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Catechol-O-Methyltransferase Val158Met Polymorphism and Antisaccade Eye Movements in Schizophrenia

机译:儿茶酚-O-甲基转移酶Val158Met多态性与精神分裂症患者抗眼球运动

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摘要

The catechol-O-methyltransferase (COMT) enzyme catabolizes dopamine. The val158met single nucleotide polymorphism (rs4680) in the COMT gene has received considerable attention as a candidate gene for schizophrenia as well as for frontally mediated cognitive functions. Antisaccade performance is a good measure of frontal lobe integrity. Deficits on the task are considered a trait marker for schizophrenia. The aim of this study was to investigate the association of COMT val158met polymorphism with antisaccade eye movements in schizophrenia patients and healthy controls. Schizophrenia patients (N = 105) and healthy controls (N = 95) underwent infrared oculographic assessment of antisaccades. Subjects were genotyped for COMT val158met and divided into 3 groups according to genotype (val/val, val/met, and met/met). Patients displayed significantly more reflexive errors, longer and more variable latency, and lower amplitude gain than controls (all P 0.1). There were no significant associations of genotype with measures of amplitude gain or spatial error (P > 0.2). The results suggest that COMT val158 carrier status is associated with better performance on the antisaccade task. Possible explanations of this finding are discussed.
机译:儿茶酚-O-甲基转移酶(COMT)酶分解多巴胺。作为精神分裂症和正面介导的认知功能的候选基因,COMT基因中的val 158 met单核苷酸多态性(rs4680)已引起了广泛的关注。抗扫视能力是额叶完整性的良好指标。任务不足被认为是精神分裂症的特征标记。这项研究的目的是调查COMT val 158 met多态性与精神分裂症患者和健康对照者的抗扫视运动有关。精神分裂症患者(N = 105)和健康对照组(N = 95)接受了抗眼球的红外眼底仪评估。对受试者的COMT val 158 met进行基因分型,并根据基因型(val / val,val / met和met / met)分为3组。与对照相比,患者表现出更多的反射错误,更长和更多的潜伏期以及更低的幅度增益(均P 0.1)。基因型与幅度增益或空间误差的度量之间无显着关联(P> 0.2)。结果表明,COMT val 158 携带者状态与反扫视任务的更好性能有关。讨论了这一发现的可能解释。

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  • 来源
    《Schizophrenia Bulletin》 |2010年第1期|p.157-164|共8页
  • 作者

    Hannes Petursson;

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  • 入库时间 2022-08-18 01:07:24

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