Makerere University-University of California, San Francisco Research Collaboration, Mulago Hospital Complex, PO Box 7475, Kampala, Uganda.
Malar J. 2012 Mar 27;11:90. doi: 10.1186/1475-2875-11-90.
In sub-Saharan Africa, malnutrition and malaria remain major causes of morbidity and mortality in young children. There are conflicting data as to whether malnutrition is associated with an increased or decreased risk of malaria. In addition, data are limited on the potential interaction between HIV infection and the association between malnutrition and the risk of malaria.
A cohort of 100 HIV-unexposed, 203 HIV-exposed (HIV negative children born to HIV-infected mothers) and 48 HIV-infected children aged 6 weeks to 1 year were recruited from an area of high malaria transmission intensity in rural Uganda and followed until the age of 2.5 years. All children were provided with insecticide-treated bed nets at enrolment and daily trimethoprim-sulphamethoxazole prophylaxis (TS) was prescribed for HIV-exposed breastfeeding and HIV-infected children. Monthly routine assessments, including measurement of height and weight, were conducted at the study clinic. Nutritional outcomes including stunting (low height-for-age) and underweight (low weight-for-age), classified as mild (mean z-scores between -1 and -2 during follow-up) and moderate-severe (mean z-scores < -2 during follow-up) were considered. Malaria was diagnosed when a child presented with fever and a positive blood smear. The incidence of malaria was compared using negative binomial regression controlling for potential confounders with measures of association expressed as an incidence rate ratio (IRR).
The overall incidence of malaria was 3.64 cases per person year. Mild stunting (IRR = 1.24, 95% CI 1.06-1.46, p = 0.008) and moderate-severe stunting (IRR = 1.24, 95% CI 1.03-1.48, p = 0.02) were associated with a similarly increased incidence of malaria compared to non-stunted children. Being mildly underweight (IRR = 1.09, 95% CI 0.95-1.25, p = 0.24) and moderate-severe underweight (IRR = 1.12, 95% CI 0.86-1.46, p = 0.39) were not associated with a significant difference in the incidence of malaria compared to children who were not underweight. There were no significant interactions between HIV-infected, HIV-exposed children taking TS and the associations between malnutrition and the incidence of malaria.
Stunting, indicative of chronic malnutrition, was associated with an increased incidence of malaria among a cohort of HIV-infected and -uninfected young children living in an area of high malaria transmission intensity. However, caution should be made when making causal inferences given the observational study design and inability to disentangle the temporal relationship between malnutrition and the incidence of malaria.
ClinicalTrials.gov: NCT00527800.
在撒哈拉以南非洲,营养不良和疟疾仍然是导致幼儿发病和死亡的主要原因。关于营养不良是否与疟疾风险增加或降低有关,存在相互矛盾的数据。此外,关于艾滋病毒感染与营养不良和疟疾风险之间的关联之间潜在相互作用的数据有限。
从乌干达农村疟疾传播强度高的地区招募了 100 名未感染艾滋病毒的儿童、203 名感染艾滋病毒的儿童(艾滋病毒阴性的母亲所生的儿童)和 48 名感染艾滋病毒的儿童,这些儿童年龄在 6 周到 1 岁之间,进行了队列研究。所有儿童在入组时都提供了经杀虫剂处理的蚊帐,并为感染艾滋病毒的哺乳期和感染艾滋病毒的儿童开具了每日甲氧苄啶-磺胺甲恶唑预防(TS)。在研究诊所每月进行常规评估,包括身高和体重测量。将包括发育迟缓(身高年龄低)和体重不足(体重年龄低)在内的营养结果,分为轻度(随访期间平均 z 分数在-1 到-2 之间)和中重度(随访期间平均 z 分数 < -2)。当儿童出现发热和阳性血涂片时诊断为疟疾。使用负二项式回归控制潜在混杂因素,用发病率比(IRR)表示关联程度,比较疟疾的发病率。
疟疾的总发病率为每 1 人年 3.64 例。与非发育迟缓儿童相比,轻度发育迟缓(IRR = 1.24,95%CI 1.06-1.46,p = 0.008)和中重度发育迟缓(IRR = 1.24,95%CI 1.03-1.48,p = 0.02)与疟疾发病率同样增加相关。轻度体重不足(IRR = 1.09,95%CI 0.95-1.25,p = 0.24)和中重度体重不足(IRR = 1.12,95%CI 0.86-1.46,p = 0.39)与未体重不足的儿童相比,疟疾发病率无显著差异。未发现感染艾滋病毒的儿童和接受 TS 治疗的感染艾滋病毒的儿童与营养不良和疟疾发病率之间的关联之间存在显著的相互作用。
在疟疾传播强度高的地区生活的感染艾滋病毒和未感染艾滋病毒的幼儿队列中,发育迟缓(表明慢性营养不良)与疟疾发病率增加有关。然而,鉴于观察性研究设计和无法厘清营养不良与疟疾发病率之间的时间关系,在进行因果推断时应谨慎。
ClinicalTrials.gov:NCT00527800。