Gender-dependent association of HSD11B1 single nucleotide polymorphisms with glucose and HDL-C levels

• Published in: Genetics and molecular biology Vol. 37; no. 3; pp. 490 - 495
• Main Authors: Turek, Luciane Viater, Leite, Neiva, Rodrigues Souza, Ricardo Lehtonen, Lima, Jovana Karoline, Milano, Gerusa Eisfeld, Timossi, Luciana da Silva, Osiecki, Ana Claudia Vecchi, Osiecki, Raul, Alle, Lupe Furtado
• Format: Journal Article
• Language: English
• Published: Brazil Sociedade Brasileira de Genética 01-09-2014
• Subjects: BIOCHEMISTRY & MOLECULAR BIOLOGY; GENETICS & HEREDITY; HSD11B1 gene; Human and Medical Genetics; men; metabolic syndrome; metabolism; women; HSD11B1 gene; metabolic syndrome; metabolism; men; women
• ISSN: 1415-4757; 1678-4685; 1415-4757; 1678-4685
• DOI: 10.1590/S1415-47572014000400003

In this study, we investigated the influence of two SNPs (rs846910 and rs12086634) of the HSD11B1 gene that encodes 11β-hydroxysteroid dehydrogenase type 1(11β-HSD1), the enzyme that catalyzes the conversion of cortisol to cortisone, on variables associated with obesity and metabolic syndrome in 215 individuals of both sexes from southern Brazil. The HSD11B1 gene variants were genotyped using the TaqMan SNP genotyping assay. Glucose, triglycerides, total cholesterol, HDL-cholesterol and LDL-cholesterol were measured by standard automated methods. Significant results were found in women, with carriers of the G allele of SNP rs12086634 having higher glucose levels than non-carriers. Carriers of the A allele of SNP rs846910 had higher levels of HDL-cholesterol. The involvement of both polymorphisms as independent factors in determining the levels of glucose and HDL-cholesterol was confirmed by multiple regression analysis (β = 0.19 ±0.09, p = 0.03 and β= 0.22 ± 0.10, p = 0.03, respectively). Our findings suggest that the HSD11B1SNPs studied may indirectly influence glucose and HDL-cholesterol metabolism in women, possibly through down-regulation of the HSD11B1 gene by estrogen.