Evidence map›Paper›PMID 30294823›Full record

ArticleBipolar disorders2018

Cluster analysis with MOODS-SR illustrates a potential bipolar disorder risk phenotype in young adults with remitted major depressive disorder.

Leah R Kling, Katie L Bessette, Sophie R DelDonno, Kelly A Ryan, Wayne C Drevets, Melvin G McInnis, Mary L Phillips, Scott A Langenecker

Abstract read
In one paragraph

Article in Bipolar disorders, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

  1. Article
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  5. Article
  6. Cognitive Control as a 5-HTFrontiers in psychology · 2019
    Article
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

8 authors.

Leah R KlingUniversity of Illinois at Chicago, Chicago, Illinois.ORCID 0000-0003-0160-9988
Katie L BessetteUniversity of Illinois at Chicago, Chicago, Illinois.
Sophie R DelDonnoUniversity of Illinois at Chicago, Chicago, Illinois.
Kelly A RyanUniversity of Michigan Medical Center, Ann Arbor, Michigan.
Wayne C DrevetsJanssen Pharmaceutical Companies of Johnson & Johnson, Inc, Titusville, New Jersey.
Melvin G McInnisUniversity of Michigan Medical Center, Ann Arbor, Michigan.
Mary L PhillipsUniversity of Pittsburg Medical Center, Pittsburg, Pennsylvania.
Scott A LangeneckerUniversity of Illinois at Chicago, Chicago, Illinois.

Funding

Strengthening Stakeholder Engagement in Human Research Protections.UL1TR002003 · NCATS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI KARNIK, NIRANJAN SUBHASH, MERMELSTEIN, ROBIN J. · 2016 to 2024
$33.7M
Center for Clinical and Translational ScienceUL1TR000050 · NCATS · UNIVERSITY OF ILLINOIS AT CHICAGO · PI AZAR, DIMITRI T, MERMELSTEIN, ROBIN J. · 2012 to 2014
$9.8M
A High-End 3 Tesla Human MRI Scanner Dedicated to ResearchS10RR028898 · NCRR · UNIVERSITY OF ILLINOIS AT CHICAGO · PI ZHOU, XIAOHONG JOE · 2010 to 2010
$2.9M
Dimensional RDoC Modeling across the Range of Negative Mood DysfunctionR01MH101487 · NIMH · UNIVERSITY OF ILLINOIS AT CHICAGO · PI LANGENECKER, SCOTT A · 2013 to 2016
$2.5M
Neurobiological Intermediate Phenotypes of Major Depressive DisorderR01MH091811 · NIMH · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI LANGENECKER, SCOTT A · 2010 to 2014
$2.3M
NCATS NIH HHS UL1 TR000050NCATS NIH HHS UL1 TR002003NCRR NIH HHS S10 RR028898NIMH NIH HHS R01 MH091811NIMH NIH HHS R01 MH101487
6 · The paper itself

Abstract

objectivesDelays in the diagnosis and detection of bipolar disorder can lead to adverse consequences, including improper treatment and increased suicide risk. The Mood Spectrum Self-Report Measure (MOODS-SR) was designed to capture the full spectrum of lifetime mood symptomology with factor scores for depression and mania symptom constellations. The utility of the MOODS-SR as a tool to investigate homogeneous subgroups was examined, with particular focus on a possible bipolar risk subgroup. Moreover, potential patterns of differences in MOODS-SR subtypes were probed using cognitive vulnerabilities, neuropsychological functioning, and ventral striatum connectivity.

methodsK-mean cluster analysis based on factor scores of MOODS-SR was used to determine homogeneous subgroupings within a healthy and remitted depressed young adult sample (N = 86). Between-group comparisons (based on cluster subgroupings) were conducted on measures of cognitive vulnerabilities, neuropsychological functioning, and ventral striatum rs-fMRI connectivity.

resultsThree groups of participants were identified: one with minimal symptomology, one with moderate primarily depressive symptomology, and one with more severe manic and depressive symptomology. Differences in impulsivity, neuroticism, conscientiousness, facial perception accuracy, and rs-fMRI connectivity exist between moderate and severe groups.

conclusionsWithin a sample of people with and without depression histories, a severe subgroup was identified with potentially increased risk of developing bipolar disorder through use of the MOODS-SR. This small subgroup had higher levels of lifetime depression and mania symptoms. Additionally, differences in traits, affective processing, and connectivity exist between those with a more prototypic unipolar subgrouping and those with potential risk for developing bipolar disorder.

Indexed as

AdultAffectBipolar DisorderCluster AnalysisFemaleHumansImpulsive BehaviorMajor Depressive DisorderMalePhenotypePsychometricsSelf ReportYoung Adultbipolar disorderdepressionneuropsychologyphenotyperesting staterisk factors

Identifiers

PMID30294823
PMCPMC6319908

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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.