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No association between Val158Met of the COMT gene and susceptibility to schizophrenia in the Syrian population

机译:COMT基因的Val158Met与叙利亚人群中的精神分裂症易感性之间没有关联

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Background:The Val158Met single nucleotide polymorphism of the COMT gene has been implicated in the aetiology of schizophrenia, although results from different populations have been conflicting.Aims:The aim of the present study was to investigate possible association between schizophrenia and Val158Met in a novel Arab population from Syria.Methods and Materials:71 unrelated schizophrenic subjects (45 men) and 102 unrelated healthy controls (62 men) were recruited to take part in this case- control study. The Val158Met of the COMT gene was genotyped for patients and controls, using a new optimized PCR-RFLP method.Results:the results demonstrated that there is no statistically significant difference between the two groups.Conclusion:This study does not support that Val158Met has an influence on susceptibility for schizophrenia in this population.
机译:背景:尽管来自不同人群的结果相互矛盾,但COMT基因的Val158Met单核苷酸多态性已与精神分裂症的病因有关。目的:本研究的目的是研究新型阿拉伯人中精神分裂症与Val158Met之间的可能关联。方法和材料:招募了71名无关的精神分裂症患者(45名男性)和102名无关的健康对照者(62名男性)参加了这项病例对照研究。使用新的优化PCR-RFLP方法对COMT基因的Val158Met进行了基因分型。结果:结果表明两组之间无统计学差异。结论:本研究不支持Val158Met具有对这个人群中精神分裂症易感性的影响。

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