Mahidol Oxford Tropical Medicine Research Unit (MORU), Faculty of Tropical Medicine, Mahidol University, Bangkok, Thailand.
Nangarhar Medical Faculty, Jalalabad, Afghanistan.
Elife. 2021 Feb 5;10:e62448. doi: 10.7554/eLife.62448.
X-linked glucose-6-phosphate dehydrogenase (G6PD) deficiency is the most common human enzymopathy. The severe Mediterranean variant (G6PD Med) found across Europe and Asia is thought to confer protection against malaria, but its effect is unclear. We fitted a Bayesian statistical model to observed G6PD Med allele frequencies in 999 Pashtun patients presenting with acute malaria and 1408 population controls. G6PD Med was associated with reductions in symptomatic malaria incidence of 76% (95% credible interval [CI], 58-88) in hemizygous males and homozygous females combined and 55% (95% CI, 38-68) in heterozygous females. Unless there is very large population stratification within the Pashtun (confounding these results), the G6PD Med genotype confers a very large and gene-dose proportional protective effect against acute vivax malaria. The proportion of patients with vivax malaria at risk of haemolysis following 8-aminoquinoline radical cure is substantially overestimated by studies measuring G6PD deficiency prevalence in healthy subjects.
X 连锁葡萄糖-6-磷酸脱氢酶(G6PD)缺乏症是最常见的人类酶病。在整个欧洲和亚洲发现的严重地中海变异型(G6PD Med)被认为对疟疾有保护作用,但作用尚不清楚。我们对 999 名患有急性疟疾的帕坦族患者和 1408 名人群对照中观察到的 G6PD Med 等位基因频率进行了贝叶斯统计模型拟合。G6PD Med 与杂合子男性和纯合子女性合并的有症状疟疾发病率降低 76%(95%可信区间,58-88)相关,杂合子女性的发病率降低 55%(95%可信区间,38-68)。除非帕坦族内部存在非常大的人群分层(混淆这些结果),否则 G6PD Med 基因型对急性间日疟具有非常大且与基因剂量成比例的保护作用。用健康受试者中 G6PD 缺乏症患病率测量方法来研究 8-氨基喹啉自由基治愈后发生溶血性贫血风险的间日疟患者比例,大大高估了。