4.5 Article

Epistatic interaction between α- and γ-adducin influences peripheral and central pulse pressures in white Europeans

Journal

JOURNAL OF HYPERTENSION
Volume 23, Issue 5, Pages 961-969

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1097/01.hjh.0000166836.70935.e7

Keywords

adducin; epistatic interaction; genetic polymorphism; large arteries; pulse pressure; sodium

Ask authors/readers for more resources

Background Adducin is a membrane skeleton protein consisting of alpha- and beta- or alpha- and gamma-subunits. Mutations in alpha- and beta-adducin are associated with hypertension. In the European Project on Genes in Hypertension, we investigated whether polymorphisms in the genes encoding alpha-adducin (Gly460Trp), beta-adducin (C1797T) and gamma-adducin (A386G), alone or in combination, affected pulse pressure (PP), an index of vascular stiffness. Methods We measured peripheral and central PP by conventional sphygmomanometry and applanation tonometry, respectively. We randomly recruited 642 subjects (1162 nuclear families and 70 unrelated individuals) from three European populations. In multivariate analyses, we used generalized estimating equations and the quantitative transmission disequilibrium test. Results Peripheral and central PP averaged 46.1 and 32.6 mmHg, respectively. Among carriers of the a-adducin Trp allele, peripheral and central PIP were 5.8 and 4.7 mmHg higher in gamma-adducin GG homozygotes than in their AA counterparts, due to an increase in systolic pressure. T-Adducin GG homozygosity was associated with lower urinary Na+/K+ ratio among alpha-adducin Trp allele carriers and with higher urinary alclosterone excretion among alpha-adducin GlyGly homozygotes. Sensitivity analyses in founders and offspring separately, and tests based on the transmission of the gamma-adducin G allele across families, confirmed the interaction between the alpha- and gamma-adducin genes. Conclusions In alpha-adducin Trp allele carriers, peripheral and central PP increased with the gamma-adducin G allele. This epistatic interaction is physiologically consistent with the heterodimeric structure of the protein and its influence on transmembranous sodium transport. (c) 2005 Lippincott Williams & Wilkins.

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.5
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available