Mmiro Francis A, Aizire Jim, Mwatha Anthony K, Eshleman Susan H, Donnell Deborah, Fowler Mary Glenn, Nakabiito Clemensia, Musoke Philippa M, Jackson J Brooks, Guay Laura A
Makerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.
J Acquir Immune Defic Syndr. 2009 Sep 1;52(1):32-9. doi: 10.1097/QAI.0b013e3181afd352.
To determine the predictors for early versus later (breastfeeding) transmission of HIV-1.
Secondary data analysis was performed on HIV Network for Prevention Trials 012, a completed randomized clinical trial assessing the relative efficacy of nevirapine (NVP) versus zidovudine in reducing mother-to-child transmission (MTCT) of HIV-1. We used Cox regression analysis to assess risk factors for MTCT. The ViroSeq HIV genotyping and a sensitive point mutation assay were used to detect NVP resistance mutations.
In this subset analyses, 122 of 610 infants were HIV infected, of whom 99 (81.1%) were infected early (first positive polymerase chain reaction < or =56 days). Incidence of MTCT after 56 days was low [0.7% per month (95% confidence interval, CI: 0.4 to 1.0)], but continued through 18 months. In multivariate analyses, early MTCT "factors" included NVP versus zidovudine (hazard ratio (HR) = 0.57, 95% CI: 0.38 to 0.86), pre-entry maternal viral load (VL, HR = 1.76, 95% CI: 1.28 to 2.41), and CD4 cell count (HR = 1.16, 95% CI: 1.05 to 1.28). Maternal VL (6-8 weeks) was associated with late MTCT (HR = 3.66, 95% CI: 1.78 to 7.50), whereas maternal NVP resistance (6-8 weeks) was not.
Maternal VL was the best predictor of both early and late transmission. Maternal NVP resistance at 6-8 weeks did not predict late transmission.
确定人类免疫缺陷病毒1型(HIV-1)早期与晚期(母乳喂养)传播的预测因素。
对预防试验HIV网络012进行二次数据分析,这是一项已完成的随机临床试验,评估奈韦拉平(NVP)与齐多夫定在降低HIV-1母婴传播(MTCT)方面的相对疗效。我们使用Cox回归分析来评估MTCT的危险因素。采用ViroSeq HIV基因分型和敏感点突变检测法检测NVP耐药突变。
在该亚组分析中,610名婴儿中有122名感染了HIV,其中99名(81.1%)为早期感染(首次聚合酶链反应阳性≤56天)。56天后MTCT的发生率较低[每月0.7%(95%置信区间,CI:0.4至1.0)],但持续至18个月。在多变量分析中,早期MTCT的“因素”包括NVP与齐多夫定(风险比(HR)=0.57,95%CI:0.38至0.86)、孕前母亲病毒载量(VL,HR=1.76,95%CI:1.28至2.41)和CD4细胞计数(HR=1.16,95%CI:1.05至1.28)。母亲VL(6至8周)与晚期MTCT相关(HR=3.66,95%CI:1.78至7.50),而母亲NVP耐药(6至8周)则无此关联。
母亲VL是早期和晚期传播的最佳预测因素。6至8周时母亲NVP耐药不能预测晚期传播。