Common and rare susceptibility genetic variants predisposing to Brugada Syndrome in Thailand
Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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Common and rare susceptibility genetic variants predisposing to Brugada Syndrome in Thailand. / Makarawate, Pattarapong; Glinge, Charlotte; Khongphatthanayothin, Apichai; Walsh, Roddy; Mauleekoonphairoj, John; Amnueypol, Montawatt; Prechawat, Somchai; Wongcharoen, Wanwarang; Krittayaphong, Rungroj; Anannab, Alisara; Lichtner, Peter; Meitinger, Thomas; Tjong, Fleur V Y; Lieve, Krystien V V; Amin, Ahmad S; Sahasatas, Dujdao; Ngarmukos, Tachapong; Wichadakul, Duangdao; Payungporn, Sanchai; Sutjaporn, Boosamas; Wandee, Pharawee; Poovorawan, Yong; Tfelt-Hansen, Jacob; Tanck, Michael W T; Tadros, Rafik; Wilde, Arthur A M; Bezzina, Connie R; Veerakul, Gumpanart; Nademanee, Koonlawee.
I: Heart Rhythm, Bind 17, Nr. 12, 30.12.2020, s. 2145-2153.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Common and rare susceptibility genetic variants predisposing to Brugada Syndrome in Thailand
AU - Makarawate, Pattarapong
AU - Glinge, Charlotte
AU - Khongphatthanayothin, Apichai
AU - Walsh, Roddy
AU - Mauleekoonphairoj, John
AU - Amnueypol, Montawatt
AU - Prechawat, Somchai
AU - Wongcharoen, Wanwarang
AU - Krittayaphong, Rungroj
AU - Anannab, Alisara
AU - Lichtner, Peter
AU - Meitinger, Thomas
AU - Tjong, Fleur V Y
AU - Lieve, Krystien V V
AU - Amin, Ahmad S
AU - Sahasatas, Dujdao
AU - Ngarmukos, Tachapong
AU - Wichadakul, Duangdao
AU - Payungporn, Sanchai
AU - Sutjaporn, Boosamas
AU - Wandee, Pharawee
AU - Poovorawan, Yong
AU - Tfelt-Hansen, Jacob
AU - Tanck, Michael W T
AU - Tadros, Rafik
AU - Wilde, Arthur A M
AU - Bezzina, Connie R
AU - Veerakul, Gumpanart
AU - Nademanee, Koonlawee
N1 - Copyright © 2020. Published by Elsevier Inc.
PY - 2020/12/30
Y1 - 2020/12/30
N2 - BACKGROUND: Mutations in SCN5A are rarely found in Thai patients with Brugada syndrome (BrS). Recent evidence suggested that common genetic variation may underlie BrS in a complex inheritance model.OBJECTIVE: To find common and rare/low frequency genetic variants predisposing to BrS 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=3x10-10). The conditional analysis identified a novel independent signal in the same locus (rs6767797; OR2.3, P=2.7x10-10). The second locus was near HEY2 (lead marker rs3734634; OR2.5, P=7x10-9). Rare (MAF<0.0001) coding variants in SCN5A were found in 8 of the 131 cases (6.1% in cases versus 2.0% in controls, P=0.046, OR=3.3 [1.0-11.1]), but an enrichment of low frequency (MAF<0.001 and >0.0001) variants was also observed in cases, with one variant (SCN5A:p.Arg965Cys), detected in 4.6% of Thai BrS patients vs 0.5% in controls (P=0.015, OR=9.8[1.2-82.3]).CONCLUSIONS: 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 trans-ethnic transferability of these two major BrS loci.
AB - BACKGROUND: Mutations in SCN5A are rarely found in Thai patients with Brugada syndrome (BrS). Recent evidence suggested that common genetic variation may underlie BrS in a complex inheritance model.OBJECTIVE: To find common and rare/low frequency genetic variants predisposing to BrS 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=3x10-10). The conditional analysis identified a novel independent signal in the same locus (rs6767797; OR2.3, P=2.7x10-10). The second locus was near HEY2 (lead marker rs3734634; OR2.5, P=7x10-9). Rare (MAF<0.0001) coding variants in SCN5A were found in 8 of the 131 cases (6.1% in cases versus 2.0% in controls, P=0.046, OR=3.3 [1.0-11.1]), but an enrichment of low frequency (MAF<0.001 and >0.0001) variants was also observed in cases, with one variant (SCN5A:p.Arg965Cys), detected in 4.6% of Thai BrS patients vs 0.5% in controls (P=0.015, OR=9.8[1.2-82.3]).CONCLUSIONS: 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 trans-ethnic transferability of these two major BrS loci.
U2 - 10.1016/j.hrthm.2020.06.027
DO - 10.1016/j.hrthm.2020.06.027
M3 - Journal article
C2 - 32619740
VL - 17
SP - 2145
EP - 2153
JO - Heart Rhythm
JF - Heart Rhythm
SN - 1547-5271
IS - 12
ER -
ID: 244528158