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首发精神分裂症患者、患者亲属和健康对照者的神经认知评估的因子结构及其家系分析。

Factor structures of the neurocognitive assessments and familial analysis in first-episode schizophrenia patients, their relatives and controls.

机构信息

Psychiatric Laboratory and Department of Psychiatry, West China Hospital, Sichuan University, Chengdu, China.

出版信息

Aust N Z J Psychiatry. 2010 Feb;44(2):109-19. doi: 10.3109/00048670903270381.

Abstract

OBJECTIVES

Schizophrenia patients have a wide range of cognitive deficits. To explore the structure of these deficits and index their psychometric properties in order to define the major separable factors, exploratory factor analysis (EFA) was performed on a series of neuropsychological test results in a sample of Han Chinese first-episode schizophrenia patients, their relatives and controls without mental illness.

METHODS

The factors derived from the composite sample were tested with confirmatory factor analysis (CFA) in each of the subsamples. The heritability of each factor was estimated by using the mixed linear model in order to determine whether the common factor scores describe the familiarity of the data.

RESULTS

A six-factor model of general mental activity, sort and shift, attention and anti-interference, logical memory, reasoning and problem-solving/executive function, and visual reproduction were extracted and confirmed on EFA and CFA. There was a hierarchy in cognitive performance deficits in relatives depending on their relatedness to probands. Patients performed more poorly than siblings/offspring in general mental activity, sort and shift, attention and anti-interference, logical memory, planning and problem-solving, but not in visual reproduction. The logical memory domain was found to be significantly heritable (h(2)=0.34), and reasoning and problem-solving had a marginal heritability of around 0.19.

CONCLUSIONS

Generalized cognitive deficit accounts for the majority of the overall variance of cognitive deficits in schizophrenia. Estimates of heritability were modest. The present results also support the hypothesis that neurocognitive deficits of schizophrenia are familial and could serve as endophenotypes, especially logical memory, which is the most heritable.

摘要

目的

精神分裂症患者存在广泛的认知缺陷。为了探索这些缺陷的结构,并对汉族首发精神分裂症患者、其亲属和无精神疾病的对照组的一系列神经心理学测试结果进行指标测量,以确定主要的可分离因素,对复合样本进行了探索性因子分析(EFA)。

方法

在每个亚组中,使用验证性因子分析(CFA)测试从综合样本中得出的因子。使用混合线性模型估计每个因子的遗传性,以确定共同因子得分是否描述数据的熟悉程度。

结果

从 EFA 和 CFA 中提取并确认了一般心理活动、分类和转移、注意力和抗干扰、逻辑记忆、推理和解决问题/执行功能以及视觉再现的六因子模型。根据与先证者的亲缘关系,亲属的认知表现缺陷存在层次结构。患者在一般心理活动、分类和转移、注意力和抗干扰、逻辑记忆、计划和解决问题方面的表现不如兄弟姐妹/子女差,但在视觉再现方面没有。逻辑记忆领域被发现具有显著的遗传性(h²=0.34),推理和解决问题的遗传性约为 0.19。

结论

广义认知缺陷解释了精神分裂症认知缺陷的大部分总体差异。遗传度的估计适中。本研究结果还支持精神分裂症神经认知缺陷是家族性的假设,可作为表型,尤其是逻辑记忆,其遗传性最强。

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