학술논문

The genetic basis of endometriosis and comorbidity with other pain and inflammatory conditions
Document Type
Original Paper
Author
Rahmioglu, NiluferMortlock, SallyGhiasi, MarziehMøller, Peter L.Stefansdottir, LiljaGalarneau, GenevièveTurman, ConstanceDanning, RebeccaLaw, Matthew H.Sapkota, YadavChristofidou, ParaskeviSkarp, SiniGiri, AyushBanasik, KarinaKrassowski, MichalLepamets, MaarjaMarciniak, BłażejNõukas, MargitPerro, DanielleSliz, EevaSobalska-Kwapis, MartaThorleifsson, GudmarTopbas-Selcuki, Nura F.Vitonis, AllisonWestergaard, DavidArnadottir, RagnheidurBurgdorf, Kristoffer S.Campbell, ArchieCheuk, Cecilia S. K.Clementi, CaterinaCook, JamesDe Vivo, ImmaculataDiVasta, AmyDorien, O.Donoghue, Jacqueline F.Edwards, ToddFontanillas, PierreFung, Jenny N.Geirsson, Reynir T.Girling, Jane E.Harkki, PaiviHarris, Holly R.Healey, MartinHeikinheimo, OskariHoldsworth-Carson, SarahHostettler, Isabel C.Houlden, HenryHoushdaran, SaharIrwin, Juan C.Jarvelin, Marjo-RiittaKamatani, YoichiroKennedy, Stephen H.Kepka, EwaKettunen, JohannesKubo, MichiakiKulig, BartoszKurra, VenlaLaivuori, HanneleLaufer, Marc R.Lindgren, Cecilia M.MacGregor, StuartMangino, MassimoMartin, Nicholas G.Matalliotaki, CharoulaMatalliotakis, MichailMurray, Alison D.Ndungu, AnneNezhat, CamranOlsen, Catherine M.Opoku-Anane, JessicaPadmanabhan, SandoshParanjpe, ManishPeters, MairePolak, GrzegorzPorteous, David J.Rabban, JosephRexrode, Kathyrn M.Romanowicz, HannaSaare, MerliSaavalainen, LiisuSchork, Andrew J.Sen, SushmitaShafrir, Amy L.Siewierska-Górska, AnnaSłomka, MarcinSmith, Blair H.Smolarz, BeataSzaflik, TomaszSzyłło, KrzysztofTakahashi, AtsushiTerry, Kathryn L.Tomassetti, CarlaTreloar, Susan A.Vanhie, ArneVincent, KatyVo, Kim C.Werring, David J.Zeggini, EleftheriaZervou, Maria I.Adachi, SosukeBuring, Julie E.Ridker, Paul M.D’Hooghe, ThomasGoulielmos, George N.Hapangama, Dharani K.Hayward, CarolineHorne, Andrew W.Low, Siew-KeeMartikainen, HannuChasman, Daniel I.Rogers, Peter A. W.Saunders, Philippa T.Sirota, MarinaSpector, TimStrapagiel, DominikTung, Joyce Y.Whiteman, David C.Giudice, Linda C.Velez-Edwards, Digna R.Uimari, OutiKraft, PeterSalumets, AndresNyholt, Dale R.Mägi, ReedikStefansson, KariBecker, Christian M.Yurttas-Beim, PirayeSteinthorsdottir, ValgerdurNyegaard, MetteMissmer, Stacey A.Montgomery, Grant W.Morris, Andrew P.Zondervan, Krina T.
Source
Nature Genetics. 55(3):423-436
Subject
Language
English
ISSN
1061-4036
1546-1718
Abstract
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.
Meta-analyses of genome-wide association studies for endometriosis identify 49 distinct association signals. Fine-mapping of causal variants explores functional effects across various tissues. Genetic correlations between endometriosis and other pain conditions are also highlighted.