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Characterisation of the opposing effects of G6PD deficiency on cerebral malaria and severe malarial anaemia

机译:G6PD缺乏症对脑疟疾和严重疟疾贫血的不利影响的特征

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Glucose-6-phosphate dehydrogenase (G6PD) deficiency is believed to confer protection against Plasmodium falciparum malaria, but the precise nature of the protective effect has proved difficult to define as G6PD deficiency has multiple allelic variants with different effects in males and females, and it has heterogeneous effects on the clinical outcome of P. falciparum infection. Here we report an analysis of multiple allelic forms of G6PD deficiency in a large multi-centre case-control study of severe malaria, using the WHO classification of G6PD mutations to estimate each individual’s level of enzyme activity from their genotype. Aggregated across all genotypes, we find that increasing levels of G6PD deficiency are associated with decreasing risk of cerebral malaria, but with increased risk of severe malarial anaemia. Models of balancing selection based on these findings indicate that an evolutionary trade-off between different clinical outcomes of P. falciparum infection could have been a major cause of the high levels of G6PD polymorphism seen in human populations.
机译:6-磷酸葡萄糖脱氢酶(G6PD)缺乏被认为可以抵抗恶性疟原虫疟疾,但是由于G6PD缺乏在男性和女性中具有多种影响不同的等位基因变异,因此已证明难以定义保护作用的确切性质。对恶性疟原虫感染的临床结果具有异质性影响。在此,我们报告了一项大型多中心严重疟疾病例对照研究中对G6PD缺乏症的多种等位基因形式的分析,该研究使用WHO对G6PD突变的分类来评估每个个体的基因型酶活性水平。综合所有基因型,我们发现G6PD缺乏水平的升高与脑疟疾的风险降低有关,但与严重疟疾贫血的风险升高有关。基于这些发现的平衡选择模型表明,恶性疟原虫感染不同临床结果之间的进化权衡可能是导致人类人群中高水平的G6PD多态性的主要原因。

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