首页> 美国卫生研究院文献>Bosnian Journal of Basic Medical Sciences >Analysis of manganese superoxide dismutase (MnSOD: Ala-9Val) and glutathione peroxidase (GSH-Px: Pro 197 Leu) gene polymorphisms in mood disorders
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Analysis of manganese superoxide dismutase (MnSOD: Ala-9Val) and glutathione peroxidase (GSH-Px: Pro 197 Leu) gene polymorphisms in mood disorders

机译:情绪障碍中锰超氧化物歧化酶(MnSOD:Ala-9Val)和谷胱甘肽过氧化物酶(GSH-Px:Pro 197 Leu)基因多态性的分析

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摘要

We investigated the etiopathogenetic role of manganese superoxide dismutase (MnSOD) (Ala-çVal) and glutathione peroxidase (GSH-Px) (Pro 197 Leu) gene polymorphisms in patients diagnosed with major depressive disorder (MDD) and bipolar I disorder (BD).Eighty patients with MDD, 82 patients with BD (total 162 patients) and 96 healthy controls were enrolled in this study and genotyped using a Real Time-Quantitative Polymer Chain Reaction (RT-qPCR)-based method.The patients with BD and MDD and the controls had a similar distribution of the genotypes and alleles in the Ala-9Val MnSOD gene polymorphism. Comparison of the MDD group and control group regarding the Pro 197 Leu GSH-Px gene polymorphism revealed similar genotype distribution but different allele distribution. The BD group and control group were similar both for genotypes and for alleles when compared regarding the Pro 197 Leu GSH-Px gene polymorphism. The combined analysis (MDD plus BD) also failed to find any association between the Ala-9Val MnSOD and Pro 197 Leu GSH-Px gene polymorphism.Although small statistical power of the current study the significant difference between patients with depression and the control group for the Pro 197 Leu GSH-Px polymorphism indicates that the distribution of these alleles may have a contribution in the physiopathogenesis of depression. One of the limitation of the current study is that the sample size is too small. Understanding of the exact role of Pro 197 Leu GSH-Px polymorphism in the development of depression needs to further studies with more sample size and high statistical power.
机译:我们调查了锰超氧化物歧化酶(MnSOD)(Ala-çVal)和谷胱甘肽过氧化物酶(GSH-Px)(Pro 197 Leu)基因多态性在诊断为重度抑郁症(MDD)和双相性I型障碍(BD)的患者中的病因。这项研究纳入了80例MDD患者,82例BD患者(总共162例患者)和96名健康对照,并使用基于实时定量聚合物链反应(RT-qPCR)的方法进行了基因分型。对照在Ala-9Val MnSOD基因多态性中的基因型和等位基因分布相似。比较MDD组和对照组的Pro 197 Leu GSH-Px基因多态性,发现相似的基因型分布,但不同的等位基因分布。当比较Pro 197 Leu GSH-Px基因多态性时,BD组和对照组在基因型和等位基因上都相似。组合分析(MDD和BD)也没有发现Ala-9Val MnSOD与Pro 197 Leu GSH-Px基因多态性之间有任何关联。尽管本研究的统计功效很小,但抑郁症患者与对照组之间的显着差异Pro 197 Leu GSH-Px多态性表明这些等位基因的分布可能与抑郁症的生理发病有关。当前研究的局限性之一是样本量太小。要了解Pro 197 Leu GSH-Px多态性在抑郁症发展中的确切作用,需要以更大的样本量和更高的统计能力进行进一步研究。

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