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Association between BDNF Val66Met polymorphism and cognitive performance in antipsychotic-na?ve patients with schizophrenia

机译:BDNF Val66Met多态性与初治精神分裂症精神分裂症患者认知能力的关系

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摘要

Cognitive impairment is one of the core symptoms in schizophrenia, which reflects the neurodevelopmental deficits in the etiology of this disease. Brain-derived neurotrophic factor (BDNF) plays an important role in various neurodevelopmental processes. Growing evidence has shown that BDNF may be involved in the etiology of schizophrenia. The aim of this study was to examine the association of the BDNF Val66Met polymorphism with cognition in patients with schizophrenia. Various neuropsychological tests including the Wechsler Adult Intelligence Scale-Revised, the Wechsler Memory Scale-Revised, and the Wisconsin Card Sorting Test (WCST) were employed in a sample of 112 antipsychotic-na?ve patients with schizophrenia and 63 healthy controls. We examined the Val66Met polymorphism in the 112 patients and 394 controls. Among the patients, cognition was compared between Met allele carriers and non-Met allele carriers. A wide range of cognitive deficits were demonstrated in the schizophrenic patients, compared with the controls (Ps<0.01). No significant differences of genotype or allele distribution were identified between patients and controls. The patients with Met allele showed more percent WCST perseverative errors than those without Met allele (P=0.007). After stratification based on gender, an association between the Met allele and a higher percentage of perseverative errors was found in male patients (P=0.014), but not in females (P=0.09). Cognitive performance is broadly impaired in schizophrenic patients. The BDNF Val66Met polymorphism may be involved in the impaired executive function. This effect may have gender-specific characteristics.
机译:认知障碍是精神分裂症的核心症状之一,反映了该病病因的神经发育缺陷。脑源性神经营养因子(BDNF)在各种神经发育过程中起重要作用。越来越多的证据表明,BDNF可能与精神分裂症的病因有关。这项研究的目的是检查BDNF Val66Met多态性与精神分裂症患者的认知之间的关系。在112名抗精神病治疗初治型精神分裂症患者和63名健康对照者的样本中,进行了各种神经心理学测试,包括修订后的Wechsler成人智力量表,Wechsler记忆量表和Wisconsin卡分类测试(WCST)。我们检查了112名患者和394名对照的Val66Met多态性。在患者中,比较了Met等位基因携带者和非Met等位基因携带者的认知。与对照组相比,精神分裂症患者表现出广泛的认知缺陷(Ps <0.01)。在患者和对照之间没有发现基因型或等位基因分布的显着差异。 Met等位基因患者的WCST持久性错误百分比高于无Met等位基因的患者(P = 0.007)。在按性别分层后,男性患者中发现Met等位基因与较高百分比的持续性错误之间存在关联(P = 0.014),而女性则没有(P = 0.09)。精神分裂症患者的认知能力广泛受损。 BDNF Val66Met多态性可能与执行功能受损有关。这种影响可能具有特定于性别的特征。

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