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The association of the rs1049353 polymorphism of the CNR1 gene with hypoadiponectinemia

机译:CNR1基因的rs1049353多态性与低脂联素血症的相关性

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The endocannabinoid system (ECS) is an important physiological system that modulates appetite, food intake, energy homeostasis, substance addiction. It is comprised of the cannabinoid receptors (CB1 and CB2), the endogenous lipid ligands of these receptors and the enzymes that mediate the endogenous ligands' biosynthesis and degradation. CB1 receptor is expressed in the brain, adipose tissue, liver, skeletal muscle, gastrointestinal tract and pancreas. The CB1 receptor is encoded by CNR1 gene located at 6q14-q15 level. The aim of our study was to investigate the possible correlation between rs1049353 polymorphism of the CNR1 gene with levels of adiponectin in a group of subjects from Romania. The study included 305 subjects divided in two groups according to their fasting adiponectin levels. Fasting adiponectin levels were determined using ELISA technique. The genotyping of the rs1049353 polymorphism of the CNR1 gene was made using the Real-Time PCR technique. The statistical analysis was performed using De Finetti's program. The differences between the allelic frequencies indicated that the presence of G-wild allele seems to confer risk for expressing low levels of adiponectin (OR=1.917; 95%C.I.=1.353-2.715; p=0.00023) and A-mutant allele seems to be protective (OR=0.522; 95%C.I.=0.368-0.739; p=0.00023). At the test of allelic positivity, the presence of the G-allele conferred risk of hypoadiponectinemia (OR=2.113; 95%C.I.=1.324-3.373). In conclusion, this study indicates that the rs1049353 polymorphism of the CNR1 gene is associated with decreased levels of adiponectin. Further research is needed in order to elucidate the link between the polymorphisms of the CNR1 gene and adiponectin levels.
机译:内源性大麻素系统(ECS)是重要的生理系统,可调节食欲,食物摄入,能量稳态,物质成瘾。它由大麻素受体(CB1和CB2),这些受体的内源性脂质配体以及介导内源性配体的生物合成和降解的酶组成。 CB1受体在脑,脂肪组织,肝脏,骨骼肌,胃肠道和胰腺中表达。 CB1受体由位于6q14-q15水平的CNR1基因编码。我们的研究目的是研究罗马尼亚的一组受试者中CNR1基因的rs1049353多态性与脂联素水平之间的可能相关性。该研究包括305名受试者,根据其禁食脂联素水平分为两组。用ELISA技术测定空腹脂联素水平。使用实时PCR技术对CNR1基因的rs1049353多态性进行基因分型。使用De Finetti的程序进行统计分析。等位基因频率之间的差异表明,G野生型等位基因的存在似乎赋予表达低水平脂联素的风险(OR = 1.917; 95%CI = 1.353-2.715; p = 0.00023),而A突变等位基因似乎是保护性的(OR = 0.522; 95%CI = 0.368-0.739; p = 0.00023)。在等位基因阳性测试中,G等位基因的存在赋予了低脂联素血症的风险(OR = 2.113; 95%C.I. = 1.324-3.373)。总之,这项研究表明CNR1基因的rs1049353多态性与脂联素水平的降低有关。为了阐明CNR1基因的多态性与脂联素水平之间的联系,需要进一步的研究。

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