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首页> 外文期刊>The Lancet >Safety and efficacy of zinc supplementation for children with HIV-1 infection in South Africa: a randomised double-blind placebo-controlled trial.
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Safety and efficacy of zinc supplementation for children with HIV-1 infection in South Africa: a randomised double-blind placebo-controlled trial.

机译:在南非,HIV-1感染儿童补充锌的安全性和有效性:一项随机双盲安慰剂对照试验。

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BACKGROUND: Zinc deficiency is associated with impaired immune function and an increased risk of infection. Supplementation can decrease the incidence of diarrhoea and pneumonia in children in resource-poor countries. However, in children with HIV-1 infection, the safety of zinc supplementation is uncertain. We aimed to assess the role of zinc in HIV-1 replication before mass zinc supplementation is recommended in regions of high HIV-1 prevalence. METHODS: We did a randomised double-blind placebo-controlled equivalence trial of zinc supplementation at Grey's Hospital in Pietermaritzburg, South Africa. 96 children with HIV-1 infection were randomly assigned to receive 10 mg of elemental zinc as sulphate or placebo daily for 6 months. Baseline measurements of plasma HIV-1 viral load and the percentage of CD4+ T lymphocytes were established at two study visits before randomisation, and measurements were repeated 3, 6, and 9 months after the start of supplementation. The primary outcome measure was plasma HIV-1 viral load. Analysis was per protocol. FINDINGS: The mean log(10) HIV-1 viral load was 5.4 (SD 0.61) for the placebo group and 5.4 (SD 0.66) for the zinc-supplemented group 6 months after supplementation began (difference 0.0002, 95% CI -0.27 to 0.27). 3 months after supplementation ended, the corresponding values were 5.5 (SD 0.77) and 5.4 (SD 0.61), a difference of 0.05 (-0.24 to 0.35). The mean percentage of CD4+ T lymphocytes and median haemoglobin concentrations were also similar between the two groups after zinc supplementation. Two deaths occurred in the zinc supplementation group and seven in the placebo group (p=0.1). Children given zinc supplementation were less likely to get watery diarrhoea than those given placebo. Watery diarrhoea was diagnosed at 30 (7.4%) of 407 clinic visits in the zinc-supplemented group versus 65 (14.5%) of 447 visits in the placebo group (p=0.001). INTERPRETATION: Zinc supplementation of HIV-1-infected children does not result in an increase in plasma HIV-1 viral load and could reduce morbidity caused by diarrhoea. RELEVANCE TO PRACTICE: Programmes to enhance zinc intake in deficient populations with a high prevalence of HIV-1 infection can be implemented without concern for adverse effects on HIV-1 replication. In view of the reductions in diarrhoea and pneumonia morbidity, zinc supplementation should be used as adjunct therapy for children with HIV-1 infection.
机译:背景:锌缺乏与免疫功能受损和感染风险增加有关。在资源贫乏的国家,补充食品可以减少儿童腹泻和肺炎的发生。但是,对于患有HIV-1感染的儿童,补充锌的安全性尚不确定。我们旨在评估在HIV-1高发地区推荐大量补充锌之前,锌在HIV-1复制中的作用。方法:我们在南非彼得马里茨堡的格雷医院,进行了一项补充锌的随机双盲安慰剂对照等效试验。随机分配96名HIV-1感染儿童,每天接受10毫克硫酸锌或安慰剂元素锌,持续6个月。在随机分组之前的两次研究访问中确定了血浆HIV-1病毒载量和CD4 + T淋巴细胞百分比的基线测量值,并在补充开始后的3、6和9个月重复进行测量。主要结果指标是血浆HIV-1病毒载量。根据方案进行分析。结果:安慰剂组的平均log(10)HIV-1病毒载量为5.4(SD 0.61),锌补充组的平均log(10)HIV-1病毒载量为开始补充6个月后(差异0.0002,95%CI -0.27至0.27)。补充结束后3个月,相应的值分别为5.5(SD 0.77)和5.4(SD 0.61),相差0.05(-0.24至0.35)。补充锌后,两组之间CD4 + T淋巴细胞的平均百分比和中值血红蛋白浓度也相似。补锌组有2例死亡,安慰剂组有7例死亡(p = 0.1)。与服用安慰剂的孩子相比,补充锌的孩子患水泻的可能性较小。补锌组407例门诊中有30例(7.4%)被诊断为水样腹泻,而安慰剂组447例中65例(14.5%)被诊断为水泻(p = 0.001)。解释:补充HIV-1感染儿童的锌不会导致血浆HIV-1病毒载量的增加,并且可以减少腹泻引起的发病率。与实践的关系:可以实施旨在提高HIV-1感染率高的缺乏人群的锌摄入量的计划,而无需担心对HIV-1复制的不利影响。鉴于腹泻和肺炎的发病率有所降低,应补充锌作为HIV-1感染儿童的辅助治疗。

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