4.7 Article

Neurocognitive subtypes in patients with bipolar disorder and their unaffected siblings

Journal

PSYCHOLOGICAL MEDICINE
Volume 47, Issue 16, Pages 2892-2905

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S003329171700143X

Keywords

Bipolar disorder; cognition; heterogeneity; unaffected sibling; verbal memory

Funding

  1. National Institute of Mental Health [R03MH079995, K23MH077807, R01MH100125]
  2. Veterans Health Administration [I01CX000995-03]

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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.

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