aCenters for Disease Control and Prevention, Atlanta, Georgia, USA bDepartment of Epidemiology and Biostatistics, School of Public Health, University of Witwatersrand, Johannesburg, South Africa cUniversity of North Carolina, Chapel Hill, North Carolina, USA dUNC Project, Lilongwe, Malawi.
AIDS. 2017 Nov 28;31(18):2455-2463. doi: 10.1097/QAD.0000000000001641.
Given the potential of cotrimoxazole preventive therapy (CPT) to prevent bacterial and malarial infections in HIV-exposed, uninfected (HEU) infants, it is important to evaluate the effects of its concurrent use with antiretroviral agents that have overlapping toxicity profiles.
We used data from the Breastfeeding, Antiretrovirals, and Nutrition study (2004-2010) to evaluate the association of CPT and antiretrovirals with hematologic measures (hemoglobin, neutrophil, and alanine aminotransferase levels) from 6 to 48 weeks of age in 2006 HEU infants in Lilongwe, Malawi. Hazards of severe outcomes (anemia, neutropenia, and elevated alanine aminotransferase), as defined by the National Institutes of Health, were compared using Cox regression models, according to time-varying CPT (implemented June 2006), antiretroviral treatment arm (maternal triple antiretroviral, infant nevirapine, or none during 6 months of breastfeeding), and their interaction. The effects of these treatments on hemoglobin, neutrophil, and alanine aminotransferase levels were assessed using linear mixed models.
In Cox models, CPT was associated with an increase in severe neutropenia [hazard ratio 1.97 (1.01, 3.86)] and a decrease in severe anemia (hazard ratio 0.65 (0.48, 0.88)]. Interactions between CPT and antiretroviral treatment were not significant. By 36 weeks, there was a significant association of CPT with increased hemoglobin levels regardless of antiretroviral drug exposure.
In addition to expected associations with increased hazard of severe neutropenia and decreased neutrophil count, CPT was associated with reduced hazard of severe anemia and higher infant blood hemoglobin. This provides further support for CPT use in HEU infants in malaria-endemic resource-limited settings where anemia is prevalent.
鉴于复方新诺明预防疗法(CPT)在预防 HIV 暴露但未感染(HEU)婴儿中的细菌和疟疾感染方面的潜力,评估其与具有重叠毒性特征的抗逆转录病毒药物同时使用的效果非常重要。
我们利用母乳喂养、抗逆转录病毒和营养研究(2004-2010 年)的数据,评估了 2006 年马拉维利隆圭的 200 名 6 至 48 周龄 HEU 婴儿中 CPT 和抗逆转录病毒药物与血液学指标(血红蛋白、中性粒细胞和丙氨酸氨基转移酶水平)之间的关系。根据时间变化的 CPT(2006 年 6 月实施)、抗逆转录病毒治疗组(产妇三联抗逆转录病毒、婴儿奈韦拉平或母乳喂养 6 个月期间均不治疗)及其相互作用,采用 Cox 回归模型比较严重结局(贫血、中性粒细胞减少和丙氨酸氨基转移酶升高,由美国国立卫生研究院定义)的风险。使用线性混合模型评估这些治疗方法对血红蛋白、中性粒细胞和丙氨酸氨基转移酶水平的影响。
在 Cox 模型中,CPT 与严重中性粒细胞减少症的发生风险增加相关(风险比 1.97(1.01,3.86)),与严重贫血的发生风险降低相关(风险比 0.65(0.48,0.88))。CPT 与抗逆转录病毒治疗之间的相互作用不显著。到 36 周时,无论抗逆转录病毒药物暴露情况如何,CPT 与血红蛋白水平升高均有显著相关性。
除了与严重中性粒细胞减少症发生风险增加和中性粒细胞计数减少的预期关联外,CPT 还与严重贫血发生风险降低和婴儿血液血红蛋白升高相关。这为在疟疾流行的资源有限环境中使用 CPT 治疗 HEU 婴儿提供了进一步的支持,因为贫血在这些环境中很常见。