A genome-wide association analysis reveals new pathogenic pathways in gout

  • Major, Tanya J.
  • Takei, Riku
  • Matsuo, Hirotaka
  • Leask, Megan P.
  • Sumpter, Nicholas A.
  • ... Lee, Chaeyoung
  • 외 92명
Citations

WEB OF SCIENCE

62
Citations

SCOPUS

58

초록

Gout is a chronic disease that is caused by an innate immune response to deposited monosodium urate crystals in the setting of hyperuricemia. Here, we provide insights into the molecular mechanism of the poorly understood inflammatory component of gout from a genome-wide association study (GWAS) of 2.6 million people, including 120,295 people with prevalent gout. We detected 377 loci and 410 genetically independent signals (149 previously unreported loci in urate and gout). An additional 65 loci with signals in urate (from a GWAS of 630,117 individuals) but not gout were identified. A prioritization scheme identified candidate genes in the inflammatory process of gout, including genes involved in epigenetic remodeling, cell osmolarity and regulation of NOD-like receptor protein 3 (NLRP3) inflammasome activity. Mendelian randomization analysis provided evidence for a causal role of clonal hematopoiesis of indeterminate potential in gout. Our study identifies candidate genes and molecular processes in the inflammatory pathogenesis of gout suitable for follow-up studies.

키워드

GENETIC ARCHITECTURECLONAL HEMATOPOIESISNLRP3 INFLAMMASOMEVARIANTCOMMONMETAANALYSISRISKIDENTIFICATIONHYPERURICEMIADEHYDROGENASE
제목
A genome-wide association analysis reveals new pathogenic pathways in gout
저자
Major, Tanya J.Takei, RikuMatsuo, HirotakaLeask, Megan P.Sumpter, Nicholas A.Topless, Ruth K.Shirai, YuyaWang, WeiCadzow, Murray J.Phipps-Green, Amanda J.Li, ZhiqiangJi, AichangMerriman, Marilyn E.Morice, EmilyKelley, Eric E.Wei, Wen-HuaMcCormick, Sally P. A.Bixley, Matthew J.Reynolds, Richard J.Saag, Kenneth G.Fadason, TayazaGolovina, EvgeniaO'Sullivan, Justin M.Stamp, Lisa K.Dalbeth, NicolaAbhishek, AbhishekDoherty, MichaelRoddy, EdwardJacobsson, Lennart T. H.Kapetanovic, Meliha C.Melander, OlleAndres, MarianoPerez-Ruiz, FernandoTorres, Rosa J.Radstake, TimothyJansen, Timothy L.Janssen, MatthijsJoosten, Leo A. B.Liu, RuiqiGaal, Orsolya I.Crisan, Tania O.Rednic, SimonaKurreeman, FinaHuizinga, Tom W. J.Toes, ReneLiote, FredericRichette, PascalBardin, ThomasEa, Hang KorngPascart, TristanMcCarthy, Geraldine M.Helbert, LauraStiburkova, BlankaTausche, Anne-K.Uhlig, TillVitart, VeroniqueBoutin, Thibaud S.Hayward, CarolineRiches, Philip L.Ralston, Stuart H.Campbell, ArchieMacDonald, Thomas M.Nakayama, AkiyoshiTakada, TappeiNakatochi, MasahiroShimizu, SeikoKawamura, YusukeToyoda, YuNakaoka, HirofumiYamamoto, KenMatsuo, KeitaroShinomiya, NariyoshiIchida, KimiyoshiLee, ChaeyoungBradbury, Linda A.Brown, Matthew A.Robinson, Philip C.Buchanan, Russell R. C.Hill, Catherine L.Lester, SusanSmith, Malcolm D.Rischmueller, MaureenChoi, Hyon K.Stahl, Eli A.Miner, Jeff N.Solomon, Daniel H.Cui, JingGiacomini, Kathleen M.Brackman, Deanna J.Jorgenson, Eric M.Liu, HongboSusztak, KatalinShringarpure, SuyashSo, AlexanderOkada, YukinoriLi, ChangguiShi, YongyongMerriman, Tony R.
DOI
10.1038/s41588-024-01921-5
발행일
2024-11
유형
Article
저널명
Nature Genetics
56
11
페이지
2392 ~ 2406