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      Neurocognitive subtypes in patients with bipolar disorder and their unaffected siblings

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          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.

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          Author and article information

          Journal
          1254142
          6777
          Psychol Med
          Psychol Med
          Psychological medicine
          0033-2917
          1469-8978
          11 March 2018
          07 June 2017
          December 2017
          01 December 2018
          : 47
          : 16
          : 2892-2905
          Affiliations
          [1 ]Department of Psychiatry, Icahn School of Medicine at Mount Sinai School of Medicine, New York, NY, USA
          [2 ]Department of Psychosis Studies, Institute of Psychiatry, Psychology & Neuroscience, King’s College London, UK
          [3 ]Melbourne Neuropsychiatry Centre, Department of Psychiatry, University of Melbourne, Melbourne, Australia
          [4 ]Brain and Psychological Sciences Research Centre, School of Health Sciences, Swinburne University, Melbourne, Australia
          [5 ]Cognitive Neuropsychiatry Laboratory, Monash Alfred Psychiatry Research Centre, The Alfred Hospital and Central Clinical School, Monash University, Melbourne, Australia
          [6 ]Zucker Hillside Hospital – Northwell Health System, Glen Oaks, NY, USA
          [7 ]Department of Neuroscience, Icahn School of Medicine at Mount Sinai School of Medicine, New York, NY, USA
          [8 ]James J Peters Veteran Administration (VA) Hospital, Bronx, NY, USA
          [9 ]Brigham and Women’s Hospital, Boston, MA, USA
          Author notes
          [* ]Address for correspondence: K. E. Burdick, Ph.D., Icahn School of Medicine at Mount Sinai, 1 Gustave L Levy Place, Box 1230, New York, NY 10029, USA. ( katherine.burdick@ 123456mssm.edu ; kburdick1@ 123456bwh.harvard.edu )
          Article
          PMC5856455 PMC5856455 5856455 nihpa949106
          10.1017/S003329171700143X
          5856455
          28587689
          d11a3edc-27be-4741-9077-0078c88f062f
          History
          Categories
          Article

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

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