Literature DB >> 21451528

Association of intima-media thickening of carotid artery with genetic polymorphisms of the regulator of G-protein signaling 2 gene in patients with hypertension and in the general population.

Kei Kamide1, Yoshihiro Kokubo, Jin Yang, Shin Takiuchi, Takeshi Horio, Sachiko Matsumoto, Mariko Banno, Tetsutaro Matayoshi, Hisayo Yasuda, Yoshikazu Miwa, Fumiki Yoshihara, Satoko Nakamura, Hajime Nakahama, Yoshio Iwashima, Ryousuke Oguro, Mitsuru Ohishi, Hiromi Rakugi, Tomonori Okamura, Toshiyuki Miyata, Yuhei Kawano.   

Abstract

Regulator of G-protein signaling 2 (RGS2) is a key molecule in signal pathways of vasoactive peptides, such as angiotensin II and endothelin 1, and is believed to have an important role in the pathophysiology of atherosclerosis. We have previously reported that common polymorphisms of RGS2 are associated with hypertension in Japanese. In this study, we studied whether the three previously identified common polymorphisms of RGS2 (-638A>G, 1026T>A and 1891-1892delTC) could be implicated in carotid atherosclerosis in Japanese patients with hypertension (459 men and 382 woman) and in a Japanese general population (814 men and 956 woman). We assessed two criteria for carotid atherosclerosis: maximal intima-media thickness (M-IMT) and mean-IMT. When subjects with atherosclerotic lesions were defined as having mean-IMT≥1.0 mm, multivariate logistic regression analysis performed after adjusting for confounding factors showed a significant association of the three common polymorphisms, -638A>G (AA versus AG+GG: odds ratio (OR), 1.55; 95% confidence interval (CI), 1.105-2.185; P=0.0113 only for the general population), 1026T>A (TT versus TA+AA: OR, 1.42; 95% CI, 1.027-1.972; P=0.034 for hypertensive subjects and OR, 1.56; 95% CI, 1.129-2.151; P=0.0071 for the general population), and 1891-1892delTC (II versus ID+DD: OR, 1.44; 95% CI, 1.043-2.008; P=0.028 for hypertensive subjects, OR, 1.32; 95% CI 1.002-1.742; P=0.048 for the total general population and OR 1.59; 95% CI 1.155-2.207; P=0.0047 for the general population), with carotid atherosclerosis. When atherosclerosis was defined as M-IMT 1.0 mm, the values of M-IMT were also significantly different between the three genotypes in the three common polymorphisms. Taken together, these data suggest that genetic polymorphisms in RGS2 are associated with intima-media thickening of carotid artery in humans.

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Year:  2011        PMID: 21451528     DOI: 10.1038/hr.2011.25

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


  4 in total

Review 1.  Genetic associations with hypertension: meta-analyses of six candidate genetic variants.

Authors:  Cheng Zhang; Lingyan Wang; Qi Liao; Lina Zhang; Leiting Xu; Cheng Chen; Huadan Ye; Xuting Xu; Meng Ye; Shiwei Duan
Journal:  Genet Test Mol Biomarkers       Date:  2013-07-16

2.  Non-dipping and arterial hypertension depend on clinical factors rather than on genetic variability of ACE and RGS2 genes in patients with type 1 diabetes.

Authors:  G Deja; M Borowiec; W Fendler; I Pietrzak; A Szadkowska; L Machnica; J Polanska; W Mlynarski; P Jarosz-Chobot
Journal:  Acta Diabetol       Date:  2014-02-23       Impact factor: 4.280

Review 3.  The downstream regulation of chemokine receptor signalling: implications for atherosclerosis.

Authors:  Jyoti Patel; Keith M Channon; Eileen McNeill
Journal:  Mediators Inflamm       Date:  2013-04-14       Impact factor: 4.711

4.  Hypertension after preeclampsia and relation to the C1114G polymorphism (rs4606) in RGS2: data from the Norwegian HUNT2 study.

Authors:  Anne Stine Kvehaugen; Øyvind Melien; Oddgeir L Holmen; Hannele Laivuori; Ralf Dechend; Anne Cathrine Staff
Journal:  BMC Med Genet       Date:  2014-03-05       Impact factor: 2.103

  4 in total

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