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首页> 外文期刊>Genetic testing and molecular biomarkers >Childhood Obesity and the Role of Dopamine D2 Receptor and Cannabinoid Receptor-1 Gene Polymorphisms
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Childhood Obesity and the Role of Dopamine D2 Receptor and Cannabinoid Receptor-1 Gene Polymorphisms

机译:儿童肥胖与多巴胺D2受体和大麻素受体1基因多态性的作用

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摘要

The dopaminergic and endocannabinoid systems are involved in regulation of feeding behavior. The aim of the study is to examine the possible relation between polymorphisms of the dopamine D2 receptor (DRD2) and cannabinoid receptor-1 (CNR1) genes and childhood obesity. Methods: A hundred obese children and 100 healthy controls were analyzed for DRD2 TaqlA and TaqlB and CNR1 1359G/A polymorphisms. Genotyping was performed by polymerase chain reaction and restriction fragment length polymorphism. Results: There were no statistically significant differences in DRD2 TaqlA and DRD2 TaqlB genotypes or allelic frequencies between obese children and controls (p>0.05). In patients with TaqlB2 allele, morbid obesity was less frequent (p = 0.010). The frequency of the A allele of CNR1 1359G/A polymorphism was significantly higher in obese children than in controls (21.0% vs. 13.0%, p = 0.0166). The frequency of genotypes AG and GG of the CNR1 1359G/A SNP was different between obese children and control subjects (for AG: 34.0% vs. 22.0%, p = 0.0294; for GG: 62.0% vs. 76.0%, p = 0.0162, respectively). Conclusions: No significant difference was found between genotypes and alleles of DRD2 TaqlA and DRD2 TaqlB polymorphism in patients and controls, while the CNR1 receptor 1359G/A polymorphism and the presence of the A allele may be one risk factor for susceptibility to obesity.
机译:多巴胺能和内源性大麻素系统参与进食行为的调节。该研究的目的是研究多巴胺D2受体(DRD2)和大麻素受体1(CNR1)基因多态性与儿童肥胖之间的可能关系。方法:分析了100名肥胖儿童和100名健康对照者的DRD2 TaqlA和TaqlB以及CNR1 1359G / A多态性。通过聚合酶链反应和限制性片段长度多态性进行基因分型。结果:肥胖儿童与对照组之间的DRD2 TaqlA和DRD2 TaqlB基因型或等位基因频率无统计学差异(p> 0.05)。在患有TaqlB2等位基因的患者中,病态肥胖症的发生率较低(p = 0.010)。肥胖儿童中CNR1 1359G / A多态性的A等位基因频率显着高于对照组(21.0%对13.0%,p = 0.0166)。肥胖儿童和对照组受试者中CNR1 1359G / A SNP基因型AG和GG的频率不同(AG:34.0%vs. 22.0%,p = 0.0294; GG:62.0%vs. 76.0%,p = 0.0162 , 分别)。结论:DRD2 TaqlA和DRD2 TaqlB多态性的基因型和等位基因在患者和对照中无显着差异,而CNR1受体1359G / A多态性和A等位基因的存在可能是肥胖易感性的危险因素之一。

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  • 来源
    《Genetic testing and molecular biomarkers》 |2012年第12期|1408-1412|共5页
  • 作者单位

    Department of Pediatrics Faculty of Medicine University of Gaziantep Gaziantep University Hospital Universite Bulvari 27310 Gaziantep Turkey;

    Departments of Pharmacology, Faculty of Medicine,University of Gaziantep, Gaziantep University Hospital, Gaziantep, Turkey;

    Departments of Medical Biology and Genetics, and Faculty of Medicine,University of Gaziantep, Gaziantep University Hospital, Gaziantep, Turkey;

    Departments of Pharmacology, Faculty of Medicine,University of Gaziantep, Gaziantep University Hospital, Gaziantep, Turkey;

    Departments of Endocrinology and Metabolism, Faculty of Medicine,University of Gaziantep, Gaziantep University Hospital, Gaziantep, Turkey;

    Departments of Medical Biology and Genetics, and Faculty of Medicine,University of Gaziantep, Gaziantep University Hospital, Gaziantep, Turkey;

    Departments of Pediatrics, Faculty of Medicine,University of Gaziantep, Gaziantep University Hospital, Gaziantep, Turkey;

    Departments of Pharmacology, Faculty of Medicine,University of Gaziantep, Gaziantep University Hospital, Gaziantep, Turkey;

  • 收录信息 美国《科学引文索引》(SCI);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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