Literature DB >> 17143180

Association of genetic polymorphisms of ACADSB and COMT with human hypertension.

Kei Kamide1, Yoshihiro Kokubo, Jing Yang, Tetsutaro Matayoshi, Nozomu Inamoto, Shin Takiuchi, Takeshi Horio, Yoshikazu Miwa, Masayoshi Yoshii, Hitonobu Tomoike, Chihiro Tanaka, Mariko Banno, Tomohiko Okuda, Yuhei Kawano, Toshiyuki Miyata.   

Abstract

OBJECTIVES: Genetically hypertensive rats provide an excellent model to investigate the genetic mechanisms of hypertension. We previously identified three differentially expressed genes, Acadsb (short/branched chain acyl-CoA dehydrogenase), Comt (catecholamine-O-methyltransferase), and Pnpo (pyridoxine 5'-phosphate oxidase), in hypertensive and normotensive rat kidneys as potential susceptibility genes for rat hypertension. We examined the association of human homologues of these genes with human hypertension.
METHODS: We sequenced three genes using samples from 48 or 96 hypertensive patients, identified single nucleotide polymorphisms, and genotyped them in a population-based sample of 1818 Japanese individuals (771 hypertensive individuals and 1047 controls).
RESULTS: After adjustments for age, body mass index, present illness (hyperlipidaemia, diabetes mellitus), and lifestyle (smoking, alcohol consumption), multivariate logistic regression analysis revealed that -512A>G in ACADSB was associated with hypertension in women (AA vs AG + GG: odds ratio = 0.70, 95% confidence interval = 0.53-0.94). This single nucleotide polymorphism was in tight linkage disequilibrium with -254G>A. Furthermore, -1187G>C in COMT was associated with hypertension in men (GG vs CG + CC: odds ratio = 0.69, 95% confidence interval = 0.52-0.93) and was in tight linkage disequilibrium with 186C>T. After adjustments described above, -512 A>G and -254G>A in ACADSB were associated with variations in systolic blood pressure. ACADSB was in tight linkage disequilibrium with MGC35392 across a distance of 18.3 kb. COMT was not in linkage disequilibrium with any adjacent genes. Analysis indicated that two haplotypes of COMT were significantly associated with hypertension in men.
CONCLUSION: Our study suggests the possible involvement of genetic polymorphisms in ACADSB and COMT in essential hypertension in the Japanese population.

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Year:  2007        PMID: 17143180     DOI: 10.1097/HJH.0b013e3280103a40

Source DB:  PubMed          Journal:  J Hypertens        ISSN: 0263-6352            Impact factor:   4.844


  10 in total

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2.  Association of polymorphisms in genes involved in the dopaminergic pathway with blood pressure and uric acid levels in Chinese females.

Authors:  Ting-Kuang Yeh; Ting-Chi Yeh; Chi-Feng Weng; Bing-Fu Shih; Hsueh-Jen Tsao; Chien-Hua Hsiao; Fu-Tai Chuang; Chung-Yi Hu; Chun-Yen Chang
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Review 3.  Meta-Analysis of the COMT Val158Met Polymorphism in Major Depressive Disorder: Effect of Ethnicity.

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Authors:  Scott H Stewart; Gabor Oroszi; Patrick K Randall; Raymond F Anton
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Journal:  Diabetol Metab Syndr       Date:  2017-12-04       Impact factor: 3.320

7.  Long-term monitoring for short/branched-chain acyl-CoA dehydrogenase deficiency: A single-center 4-year experience and open issues.

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8.  Low enzymatic activity haplotypes of the human catechol-O-methyltransferase gene: enrichment for marker SNPs.

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Journal:  PLoS One       Date:  2009-04-13       Impact factor: 3.240

9.  Pulse Pressure Magnifies the Effect of COMT Val(158)Met on 15 Years Episodic Memory Trajectories.

Authors:  Ninni Persson; Catharina Lavebratt; Anna Sundström; Håkan Fischer
Journal:  Front Aging Neurosci       Date:  2016-03-02       Impact factor: 5.750

10.  Interleukin-1β enhances cell adhesion in human endothelial cells via microRNA-1914-5p suppression.

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Journal:  Biochem Biophys Rep       Date:  2021-06-12
  10 in total

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