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Lahrouchi, N.* ; Tadros, R.* ; Mizusawa, Y.* ; Postema, P.G.* ; Beekman, L.* ; Walsh, R.* ; Hasegawa, K.* ; Barc, J.* ; Ernsting, M.* ; Turkowski, K.L.* ; Mazzanti, A.* ; Beckmann, B.M.* ; Shimamoto, K.* ; Diamant, U.B.* ; Wijeyeratne, Y.D.* ; Kucho, Y.* ; Robyns, T.* ; Ishikawa, T.* ; Arbelo, E.* ; Christiansen, M.* ; Winbo, A.* ; Jabbari, R.* ; Lubitz, S.A.* ; Steinfurt, J.* ; Rudic, B.* ; Loeys, B.* ; Shoemaker, M.B.* ; Weeke, P.E.* ; Pfeiffer, R.* ; Davies, B.* ; Andorin, A.* ; Hofman, N.* ; Dagradi, F.* ; Pedrazzini, M.* ; Tester, D.J.* ; Bos, J.M.* ; Sarquella-Brugada, G.* ; Campuzano, Ó.* ; Platonov, P.G.* ; Stallmeyer, B.* ; Zumhagen, S.* ; Nannenberg, E.A.* ; Veldink, J.H.* ; van den Berg, L.H.* ; Al-Chalabi, A.* ; Shaw, C.E.* ; Shaw, P.J.* ; Morrison, K.E.* ; Andersen, P.M.* ; Müller-Nurasyid, M. ; Cusi, D.* ; Barlassina, C.* ; Galan, P.* ; Lathrop, M.* ; Munter, M.* ; Werge, T.* ; Ribasés, M.* ; Aung, T.* ; Khor, C.C.* ; Ozaki, M.* ; Lichtner, P. ; Meitinger, T. ; van Tintelen, J.P.* ; Hoedemaekers, Y.* ; Denjoy, I.* ; Leenhardt, A.* ; Napolitano, C.* ; Shimizu, W.* ; Schott, J.J.* ; Gourraud, J.B.* ; Makiyama, T.* ; Ohno, S.* ; Itoh, H.* ; Krahn, A.D.* ; Antzelevitch, C.* ; Roden, D.M.* ; Saenen, J.* ; Borggrefe, M.* ; Odening, K.E.* ; Ellinor, P.T.* ; Tfelt-Hansen, J.* ; Skinner, J.R.* ; van den Berg, M.P.* ; Olesen, M.S.* ; Brugada, J.* ; Brugada, R.* ; Makita, N.* ; Breckpot, J.* ; Yoshinaga, M.* ; Behr, E.R.* ; Rydberg, A.* ; Aiba, T.* ; Kääb, S.* ; Priori, S.G.* ; Guicheney, P.* ; Tan, H.L.* ; Newton-Cheh, C.* ; Ackerman, M.J.* ; Schulze-Bahr, E.* ; Probst, V.* ; Horie, M.* ; Wilde, A.A.* ; Tanck, M.W.T.* ; Bezzina, C.R.*

Transethnic genome-wide association study provides insights in the genetic architecture and heritability of long QT syndrome.

Circulation 142, 324-338 (2020)
Publ. Version/Full Text DOI
Open Access Gold (Paid Option)
Creative Commons Lizenzvertrag
Background: Long QT syndrome (LQTS) is a rare genetic disorder and a major preventable cause of sudden cardiac death in the young. A causal rare genetic variant with large effect size is identified in up to 80% of probands (genotype positive) and cascade family screening shows incomplete penetrance of genetic variants. Furthermore, a proportion of cases meeting diagnostic criteria for LQTS remain genetically elusive despite genetic testing of established genes (genotype negative). These observations raise the possibility that common genetic variants with small effect size contribute to the clinical picture of LQTS. This study aimed to characterize and quantify the contribution of common genetic variation to LQTS disease susceptibility. Methods: We conducted genome-wide association studies followed by transethnic meta-analysis in 1656 unrelated patients with LQTS of European or Japanese ancestry and 9890 controls to identify susceptibility single nucleotide polymorphisms. We estimated the common variant heritability of LQTS and tested the genetic correlation between LQTS susceptibility and other cardiac traits. Furthermore, we tested the aggregate effect of the 68 single nucleotide polymorphisms previously associated with the QT-interval in the general population using a polygenic risk score. Results: Genome-wide association analysis identified 3 loci associated with LQTS at genome-wide statistical significance (P<5x10(-8)) nearNOS1AP,KCNQ1, andKLF12, and 1 missense variant inKCNE1(p.Asp85Asn) at the suggestive threshold (P<10(-6)). Heritability analyses showed that approximate to 15% of variance in overall LQTS susceptibility was attributable to common genetic variation (h2SNP0.148; standard error 0.019). LQTS susceptibility showed a strong genome-wide genetic correlation with the QT-interval in the general population (r(g)=0.40;P=3.2x10(-3)). The polygenic risk score comprising common variants previously associated with the QT-interval in the general population was greater in LQTS cases compared with controls (P<10-13), and it is notable that, among patients with LQTS, this polygenic risk score was greater in patients who were genotype negative compared with those who were genotype positive (P<0.005). Conclusions: This work establishes an important role for common genetic variation in susceptibility to LQTS. We demonstrate overlap between genetic control of the QT-interval in the general population and genetic factors contributing to LQTS susceptibility. Using polygenic risk score analyses aggregating common genetic variants that modulate the QT-interval in the general population, we provide evidence for a polygenic architecture in genotype negative LQTS.
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Publication type Article: Journal article
Document type Scientific Article
Keywords Genome-wide Association Study ; Inheritance Patterns ; Long Qt Syndrome; Common Variants; Risk; Interval; Disease; Mutations; Duration; Identification; Polymorphism; Modifier; Events
ISSN (print) / ISBN 0009-7322
e-ISSN 1524-4539
Journal Circulation
Quellenangaben Volume: 142, Issue: 4, Pages: 324-338 Article Number: , Supplement: ,
Publisher Lippincott Williams & Wilkins
Publishing Place Two Commerce Sq, 2001 Market St, Philadelphia, Pa 19103 Usa
Reviewing status Peer reviewed