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向显性疾病转变过程中的神经认知功能变化:精神分裂症和双相情感性精神病风险个体的比较。

Changes in neurocognitive functioning during transition to manifest disease: comparison of individuals at risk for schizophrenic and bipolar affective psychoses.

作者信息

Metzler S, Dvorsky D, Wyss C, Müller M, Gerstenberg M, Traber-Walker N, Walitza S, Theodoridou A, Rössler W, Heekeren K

机构信息

The Zurich Program for Sustainable Development of Mental Health Services (ZInEP),University Hospital of Psychiatry Zurich,Switzerland.

Department of Child and Adolescent Psychiatry,University of Zurich,Switzerland.

出版信息

Psychol Med. 2015 Jul;45(10):2123-34. doi: 10.1017/S0033291715000057. Epub 2015 Feb 2.

Abstract

BACKGROUND

Neurocognitive deficits are important aspects of schizophrenic disorder because they have a strong impact on social and vocational outcomes. Previously it was assumed that cognitive abilities progressively deteriorate with illness onset. However, recent research results have contradicted this with observations of continuous or even improved performance in individuals at risk for psychosis or manifest schizophrenia. The objective of our longitudinal study was to examine neurocognitive functioning in help-seeking individuals meeting basic symptoms or ultra-high-risk criteria for schizophrenic psychosis (HRSchiz) or risk criteria for affective psychosis (HRBip). The progression of cognitive functioning in individuals converting to psychosis was compared with that of at-risk individuals who did not convert during the follow-up period.

METHOD

Data were available from 86 study participants who completed neurocognitive and clinical assessments at baseline and, on average, 12.8 (s.d. = 1.5) months later. Neurocognitive measures were grouped according to their load in factor analysis to five cognitive domains: speed, attention, fluency, learning and memory, and working memory.

RESULTS

Neurocognitive functioning in HRSchiz and HRBip individuals generally improved over time. Subjects converting to manifest psychosis displayed a stable neurocognitive profile from baseline to follow-up. Compared with non-converters, they had already demonstrated a significantly lower level of performance during their baseline examinations.

CONCLUSIONS

Our data provide no evidence for a progressive cognitive decline in individuals at risk of psychosis. In line with the neurodevelopmental model, our findings suggest that cognitive deficits are already present very early, before or during the prodromal stage of the illness.

摘要

背景

神经认知缺陷是精神分裂症的重要方面,因为它们对社会和职业结局有很大影响。以前认为认知能力会随着疾病发作而逐渐恶化。然而,最近的研究结果与之相矛盾,观察到有精神病风险或明显精神分裂症的个体的表现持续甚至有所改善。我们纵向研究的目的是检查符合精神分裂症精神病基本症状或超高风险标准(HRSchiz)或情感性精神病风险标准(HRBip)的求助个体的神经认知功能。将转化为精神病的个体的认知功能进展与随访期间未转化的高危个体进行比较。

方法

数据来自86名研究参与者,他们在基线时完成了神经认知和临床评估,平均在12.8(标准差 = 1.5)个月后再次评估。神经认知测量根据其在因子分析中的负荷分为五个认知领域:速度、注意力、流畅性、学习和记忆以及工作记忆。

结果

HRSchiz和HRBip个体的神经认知功能一般随时间改善。转化为明显精神病的受试者从基线到随访显示出稳定的神经认知特征。与未转化者相比,他们在基线检查期间的表现水平已经显著较低。

结论

我们的数据没有提供证据表明有精神病风险的个体存在渐进性认知下降。与神经发育模型一致,我们的研究结果表明认知缺陷在疾病前驱期之前或期间就已经很早就存在了。

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