학술논문

Multi-trait analysis characterizes the genetics of thyroid function and identifies causal associations with clinical implications
Document Type
article
Author
Rosalie B. T. M. SterenborgInga SteinbrennerYong LiMelissa N. BujnisTatsuhiko NaitoEirini MarouliTessel E. GaleslootOladapo BabajideLaura AndreasenArne AstrupBjørn Olav ÅsvoldStefania BandinelliMarian BeekmanJohn P. BeilbyJette Bork-JensenThibaud BoutinJennifer A. BrodySuzanne J. BrownBen BrumptonPurdey J. CampbellAnne R. CappolaGraziano CeresiniLayal ChakerDaniel I. ChasmanMaria Pina ConcasRodrigo Coutinho de AlmeidaSimone M. CrossFrancesco CuccaIan J. DearyAlisa Devedzic KjaergaardJustin B. Echouffo TcheuguiChristina EllervikJohan G. ErikssonLuigi FerrucciJan FreudenbergGHS DiscovEHRRegeneron Genetics CenterChristian FuchsbergerChristian GiegerFranco GiulianiniMartin GögeleSarah E. GrahamNiels GrarupIvana GunjačaTorben HansenBarbara N. HardingSarah E. HarrisStig HaunsøCaroline HaywardJennie HuiTill IttermannJ. Wouter JukemaEero KajantieJørgen K. KantersLine L. KårhusLambertus A. L. M. KiemeneyMargreet KloppenburgBrigitte KühnelJari LahtiClaudia LangenbergBruno LapauwGraham LeeseShuo LiDavid C. M. LiewaldAllan LinnebergJesus V. T. LomincharJian’an LuanNicholas G. MartinAntonela MatanaMarcel E. MeimaThomas MeitingerIngrid MeulenbeltBraxton D. MitchellLine T. MøllehaveSamia MoraSilvia NaitzaMatthias NauckRomana T. Netea-MaierRaymond NoordamCasia NursyifaYukinori OkadaStefano OnanoAreti PapadopoulouColin N. A. PalmerCristian PattaroOluf PedersenAnnette PetersMaik PietznerOzren PolašekPeter P. PramstallerBruce M. PsatyAnte PundaDebashree RayPaul RedmondJ. Brent RichardsPaul M. RidkerTom C. RussKathleen A. RyanMorten Salling OlesenUlla T. SchultheissElizabeth SelvinMoneeza K. SiddiquiCarlo SidoreP. Eline SlagboomThorkild I. A. SørensenEnrique Soto-PedreTim D. SpectorBeatrice SpedicatiSundararajan SrinivasanJohn M. StarrDavid J. StottToshiko TanakaVesela TorlakStella TrompetJohanna TuhkanenAndré G. UitterlindenErik B. van den AkkerTibbert van den EyndeMelanie M. van der KlauwDiana van HeemstCharlotte VerrokenW. Edward VisserDina VojinovicHenry VölzkeMelanie WaldenbergerJohn P. WalshNicholas J. WarehamStefan WeissCristen J. WillerScott G. WilsonBruce H. R. WolffenbuttelHanneke J. C. M. WoutersMargaret J. WrightQiong YangTatijana ZemunikWei ZhouGu ZhuSebastian ZöllnerJohannes W. A. SmitRobin P. PeetersAnna KöttgenAlexander TeumerMarco Medici
Source
Nature Communications, Vol 15, Iss 1, Pp 1-18 (2024)
Subject
Science
Language
English
ISSN
2041-1723
Abstract
Abstract To date only a fraction of the genetic footprint of thyroid function has been clarified. We report a genome-wide association study meta-analysis of thyroid function in up to 271,040 individuals of European ancestry, including reference range thyrotropin (TSH), free thyroxine (FT4), free and total triiodothyronine (T3), proxies for metabolism (T3/FT4 ratio) as well as dichotomized high and low TSH levels. We revealed 259 independent significant associations for TSH (61% novel), 85 for FT4 (67% novel), and 62 novel signals for the T3 related traits. The loci explained 14.1%, 6.0%, 9.5% and 1.1% of the total variation in TSH, FT4, total T3 and free T3 concentrations, respectively. Genetic correlations indicate that TSH associated loci reflect the thyroid function determined by free T3, whereas the FT4 associations represent the thyroid hormone metabolism. Polygenic risk score and Mendelian randomization analyses showed the effects of genetically determined variation in thyroid function on various clinical outcomes, including cardiovascular risk factors and diseases, autoimmune diseases, and cancer. In conclusion, our results improve the understanding of thyroid hormone physiology and highlight the pleiotropic effects of thyroid function on various diseases.