Evidence map›Paper›PMID 28587689›Full record

ArticlePsychological medicine2017

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

M Russo, T E Van Rheenen, M Shanahan, K Mahon, M M Perez-Rodriguez, A Cuesta-Diaz, E Larsen, A K Malhotra, K E Burdick

Open access · greenAbstract read
In one paragraph

Article in Psychological medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 25 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed, 2 pooled it
6.2field-weighted citation impact, top 3% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 2 syntheses or guidelines pooled it, 73 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
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  6. Transdiagnostic subgroups of cognitive impairment in early affective and psychotic illness.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2024
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  11. Review
  12. Facial processing in bipolar disorder is mediated by clinical and biological aspects.Revista brasileira de psiquiatria (Sao Paulo, Brazil : 1999) · 2022
    Article
  13. Article
  14. Article
  15. Cognitive heterogeneity is a key predictor of differential functional outcome in patients with bipolar disorder.European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology · 2021
    Article
  16. Article
  17. Neuropsychology of Bipolar Disorder.Current topics in behavioral neurosciences · 2021
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 3 countries.

M RussoDepartment of Psychiatry,Icahn School of Medicine at Mount Sinai School of Medicine,New York, NY,USA.
T E Van RheenenMelbourne Neuropsychiatry Centre,Department of Psychiatry,University of Melbourne,Melbourne,Australia.
M ShanahanDepartment of Psychiatry,Icahn School of Medicine at Mount Sinai School of Medicine,New York, NY,USA.
K MahonDepartment of Psychiatry,Icahn School of Medicine at Mount Sinai School of Medicine,New York, NY,USA.
M M Perez-RodriguezDepartment of Psychiatry,Icahn School of Medicine at Mount Sinai School of Medicine,New York, NY,USA.
A Cuesta-DiazDepartment of Psychiatry,Icahn School of Medicine at Mount Sinai School of Medicine,New York, NY,USA.
E LarsenDepartment of Psychiatry,Icahn School of Medicine at Mount Sinai School of Medicine,New York, NY,USA.
A K MalhotraZucker Hillside Hospital - Northwell Health System,Glen Oaks, NY,USA.
K E BurdickDepartment of Psychiatry,Icahn School of Medicine at Mount Sinai School of Medicine,New York, NY,USA.
Icahn School of Medicine at Mount Sinai · USBrigham and Women's Hospital · USKing's College London · GBThe Alfred Hospital · AUZucker Hillside Hospital · US

Funding

MSHS Translational Science HubKL2TR001435 · NCATS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MOSKOWITZ, ALAN J · 2015 to 2019
$3.8M
Understanding the Neurocognitive Heterogeneity in Bipolar DisorderR01MH100125 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BURDICK, KATHERINE ELIZABETH · 2013 to 2017
$2.1M
Neurocognition as an endophenotype in bipolar disorderK23MH077807 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI BURDICK, KATHERINE ELIZABETH · 2008 to 2012
$774k
Correlates of Suicidal Ideation in Bipolar DisorderR03MH079995 · NIMH · FEINSTEIN INSTITUTE FOR MEDICAL RESEARCH · PI BURDICK, KATHERINE ELIZABETH · 2007 to 2007
$83k
Neurocognitive Heterogeneity in Patients with Psychosis _ A Dimensional ApproachI01CX000995 · VA · JAMES J PETERS VA MEDICAL CENTER · PI BURDICK, KATHERINE ELIZABETH · 2014 to 2019
–
CSRD VA I01 CX000995NCATS NIH HHS KL2 TR001435NIMH NIH HHS K23 MH077807NIMH NIH HHS R01 MH100125NIMH NIH HHS R03 MH079995
6 · The paper itself

Abstract

backgroundOur 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.

methodsCluster 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).

resultsThree 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.

conclusionsThis 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.

Indexed as

SiblingsAdultBipolar DisorderCluster AnalysisCognitive DysfunctionFemaleHumansMaleMiddle AgedBipolar disordercognitionheterogeneityunaffected siblingverbal memory

Identifiers

PMID28587689
PMCPMC5856455
OpenAlexW2621825852

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.