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Free keywords:
LIFE-STYLE INTERVENTION; FATTY LIVER-DISEASE; INSULIN-RESISTANCE;
INDEPENDENT PREDICTOR; SENSITIVITY; ATHEROSCLEROSIS; IDENTIFICATION;
INTERACTOME; INHIBITION; GLUCOSEScience & Technology - Other Topics;
Abstract:
Genetically modified mice models suggest an important role for G-protein-coupled receptor kinase 5 (GRK5) in the pathophysiology of obesity and related disorders. We investigated whether single nucleotide polymorphisms (SNPs) in the gene encoding GRK5 affect cardiometabolic traits in humans. We genotyped 3 common SNPs in intron 1 (rsl980030, rsl0466210, rs9325562) and one SNP in intron 3 (rsl0886471) of GRK5 in 2332 subjects at risk for type 2 diabetes. Total- and visceral fat mass were measured by magnetic resonance (MR) tomography and liver fat content by H-1-MR spectroscopy. Insulin secretion and sensitivity were estimated during an OGTT and measured during the euglycemic, hyperinsulinemic clamp (n = 498). Carriers of the minor allele of rsl0466210 and rsl980030 had higher total- and LDL-cholesterol levels (p = 0.0018 and p = 0.0031, respectively, for rsl0466210; p = 0.0035 and p = 0.0081, respectively, for rsl980030), independently of gender, age, BMI and lipid-lowering drugs. The effects of rsl0466210 withstood Bonferroni correction. Similar associations were observed with apolipoprotein B levels (p = 0.0034 and p = 0.0122, respectively). Carriers of the minor allele of rsl0466210 additionally displayed a trend for higher intima-media thickness of the carotid artery (p = 0.075). GRK5 may represent a novel target for strategies aiming at lowering LDL-cholesterol levels and at modifying cardiovascular risk.
