The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

  • Nilufer Rahmioglu
  • Sally Mortlock
  • Marzieh Ghiasi
  • Peter L. Møller
  • Lilja Stefansdottir
  • Geneviève Galarneau
  • Constance Turman
  • Rebecca Danning
  • Matthew H. Law
  • Yadav Sapkota
  • Paraskevi Christofidou
  • Sini Skarp
  • Ayush Giri
  • Banasik, Karina
  • Michal Krassowski
  • Maarja Lepamets
  • Błażej Marciniak
  • Margit Nõukas
  • Danielle Perro
  • Eeva Sliz
  • Marta Sobalska-Kwapis
  • Gudmar Thorleifsson
  • Nura F. Topbas-Selcuki
  • Allison Vitonis
  • Westergaard, David
  • Ragnheidur Arnadottir
  • Burgdorf, Kristoffer Sølvsten
  • Archie Campbell
  • Cecilia S.K. Cheuk
  • Caterina Clementi
  • James Cook
  • Immaculata De Vivo
  • Amy DiVasta
  • O. Dorien
  • Jacqueline F. Donoghue
  • Todd Edwards
  • Pierre Fontanillas
  • Jenny N. Fung
  • Reynir T. Geirsson
  • Jane E. Girling
  • Paivi Harkki
  • Holly R. Harris
  • Martin Healey
  • Oskari Heikinheimo
  • Sarah Holdsworth-Carson
  • Isabel C. Hostettler
  • Henry Houlden
  • Sahar Houshdaran
  • Andrew J. Schork
  • Mette Nyegaard
  • DBDS Genomic Consortium
  • FinnGen Study
  • FinnGen Endometriosis Taskforce
  • Celmatix Research Team
  • 23andMe Research Team

Endometriosis is a common condition associated with debilitating pelvic pain and infertility. A genome-wide association study meta-analysis, including 60,674 cases and 701,926 controls of European and East Asian descent, identified 42 genome-wide significant loci comprising 49 distinct association signals. Effect sizes were largest for stage 3/4 disease, driven by ovarian endometriosis. Identified signals explained up to 5.01% of disease variance and regulated expression or methylation of genes in endometrium and blood, many of which were associated with pain perception/maintenance (SRP14/BMF, GDAP1, MLLT10, BSN and NGF). We observed significant genetic correlations between endometriosis and 11 pain conditions, including migraine, back and multisite chronic pain (MCP), as well as inflammatory conditions, including asthma and osteoarthritis. Multitrait genetic analyses identified substantial sharing of variants associated with endometriosis and MCP/migraine. Targeted investigations of genetically regulated mechanisms shared between endometriosis and other pain conditions are needed to aid the development of new treatments and facilitate early symptomatic intervention.

OriginalsprogEngelsk
TidsskriftNature Genetics
Vol/bind55
Udgave nummer3
Sider (fra-til)423-436
Antal sider14
ISSN1061-4036
DOI
StatusUdgivet - 2023

Bibliografisk note

Publisher Copyright:
© 2023. The Author(s), under exclusive licence to Springer Nature America, Inc.

ID: 341018992