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Common Variation at the 11-beta Hydroxysteroid Dehydrogenase Type 1 Gene Is Associated With Left Ventricular Mass

Lookup NU author(s): Dr Thahira Rahman, Dr Peter Avery, Professor Bernard Keavney

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Abstract

Background-Polymorphisms in 11-beta hydroxysteroid dehydrogenase type 1 (11 beta-HSD1, encoded by HSD11B1) have been reported to be associated with obesity-related cardiovascular risk factors, such as type II diabetes and hypertension. Left ventricular hypertrophy (LVH) is an independent risk factor for cardiovascular death associated with these factors but has significant additional heritability, the cause of which is undetermined. The 11 beta-HSD1 is believed to maintain tonic inhibition of the mineralocorticoid receptor in cardiomyocytes, and mineralocorticoid receptor activation is involved in the pathophysiology of LVH. We assessed the association between polymorphisms in the HSD11B1 gene and left ventricular mass (LVM) in 248 families ascertained through a proband with hypertension. Methods and Results-LVM was measured by electrocardiography and echocardiography in 868 and 829 participants, respectively. Single-nucleotide polymorphisms (SNPs) tagging common variation in the HSD11B1 gene were genotyped by mass spectrometry. The rs846910 SNP, which lies in the flanking region 5' to exon 1B of HSD11B1, was associated with LVM both by electrocardiography (approximate to 5% lower LVM per copy of the rare allele, P = 0.02) and by echocardiography (approximate to 10% lower LVM per copy of the rare allele, P = 0.003). Genotype explained 1% to 2% of the population variability in LVM, or approximately 5% of the heritable fraction. There were no significant associations between any HSD11B1 SNP and blood pressure or body mass index that could have confounded the association with LVM. Conclusions-Genotype at HSD11B1 has a small, but significant effect on LVM, apparently independently of any effect on obesity-related traits. These findings suggest a novel action of 11 beta-HSD1 in the human cardiomyocyte, which may be of therapeutic importance. (Circ Cardiovasc Genet. 2011;4:156-162.)


Publication metadata

Author(s): Rahman TJ, Mayosi BM, Hall D, Avery PJ, Stewart PM, Connell JMC, Watkins H, Keavney B

Publication type: Article

Publication status: Published

Journal: Circulation: Cardiovascular Genetics

Year: 2011

Volume: 4

Issue: 2

Pages: 156-U196

Print publication date: 14/03/2011

ISSN (print): 1942-325X

ISSN (electronic): 1942-3268

Publisher: Lippincott Williams & Wilkins

URL: http://dx.doi.org/10.1161/CIRCGENETICS.110.958496

DOI: 10.1161/CIRCGENETICS.110.958496


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