自身免疫性肝炎
孟德尔随机化
全基因组关联研究
医学
优势比
原发性硬化性胆管炎
内科学
自身免疫性疾病
免疫学
遗传关联
红斑狼疮
胃肠病学
肝炎
单核苷酸多态性
疾病
基因型
遗传变异
遗传学
生物
抗体
基因
作者
Wei Huang,Tianyu Jin,Wei Zheng,Qiaoqiao Yin,Qiqi Yan,Hongying Pan,Chengan Xu
标识
DOI:10.1016/j.jaut.2024.103188
摘要
Previous studies on the relationship between systemic lupus erythematosus (SLE) and autoimmune liver diseases (AILDs) are inconclusive. Therefore, we employed Mendelian randomization (MR) to explore the causal associations between SLE and AILDs. A two-sample MR analysis was performed using summary-level statistics sourced from genome-wide association study (GWAS) datasets. Inverse-variance weighting (IVW), MR‒Egger, and weighted median (WM) were further supported by several sensitivity analyses. We detected causal genetic associations between SLE and primary biliary cholangitis (PBC) (odds ratio (OR) = 1.31, 95% CI = 1.15–1.51, P < 0.01; adjusted OR = 1.63, 95% CI = 1.39–1.90, P < 0.01) and between SLE and primary sclerosing cholangitis (PSC) (OR = 1.09, 95% CI = 1.01–1.08, P = 0.03; adjusted OR = 1.10, 95% CI = 1.00–1.21, P = 0.04). No causal association was found between SLE and autoimmune hepatitis. We are the first to use MR analysis to explore the causal relationships between SLE and various AILDs, revealing an increased risk of PBC and PSC in individuals with SLE.
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