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 E. Mitchell,Andrei‐Emil Constantinescu,David A. 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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