医学
孟德尔随机化
炎症性肠病
优势比
溃疡性结肠炎
免疫学
内科学
疾病
置信区间
基因型
遗传学
遗传变异
基因
生物
作者
Haojia Li,Qing Xin,Liping Hong,Yuqi Hu,Lie Lin,Mingkai Guo,Huixin Jiang,Chengcheng He,Shanping Wang,Mingsong Li
标识
DOI:10.1016/j.dld.2023.08.044
摘要
Abstract
Background
Emerging clinical evidence has been discovered associating Inflammatory bowel disease (IBD) with Henoch-Schönlein purpura (HSP) and immune thrombocytopenia (ITP). However, it is unclear whether a cause-effect relationship exists between them. We aimed to examine the casual effect of IBD on the risk of HSP and ITP. Methods
Based on summary statistics from International IBD Genetics (IIBDG) Consortium and FinnGen study, a two-sample Mendelian randomization study was carried out to determine whether IBD including ulcerative colitis (UC) and Crohn's disease (CD) is causally related to HSP, ITP or secondary thrombocytopenia. To support the results, a variety of sensitivity analyses were performed. Results
Significant causal relationships between IBD and HSP (odds ratios = 1.20, 95% confidence interval: 1.07–1.36, adjusted P = 0.006) and ITP (odds ratios=1.22, 95% confidence interval: 1.08–1.38, adjusted P = 0.006) were found. Both genetically predicted UC and CD were positively related with ITP, while CD alone may be responsible for the higher risk of HSP. Besides, no significant association was observed between IBD and secondary thrombocytopenia. Conclusions
The results of this Mendelian randomization study supported the causal association of IBD with HSP and ITP. Taken together, our findings may present implications for management of IBD.
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