Jao Jennifer, Kacanek Deborah, Williams Paige L, Geffner Mitchell E, Livingston Elizabeth G, Sperling Rhoda S, Patel Kunjal, Bardeguez Arlene D, Burchett Sandra K, Chakhtoura Nahida, Scott Gwendolyn B, Van Dyke Russell B, Abrams Elaine J
Departments of Medicine and Obstetrics, Gynecology, and Reproductive Science, Icahn School of Medicine at Mount Sinai, New York, New York.
Department of Biostatistics, Center for Biostatistics in AIDS Research, Harvard T. H. Chan School of Public Health, Boston, Massachusetts.
Clin Infect Dis. 2017 Sep 15;65(6):982-989. doi: 10.1093/cid/cix488.
Pregnancy outcomes of perinatally human immunodeficiency virus-infected women (PHIV) are poorly defined.
We compared preterm delivery and birth weight (BW) outcomes (low BW [LBW], <2500 g), small-for-gestational-age [SGA], and BW z scores [BWZ]) in HIV-exposed uninfected infants of PHIV vs nonperinatally HIV-infected (NPHIV) pregnant women in the Pediatric HIV/AIDS Cohort Study Surveillance Monitoring of ART Toxicities or International Maternal Pediatric Adolescent AIDS Clinical Trials P1025 studies. Mixed effects models and log binomial models were used to assess the association of maternal PHIV status with infant outcomes. Age-stratified analyses were performed.
From 1998 to 2013, 2270 HIV-infected pregnant women delivered 2692 newborns (270 born to PHIV and 2422 to NPHIV women). PHIV women were younger, (mean age 21 vs 25 years, P < .01) and more likely to have a pregnancy CD4 count <200 cells/mm3 (19% vs 11%, P = .01). No associations between maternal PHIV status and preterm delivery, SGA, or LBW were observed. After adjustment, BWZ was 0.12 lower in infants of PHIV vs NPHIV women (adjusted mean, -0.45 vs -0.33; P = .04). Among women aged 23-30 years (n = 1770), maternal PHIV was associated with LBW (aRR = 1.74; 95% confidence interval, 1.18, 2.58; P < .01).
The overall lack of association between maternal PHIV status and preterm delivery or infant BW outcomes is reassuring. The higher rates of LBW observed in PHIV women aged 23-30 years warrants further mechanism-based investigations as this is a rapidly growing and aging population worldwide.
PHACS SMARTT study, NCT01310023.
IMPAACT 1025, NCT00028145.
围产期感染人类免疫缺陷病毒(PHIV)的女性的妊娠结局尚不明确。
在儿科HIV/AIDS队列研究抗逆转录病毒治疗毒性监测或国际孕产妇儿科青少年艾滋病临床试验P1025研究中,我们比较了PHIV感染孕妇的未感染HIV的婴儿与非围产期感染HIV(NPHIV)的孕妇的未感染HIV的婴儿的早产和出生体重(BW)结局(低出生体重[LBW],<2500g)、小于胎龄儿[SGA]和BW z评分[BWZ]。采用混合效应模型和对数二项模型评估母亲的PHIV状态与婴儿结局之间的关联。进行了年龄分层分析。
1998年至2013年,2270名感染HIV的孕妇分娩了2692名新生儿(270名由PHIV感染的孕妇分娩,2422名由NPHIV感染的孕妇分娩)。感染PHIV的女性更年轻(平均年龄21岁对25岁,P<.01),且更有可能妊娠时CD4细胞计数<200个/mm³(19%对11%,P=.01)。未观察到母亲的PHIV状态与早产、SGA或LBW之间存在关联。调整后,感染PHIV的孕妇的婴儿的BWZ比NPHIV感染的孕妇的婴儿低0.12(调整后均值,-0.45对-0.33;P=.04)。在23至30岁的女性(n=1770)中,母亲感染PHIV与LBW相关(aRR=1.74;95%置信区间,1.18,2.58;P<.01)。
母亲的PHIV状态与早产或婴儿BW结局之间总体缺乏关联,这令人安心。在23至30岁的感染PHIV的女性中观察到的较高LBW发生率值得进一步进行基于机制的研究,因为这是全球一个快速增长且老龄化的人群。
PHACS SMARTT研究,NCT01310023。
IMPAACT 1025,NCT00028145。