Literature DB >> 17510502

NADH dehydrogenase subunit-2 237 Leu/Met polymorphism modifies the effects of alcohol consumption on risk for hypertension in middle-aged Japanese men.

Akatsuki Kokaze1, Mamoru Ishikawa, Naomi Matsunaga, Masao Yoshida, Masao Satoh, Koji Teruya, Yumi Masuda, Rie Honmyo, Yoshiko Uchida, Yutaka Takashima.   

Abstract

NADH dehydrogenase subunit-2 237 leucine/methionine (ND2-237 Leu/Met) polymorphism is associated with longevity in the Japanese population, and the ND2-237Met genotype may exert antiatherogenic effects. To investigate whether ND2-237 Leu/Met polymorphism is associated with risk of hypertension, we conducted a cross-sectional study of 398 Japanese male subjects. The frequency of hypertension was significantly higher in ND2-237Leu genotypic men than in ND2-237Met genotypic men. On analysis of covariance, the interaction between ND2-237 Leu/Met polymorphism and habitual drinking was significantly associated with both systolic blood pressure and diastolic blood pressure. Multiple logistic regression analysis revealed that the ND2-237Met genotype, particularly in younger subjects (age <60 years), had a lower odds ratio for hypertension than the ND2-237Leu genotype. Moreover, the association of ND2-237 Leu/Met polymorphism with hypertension may depend on the frequency of alcohol consumption. The odds ratio for hypertension was significantly higher in daily drinkers with ND2-237Leu when compared with non- or ex-drinkers with ND2-237Leu. However, the association between the ND2-237Met genotype and hypertension may not depend on the frequency of alcohol consumption. The present results suggest that ND2-237 Leu/Met polymorphism is associated with hypertension and that modification of hypertension risk is dependent on alcohol consumption in middle-aged Japanese men.

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Year:  2007        PMID: 17510502     DOI: 10.1291/hypres.30.213

Source DB:  PubMed          Journal:  Hypertens Res        ISSN: 0916-9636            Impact factor:   3.872


  16 in total

1.  Longevity-associated mitochondrial DNA 5178 C/A polymorphism and its interaction with cigarette consumption are associated with pulmonary function in middle-aged Japanese men.

Authors:  Akatsuki Kokaze; Mamoru Ishikawa; Naomi Matsunaga; Masao Yoshida; Masao Satoh; Koji Teruya; Rie Honmyo; Takako Shirasawa; Hiromi Hoshino; Yutaka Takashima
Journal:  J Hum Genet       Date:  2007-07-17       Impact factor: 3.172

2.  Mitochondria-wide association study of common variants in osteoporosis.

Authors:  Yan Guo; Tie-Lin Yang; Yao-Zhong Liu; Hui Shen; Shu-Feng Lei; Na Yu; Jia Chen; Ting Xu; Yu Cheng; Qing Tian; Ping Yu; Hong-Wen Deng
Journal:  Ann Hum Genet       Date:  2011-07-18       Impact factor: 1.670

3.  Joint effect of longevity-associated mitochondrial DNA 5178 C/A polymorphism and alcohol consumption on risk of hyper-LDL cholesterolemia in middle-aged Japanese men.

Authors:  Teruyoshi Kawamoto; Akatsuki Kokaze; Mamoru Ishikawa; Naomi Matsunaga; Kanae Karita; Masao Yoshida; Naoki Shimada; Tadahiro Ohtsu; Takako Shirasawa; Hirotaka Ochiai; Taku Ito; Hiromi Hoshino; Yutaka Takashima
Journal:  Lipids Health Dis       Date:  2011-06-25       Impact factor: 3.876

4.  Difference in effects of cigarette smoking or alcohol consumption on serum non-high-density lipoprotein cholesterol levels is related to mitochondrial DNA 5178 C/A polymorphism in middle-aged Japanese men: a cross-sectional study.

Authors:  Akatsuki Kokaze; Mamoru Ishikawa; Naomi Matsunaga; Kanae Karita; Masao Yoshida; Tadahiro Ohtsu; Hirotaka Ochiai; Takako Shirasawa; Hinako Nanri; Hiromi Hoshino; Yutaka Takashima
Journal:  J Physiol Anthropol       Date:  2014-01-03       Impact factor: 2.867

5.  Joint effects of mitochondrial DNA 5178 C/A polymorphism and coffee consumption or alcohol consumption on clustering of cardiovascular risk factors in middle-aged Japanese men: a cross-sectional study.

Authors:  Taku Ito; Akatsuki Kokaze; Mamoru Ishikawa; Naomi Matsunaga; Kanae Karita; Masao Yoshida; Tadahiro Ohtsu; Hirotaka Ochiai; Takako Shirasawa; Hinako Nanri; Hiromi Hoshino; Yutaka Takashima
Journal:  J Diabetes Metab Disord       Date:  2014-01-06

6.  Unexpected combined effects of NADH dehydrogenase subunit-2 237 Leu/Met polymorphism and green tea consumption on renal function in male Japanese health check-up examinees: a cross-sectional study.

Authors:  Akatsuki Kokaze; Mamoru Ishikawa; Naomi Matsunaga; Kanae Karita; Masao Yoshida; Tadahiro Ohtsu; Hirotaka Ochiai; Takako Shirasawa; Hinako Nanri; Hiromi Hoshino; Yutaka Takashima
Journal:  J Negat Results Biomed       Date:  2013-11-20

7.  NADH dehydrogenase subunit-2 237 Leu/Met polymorphism modulates the effects of coffee consumption on the risk of hypertension in middle-aged Japanese men.

Authors:  Akatsuki Kokaze; Mamoru Ishikawa; Naomi Matsunaga; Kanae Karita; Masao Yoshida; Tadahiro Ohtsu; Takako Shirasawa; Hideaki Sekii; Taku Ito; Teruyoshi Kawamoto; Yutaka Takashima
Journal:  J Epidemiol       Date:  2009-08-08       Impact factor: 3.211

8.  Combined effect of mitochondrial DNA 5178 C/A polymorphism and alcohol consumption on estimated glomerular filtration rate in male Japanese health check-up examinees: a cross-sectional study.

Authors:  Akatsuki Kokaze; Mamoru Ishikawa; Naomi Matsunaga; Kanae Karita; Masao Yoshida; Naoki Shimada; Tadahiro Ohtsu; Takako Shirasawa; Hirotaka Ochiai; Hiromi Hoshino; Yutaka Takashima
Journal:  BMC Nephrol       Date:  2013-02-12       Impact factor: 2.388

9.  Mitochondrial DNA 5178 C/A polymorphism influences the effects of habitual smoking on the risk of dyslipidemia in middle-aged Japanese men.

Authors:  Akatsuki Kokaze; Mamoru Ishikawa; Naomi Matsunaga; Kanae Karita; Masao Yoshida; Naoki Shimada; Tadahiro Ohtsu; Takako Shirasawa; Hirotaka Ochiai; Masao Satoh; Masayasu Hashimoto; Hiromi Hoshino; Yutaka Takashima
Journal:  Lipids Health Dis       Date:  2012-08-02       Impact factor: 3.876

10.  Gene-alcohol interactions identify several novel blood pressure loci including a promising locus near SLC16A9.

Authors:  Jeannette Simino; Yun Ju Sung; Rezart Kume; Karen Schwander; D C Rao
Journal:  Front Genet       Date:  2013-12-12       Impact factor: 4.599

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