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

Fei Yang, Yeda Wu, Richard Hockey, The International Endometriosis Genetics Consortium, Jenny Doust, Gita D. Mishra, Grant W. Montgomery, Sally Mortlock*

*Corresponding author for this work

Research output: Contribution to journalArticlepeer-review

12 Citations (Scopus)
8 Downloads (Pure)

Abstract

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.
Original languageEnglish
Article number101250
Pages (from-to)1-14, e1-e5
Number of pages20
JournalCell Reports Medicine
Volume4
Issue number11
DOIs
Publication statusPublished - 21 Nov 2023
Externally publishedYes

Bibliographical note

Copyright the Author(s) 2023. Version archived for private and non-commercial use with the permission of the author/s and according to publisher conditions. For further rights please contact the publisher.

Keywords

  • clinical implications
  • co-occurrence
  • drug contraindications
  • drug repositioning
  • endometriosis
  • gastrointestinal disorders
  • irritable bowel syndrome
  • Mendelian randomization
  • prescription drug usage
  • shared genetic components

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