孟德尔随机化
疟疾
单核苷酸多态性
优势比
SNP公司
置信区间
严重疟疾
免疫学
生物
医学
内科学
恶性疟原虫
生物信息学
基因型
遗传学
基因
遗传变异
作者
Fergus Hamilton,Ruth Mitchell,Andrei Constantinescu,David Hughes,Aubrey J. Cunnington,Peter Ghazal,Nicholas J. Timpson
标识
DOI:10.1016/j.ijid.2023.02.008
摘要
Severe malaria remains a deadly disease for many young children in low- and middle-income countries. Levels of interleukin (IL)-6 have been shown to identify cases of severe malaria and associate with severity, but it is unknown if this association is causal.A single nucleotide polymorphism (SNP; rs2228145) in the IL-6 receptor was chosen as a genetic variant that is known to alter IL-6 signaling. We tested this, then took this forward as an instrument to perform Mendelian randomization (MR) in MalariaGEN, a large cohort study of patients with severe malaria at 11 worldwide sites.In MR analyses using rs2228145, we did not identify an effect of decreased IL-6 signaling on severe malaria (odds ratio 1.14, 95% confidence interval 0.56-2.34, P = 0.713). The estimates of the association with any severe malaria subphenotype were similarly null, although with some imprecision. Further analyses using other MR approaches had similar results.These analyses do not support a causal role for IL-6 signaling in the development of severe malaria. This result suggests IL-6 may not be causal for severe outcomes in malaria, and that therapeutic manipulation of IL-6 is unlikely to be a suitable treatment for severe malaria.
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