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Molecular Genetic Studies of Cognitive Deficit in Schizophrenia

机译:精神分裂症认知缺陷的分子遗传学研究

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Cognitive deficit is a key feature of schizophrenia. Genetic factors are thought to contribute to cognitive disturbances in schizophrenic patients. However, the role of specific genes in the development of cognitive deficit remains elusive. The review considers the current studies on the association between gene polymorphisms and cognitive dysfunction in schizophrenics. Main attention is drawn to the consistently reproducible association between the COMT polymorphism Val 158Met and cognitive traits, which has a biological and neuropsychological support. The association studies with the genes for the dopamine and serotonin receptors, brain-derived neurotrophic factor, dysbindin, DISC1, D-amino acid oxidase, and D-amino acid oxidase activator are reviewed as well.
机译:认知缺陷是精神分裂症的关键特征。人们认为遗传因素会导致精神分裂症患者的认知障碍。然而,特定基因在认知缺陷发展中的作用仍然难以捉摸。审查认为目前有关精神分裂症的基因多态性与认知功能障碍之间的关联的研究。主要关注的是COMT多态性Val 158Met与认知特征之间的一致可重复关联,该关联具有生物学和神经心理学支持。还审查了与多巴胺和5-羟色胺受体基因,脑源性神经营养因子,dysbindin,DISC1,D-氨基酸氧化酶和D-氨基酸氧化酶激活剂的关联研究。

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