Genetic analyses identify brain imaging-derived phenotypes associated with the risk of intracerebral hemorrhage

孟德尔随机化 内囊 全基因组关联研究 脑出血 医学 遗传关联 观察研究 生命银行 磁共振成像 单核苷酸多态性 内科学 遗传变异 生物信息学 遗传学 放射科 白质 生物 基因型 基因 蛛网膜下腔出血
作者
Yi Liu,Yiming Jia,Hongyan Sun,Lulu Sun,Yinan Wang,Qingyun Xu,Yu He,Xinyue Chang,Daoxia Guo,Mengyao Shi,Guo‐Chong Chen,Jin Zheng,Zhengbao Zhu
出处
期刊:Cerebral Cortex [Oxford University Press]
标识
DOI:10.1093/cercor/bhad518
摘要

Abstract Previous observational studies have reported associations between brain imaging-derived phenotypes (IDPs) and intracerebral hemorrhage (ICH), but the causality between them remains uncertain. We aimed to investigate the potential causal relationship between IDPs and ICH by a two-sample Mendelian randomization (MR) study. We selected genetic instruments for 363 IDPs from a genome-wide association study (GWASs) based on the UK Biobank (n = 33,224). Summary-level data on ICH was derived from a European-descent GWAS with 1,545 cases and 1,481 controls. Inverse variance weighted MR method was applied in the main analysis to investigate the associations between IDPs and ICH. Reverse MR analyses were performed for significant IDPs to examine the reverse causation for the identified associations. Among the 363 IDPs, isotropic or free water volume fraction (ISOVF) in the anterior limb of the left internal capsule was identified to be associated with the risk of ICH (OR per 1-SD increase, 4.62 [95% CI, 2.18–9.81], P = 6.63 × 10−5). In addition, the reverse MR analysis indicated that ICH had no effect on ISOVF in the anterior limb of the left internal capsule (beta, 0.010 [95% CI, −0.010-0.030], P = 0.33). MR-Egger regression analysis showed no directional pleiotropy for the association between ISOVF and ICH, and sensitivity analyses with different MR models further confirmed these findings. ISOVF in the anterior limb of the left internal capsule might be a potential causal mediator of ICH, which may provide predictive guidance for the prevention of ICH. Further studies are warranted to replicate our findings and clarify the underlying mechanisms.
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