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
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.