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首页> 外文期刊>Brain research bulletin >Neurocognitive functioning in a group of offspring genetically at high-risk for schizophrenia in Eastern Turkey.
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Neurocognitive functioning in a group of offspring genetically at high-risk for schizophrenia in Eastern Turkey.

机译:土耳其东部精神分裂症高危人群的后代中有神经认知功能。

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摘要

We assessed major cognitive domains in symptom-free children of patients with schizophrenia compared to the healthy children of parents with no psychopathology using neurocognitive tests. We hypothesized that, offspring at high-risk for schizophrenia would have significant impairment in major domains: attention, memory, verbal-linguistic ability and executive functions. Thirty symptom-free children (17-males, 13-females; intelligence quotient=99.6+/-13.6; age=12.69+/-2.32 and education=5.8+/-2.3 years) having a parent diagnosed with schizophrenia and 37 healthy children matched for gender (19-males, 18-females), IQ (106.05+/-14.70), age (12.48+/-2.58) and years of education (6.0+/-2.5) were evaluated. The study group showed significant poor performance in cognitive domains, such as working memory (assessed with Auditory consonant trigram test), focused attention (Stroop test), attention speed (Trail making test), divided attention (Auditory consonant trigram test), executive functions (Wisconsin card sorting test), verbal fluency (Controlled word association test) and declarative memory (Rey verbal learning and Short-term memory test). However, no group differences were detected either on verbal attention (Digit span forward test) or sustained attention (TOVA, a continuous performance task); the latter as consistently reported to be a predictor of schizophrenia. In order to determine the cognitive endophenotype of schizophrenia, it seems more rational to conduct comprehensive evaluation of neurocognitive domains in well-matched groups via using sufficiently challenging tests to detect slight deficits. In addition, longitudinal studies with a larger sample size evaluating neurocognitive functions combined with genetic analysis may provide clues about explaining the genetic background of the disorder within the endophenocognitype concept and serve as new targets for early interventions.
机译:使用神经认知测验,我们评估了精神分裂症患者无症状儿童与没有心理病理学父母的健康儿童相比的主要认知领域。我们假设,精神分裂症高风险的后代将在以下主要领域显着受损:注意力,记忆力,语言能力和执行功能。 30名无症状儿童(男17例,女13例;智商= 99.6 +/- 13.6;年龄= 12.69 +/- 2.32和受教育程度= 5.8 +/- 2.3岁),其父母被诊断患有精神分裂症,另有37名健康儿童对性别(19位男性,18位女性),智商(106.05 +/- 14.70),年龄(12.48 +/- 2.58)和受教育年限(6.0 +/- 2.5)进行了匹配。该研究组在认知领域表现出显着差的表现,例如工作记忆(听觉辅音三语测验),注意力集中(Stroop测验),注意力速度(跟踪制作测验),注意力分散(听觉辅音三语测验),执行功能(威斯康星卡片分类测试),语言流利度(受控单词联想测试)和陈述式记忆(雷伊语言学习和短期记忆测试)。但是,无论是口头注意(数字跨度向前测试)还是持续注意(TOVA,一项持续的表演任务),都没有发现组间差异。后者一直被认为是精神分裂症的预测因子。为了确定精神分裂症的认知内表型,通过使用足够具有挑战性的测试来检测轻度缺陷,对完全匹配组中的神经认知域进行全面评估似乎更为合理。此外,纵向研究以更大的样本量评估神经认知功能并结合遗传分析,可以为解释内表型识别概念内疾病的遗传背景提供线索,并作为早期干预的新目标。

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