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Rigshospitalet - en del af Københavns Universitetshospital
Udgivet

Genetic insight into sick sinus syndrome

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

DOI

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  • Rosa B Thorolfsdottir
  • Gardar Sveinbjornsson
  • Hildur M Aegisdottir
  • Stefania Benonisdottir
  • Lilja Stefansdottir
  • Erna V Ivarsdottir
  • Gisli H Halldorsson
  • Jon K Sigurdsson
  • Christian Torp-Pedersen
  • Peter E Weeke
  • Søren Brunak
  • David Westergaard
  • Ole B Pedersen
  • Erik Sorensen
  • Kaspar R Nielsen
  • Kristoffer S Burgdorf
  • Karina Banasik
  • Ben Brumpton
  • Wei Zhou
  • Asmundur Oddsson
  • Vinicius Tragante
  • Kristjan E Hjorleifsson
  • Olafur B Davidsson
  • Sridharan Rajamani
  • Stefan Jonsson
  • Bjarni Torfason
  • Atli S Valgardsson
  • Gudmundur Thorgeirsson
  • Michael L Frigge
  • Gudmar Thorleifsson
  • Gudmundur L Norddahl
  • Anna Helgadottir
  • Solveig Gretarsdottir
  • Patrick Sulem
  • Ingileif Jonsdottir
  • Cristen J Willer
  • Kristian Hveem
  • Henning Bundgaard
  • Henrik Ullum
  • David O Arnar
  • Unnur Thorsteinsdottir
  • Daniel F Gudbjartsson
  • Hilma Holm
  • Kari Stefansson
  • DBDS Genomic Consortium
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AIMS: The aim of this study was to use human genetics to investigate the pathogenesis of sick sinus syndrome (SSS) and the role of risk factors in its development.

METHODS AND RESULTS: We performed a genome-wide association study of 6469 SSS cases and 1 000 187 controls from deCODE genetics, the Copenhagen Hospital Biobank, UK Biobank, and the HUNT study. Variants at six loci associated with SSS, a reported missense variant in MYH6, known atrial fibrillation (AF)/electrocardiogram variants at PITX2, ZFHX3, TTN/CCDC141, and SCN10A and a low-frequency (MAF = 1.1-1.8%) missense variant, p.Gly62Cys in KRT8 encoding the intermediate filament protein keratin 8. A full genotypic model best described the p.Gly62Cys association (P = 1.6 × 10-20), with an odds ratio (OR) of 1.44 for heterozygotes and a disproportionally large OR of 13.99 for homozygotes. All the SSS variants increased the risk of pacemaker implantation. Their association with AF varied and p.Gly62Cys was the only variant not associating with any other arrhythmia or cardiovascular disease. We tested 17 exposure phenotypes in polygenic score (PGS) and Mendelian randomization analyses. Only two associated with the risk of SSS in Mendelian randomization, AF, and lower heart rate, suggesting causality. Powerful PGS analyses provided convincing evidence against causal associations for body mass index, cholesterol, triglycerides, and type 2 diabetes (P > 0.05).

CONCLUSION: We report the associations of variants at six loci with SSS, including a missense variant in KRT8 that confers high risk in homozygotes and points to a mechanism specific to SSS development. Mendelian randomization supports a causal role for AF in the development of SSS.

OriginalsprogEngelsk
TidsskriftEuropean Heart Journal
Vol/bind42
Udgave nummer20
Sider (fra-til)1959-1971
Antal sider13
ISSN0195-668X
DOI
StatusUdgivet - 21 maj 2021

Bibliografisk note

© The Author(s) 2021. Published by Oxford University Press on behalf of the European Society of Cardiology.

ID: 62373710