A meta-analysis of neurocognition in youth with familial high risk for bipolar disorder

被引:60
|
作者
Bora, E. [1 ,2 ,3 ]
Ozerdem, A. [1 ,4 ]
机构
[1] Dokuz Eylul Univ, Fac Med, Dept Psychiat, Izmir, Turkey
[2] Univ Melbourne, Dept Psychiat, Melbourne Neuropsychiat Ctr, Carlton, Vic 3053, Australia
[3] Melbourne Hlth, Carlton, Vic 3053, Australia
[4] Dokuz Eylul Univ, Hlth Sci Inst, Dept Neurosci, Izmir, Turkey
关键词
Bipolar disorder; High-risk; Familial; Cognition; COGNITIVE IMPAIRMENT; EUTHYMIC PATIENTS; YOUNG-ADULTS; I DISORDER; SCHIZOPHRENIA; CHILDREN; PSYCHOSIS; DEFICITS; ENDOPHENOTYPES; IDENTIFICATION;
D O I
10.1016/j.eurpsy.2017.02.483
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Objective: Neuropsychological impairment, including deficits in social cognition is evident in subjects at genetic high-risk for psychosis. However, findings in youth at genetic risk to bipolar disorder (BP) have been suggested to be less supportive of premorbid deficits. We aimed to conduct a meta-analysis of cognitive deficits in youth with familiar risk for bipolar disorder (FHR-BD). Methods: A novel meta-analysis of FHR-BD (mean age 10-25), including 18 studies (786 offsprings/siblings of patients with BD and 794 healthy controls), was conducted. Results: Both general cognition (d = 0.29, CI = 0.15-0.44) and social cognition (d = 0.23, CI = 0-0.45) were impaired in FHR-BD. In comparison to controls, FHR-BD had significant deficits in several cognitive domains, including visual memory (d = 0.35), verbal memory (d = 0.21), processing speed (d = 0.26) and sustained attention (d = 0.36). There was no significant difference between FHR-BD and controls in planning and working memory. Conclusions: Cognitive deficits are evident in individuals who are at genetic high-risk for developing BD. Neurodevelopmental abnormalities are likely playing a role not only in schizophrenia but also in BD. (C) 2017 Elsevier Masson SAS. All rights reserved.
引用
收藏
页码:17 / 23
页数:7
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