-354. doi: 10.1097/QAI.0000000000002445.
Birth rates among women living with HIV (WLHIV) have increased recently, with many experiencing multiple pregnancies. Yet, viral suppression is often not sustained between pregnancies. In addition, protease inhibitors (PIs) have been associated with preterm birth, but associations between integrase strand transfer inhibitors (INSTIs) and preterm birth are less well characterized.
We studied WLHIV with ≥2 live-born infants enrolled into the Pediatric HIV/AIDS Cohort Study Surveillance Monitoring for Antiretroviral Treatment Toxicities (SMARTT) study between 2007 and 2018, comparing CD4 counts and viral loads (VLs) between 2 consecutive SMARTT pregnancies. We evaluated associations of covariates with CD4 and viral suppression and the association of PI/INSTI use during pregnancy with odds of preterm birth.
There were 736 women who had ≥2 live-born children enrolled in SMARTT (1695 pregnancies). Median CD4 counts remained stable over repeat pregnancies. Although >80% of women achieved VL suppression during pregnancy, more than half had a detectable VL early in their subsequent pregnancy. In adjusted models including all singleton pregnancies, an increased odds of preterm birth was observed for women with first trimester PI initiation (adjusted odds ratio: 1.97; 95% confidence interval: 1.27 to 3.07) compared with those not receiving PIs during pregnancy and for first trimester INSTI initiation (adjusted odds ratio: 2.39; 95% confidence interval: 1.04 to 5.46) compared with those never using INSTIs during pregnancy.
Most WLHIV achieved VL suppression by late pregnancy but many were viremic early in subsequent pregnancies. First trimester initiation of PIs or INSTIs was associated with a higher risk of preterm birth.
感染 HIV 的女性(WLHIV)的出生率最近有所增加,许多人经历了多次妊娠。然而,病毒抑制在妊娠之间往往不能持续。此外,蛋白酶抑制剂(PIs)与早产有关,但整合酶抑制剂(INSTIs)与早产之间的关联尚未得到充分描述。
我们研究了 2007 年至 2018 年间纳入儿科 HIV/AIDS 队列研究监测抗逆转录病毒治疗毒性(SMARTT)研究的至少有 2 个活产婴儿的 WLHIV,比较了连续 2 次 SMARTT 妊娠之间的 CD4 计数和病毒载量(VL)。我们评估了协变量与 CD4 和病毒抑制的关系,以及妊娠期间使用 PI/INSTI 与早产几率的关系。
共有 736 名至少有 2 个活产子女的妇女被纳入 SMARTT(1695 例妊娠)。重复妊娠时,CD4 计数中位数保持稳定。尽管超过 80%的妇女在妊娠期间实现了 VL 抑制,但超过一半的妇女在随后的妊娠早期 VL 可检测到。在包括所有单胎妊娠的调整模型中,与妊娠期间未接受 PIs 的妇女相比,首次孕期使用 PI 的妇女早产的几率增加(调整后的优势比:1.97;95%置信区间:1.27 至 3.07),与妊娠期间从未使用过 INSTIs 的妇女相比,首次孕期使用 INSTIs 的妇女早产的几率增加(调整后的优势比:2.39;95%置信区间:1.04 至 5.46)。
大多数 WLHIV 在妊娠晚期实现了 VL 抑制,但许多妇女在随后的妊娠早期 VL 可检测到。首次孕期使用 PIs 或 INSTIs 与早产风险增加相关。