Genome-wide association analysis of plasma B-type natriuretic Peptide in blacks: the jackson heart study.

TitleGenome-wide association analysis of plasma B-type natriuretic Peptide in blacks: the jackson heart study.
Publication TypeJournal Article
Year of Publication2015
AuthorsMusani, S. K., Fox E. R., Kraja A., Bidulescu A., Lieb W., Lin H., Beecham A., Chen M-H., Felix J. F., Fox C. S., Kao W. H. Linda, Kardia S. L. R., Liu C-T., Nalls M. A., Rundek T., Sacco R. L., Smith J., Sun Y. V., Wilson G., Zhang Z., Mosley T. H., & Taylor H. A.
JournalCirc Cardiovasc Genet
Volume8
Issue1
Pagination122-30
Date Published2015 Feb
ISSN1942-3268
Abstract

BACKGROUND: Numerous experimental studies suggest that B-type natriuretic peptide (BNP) is cardioprotective; however, in clinical studies, higher plasma BNP concentrations have been associated with incident cardiovascular disease and higher left ventricular mass. Genetic association studies may allow us to determine the true causal directions without confounding by compensatory mechanisms.

METHODS AND RESULTS: We performed a meta-analysis of 2 genome-wide association results from a total of 2790 blacks. We assumed an additive genetic model in an association analysis of imputed 2.5 million single-nucleotide polymorphism dosages with residuals generated from multivariable-adjusted logarithmically transformed BNP controlling for relevant covariates and population stratification. Two loci were genome-wide significant, a candidate gene locus NPPB (rs198389, P=1.18×10(-09)) and a novel missense variant in the KLKB1 locus (rs3733402, P=1.75×10(-11)) that explained 0.4% and 1.9% of variation in log BNP concentration, respectively. The observed increase in BNP concentration was proportional to the number of effect allele copies, and an average of 8.1 pg/mL increase was associated with 2 allele copies. In a companion study, single-nucleotide polymorphisms in this loci were cross-checked with genome-wide association results for the aldosterone/renin ratio in individuals of European ancestry, and rs3733402 was genome-wide significant (P<5.0×10(-8)), suggesting possible shared genetic architecture for these 2 pathways. Other statistically significant relations for these single-nucleotide polymorphisms included the following: rs198389 with systolic blood pressure in blacks (COGENT consortium) and rs198389 and rs3733402 with left ventricular mass in whites (EchoGEN consortium).

CONCLUSIONS: These findings improve our knowledge of the genetic basis of BNP variation in blacks, demonstrate a possible shared allelic architecture for BNP with aldosterone-renin ratio, and motivate further studies of underlying mechanisms.

DOI10.1161/CIRCGENETICS.114.000900
Alternate JournalCirc Cardiovasc Genet
PubMed ID25561047