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马来西亚受试者中α-肾上腺素能受体基因插入/缺失多态性与伴或不伴2型糖尿病的原发性高血压的关联。

Association of insertion/deletion polymorphism of alpha-adrenoceptor gene in essential hypertension with or without type 2 diabetes mellitus in Malaysian subjects.

作者信息

Vasudevan R, Ismail Patimah, Stanslas Johnson, Shamsudin Norashikin, Ali Aisyah Binti

机构信息

Molecular Biology Lab, Department of Biomedical Science, Universiti Putra Malaysia, Serdang 43400, Malaysia.

出版信息

Int J Biol Sci. 2008;4(6):362-7. doi: 10.7150/ijbs.4.362. Epub 2008 Oct 5.

DOI:10.7150/ijbs.4.362
PMID:18953403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC2567812/
Abstract

An insertion/deletion (I/D) polymorphism of Alpha2B-Adrenoceptor (ADRA2B) gene located on chromosome 2 has been studied extensively in related to cardiovascular diseases. The main aim of the present study was to examine the potential association of D allele frequency of I/D polymorphism of ADRA2B gene in Malaysian essential hypertensive subjects with or without type 2 diabetes mellitus (T2DM). This study includes 70 hypertensive subjects without T2DM, 65 hypertensive subjects with T2DM and 75 healthy volunteers as control subjects. Genotyping of I/D polymorphism was performed by conventional PCR method. There was significant difference found in age, body mass index, systolic/diastolic blood pressure and high density lipoprotein cholesterol level between the case and control subjects. DD genotypic frequency of I/D polymorphism was significantly higher in hypertensive subjects (42.84% vs. 29.33%; P-=0.029) and in hypertensive with T2DM subjects (46.15% vs. 29.33%; P=0.046) than control group. D allele frequency was higher in hypertensive group (67.41%) than control subjects (52.67%). However, no significant difference was found between the three genotypes of I/D polymorphism of ADRA2B gene and the clinical characteristics of the subjects. The result obtained in this study show D allele of ADRA2B gene was associated with essential hypertension with or without T2DM in Malaysian subjects.

摘要

位于2号染色体上的α2B -肾上腺素能受体(ADRA2B)基因的插入/缺失(I/D)多态性已被广泛研究,与心血管疾病相关。本研究的主要目的是检测马来西亚原发性高血压患者中,无论有无2型糖尿病(T2DM),ADRA2B基因I/D多态性的D等位基因频率的潜在关联。本研究纳入70例无T2DM的高血压患者、65例有T2DM的高血压患者以及75名健康志愿者作为对照。采用常规PCR方法对I/D多态性进行基因分型。病例组和对照组在年龄、体重指数、收缩压/舒张压以及高密度脂蛋白胆固醇水平方面存在显著差异。I/D多态性的DD基因型频率在高血压患者(42.84%对29.33%;P = 0.029)和伴有T2DM的高血压患者(46.15%对29.33%;P = 0.046)中显著高于对照组。高血压组的D等位基因频率(67.41%)高于对照组(52.67%)。然而,ADRA2B基因I/D多态性的三种基因型与受试者的临床特征之间未发现显著差异。本研究结果表明,在马来西亚受试者中,ADRA2B基因的D等位基因与有或无T2DM的原发性高血压相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113a/2567812/749ddddcd711/ijbsv04p0362g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113a/2567812/749ddddcd711/ijbsv04p0362g01.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/113a/2567812/749ddddcd711/ijbsv04p0362g01.jpg

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