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Convergence, preliminary findings and future directions across the four human connectome projects investigating mood and anxiety disorders

In this paper we provide an overview of the rationale, methods, and preliminary results of the four Connectome Studies Related to Human Disease investigating mood and anxiety disorders. The first study, “Dimensional connectomics of anxious misery” (HCP-DAM), characterizes brain-symptom relations of...

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Autores principales: Tozzi, Leonardo, Anene, Esther T., Gotlib, Ian H., Wintermark, Max, Kerr, Adam B., Wu, Hua, Seok, Darsol, Narr, Katherine L., Sheline, Yvette I., Whitfield-Gabrieli, Susan, Williams, Leanne M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727513/
https://www.ncbi.nlm.nih.gov/pubmed/34732328
http://dx.doi.org/10.1016/j.neuroimage.2021.118694
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author Tozzi, Leonardo
Anene, Esther T.
Gotlib, Ian H.
Wintermark, Max
Kerr, Adam B.
Wu, Hua
Seok, Darsol
Narr, Katherine L.
Sheline, Yvette I.
Whitfield-Gabrieli, Susan
Williams, Leanne M.
author_facet Tozzi, Leonardo
Anene, Esther T.
Gotlib, Ian H.
Wintermark, Max
Kerr, Adam B.
Wu, Hua
Seok, Darsol
Narr, Katherine L.
Sheline, Yvette I.
Whitfield-Gabrieli, Susan
Williams, Leanne M.
author_sort Tozzi, Leonardo
collection PubMed
description In this paper we provide an overview of the rationale, methods, and preliminary results of the four Connectome Studies Related to Human Disease investigating mood and anxiety disorders. The first study, “Dimensional connectomics of anxious misery” (HCP-DAM), characterizes brain-symptom relations of a transdiagnostic sample of anxious misery disorders. The second study, “Human connectome Project for disordered emotional states” (HCP-DES), tests a hypothesis-driven model of brain circuit dysfunction in a sample of untreated young adults with symptoms of depression and anxiety. The third study, “Perturbation of the treatment resistant depression connectome by fast-acting therapies” (HCP-MDD), quantifies alterations of the structural and functional connectome as a result of three fast-acting interventions: electroconvulsive therapy, serial ketamine therapy, and total sleep deprivation. Finally, the fourth study, “Connectomes related to anxiety and depression in adolescents” (HCP-ADA), investigates developmental trajectories of subtypes of anxiety and depression in adolescence. The four projects use comparable and standardized Human Connectome Project magnetic resonance imaging (MRI) protocols, including structural MRI, diffusion-weighted MRI, and both task and resting state functional MRI. All four projects also conducted comprehensive and convergent clinical and neuropsychological assessments, including (but not limited to) demographic information, clinical diagnoses, symptoms of mood and anxiety disorders, negative and positive affect, cognitive function, and exposure to early life stress. The first round of analyses conducted in the four projects offered novel methods to investigate relations between functional connectomes and self-reports in large datasets, identified new functional correlates of symptoms of mood and anxiety disorders, characterized the trajectory of connectome-symptom profiles over time, and quantified the impact of novel treatments on aberrant connectivity. Taken together, the data obtained and reported by the four Connectome Studies Related to Human Disease investigating mood and anxiety disorders describe a rich constellation of convergent biological, clinical, and behavioral phenotypes that span the peak ages for the onset of emotional disorders. These data are being prepared for open sharing with the scientific community following screens for quality by the Connectome Coordinating Facility (CCF). The CCF also plans to release data from all projects that have been pre-processed using identical state-of-the-art pipelines. The resultant dataset will give researchers the opportunity to pool complementary data across the four projects to study circuit dysfunctions that may underlie mood and anxiety disorders, to map cohesive relations among circuits and symptoms, and to probe how these relations change as a function of age and acute interventions. This large and combined dataset may also be ideal for using data-driven analytic approaches to inform neurobiological targets for future clinical trials and interventions focused on clinical or behavioral outcomes.
