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Measurement of the levels of leptin, BDNF associated with polymorphisms LEP G2548A, LEPR Gln223Arg and BDNF Val66Met in Thai with metabolic syndrome

机译:患有代谢综合征的泰国人瘦素,BDNF水平与多态性LEP G2548A,LEPR Gln223Arg和BDNF Val66Met的相关性

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Background Metabolic syndrome is a cluster of metabolic risk factors including dyslipidemia, impaired glucose tolerance, hypertension and central obesity. BDNF (Brain-derived neurotrophic factor) and leptin have been implied in the energy homeostasis. The purposes of this study were to examine concentrations of leptin, BDNF and biochemical parameters in metabolic-syndrome subjects and healthy controls, and also to search for associations of leptin gene (LEP) G2548A, leptin receptor gene (LEPR) Gln223Arg, and BDNF gene (BDNF) Val66Met polymorphisms with leptin levels, BDNF levels and metabolic syndrome among Thais. Methods The case-controlled design was performed using 322 Thai volunteers (160 metabolic-syndrome subjects; 162 controls) during the health screening program. Metabolic syndrome was assessed by using the modified National Cholesterol Education Program, Adult Treatment Panel III criteria. The levels of leptin, BDNF, insulin, glucose and lipids were measured in samples. Genotyping of LEP G2548A, LEPR Gln223Arg and BDNF Val66Met was carried out using polymerase chain reaction-restriction fragment length polymorphism technique. Results Serum leptin levels were significantly higher in the metabolic-syndrome group than the control group (p < 0.01), but the BDNF difference between them was not significant. Significant associations of LEPR Gln223Arg polymorphism were found with leptin and glucose levels (p < 0.05), after adjusting for potential covariates. This LEPR polymorphism in the metabolic-syndrome group was also significantly more frequent than in the control group (p < 0.05). However, other gene polymorphisms, LEP G2548A and BDNF Val66Met, showed no significant relationship with leptin levels, BDNF levels or metabolic syndrome. Conclusion These findings suggest leptin levels are linked with metabolic syndrome. LEPR Gln223Arg polymorphism impacted leptin concentrations, and this gene polymorphism may influence susceptibility to metabolic syndrome among Thais.
机译:背景代谢综合征是一组代谢风险因素,包括血脂异常,糖耐量减低,高血压和中枢性肥胖。 BDNF(脑源性神经营养因子)和瘦素已被隐含在能量稳态中。这项研究的目的是检查代谢综合征患者和健康对照者的瘦素,BDNF浓度和生化参数,以及寻找瘦素基因(LEP)G2548A,瘦素受体基因(LEPR)Gln223Arg和BDNF基因的关联(BDNF)Val66Met多态性与泰国人的瘦素水平,BDNF水平和代谢综合征有关。方法在健康筛查程序中,对322名泰国志愿者(160名代谢综合征患者; 162名对照)进行了病例对照设计。代谢综合征是通过修改后的《全国胆固醇教育计划》(成人治疗小组III)标准进行评估的。测量样品中瘦素,BDNF,胰岛素,葡萄糖和脂质的水平。使用聚合酶链反应-限制性片段长度多态性技术对LEP G2548A,LEPR Gln223Arg和BDNF Val66Met进行基因分型。结果代谢综合征组血清瘦素水平明显高于对照组(p <0.01),但两者之间的BDNF差异无统计学意义。调整潜在的协变量后,发现LEPR Gln223Arg多态性与瘦素和葡萄糖水平显着相关(p <0.05)。代谢综合征组的这种LEPR多态性也显着高于对照组(p <0.05)。然而,其他基因多态性,LEP G2548A和BDNF Val66Met,与瘦素水平,BDNF水平或代谢综合征无显着相关性。结论这些发现表明瘦素水平与代谢综合征有关。 LEPR Gln223Arg多态性影响了瘦素的浓度,该基因多态性可能影响泰国人对代谢综合征的易感性。

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