Mackinnon Margaret J, Mwangi Tabitha W, Snow Robert W, Marsh Kevin, Williams Thomas N
School of Biological Sciences, University of Edinburgh, Edinburgh, United Kingdom.
PLoS Med. 2005 Dec;2(12):e340. doi: 10.1371/journal.pmed.0020340. Epub 2005 Nov 8.
While many individual genes have been identified that confer protection against malaria, the overall impact of host genetics on malarial risk remains unknown.
We have used pedigree-based genetic variance component analysis to determine the relative contributions of genetic and other factors to the variability in incidence of malaria and other infectious diseases in two cohorts of children living on the coast of Kenya. In the first, we monitored the incidence of mild clinical malaria and other febrile diseases through active surveillance of 640 children 10 y old or younger, living in 77 different households for an average of 2.7 y. In the second, we recorded hospital admissions with malaria and other infectious diseases in a birth cohort of 2,914 children for an average of 4.1 y. Mean annual incidence rates for mild and hospital-admitted malaria were 1.6 and 0.054 episodes per person per year, respectively. Twenty-four percent and 25% of the total variation in these outcomes was explained by additively acting host genes, and household explained a further 29% and 14%, respectively. The haemoglobin S gene explained only 2% of the total variation. For nonmalarial infections, additive genetics explained 39% and 13% of the variability in fevers and hospital-admitted infections, while household explained a further 9% and 30%, respectively.
Genetic and unidentified household factors each accounted for around one quarter of the total variability in malaria incidence in our study population. The genetic effect was well beyond that explained by the anticipated effects of the haemoglobinopathies alone, suggesting the existence of many protective genes, each individually resulting in small population effects. While studying these genes may well provide insights into pathogenesis and resistance in human malaria, identifying and tackling the household effects must be the more efficient route to reducing the burden of disease in malaria-endemic areas.
虽然已经鉴定出许多可提供疟疾防护的个体基因,但宿主遗传学对疟疾风险的总体影响仍不清楚。
我们采用基于家系的遗传方差成分分析,以确定遗传因素和其他因素对肯尼亚沿海两个儿童队列中疟疾及其他传染病发病率变异性的相对贡献。在第一个队列中,我们通过对640名10岁及以下儿童进行主动监测,这些儿童居住在77个不同家庭中,平均监测时间为2.7年,以监测轻度临床疟疾和其他发热性疾病的发病率。在第二个队列中,我们记录了2914名儿童出生队列中因疟疾和其他传染病的住院情况,平均记录时间为4.1年。轻度和住院疟疾的年平均发病率分别为每人每年1.6次和0.054次。这些结果中总变异的24%和25%分别由具有累加作用的宿主基因解释,家庭因素分别进一步解释了29%和14%。血红蛋白S基因仅解释了总变异的2%。对于非疟疾感染,累加遗传学分别解释了发热和住院感染变异性的39%和13%,而家庭因素分别进一步解释了9%和30%。
在我们的研究人群中,遗传因素和未明确的家庭因素各占疟疾发病率总变异性的约四分之一。遗传效应远超过仅由预期的血红蛋白病效应所解释的范围,这表明存在许多保护性基因,每个基因单独导致的群体效应较小。虽然研究这些基因可能会为人类疟疾的发病机制和抗性提供见解,但识别和解决家庭因素的影响必定是减轻疟疾流行地区疾病负担的更有效途径。