Evidence of shared genetic factors in the etiology of gastrointestinal disorders and endometriosis and clinical implications for disease management

被引:12
作者
Yang, Fei [1 ]
Wu, Yeda [1 ]
Hockey, Richard [2 ]
Doust, Jenny [2 ]
Mishra, Gita D. [2 ]
Montgomery, Grant W. [1 ]
Mortlock, Sally [1 ]
机构
[1] Univ Queensland, Inst Mol Biosci, Brisbane, Qld 4072, Australia
[2] Univ Queensland, NHMRC Ctr Res Excellence Women & Noncommunicable, Sch Publ Hlth, Herston Rd, Herston, Qld, Australia
基金
英国医学研究理事会;
关键词
IRRITABLE-BOWEL-SYNDROME; GASTROESOPHAGEAL-REFLUX DISEASE; MENDELIAN RANDOMIZATION; EXPRESSION; EPIDEMIOLOGY; PATHOGENESIS; METAANALYSIS; ASSOCIATION; PREVALENCE; DIAGNOSIS;
D O I
10.1016/j.xcrm.2023.101250
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
In clinical practice, the co-existence of endometriosis and gastrointestinal symptoms is often observed. Using large-scale datasets, we report a genetic correlation between endometriosis and irritable bowel syndrome (IBS), peptic ulcer disease (PUD), gastro-esophageal reflux disease (GORD), and a combined GORD/ PUD medicated (GPM) phenotype. Mendelian randomization analyses support a causal relationship between genetic predisposition to endometriosis and IBS and GPM. Identification of shared risk loci highlights biological pathways that may contribute to the pathogenesis of both diseases, including estrogen regulation and inflammation, and potential therapeutic drug targets (CCKBR; PDE4B). Higher use of IBS, GORD, and PUD medications in women with endometriosis and higher use of hormone therapies in women with IBS, GORD, and PUD, support the co-occurrence of these conditions and highlight the potential for drug repositioning and drug contraindications. Our results provide evidence of shared disease etiology and have important clinical implications for diagnostic and treatment decisions for both diseases.
引用
收藏
页数:20
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