Evidence map›Paper›PMID 37841877›Full record

ArticleResearch square2023

Brain-based graph-theoretical predictive modeling to map the trajectory of transdiagnostic symptoms of anhedonia, impulsivity, and hypomania from the human functional connectome.

Diego Pizzagalli, Alexis Whitton, Michael Treadway, Ashleigh Rutherford, Poornima Kumar, Manon Ironside, Roselinde Kaiser, Boyu Ren, Rotem Dan

Registry-linked trialOpen access · greenAbstract readPreprint
In one paragraph

Article in Research square, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT01976975 (Multi Level Analysis of Positive Valence Systems Across Mood Disorders), which is not on this map. Not yet cited in PubMed.

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

What it found

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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.

NCT01976975 completednot on this map

Multi Level Analysis of Positive Valence Systems Across Mood Disorders

TypeobservationalSponsorMclean HospitalRan2013 to 2018Enrolled270ConditionsMajor Depressive Disorder, Bipolar Disorder
3 · Its place in the literature

Who cites it

0 citing papers in PubMed, 1 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

9 authors at 1 institution in 3 countries.

Diego PizzagalliHarvard Medical School/McLean Hospital.ORCID 0000-0002-7772-1143
Alexis WhittonBlack Dog Institute, University of New South Wales, Sydney.ORCID 0000-0002-7944-2172
Michael TreadwayEmory University.ORCID 0000-0002-5913-114X
Ashleigh RutherfordMcLean Hospital.
Poornima KumarMcLean Hospital.ORCID 0000-0002-9548-3281
Manon IronsideMcLean Hospital / Harvard Medical School.
Roselinde KaiserMcLean Hospital / Harvard Medical School.
Boyu RenMcLean Hospital / Harvard Medical School.
Rotem DanMcLean Hospital / Harvard Medical School.ORCID 0000-0003-4341-330X
Harvard University · US

Funding

Neuroimaging Studies of Reward Processing in DepressionR37MH068376 · NIMH · UNIVERSITY OF CALIFORNIA-IRVINE · PI Diego A Pizzagalli · 2016 to 2026
$7.4M
Multi level Analysis of Positive Valence Systems Across Mood DisordersR01MH101521 · NIMH · MCLEAN HOSPITAL · PI PIZZAGALLI, DIEGO A · 2013 to 2016
$2.1M
NIMH NIH HHS R01 MH101521NIMH NIH HHS R37 MH068376Wellcome Trust
6 · The paper itself

Abstract

Clinical assessments often fail to discriminate between unipolar and bipolar depression and identify individuals who will develop future (hypo)manic episodes. To address this challenge, we developed a brain-based graph-theoretical predictive model (GPM) to prospectively map symptoms of anhedonia, impulsivity, and (hypo)mania. Individuals seeking treatment for mood disorders (n = 80) underwent an fMRI scan, including (i) resting-state and (ii) a reinforcement-learning (RL) task. Symptoms were assessed at baseline as well as at 3- and 6-month follow-ups. A whole-brain functional connectome was computed for each fMRI task, and the GPM was applied for symptom prediction using cross-validation. Prediction performance was evaluated by comparing the GPM's mean square error (MSE) to that of a corresponding null model. In addition, the GPM was compared to the connectome-based predictive modeling (CPM). Cross-sectionally, the GPM predicted anhedonia from the global efficiency (a graph theory metric that quantifies information transfer across the connectome) during the RL task, and impulsivity from the centrality (a metric that captures the importance of a region for information spread) of the left anterior cingulate cortex during resting-state. At 6-month follow-up, the GPM predicted (hypo)manic symptoms from the local efficiency of the left nucleus accumbens during the RL task and anhedonia from the centrality of the left caudate during resting-state. Notably, the GPM outperformed the CPM, and GPM derived from individuals with unipolar disorders predicted anhedonia and impulsivity symptoms for individuals with bipolar disorders, highlighting transdiagnostic generalization. Taken together, across DSM mood diagnoses, efficiency and centrality of the reward circuit predicted symptoms of anhedonia, impulsivity, and (hypo)mania, cross-sectionally and prospectively. The GPM is an innovative modeling approach that may ultimately inform clinical prediction at the individual level. ClinicalTrials.gov identifier: NCT01976975.

Identifiers

PMID37841877
PMCPMC10571608
OpenAlexW4387131317

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Registered trials

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.