Mendelian randomization analysis reveals causality of inflammatory bowel disease on risks of Henoch-Schönlein purpura and immune thrombocytopenia

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 生物 基因 遗传变异
作者
Haojia Li,Qing Xin,Liping Hong,Yuqi Hu,Lie Lin,Mingkai Guo,Huixin Jiang,Chengcheng He,Shanping Wang,Mingsong Li
出处
期刊:Digestive and Liver Disease [Elsevier BV]
卷期号:56 (1): 92-97 被引量:1
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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