Coutsoudis Anna, Dabis Francois, Fawzi Wafaie, Gaillard Philippe, Haverkamp Geert, Harris D Robert, Jackson J Brooks, Leroy Valerie, Meda Nicolas, Msellati Philippe, Newell Marie-Louise, Nsuati Ruth, Read Jennifer S, Wiktor Stefan
J Infect Dis. 2004 Jun 15;189(12):2154-66. doi: 10.1086/420834. Epub 2004 May 26.
We analyzed individual patient data to determine the contribution of late postnatal transmission to the overall risk of mother-to-child transmission of human immunodeficiency virus type 1 (HIV-1) and the timing and determinants of late postnatal transmission.
Eligible trials were conducted where breast-feeding was common; included >/=2 HIV-1 tests by 3 months, and, if follow-up continued, >/=2 tests at 3-12 months; and regularly assessed infant-feeding modality. Data on children born before January 2000 were analyzed.
Of 4085 children from 9 trials (breast-fed singletons for whom HIV-1 testing was performed), 993 (24%) were definitively infected (placebo arms, 25.9%; treatment arms, 23.4%; P=.08). Of 539 children with known timing of infection, 225 (42%) had late postnatal transmission. Late postnatal transmission occurred throughout breast-feeding. The estimated hazard function for time to late postnatal transmission was roughly constant. The cumulative probability of late postnatal transmission at 18 months was 9.3%. The overall risk of late postnatal transmission was 8.9 transmissions/100 child-years of breast-feeding and was significantly higher with lower maternal CD4(+) cell counts and male sex.
Late postnatal transmission contributes substantially to overall mother-to-child transmission of HIV-1. The risk of late postnatal transmission is generally constant throughout breast-feeding, and late postnatal transmission is associated with a lower maternal CD4(+) cell count and male sex. Biological and cultural mechanisms underlying the association between sex and late postnatal transmission should be further investigated. Interventions to decrease transmission of HIV-1 through breast-feeding are urgently needed.
我们分析了个体患者数据,以确定产后晚期传播对1型人类免疫缺陷病毒(HIV-1)母婴传播总体风险的影响,以及产后晚期传播的时间和决定因素。
在母乳喂养普遍的情况下开展符合条件的试验;在3个月时进行≥2次HIV-1检测,若随访持续,则在3至12个月时进行≥2次检测;并定期评估婴儿喂养方式。对2000年1月之前出生的儿童数据进行分析。
在9项试验中的4085名儿童(进行了HIV-1检测的母乳喂养单胎婴儿)中,993名(24%)被确诊感染(安慰剂组,25.9%;治疗组,23.4%;P = 0.08)。在539名已知感染时间的儿童中,225名(42%)发生了产后晚期传播。产后晚期传播在整个母乳喂养期间均有发生。产后晚期传播时间的估计风险函数大致恒定。18个月时产后晚期传播的累积概率为9.3%。产后晚期传播的总体风险为每100儿童母乳喂养年8.9例传播,且随着母亲CD4(+)细胞计数降低和男性性别而显著升高。
产后晚期传播对HIV-1母婴传播的总体影响很大。产后晚期传播的风险在整个母乳喂养期间通常是恒定的,且产后晚期传播与母亲较低的CD4(+)细胞计数和男性性别有关。性别与产后晚期传播之间关联的生物学和文化机制应进一步研究。迫切需要采取干预措施以减少通过母乳喂养传播HIV-1。