Sitali Lungowe, Chipeta James, Miller John M, Moonga Hawela B, Kumar Nirbhay, Moss William J, Michelo Charles
Department of Biomedical Science, University of Zambia, School of Medicine, Lusaka, Zambia.
Department of Paediatrics and Child Health, School of Medicine, Malaria Research Unit (SMUTH-MRU), Lusaka, Zambia.
BMC Infect Dis. 2015 May 2;15:204. doi: 10.1186/s12879-015-0935-7.
Although malaria is preventable and treatable, it still claims 660,000 lives every year globally with children under five years of age having the highest burden. In Zambia, malaria rapid diagnostic tests (RDTs) that only detect Plasmodium falciparum are the main confirmatory means for malaria diagnosis in most health facilities without microscopy services. As a consequence of this P. falciparum species diagnostic approach, non-falciparum malaria is not only under-diagnosed but entirely missed, thereby making the exact disease burden unknown. We thus investigated the prevalence of various Plasmodium spp. and associated burden of infection in selected communities in Zambia.
Data from two malaria hyper-endemic provinces (Eastern and Luapula) of the 2012 National Malaria Indicator Survey (MIS), conducted between April and May 2012, were used. The MIS is a nationally representative, two-stage cluster survey conducted to coincide with the end of the malaria transmission season. Social, behavioural and background information were collected from households as part of the survey. Thick blood smears, RDTs and dried blood spots (DBS) were collected from children below six years of age. Slides were stained using Giemsa and examined by microscopy while polymerase chain reaction (PCR) was used to analyse the DBS for malaria Plasmodium spp. Multivariate logistic regression was employed to examine the association between background factors and malaria.
Overall, 873 children younger than six years of age were surveyed. The overall prevalence of Plasmodium spp. by PCR was 54.3% (95% CI 51-57.6%). Of the total Plasmodium isolates, 88% were P. falciparum, 10.6% were mixed infections and 1.4% were non-falciparum mono infections. Among the mixed infections, the majority were a combination of P. falciparum and P. malariae (6.5% of all mixed infections). Children two years and older (2-5 years) had three-fold higher risk of mixed malaria infections (aOR 2.8 CI 1.31-5.69) than children younger than two years of age.
The high prevalence of mixed Plasmodium spp. infections in this population stresses review of the current malaria RDT diagnostic approaches. The observed less incidence of mixed infections in children under two years of age compared to their older two-to-five-year-old counterparts is probably due to the protective maternal passive immunity, among other factors, in that age group.
尽管疟疾是可预防和可治疗的,但全球每年仍有66万人死于疟疾,其中五岁以下儿童负担最重。在赞比亚,大多数没有显微镜检测服务的医疗机构中,仅检测恶性疟原虫的疟疾快速诊断检测(RDT)是疟疾诊断的主要确诊手段。由于这种仅针对恶性疟原虫的诊断方法,非恶性疟原虫疟疾不仅诊断不足,甚至完全被漏诊,因此确切的疾病负担未知。因此,我们调查了赞比亚部分社区各种疟原虫的流行情况及相关感染负担。
使用了2012年4月至5月期间进行的2012年全国疟疾指标调查(MIS)中两个疟疾高度流行省份(东部和卢阿普拉)的数据。MIS是一项具有全国代表性的两阶段整群调查,与疟疾传播季节结束时间一致。作为调查的一部分,收集了家庭的社会、行为和背景信息。从六岁以下儿童中采集了厚血涂片、RDT检测样本和干血斑(DBS)。玻片用吉姆萨染色后进行显微镜检查,同时使用聚合酶链反应(PCR)分析DBS中的疟原虫种类。采用多变量逻辑回归分析背景因素与疟疾之间的关联。
总体而言,共调查了873名六岁以下儿童。通过PCR检测的疟原虫总体流行率为54.3%(95%置信区间51 - 57.6%)。在所有疟原虫分离株中,88%为恶性疟原虫,10.6%为混合感染,1.4%为非恶性疟原虫单一感染。在混合感染中,大多数是恶性疟原虫和三日疟原虫的组合(占所有混合感染的6.5%)。两岁及以上(2 - 5岁)儿童混合疟疾感染的风险是两岁以下儿童的三倍(调整后比值比2.8,置信区间1.31 - 5.69)。
该人群中疟原虫混合感染的高流行率强调了对当前疟疾RDT诊断方法进行审查的必要性。与两岁至五岁的大龄儿童相比,两岁以下儿童混合感染的发生率较低,这可能是由于该年龄组存在母体被动免疫等保护因素。