Human beta(2)-adrenergic receptor polymorphisms: No association with essential hypertension in black or white Americans

Citation
Hg. Xie et al., Human beta(2)-adrenergic receptor polymorphisms: No association with essential hypertension in black or white Americans, CLIN PHARM, 67(6), 2000, pp. 670-675
Citations number
38
Categorie Soggetti
Pharmacology,"Pharmacology & Toxicology
Journal title
CLINICAL PHARMACOLOGY & THERAPEUTICS
ISSN journal
00099236 → ACNP
Volume
67
Issue
6
Year of publication
2000
Pages
670 - 675
Database
ISI
SICI code
0009-9236(200006)67:6<670:HBRPNA>2.0.ZU;2-7
Abstract
Background and Objectives: The most common polymorphisms of the human beta( 2)-adrenergic receptor - Arg16 --> Gly and Gln27 --> Glu - are associated w ith alterations in beta(2)-adrenergic receptor responses, both in vitro and in vivo. beta(2)-Adrenergic receptor-mediated vascular responses are affec ted by ethnicity, blood pressure, and genotype. We tested the hypothesis th at these two common beta(2)-adrenergic receptor genetic variants are associ ated with essential hypertension in black or white Americans. Subjects and Methods: In a population-based case-control association study, the relationship between beta(2)-adrenergic receptor genotypes and hyperte nsion was examined in 307 normotensive subjects (128 black and 179 white) a nd 356 hypertensive subjects (155 black and 201 white). A polymerase chain reaction-based single-stranded conformational polymorphism method with dire ct sequencing of the bands of interest was used to detect the two frequentl y occurring beta(2)-adrenergic receptor variants (Arg16-->Gly, Gln27-->Glu) . Results: No significant differences in the distributions of alleles and gen otypes of the tested beta(2)-adrenergic receptor variants were found betwee n normotensive and hypertensive groups from either black or white Americans (all P >.05). There was a marked interethnic difference in the frequency o f the Gln27-->Glu beta(2)-adrenergic receptor polymorphism in both normoten sive and hypertensive subjects. Ln normotensive white: subjects, the varian t Glu27 allele (35.2% versus 18.0%; P <.0001) and Glu27 homozygous genotype (14.0% versus 4.7%; P <.01) mere more common than in black subjects. Simil arly, in hypertensive white subjects, the variant Glu27 allele (35.8% versu s 18.4%; P <.0001) and the Glu27 homozygous genotype (15.9% ret sus 2.6%; P <.0001) were more common than in black subjects. Conclusions: These data suggest that although there are marked ethnic diffe rences in their distribution, the common genetic polymorphisms of the human beta(2)-adrenergic receptor gene do not cosegregate with the presence of h ypertension in either black or white Americans.