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双相障碍患者及其未受影响的兄弟姐妹的神经认知亚型。

Neurocognitive subtypes in patients with bipolar disorder and their unaffected siblings.

机构信息

Department of Psychiatry,Icahn School of Medicine at Mount Sinai School of Medicine,New York, NY,USA.

Melbourne Neuropsychiatry Centre,Department of Psychiatry,University of Melbourne,Melbourne,Australia.

出版信息

Psychol Med. 2017 Dec;47(16):2892-2905. doi: 10.1017/S003329171700143X. Epub 2017 Jun 7.

Abstract

BACKGROUND

Our previous work revealed substantial heterogeneity in the cognitive profile of bipolar disorder (BD) due to the presence of three underlying cognitive subgroups characterized as: globally impaired, selectively impaired, or cognitively intact. In an effort to determine whether these subgroups are differentially related to genetic risk for the illness, we investigated whether cognitive deficits were more pronounced in unaffected siblings (UAS) of BD probands within identified clusters.

METHODS

Cluster analysis was used to identify cognitive clusters in BD (N = 60). UAS (N = 49) were classified into groups according to their proband sibling's cluster assignment; comparisons were made across all clusters and healthy controls (HCs; N = 71).

RESULTS

Three cognitive clusters in BD emerged: a globally impaired (36.7%), a selectively impaired (30%), and a cognitively intact cluster (33.3%). UAS showed a qualitatively similar pattern to their BD siblings; UAS of the globally impaired BD cluster showed verbal memory and general cognitive impairments relative to HCs. In contrast, UAS of the other two clusters did not differ from HCs.

CONCLUSIONS

This study corroborates findings from prior work regarding the presence of cognitive heterogeneity in BD. UAS of subjects in the globally impaired BD cluster presented with a qualitatively similar cognitive profile to their siblings and performed worse than all other BD clusters and UAS groups. This suggests that inherited risk factors may be contributing to cognitive deficits more notably in one subgroup of patients with BD, pointing toward differential causes of cognitive deficits in discrete subgroups of patients with the disorder.

摘要

背景

我们之前的研究发现,由于存在三种认知亚组,双相情感障碍(BD)的认知特征存在很大的异质性,这三种亚组分别为:整体受损、选择性受损和认知正常。为了确定这些亚组是否与疾病的遗传风险存在差异,我们研究了在确定的聚类中,BD 先证者的未受影响的同胞(UAS)中是否存在更明显的认知缺陷。

方法

采用聚类分析对 BD(N=60)进行认知聚类。根据其先证者兄弟姐妹的聚类分配,将 UAS(N=49)分为不同的组;并对所有聚类和健康对照组(HCs;N=71)进行了比较。

结果

BD 中出现了三个认知聚类:整体受损(36.7%)、选择性受损(30%)和认知正常聚类(33.3%)。UAS 与其 BD 兄弟姐妹表现出相似的模式;与 HCs 相比,BD 聚类中整体受损的 UAS 表现出言语记忆和一般认知障碍。相比之下,其他两个聚类的 UAS 与 HCs 没有差异。

结论

本研究证实了先前关于 BD 认知异质性存在的研究结果。BD 聚类中整体受损的 UAS 与其兄弟姐妹表现出相似的认知特征,表现不如所有其他 BD 聚类和 UAS 组差。这表明遗传风险因素可能在 BD 患者的一个亚组中更显著地导致认知缺陷,这指向了离散亚组患者认知缺陷的不同原因。

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本文引用的文献

1
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2
Discrete neurocognitive subgroups in fully or partially remitted bipolar disorder: Associations with functional abilities.
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4
Cognitive variability in bipolar II disorder: who is cognitively impaired and who is preserved.
Bipolar Disord. 2016 May;18(3):288-99. doi: 10.1111/bdi.12385. Epub 2016 Apr 26.
5
Cognitive reserve in bipolar disorder: relation to cognition, psychosocial functioning and quality of life.
Acta Psychiatr Scand. 2016 May;133(5):386-98. doi: 10.1111/acps.12535. Epub 2015 Dec 30.
6
Identification of Distinct Psychosis Biotypes Using Brain-Based Biomarkers.
Am J Psychiatry. 2016 Apr 1;173(4):373-84. doi: 10.1176/appi.ajp.2015.14091200. Epub 2015 Dec 7.
8
Exploring cognitive heterogeneity in first-episode psychosis: What cluster analysis can reveal.
Psychiatry Res. 2015 Oct 30;229(3):819-27. doi: 10.1016/j.psychres.2015.07.084. Epub 2015 Jul 31.
10
Genetic Sources of Subcomponents of Event-Related Potential in the Dimension of Psychosis Analyzed From the B-SNIP Study.
Am J Psychiatry. 2015 May;172(5):466-78. doi: 10.1176/appi.ajp.2014.13101411. Epub 2015 Jan 23.

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