精神分裂症和双相情感谱系障碍的个体内和个体间认知变异:跨多个认知领域的研究。

IF 3 Q2 PSYCHIATRY
Beathe Haatveit, Lars T Westlye, Anja Vaskinn, Camilla Bärthel Flaaten, Christine Mohn, Thomas Bjella, Linn Sofie Sæther, Kjetil Sundet, Ingrid Melle, Ole A Andreassen, Dag Alnæs, Torill Ueland
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引用次数: 0

摘要

精神分裂症(SZ)和双相情感障碍(BD)患者的认知存在很大的异质性。更多地了解认知能力变异的程度和临床相关性,可以提高我们对认知障碍的理解。我们使用双广义线性模型(DGLMs)研究了 SZ(905 人)和 BD 谱系障碍(522 人)患者与健康对照组(1170 人)在 22 个变量上的认知平均值和变异性差异。分析显示,90%的变量存在明显的病例对照差异。与健康对照组相比,在精细运动速度、心理处理速度和抑制控制(SZ 和 BD)以及言语学习、记忆和智力功能(SZ)方面,患者在不同测试中表现出更大的个体内(主体内)变异性和更大的个体间(主体间)变异性。我们发现,在 SZ 中,个体内部和个体之间(抑制控制和速度功能)的变异性越大,其功能越低,负面症状越多。在记忆和智力功能的单项测量中,个体间的差异性还与紊乱和阳性症状以及抗抑郁药物的使用有关。在 BD 中,受试者内部与症状严重程度没有关联。然而,个体间更大的变异性(主要是抑制控制和加速功能)与功能低下、更多的消极和紊乱症状、更早的发病年龄、更长的病程以及更多的药物使用有关。这些结果突显出,与对照组相比,患者在各个认知领域的个体差异更大。我们有必要进一步研究认知功能个体差异的原因和相关因素。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Intra- and inter-individual cognitive variability in schizophrenia and bipolar spectrum disorder: an investigation across multiple cognitive domains.

Intra- and inter-individual cognitive variability in schizophrenia and bipolar spectrum disorder: an investigation across multiple cognitive domains.

There is substantial cognitive heterogeneity among patients with schizophrenia (SZ) and bipolar disorders (BD). More knowledge about the magnitude and clinical correlates of performance variability could improve our understanding of cognitive impairments. Using double generalized linear models (DGLMs) we investigated cognitive mean and variability differences between patients with SZ (n = 905) and BD spectrum disorders (n = 522), and healthy controls (HC, n = 1170) on twenty-two variables. The analysis revealed significant case-control differences on 90% of the variables. Compared to HC, patients showed larger intra-individual (within subject) variability across tests and larger inter-individual (between subject) variability in measures of fine-motor speed, mental processing speed, and inhibitory control (SZ and BD), and in verbal learning and memory and intellectual functioning (SZ). In SZ, we found that lager intra -and inter (on inhibitory control and speed functions) individual variability, was associated with lower functioning and more negative symptoms. Inter-individual variability on single measures of memory and intellectual function was additionally associated with disorganized and positive symptoms, and use of antidepressants. In BD, there were no within-subject associations with symptom severity. However, greater inter-individual variability (primarily on inhibitory control and speeded functions) was associated with lower functioning, more negative -and disorganized symptoms, earlier age at onset, longer duration of illness, and increased medication use. These results highlight larger individual differences in patients compared to controls on various cognitive domains. Further investigations of the causes and correlates of individual differences in cognitive function are warranted.

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