Neurocognitive subtypes in patients with bipolar disorder and their unaffected siblings

被引:55
|
作者
Russo, M. [1 ,2 ]
Van Rheenen, T. E. [3 ,4 ,5 ,6 ]
Shanahan, M. [1 ]
Mahon, K. [1 ]
Perez-Rodriguez, M. M. [1 ]
Cuesta-Diaz, A. [1 ]
Larsen, E. [1 ]
Malhotra, A. K. [7 ]
Burdick, K. E. [1 ,8 ,9 ,10 ]
机构
[1] Icahn Sch Med Mt Sinai, Dept Psychiat, Sch Med, New York, NY 10029 USA
[2] Kings Coll London, Dept Psychosis Studies, Inst Psychiat Psychol & Neurosci, London, England
[3] Univ Melbourne, Melbourne Neuropsychiat Ctr, Dept Psychiat, Melbourne, Vic, Australia
[4] Swinburne Univ, Brain & Psychol Sci Res Ctr, Sch Hlth Sci, Melbourne, Vic, Australia
[5] Monash Univ, Cognit Neuropsychiat Lab, Monash Alfred Psychiat Res Ctr, Alfred Hosp, Melbourne, Vic, Australia
[6] Monash Univ, Cent Clin Sch, Melbourne, Vic, Australia
[7] Northwell Hlth Syst, Zucker Hillside Hosp, Glen Oaks, NY USA
[8] Icahn Sch Med Mt Sinai, Dept Neurosci, Sch Med, New York, NY 10029 USA
[9] James J Peters Veteran Adm VA Hosp, Bronx, NY USA
[10] Brigham & Womens Hosp, 75 Francis St, Boston, MA 02115 USA
关键词
Bipolar disorder; cognition; heterogeneity; unaffected sibling; verbal memory; CONSENSUS COGNITIVE BATTERY; CLUSTER-ANALYSIS; I DISORDER; SCHIZOPHRENIA; PSYCHOSIS; IDENTIFICATION; HETEROGENEITY; METAANALYSIS; VARIABILITY; RELIABILITY;
D O I
10.1017/S003329171700143X
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
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.
引用
收藏
页码:2892 / 2905
页数:14
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