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乌干达坎帕拉母乳喂养人群中HIV母婴早期和晚期传播的预测因素:预防试验HIV网络012的经验

Predictors of early and late mother-to-child transmission of HIV in a breastfeeding population: HIV Network for Prevention Trials 012 experience, Kampala, Uganda.

作者信息

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

机构信息

Makerere University-Johns Hopkins University Research Collaboration, Kampala, Uganda.

出版信息

J Acquir Immune Defic Syndr. 2009 Sep 1;52(1):32-9. doi: 10.1097/QAI.0b013e3181afd352.

Abstract

OBJECTIVE

To determine the predictors for early versus later (breastfeeding) transmission of HIV-1.

METHODS

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.

RESULTS

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.

CONCLUSIONS

Maternal VL was the best predictor of both early and late transmission. Maternal NVP resistance at 6-8 weeks did not predict late transmission.

摘要

目的

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。

方法

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。

结果

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。

结论

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。

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