A Biallelic Gene Polymorphism of CYP11B2 Predicts Increased Aldosterone to Renin Ratio in Selected Hypertensive Patients

• Published in: The journal of clinical endocrinology and metabolism Vol. 88; no. 6; pp. 2495 - 2500
• Main Authors: Nicod, Jérôme, Bruhin, David, Auer, Lucas, Vogt, Bruno, Frey, Felix J., Ferrari, Paolo
• Format: Journal Article
• Language: English
• Published: United States Oxford University Press 01.06.2003; Copyright Oxford University Press
• Subjects: Adult; Aldosterone; Aldosterone - blood; Aldosterone synthase; Alleles; Cytochrome P-450 CYP11B2 - genetics; Female; Gene Frequency; Gene polymorphism; Genotype; Haplotypes; Humans; Hypertension; Hypertension - blood; Hypertension - genetics; Linkage disequilibrium; Male; Middle Aged; Polymorphism, Genetic; Prognosis; Renin; Renin - blood
• ISSN: 0021-972X; 1945-7197
• DOI: 10.1210/jc.2002-021598

Altered control of aldosterone synthase (CYP11B2) gene expression may modulate aldosterone secretion, as suggested by a raised aldosterone to renin ratio (ARR) in some patients with essential hypertension.We compared the frequency of two linked CYP11B2 polymorphisms, one in the steroidogenic factor-1 (SF-1) binding site and the other an intronic conversion (Int2) in relation to ARR in 141 hypertensive patients. Patients were divided into groups with either normal or high supine ARR using a cut-off threshold of 145 pmol/liter per ng/liter. Supine ARR was normal in 104 patients and raised in 37 patients. The two polymorphisms were in strong linkage disequilibrium (χ2 = 123.8; P < 0.0001). The SF-1 T and Int2 C alleles were more prevalent among patients with high ARR (46% and 43%, respectively) than with normal ARR (22% and 17%; P < 0.01 and P < 0.005, respectively). Odds ratios for raised ARR in subjects with a homozygous SF-1 T and Int2 C haplotype were 6.1 (95% confidence interval, 1.6–22.5; P < 0.005) when compared with the contrasting haplotype. Linear modeling of individual postural changes in renin and aldosterone showed a maximal achievable aldosterone increase of 110 pmol/liter with no mutated haplotype and 500 pmol/liter with two mutated haplotypes. These findings support the view of a molecular basis regulating aldosterone production.