Polymorphisms in the GNB3 and ADD1 genes and blood pressure in a Chinese population

被引:6
|
作者
Chen, Shufeng [1 ]
Wang, Hongwei [1 ]
Lu, Xiangfeng [1 ]
Liu, De-Pei [3 ]
Chen, Jing [4 ,5 ]
Jaquish, Cashell E. [6 ]
Rao, Dabeeru C. [7 ]
Hixson, James E. [8 ]
Kelly, Tanika N. [4 ]
Hou, Liping [1 ]
Wang, Laiyuan [1 ]
Huang, Jianfeng [1 ]
Chen, Chung-Shiuan [4 ]
Rice, Treva K. [7 ]
Whelton, Paul K. [9 ]
He, Jiang [4 ,5 ]
Gu, Dongfeng [1 ,2 ]
机构
[1] Chinese Acad Med Sci, Peking Union Med Coll, Div Populat Genet,Dept Evidence Based Med, Cardiovasc Inst,Fu Wai Hosp, 167 Beilishi Rd, Beijing 100037, Peoples R China
[2] Chinese Natl Human Genome Ctr, Beijing, Peoples R China
[3] Chinese Acad Med Sci, Peking Union Med Coll, Inst Basic Med Sci, Natl Lab Med Mol Biol, Beijing 100037, Peoples R China
[4] Tulane Univ, Sch Publ Hlth & Trop Med, Dept Epidemiol, New Orleans, LA 70112 USA
[5] Tulane Univ, Sch Med, Dept Med, New Orleans, LA 70112 USA
[6] NHLBI, NIH, Bethesda, MD 20892 USA
[7] Washington Univ, Sch Med, St Louis, MO USA
[8] Univ Texas Sch Publ Hlth, Houston, TX USA
[9] Loyola Univ Med Ctr, Maywood, IL 60153 USA
基金
美国国家卫生研究院;
关键词
BETA-3 SUBUNIT GENE; ESSENTIAL-HYPERTENSION; ALPHA-ADDUCIN; JAPANESE POPULATION; NO ASSOCIATION; VARIANTS; RENIN;
D O I
10.1007/s00439-010-0834-3
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
A large proportion of the phenotypic variation in blood pressure (BP) appears to be inherited as a polygenic trait. This study examined the association between 12 single nucleotide polymorphisms (SNPs) in the guanine nucleotide binding protein beta polypeptide 3 (GNB3) and adducin 1 alpha (ADD1) genes and systolic (SBP), diastolic (DBP), and mean arterial (MAP) BP. A total of 3,142 individuals from 636 families were recruited from rural north China, and 2,746 met the eligibility criteria for analysis. BP measurements were obtained using a random-zero sphygmomanometer. Genetic variants were determined using SNPlex assays on an automated DNA Sequencer. A mixed linear model was used to estimate the association between each SNP and BP level. After Bonferroni correction, marker rs4963516 of the GNB3 gene remained significantly associated with DBP (corrected P values = 0.006, 0.007 and 0.002 for co-dominant, additive, and recessive models, respectively) and MAP (corrected P values = 0.02, 0.049, and 0.005, respectively). Compared to carriers of the major A allele, CC homozygotes had higher mean DBP (75.81 +/- A 0.62 vs. 73.46 +/- A 0.25 mmHg, P = 0.0002) and MAP (91.87 +/- A 0.68 vs. 89.42 +/- A 0.28 mmHg, P = 0.0004) after adjusting for covariates of age, gender, BMI, study site, and room temperature during BP measurement. In summary, these data support a role for the GNB3 gene in BP regulation in the Chinese population. Future studies aimed at replicating these novel findings are warranted.
引用
收藏
页码:137 / 143
页数:7
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