Literature DB >> 20479155

Blood pressure and hypertension are associated with 7 loci in the Japanese population.

Fumihiko Takeuchi1, Masato Isono, Tomohiro Katsuya, Ken Yamamoto, Mitsuhiro Yokota, Takao Sugiyama, Toru Nabika, Akihiro Fujioka, Keizo Ohnaka, Hiroyuki Asano, Yukio Yamori, Shuhei Yamaguchi, Shotai Kobayashi, Ryoichi Takayanagi, Toshio Ogihara, Norihiro Kato.   

Abstract

BACKGROUND: Two consortium-based genome-wide association studies have recently identified robust and significant associations of common variants with systolic and diastolic blood pressures in populations of European descent, warranting further investigation in populations of non-European descent. METHODS AND
RESULTS: We examined the associations at 27 loci reported by the genome-wide association studies on Europeans in a screening panel of Japanese subjects (n=1526) and chose 11 loci showing association signals (1-tailed test in the screening, P<0.3) for an extensive replication study with a follow-up panel of 3 Japanese general-population cohorts (n < or =24 300). Significant associations were replicated for 7 loci-CASZ1, MTHFR, ITGA9, FGF5, CYP17A1-CNNM2, ATP2B1, and CSK-ULK3-with any or all of these 3 traits: systolic blood pressure (P=1.4x10(-14) to 0.05), diastolic blood pressure (P=1.9x10(-12) to 0.05), and hypertension (P=2.0x10(-14) to 0.006; odds ratio, 1.10 to 1.29). The strongest association was observed for FGF5. In the whole study panel, the variance (R(2)) for blood pressure explained by the 7 single-nucleotide polymorphism loci was calculated to be R(2)=0.003 for male and 0.006 for female participants. Stratified analysis implied the potential presence of a gene-age-sex interaction, although it did not reach a conclusive level of statistical significance after adjustment for multiple testing.
CONCLUSIONS: We have confirmed 7 loci associated with blood pressure and/or hypertension in the Japanese. These loci can guide fine-mapping efforts to pinpoint causal variants and causal genes with the integration of multiethnic results.

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Year:  2010        PMID: 20479155     DOI: 10.1161/CIRCULATIONAHA.109.904664

Source DB:  PubMed          Journal:  Circulation        ISSN: 0009-7322            Impact factor:   29.690


  79 in total

Review 1.  Between candidate genes and whole genomes: time for alternative approaches in blood pressure genetics.

Authors:  Jacob Basson; Jeannette Simino; D C Rao
Journal:  Curr Hypertens Rep       Date:  2012-02       Impact factor: 5.369

2.  Discovery and replication of novel blood pressure genetic loci in the Women's Genome Health Study.

Authors:  Jennifer E Ho; Daniel Levy; Lynda Rose; Andrew D Johnson; Paul M Ridker; Daniel I Chasman
Journal:  J Hypertens       Date:  2011-01       Impact factor: 4.844

3.  Detection of common single nucleotide polymorphisms synthesizing quantitative trait association of rarer causal variants.

Authors:  Fumihiko Takeuchi; Shotai Kobayashi; Toshio Ogihara; Akihiro Fujioka; Norihiro Kato
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Review 4.  Over 1000 genetic loci influencing blood pressure with multiple systems and tissues implicated.

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8.  Common variants in the ATP2B1 gene are associated with hypertension and arterial stiffness in Chinese population.

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9.  Congenital heart disease protein 5 associates with CASZ1 to maintain myocardial tissue integrity.

Authors:  Stephen Sojka; Nirav M Amin; Devin Gibbs; Kathleen S Christine; Marta S Charpentier; Frank L Conlon
Journal:  Development       Date:  2014-07-03       Impact factor: 6.868

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Authors:  Zinia Islam; Naoko Hayashi; Hana Inoue; Takahiro Umezawa; Yuuri Kimura; Hiroyuki Doi; Michael F Romero; Shigehisa Hirose; Akira Kato
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