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BDNF Val66Met 基因变异及其在病态肥胖患者中的血浆水平:一项病例对照研究。

BDNF Val66Met genetic variation and its plasma level in patients with morbid obesity: A case-control study.

机构信息

Colorectal Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.

Department of Biochemistry, School of Medicine, Shiraz University of Medical Sciences, Shiraz, Iran.

出版信息

Gene. 2019 Jul 15;705:51-54. doi: 10.1016/j.gene.2019.04.045. Epub 2019 Apr 17.

Abstract

Obesity is a major public health concern worldwide. Genetic, behavioral, and environmental factors contribute to the multifactorial etiology of obesity. Evidence suggests an association between human Brain-Derived Neurotrophic Factor (BDNF) Val66Met single nucleotide polymorphism (SNP) and obesity. Reduced plasma BDNF levels have also been reported in patients with eating disorders and obesity. We aimed to evaluate the BDNF Val66Met (rs6265) SNP and also plasma BDNF levels in morbidly obese patients compared with healthy normal controls in southern Iran. One hundred morbidly obese patients and one hundred eight healthy normal controls were enrolled. Blood-derived DNA samples were genotyped using the polymerase chain reaction-restriction fragment length polymorphism (PCR-RFLP) method and confirmed by DNA sequencing. Plasma BDNF levels were evaluated using a commercially available sandwich enzyme-linked immunosorbent assay (ELISA) kit for human BDNF. Data analysis was performed by SPSS software, version 18.0. Genotype distribution was not significantly different between obese patients and controls. However, plasma BDNF levels were significantly lower in obese patients compared with controls. Interestingly, a significant association was found between BDNF Val66Met SNP and plasma BDNF levels. No relationship was observed between BDNF Val66Met SNP and all assessed demographic and clinical characteristics of obese patients. It seems that plasma BDNF levels were associated with both obesity and BDNF Val66Met SNP. However, this association was not found between BDNF Val66Met SNP and obesity. Further studies with larger sample sizes are needed for more detailed assessment of this genetic variation as a potential biomarker for obesity.

摘要

肥胖是全球范围内一个主要的公共健康关注点。遗传、行为和环境因素促成了肥胖的多因素病因。有证据表明,人类脑源性神经营养因子(BDNF)Val66Met 单核苷酸多态性(SNP)与肥胖之间存在关联。也有报道称,饮食失调和肥胖患者的血浆 BDNF 水平降低。我们旨在评估伊朗南部病态肥胖患者与健康正常对照组之间 BDNF Val66Met(rs6265)SNP 以及血浆 BDNF 水平。共纳入 100 例病态肥胖患者和 108 例健康正常对照者。采用聚合酶链反应-限制性片段长度多态性(PCR-RFLP)方法对血源性 DNA 样本进行基因分型,并通过 DNA 测序进行确认。使用人 BDNF 的商业夹心酶联免疫吸附测定(ELISA)试剂盒评估血浆 BDNF 水平。数据分析采用 SPSS 软件,版本 18.0。肥胖患者和对照组之间的基因型分布无显著差异。然而,肥胖患者的血浆 BDNF 水平明显低于对照组。有趣的是,BDNF Val66Met SNP 与血浆 BDNF 水平之间存在显著关联。BDNF Val66Met SNP 与肥胖患者所有评估的人口统计学和临床特征之间均未观察到相关性。似乎血浆 BDNF 水平与肥胖和 BDNF Val66Met SNP 均相关。然而,BDNF Val66Met SNP 与肥胖之间未发现这种关联。需要进一步开展更大样本量的研究,以更详细地评估这种遗传变异作为肥胖潜在生物标志物的作用。

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