Effect of transmission intensity on hotspots and micro-epidemiology of malaria in sub-Saharan Africa

被引:26
|
作者
Mogeni, Polycarp [1 ]
Omedo, Irene [1 ]
Nyundo, Christopher [1 ]
Kamau, Alice [1 ]
Noor, Abdisalan [2 ,3 ]
Bejon, Philip [1 ,2 ]
机构
[1] CGMR Coast, KEMRI Wellcome Trust Res Programme, Kilifi, Kenya
[2] Univ Oxford, Nuffield Dept Clin Med, Ctr Trop Med & Global Hlth, CCVTM, Oxford, England
[3] Kenya Govt Med Res Ctr, Spatial Hlth Metr Grp, Wellcome Trust Res Programme, Nairobi, Kenya
来源
BMC MEDICINE | 2017年 / 15卷
基金
英国惠康基金; 英国医学研究理事会;
关键词
Malaria; Micro-epidemiology; Hotspots; Sub-Saharan Africa; Stability of hotspots; D function; Moran's I; Symptomatic malaria; Asymptomatic parasitaemia; Age; Meta-analysis; PLASMODIUM-FALCIPARUM; WESTERN KENYA; FRACTIONAL POLYNOMIALS; CLINICAL MALARIA; KILIFI DISTRICT; RISK-FACTORS; INFECTION; CHILDREN; AREA; INTERVENTION;
D O I
10.1186/s12916-017-0887-4
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Malaria transmission intensity is heterogeneous, complicating the implementation of malaria control interventions. We provide a description of the spatial micro-epidemiology of symptomatic malaria and asymptomatic parasitaemia in multiple sites. Methods: We assembled data from 19 studies conducted between 1996 and 2015 in seven countries of sub-Saharan Africa with homestead-level geospatial data. Data from each site were used to quantify spatial autocorrelation and examine the temporal stability of hotspots. Parameters from these analyses were examined to identify trends over varying transmission intensity. Results: Significant hotspots of malaria transmission were observed in most years and sites. The risk ratios of malaria within hotspots were highest at low malaria positive fractions (MPFs) and decreased with increasing MPF (p < 0.001). However, statistical significance of hotspots was lowest at extremely low and extremely high MPFs, with a peak in statistical significance at an MPF of similar to 0.3. In four sites with longitudinal data we noted temporal instability and variable negative correlations between MPF and average age of symptomatic malaria across all sites, suggesting varying degrees of temporal stability. Conclusions: We observed geographical micro-variation in malaria transmission at sites with a variety of transmission intensities across sub-Saharan Africa. Hotspots are marked at lower transmission intensity, but it becomes difficult to show statistical significance when cases are sparse at very low transmission intensity. Given the predictability with which hotspots occur as transmission intensity falls, malaria control programmes should have a low threshold for responding to apparent clustering of cases.
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页数:11
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