Identification of six new genetic loci associated with atrial fibrillation in the Japanese population

Kaoru Ito, Yoichiro Kamatani, Toshihiro Tanaka and colleagues report a genome-wide association study for atrial fibrillation in the Japanese population. They identify six new loci, five of which are not associated with atrial fibrillation in individuals of European ancestry, suggesting that they may...

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Published inNature genetics Vol. 49; no. 6; pp. 953 - 958
Main Authors Low, Siew-Kee, Takahashi, Atsushi, Ebana, Yusuke, Ozaki, Kouichi, Christophersen, Ingrid E, Ellinor, Patrick T, Ogishima, Soichi, Yamamoto, Masayuki, Satoh, Mamoru, Sasaki, Makoto, Yamaji, Taiki, Iwasaki, Motoki, Tsugane, Shoichiro, Tanaka, Keitaro, Naito, Mariko, Wakai, Kenji, Tanaka, Hideo, Furukawa, Tetsushi, Kubo, Michiaki, Ito, Kaoru, Kamatani, Yoichiro, Tanaka, Toshihiro
Format Journal Article
LanguageEnglish
Published New York Nature Publishing Group US 01.06.2017
Nature Publishing Group
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ISSN1061-4036
1546-1718
1546-1718
DOI10.1038/ng.3842

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Summary:Kaoru Ito, Yoichiro Kamatani, Toshihiro Tanaka and colleagues report a genome-wide association study for atrial fibrillation in the Japanese population. They identify six new loci, five of which are not associated with atrial fibrillation in individuals of European ancestry, suggesting that they may be specific to the Japanese population. Atrial fibrillation is the most common cardiac arrhythmia and leads to stroke. To investigate genetic loci associated with atrial fibrillation in the Japanese population, we performed a genome-wide association study (GWAS) that included 8,180 atrial fibrillation cases and 28,612 controls with follow-up in an additional 3,120 cases and 125,064 controls. We replicated previously reported loci and identified six new loci, near the KCND3 , PPFIA4 , SLC1A4 – CEP68 , HAND2 , NEBL and SH3PXD2A genes. Five of the six new loci were specifically associated with atrial fibrillation in the Japanese population after comparing our data to those from individuals of European ancestry, suggesting that there might be different genetic factors affecting susceptibility across ancestry groups. Our study discovered variants in the HAND2 , KCND3 and NEBL genes, which are relevant to atrial fibrillation susceptibility. The involvement of PPFIA4 and SH3PXD2A in axon guidance also suggested a role in disease pathogenesis. Our findings may contribute to a better understanding of atrial fibrillation susceptibility and pathogenesis.
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ISSN:1061-4036
1546-1718
1546-1718
DOI:10.1038/ng.3842