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spelling pubmed-87275132022-01-05 Convergence, preliminary findings and future directions across the four human connectome projects investigating mood and anxiety disorders Tozzi, Leonardo Anene, Esther T. Gotlib, Ian H. Wintermark, Max Kerr, Adam B. Wu, Hua Seok, Darsol Narr, Katherine L. Sheline, Yvette I. Whitfield-Gabrieli, Susan Williams, Leanne M. Neuroimage Article In this paper we provide an overview of the rationale, methods, and preliminary results of the four Connectome Studies Related to Human Disease investigating mood and anxiety disorders. The first study, “Dimensional connectomics of anxious misery” (HCP-DAM), characterizes brain-symptom relations of a transdiagnostic sample of anxious misery disorders. The second study, “Human connectome Project for disordered emotional states” (HCP-DES), tests a hypothesis-driven model of brain circuit dysfunction in a sample of untreated young adults with symptoms of depression and anxiety. The third study, “Perturbation of the treatment resistant depression connectome by fast-acting therapies” (HCP-MDD), quantifies alterations of the structural and functional connectome as a result of three fast-acting interventions: electroconvulsive therapy, serial ketamine therapy, and total sleep deprivation. Finally, the fourth study, “Connectomes related to anxiety and depression in adolescents” (HCP-ADA), investigates developmental trajectories of subtypes of anxiety and depression in adolescence. The four projects use comparable and standardized Human Connectome Project magnetic resonance imaging (MRI) protocols, including structural MRI, diffusion-weighted MRI, and both task and resting state functional MRI. All four projects also conducted comprehensive and convergent clinical and neuropsychological assessments, including (but not limited to) demographic information, clinical diagnoses, symptoms of mood and anxiety disorders, negative and positive affect, cognitive function, and exposure to early life stress. The first round of analyses conducted in the four projects offered novel methods to investigate relations between functional connectomes and self-reports in large datasets, identified new functional correlates of symptoms of mood and anxiety disorders, characterized the trajectory of connectome-symptom profiles over time, and quantified the impact of novel treatments on aberrant connectivity. Taken together, the data obtained and reported by the four Connectome Studies Related to Human Disease investigating mood and anxiety disorders describe a rich constellation of convergent biological, clinical, and behavioral phenotypes that span the peak ages for the onset of emotional disorders. These data are being prepared for open sharing with the scientific community following screens for quality by the Connectome Coordinating Facility (CCF). The CCF also plans to release data from all projects that have been pre-processed using identical state-of-the-art pipelines. The resultant dataset will give researchers the opportunity to pool complementary data across the four projects to study circuit dysfunctions that may underlie mood and anxiety disorders, to map cohesive relations among circuits and symptoms, and to probe how these relations change as a function of age and acute interventions. This large and combined dataset may also be ideal for using data-driven analytic approaches to inform neurobiological targets for future clinical trials and interventions focused on clinical or behavioral outcomes. 2021-10-31 2021-12-15 /pmc/articles/PMC8727513/ /pubmed/34732328 http://dx.doi.org/10.1016/j.neuroimage.2021.118694 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) )
spellingShingle Article
Tozzi, Leonardo
Anene, Esther T.
Gotlib, Ian H.
Wintermark, Max
Kerr, Adam B.
Wu, Hua
Seok, Darsol
Narr, Katherine L.
Sheline, Yvette I.
Whitfield-Gabrieli, Susan
Williams, Leanne M.
Convergence, preliminary findings and future directions across the four human connectome projects investigating mood and anxiety disorders
title Convergence, preliminary findings and future directions across the four human connectome projects investigating mood and anxiety disorders
title_full Convergence, preliminary findings and future directions across the four human connectome projects investigating mood and anxiety disorders
title_fullStr Convergence, preliminary findings and future directions across the four human connectome projects investigating mood and anxiety disorders
title_full_unstemmed Convergence, preliminary findings and future directions across the four human connectome projects investigating mood and anxiety disorders
title_short Convergence, preliminary findings and future directions across the four human connectome projects investigating mood and anxiety disorders
title_sort convergence, preliminary findings and future directions across the four human connectome projects investigating mood and anxiety disorders
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8727513/
https://www.ncbi.nlm.nih.gov/pubmed/34732328
http://dx.doi.org/10.1016/j.neuroimage.2021.118694
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