Powis Kathleen M, Smeaton Laura, Hughes Michael D, Tumbare Esther A, Souda Sajini, Jao Jennifer, Wirth Kathleen E, Makhema Joseph, Lockman Shahin, Fawzi Wafaie, Essex Max, Shapiro Roger L
aDepartments of Medicine and Pediatrics, Massachusetts General Hospital, Boston bDepartment of Immunology and Infectious Diseases, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA cBotswana Harvard AIDS Institute Partnership, Gaborone, Botswana dDepartment of Biostatistics, Harvard T.H. Chan School of Public Health, Boston, Massachusetts, USA eElizabeth Glaser Pediatric AIDS Foundation, Harare, Zimbabwe fFaculty of Medicine, University of Botswana, Gabarone, Botswana gDivisions of Infectious Diseases and General Medicine, Department of Obstetrics, Gynecology, and Reproductive Science, Icahn School of Medicine, Mount Sinai, New York City, New York, USA hDepartment of Epidemiology, Harvard T.H. Chan School of Public Health iInfectious Disease Division, Brigham and Women's Hospital, Boston jDepartments of Global Health and Population, Nutrition and Epidemiology, Harvard T.H. Chan School of Public Health kBeth Israel Deaconess Medical Center, Infectious Diseases Department, Boston, Massachusetts, USA.
AIDS. 2016 Jan;30(2):211-20. doi: 10.1097/QAD.0000000000000895.
To assess associations between in-utero triple antiretrovirals (cART) versus zidovudine (ZDV) monotherapy exposure and growth among HIV-uninfected children of HIV-infected women in Botswana.
Secondary retrospective data analysis from two randomized intervention trials of mother-to-child HIV transmission prevention.
The Mashi and Mma Bana studies enrolled HIV-infected pregnant women, following their children through 24 months of age. This analysis includes singleton, full-term, HIV-exposed uninfected children. Mothers received cART or ZDV at least 2 weeks predelivery, and breastfed up to 6 months. Weight-for-age (WAZ), length-for-age (LAZ) and weight-for-length (WLZ) z-scores were derived. Mean z-scores were compared by exposure group at 24 months (t-test, linear regression).
Of 819 children, 303 were ZDV- and 516 cART-exposed in utero. Maternal median enrolment CD4 was higher among ZDV versus cART-treated mothers (393 versus 324 cells/μl; P < 0.0001). Median duration of antepartum antiretroviral use was shorter among ZDV-treated women (5.7 versus 12.0 weeks; P < 0.0001). Median months breastfed were similar (5.9 and 6.0; P = 0.43). At 24 months, mean LAZ and WAZ were significantly lower among cART-exposed children (LAZ -1.01 versus -0.74; P = 0.003) (WAZ -0.53 versus -0.30; P = 0.002) in unadjusted analyses. Adjusting for maternal CD4, viral load, enrolment site and maternal anthropometric measures, cART-exposed children had significantly lower LAZ and WAZ at 24 months (P = 0.0004 for both).
At 24 months, in-utero cART-exposed children had significantly lower LAZ and WAZ. Poor growth impacts childhood and adult mortality. These findings raise concerns for potential lasting health impacts among HIV-exposed uninfected children with in-utero cART exposure.
评估博茨瓦纳感染艾滋病毒妇女的未感染艾滋病毒儿童在子宫内接受三联抗逆转录病毒疗法(cART)与齐多夫定(ZDV)单药治疗的暴露情况与生长之间的关联。
两项预防母婴艾滋病毒传播的随机干预试验的二次回顾性数据分析。
马希研究和玛玛·巴纳研究纳入了感染艾滋病毒的孕妇,并对其子女进行追踪至24个月龄。该分析包括单胎、足月、暴露于艾滋病毒但未感染的儿童。母亲们在分娩前至少2周接受cART或ZDV治疗,并进行长达6个月的母乳喂养。得出年龄别体重(WAZ)、年龄别身长(LAZ)和身长别体重(WLZ)z评分。在24个月时按暴露组比较平均z评分(t检验、线性回归)。
在819名儿童中,303名在子宫内暴露于ZDV,516名暴露于cART。与接受cART治疗的母亲相比,接受ZDV治疗的母亲孕期登记时的CD4中位数更高(393对324个细胞/μl;P<0.0001)。接受ZDV治疗的妇女产前抗逆转录病毒药物使用的中位数持续时间较短(5.7对12.0周;P<0.0001)。母乳喂养的中位数月份相似(5.9和6.0;P=0.43)。在24个月时,未经调整的分析显示,暴露于cART的儿童的平均LAZ和WAZ显著更低(LAZ -1.01对-0.74;P=0.003)(WAZ -0.53对-0.30;P=0.002)。在对母亲的CD4、病毒载量、登记地点和母亲人体测量指标进行调整后,暴露于cART的儿童在24个月时的LAZ和WAZ显著更低(两者P均=0.0004)。
在24个月时,子宫内暴露于cART的儿童的LAZ和WAZ显著更低。生长发育不良会影响儿童期和成人期死亡率。这些发现引发了对子宫内暴露于cART的暴露于艾滋病毒但未感染儿童潜在长期健康影响的担忧。