Abstract
OBJECTIVE: To assess in a US general adult population the effect of the functional single-nucleotide polymorphism rs198389 in the promoter region of the gene of brain-type natriuretic peptide (BNP) on 3 commonly used BNP assays, clinical phenotype, disease prevalence, overall survival, and diagnostic test characteristics of BNP as a biomarker. PATIENTS AND METHODS: We genotyped for rs198389 in a random sample of the general population (aged ≥45 years; n=1970; enrolled between June 1, 1997, and September 30, 2000) from Olmsted County, Minnesota. Patients were characterized biochemically, clinically, echocardiographically, and regarding BNP molecular forms (2 assays for BNP and 1 assay for amino-terminal proBNP). Median follow-up was 9 years. RESULTS: Genotype frequencies were in Hardy-Weinberg equilibrium (P=.98): TT genotype, n=645 (32.7%); TC genotype, n=983 (49.9%); and CC genotype, n=342 (17.4%). The C allele independently predicted higher BNP forms (P
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Costello-Boerrigter, L. C., Boerrigter, G., Ameenuddin, S., Mahoney, D. W., Slusser, J. P., Heublein, D. M., … Burnett, J. C. (2011). The effect of the brain-type natriuretic peptide single-nucleotide polymorphism rs198389 on test characteristics of common assays. Mayo Clinic Proceedings, 86(3), 210–218. https://doi.org/10.4065/mcp.2010.0708
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