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

被引:0
|
作者
Shufeng Chen
Hongwei Wang
Xiangfeng Lu
De-Pei Liu
Jing Chen
Cashell E. Jaquish
Dabeeru C. Rao
James E. Hixson
Tanika N. Kelly
Liping Hou
Laiyuan Wang
Jianfeng Huang
Chung-Shiuan Chen
Treva K. Rice
Paul K. Whelton
Jiang He
Dongfeng Gu
机构
[1] Chinese Academy of Medical Sciences,Division of Population Genetics, Department of Evidence Based Medicine, Cardiovascular Institute, Fu Wai Hospital, Peking Union Medical College
[2] Chinese National Human Genome Center,National Laboratory of Medical Molecular Biology, Institute of Basic Medical Sciences, Peking Union Medical College
[3] Chinese Academy of Medical Sciences,Department of Epidemiology
[4] Tulane University School of Public Health and Tropical Medicine,Department of Medicine
[5] Tulane University School of Medicine,National Heart, Lung, and Blood Institute
[6] National Institute of Health,undefined
[7] Washington University in St. Louis School of Medicine,undefined
[8] University of Texas School of Public Health,undefined
[9] Loyola University Medical Center,undefined
来源
Human Genetics | 2010年 / 128卷
关键词
Blood Pressure Level; Guanine Nucleotide Binding Protein; Recessive Genetic Model; Genotyping Call Rate; Marker Rs4963516;
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中图分类号
学科分类号
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 ± 0.62 vs. 73.46 ± 0.25 mmHg, P = 0.0002) and MAP (91.87 ± 0.68 vs. 89.42 ± 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.
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页码:137 / 143
页数:6
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