Cargando…

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

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, im...

Descripción completa

Detalles Bibliográficos
Autores principales: Pizzagalli, Diego, Whitton, Alexis, Treadway, Michael, Rutherford, Ashleigh, Kumar, Poornima, Ironside, Manon, Kaiser, Roselinde, Ren, Boyu, Dan, Rotem
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Journal Experts 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571608/
https://www.ncbi.nlm.nih.gov/pubmed/37841877
http://dx.doi.org/10.21203/rs.3.rs-3168186/v1
_version_ 1785120040658403328
author Pizzagalli, Diego
Whitton, Alexis
Treadway, Michael
Rutherford, Ashleigh
Kumar, Poornima
Ironside, Manon
Kaiser, Roselinde
Ren, Boyu
Dan, Rotem
author_facet Pizzagalli, Diego
Whitton, Alexis
Treadway, Michael
Rutherford, Ashleigh
Kumar, Poornima
Ironside, Manon
Kaiser, Roselinde
Ren, Boyu
Dan, Rotem
author_sort Pizzagalli, Diego
collection PubMed
description 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
format Online
Article
Text
id pubmed-10571608
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher American Journal Experts
record_format MEDLINE/PubMed
spelling pubmed-105716082023-10-14 Brain-based graph-theoretical predictive modeling to map the trajectory of transdiagnostic symptoms of anhedonia, impulsivity, and hypomania from the human functional connectome Pizzagalli, Diego Whitton, Alexis Treadway, Michael Rutherford, Ashleigh Kumar, Poornima Ironside, Manon Kaiser, Roselinde Ren, Boyu Dan, Rotem Res Sq Article 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 American Journal Experts 2023-09-28 /pmc/articles/PMC10571608/ /pubmed/37841877 http://dx.doi.org/10.21203/rs.3.rs-3168186/v1 Text en https://creativecommons.org/licenses/by/4.0/This work is licensed under a Creative Commons Attribution 4.0 International License (https://creativecommons.org/licenses/by/4.0/) , which allows reusers to distribute, remix, adapt, and build upon the material in any medium or format, so long as attribution is given to the creator. The license allows for commercial use. https://creativecommons.org/licenses/by/4.0/License: This work is licensed under a Creative Commons Attribution 4.0 International License. Read Full License (https://creativecommons.org/licenses/by/4.0/)
spellingShingle Article
Pizzagalli, Diego
Whitton, Alexis
Treadway, Michael
Rutherford, Ashleigh
Kumar, Poornima
Ironside, Manon
Kaiser, Roselinde
Ren, Boyu
Dan, Rotem
Brain-based graph-theoretical predictive modeling to map the trajectory of transdiagnostic symptoms of anhedonia, impulsivity, and hypomania from the human functional connectome
title Brain-based graph-theoretical predictive modeling to map the trajectory of transdiagnostic symptoms of anhedonia, impulsivity, and hypomania from the human functional connectome
title_full Brain-based graph-theoretical predictive modeling to map the trajectory of transdiagnostic symptoms of anhedonia, impulsivity, and hypomania from the human functional connectome
title_fullStr Brain-based graph-theoretical predictive modeling to map the trajectory of transdiagnostic symptoms of anhedonia, impulsivity, and hypomania from the human functional connectome
title_full_unstemmed Brain-based graph-theoretical predictive modeling to map the trajectory of transdiagnostic symptoms of anhedonia, impulsivity, and hypomania from the human functional connectome
title_short Brain-based graph-theoretical predictive modeling to map the trajectory of transdiagnostic symptoms of anhedonia, impulsivity, and hypomania from the human functional connectome
title_sort brain-based graph-theoretical predictive modeling to map the trajectory of transdiagnostic symptoms of anhedonia, impulsivity, and hypomania from the human functional connectome
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10571608/
https://www.ncbi.nlm.nih.gov/pubmed/37841877
http://dx.doi.org/10.21203/rs.3.rs-3168186/v1
work_keys_str_mv AT pizzagallidiego brainbasedgraphtheoreticalpredictivemodelingtomapthetrajectoryoftransdiagnosticsymptomsofanhedoniaimpulsivityandhypomaniafromthehumanfunctionalconnectome
AT whittonalexis brainbasedgraphtheoreticalpredictivemodelingtomapthetrajectoryoftransdiagnosticsymptomsofanhedoniaimpulsivityandhypomaniafromthehumanfunctionalconnectome
AT treadwaymichael brainbasedgraphtheoreticalpredictivemodelingtomapthetrajectoryoftransdiagnosticsymptomsofanhedoniaimpulsivityandhypomaniafromthehumanfunctionalconnectome
AT rutherfordashleigh brainbasedgraphtheoreticalpredictivemodelingtomapthetrajectoryoftransdiagnosticsymptomsofanhedoniaimpulsivityandhypomaniafromthehumanfunctionalconnectome
AT kumarpoornima brainbasedgraphtheoreticalpredictivemodelingtomapthetrajectoryoftransdiagnosticsymptomsofanhedoniaimpulsivityandhypomaniafromthehumanfunctionalconnectome
AT ironsidemanon brainbasedgraphtheoreticalpredictivemodelingtomapthetrajectoryoftransdiagnosticsymptomsofanhedoniaimpulsivityandhypomaniafromthehumanfunctionalconnectome
AT kaiserroselinde brainbasedgraphtheoreticalpredictivemodelingtomapthetrajectoryoftransdiagnosticsymptomsofanhedoniaimpulsivityandhypomaniafromthehumanfunctionalconnectome
AT renboyu brainbasedgraphtheoreticalpredictivemodelingtomapthetrajectoryoftransdiagnosticsymptomsofanhedoniaimpulsivityandhypomaniafromthehumanfunctionalconnectome
AT danrotem brainbasedgraphtheoreticalpredictivemodelingtomapthetrajectoryoftransdiagnosticsymptomsofanhedoniaimpulsivityandhypomaniafromthehumanfunctionalconnectome