Department of Cardiovascular Medicine, The Second Affiliated Hospital of Nanchang University, Nanchang, 330006, China.
Sci Rep. 2023 Nov 1;13(1):18807. doi: 10.1038/s41598-023-46117-9.
Gallstone disease (GSD) is thought to be associated with the risk of coronary heart disease (CHD) or acute myocardial infarction (AMI), which may be due to abnormal cholesterol metabolism. We used multiple Mendelian randomization (MR) methods based on publicly available genome-wide association study data to assess whether this association is genetically causal and to search for loci driving causality. Pooled data for GSD were obtained from FinnGen Biobank and Biobank Japan, while CHD and AMI were obtained as pooled data from the CARDIoGRAMplusC4D consortium. In this MR study, we found a significant negative causal effect of genetic susceptibility to GSD on AMI in the Finnish population, but no causal effect was found on CHD. This causal effect was not confounded by reverse causality and the same findings were obtained in the Japanese population. Furthermore, the negative causal effect of GSD on AMI risk may be driven by the rs4245791-regulated ABCG5/8 protein. In conclusion, the results of this MR study support a negative causal effect of GSD on AMI and suggest that rs4245791 is the causal driver locus of this effect, which provides new ideas and evidence for the prevention and etiologic study of AMI in patients with GSD.
胆石病(GSD)被认为与冠心病(CHD)或急性心肌梗死(AMI)的风险相关,这可能是由于胆固醇代谢异常所致。我们使用了基于公开的全基因组关联研究数据的多种孟德尔随机化(MR)方法,以评估这种关联是否具有遗传因果关系,并寻找驱动因果关系的基因座。GSD 的汇总数据来自芬兰基因生物银行和日本生物银行,而 CHD 和 AMI 则作为来自 CARDIoGRAMplusC4D 联盟的汇总数据获得。在这项 MR 研究中,我们发现芬兰人群中 GSD 的遗传易感性对 AMI 有显著的负向因果效应,但对 CHD 没有因果效应。这种因果效应不受反向因果关系的影响,在日本人群中也得到了相同的发现。此外,GSD 对 AMI 风险的负向因果效应可能是由 rs4245791 调节的 ABCG5/8 蛋白驱动的。总之,这项 MR 研究的结果支持 GSD 对 AMI 的负向因果效应,并表明 rs4245791 是该效应的因果驱动基因座,为 GSD 患者的 AMI 预防和病因研究提供了新的思路和证据。