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Rigshospitalet - en del af Københavns Universitetshospital
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Common and rare susceptibility genetic variants predisposing to Brugada syndrome in Thailand

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DOI

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  • Pattarapong Makarawate
  • Charlotte Glinge
  • Apichai Khongphatthanayothin
  • Roddy Walsh
  • John Mauleekoonphairoj
  • Montawatt Amnueypol
  • Somchai Prechawat
  • Wanwarang Wongcharoen
  • Rungroj Krittayaphong
  • Alisara Anannab
  • Peter Lichtner
  • Thomas Meitinger
  • Fleur V Y Tjong
  • Krystien V V Lieve
  • Ahmad S Amin
  • Dujdao Sahasatas
  • Tachapong Ngarmukos
  • Duangdao Wichadakul
  • Sunchai Payungporn
  • Boosamas Sutjaporn
  • Pharawee Wandee
  • Yong Poovorawan
  • Jacob Tfelt-Hansen
  • Michael W T Tanck
  • Rafik Tadros
  • Arthur A M Wilde
  • Connie R Bezzina
  • Gumpanart Veerakul
  • Koonlawee Nademanee
Vis graf over relationer

BACKGROUND: Mutations in SCN5A are rarely found in Thai patients with Brugada syndrome (BrS). Recent evidence suggested that common genetic variations may underlie BrS in a complex inheritance model.

OBJECTIVE: The purpose of this study was to find common and rare/low-frequency genetic variants predisposing to BrS in persons in Thailand.

METHODS: We conducted a genome-wide association study (GWAS) to explore the association of common variants in 154 Thai BrS cases and 432 controls. We sequenced SCN5A in 131 cases and 205 controls. Variants were classified according to current guidelines, and case-control association testing was performed for rare and low-frequency variants.

RESULTS: Two loci were significantly associated with BrS. The first was near SCN5A/SCN10A (lead marker rs10428132; odds ratio [OR] 2.4; P = 3 × 10-10). Conditional analysis identified a novel independent signal in the same locus (rs6767797; OR 2.3; P = 2.7 × 10-10). The second locus was near HEY2 (lead marker rs3734634; OR 2.5; P = 7 × 10-9). Rare (minor allele frequency [MAF] <0.0001) coding variants in SCN5A were found in 8 of the 131 cases (6.1% in cases vs 2.0% in controls; P = .046; OR 3.3; 95% confident interval [CI] 1.0-11.1), but an enrichment of low-frequency (MAF<0.001 and >0.0001) variants also was observed in cases, with 1 variant (SCN5A: p.Arg965Cys) detected in 4.6% of Thai BrS patients vs 0.5% in controls (P = 0.015; OR 9.8; 95% CI 1.2-82.3).

CONCLUSION: The genetic basis of BrS in Thailand includes a wide spectrum of variant frequencies and effect sizes. As previously shown in European and Japanese populations, common variants near SCN5A and HEY2 are associated with BrS in the Thai population, confirming the transethnic transferability of these 2 major BrS loci.

OriginalsprogEngelsk
TidsskriftHeart Rhythm
Vol/bind17
Udgave nummer12
Sider (fra-til)2145-2153
Antal sider9
ISSN1547-5271
DOI
StatusUdgivet - dec. 2020

Bibliografisk note

Copyright © 2020 Heart Rhythm Society. Published by Elsevier Inc. All rights reserved.

ID: 62373982