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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Online AccessGet full text
ISSN1061-4036
1546-1718
1546-1718
DOI10.1038/ng.3842

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Abstract 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.
AbstractList 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.
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.
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.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.
Audience Academic
Author Tsugane, Shoichiro
Christophersen, Ingrid E
Yamamoto, Masayuki
Tanaka, Hideo
Ellinor, Patrick T
Tanaka, Keitaro
Kamatani, Yoichiro
Furukawa, Tetsushi
Sasaki, Makoto
Ebana, Yusuke
Ozaki, Kouichi
Takahashi, Atsushi
Iwasaki, Motoki
Kubo, Michiaki
Ito, Kaoru
Wakai, Kenji
Ogishima, Soichi
Satoh, Mamoru
Yamaji, Taiki
Low, Siew-Kee
Tanaka, Toshihiro
Naito, Mariko
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/28416822$$D View this record in MEDLINE/PubMed
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ContentType Journal Article
Copyright Springer Nature America, Inc. 2017
COPYRIGHT 2017 Nature Publishing Group
Copyright Nature Publishing Group Jun 2017
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– notice: COPYRIGHT 2017 Nature Publishing Group
– notice: Copyright Nature Publishing Group Jun 2017
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Snippet Kaoru Ito, Yoichiro Kamatani, Toshihiro Tanaka and colleagues report a genome-wide association study for atrial fibrillation in the Japanese population. They...
Atrial fibrillation is the most common cardiac arrhythmia and leads to stroke. To investigate genetic loci associated with atrial fibrillation in the Japanese...
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SubjectTerms 45/43
631/208/205/2138
631/208/457
692/699/75/29/1309
Adult
Aged
Agriculture
Animal Genetics and Genomics
Arrhythmia
Asian Continental Ancestry Group - genetics
Atrial fibrillation
Atrial Fibrillation - genetics
Axon guidance
Basic Helix-Loop-Helix Transcription Factors - genetics
Biomedicine
Cancer Research
Cardiac arrhythmia
Chromosomes, Human, Pair 4
Electrocardiography
Fibrillation
Gene Function
Gene loci
Genes
Genetic aspects
Genetic factors
Genetic Loci
Genetic Predisposition to Disease
Genetic research
Genetic susceptibility
Genome-wide association studies
Genome-Wide Association Study - methods
Genomes
Heart diseases
Human Genetics
Humans
Identification and classification
letter
Loci
Middle Aged
Pathogenesis
Polymorphism, Single Nucleotide
Preventive medicine
Quantitative trait loci
Risk factors
Shal Potassium Channels - genetics
Stroke
Title Identification of six new genetic loci associated with atrial fibrillation in the Japanese population
URI https://link.springer.com/article/10.1038/ng.3842
https://www.ncbi.nlm.nih.gov/pubmed/28416822
https://www.proquest.com/docview/1905668804
https://www.proquest.com/docview/1889387022
Volume 49
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