Cargando…
A generalizable functional connectivity signature characterizes brain dysfunction and links to rTMS treatment response in cocaine use disorder
Cocaine use disorder (CUD) is a prevalent substance abuse disorder, and repetitive transcranial magnetic stimulation (rTMS) has shown potential in reducing cocaine cravings. However, a robust and replicable biomarker for CUD phenotyping is lacking, and the association between CUD brain phenotypes an...
Autores principales: | , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2023
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168499/ https://www.ncbi.nlm.nih.gov/pubmed/37162878 http://dx.doi.org/10.1101/2023.04.21.23288948 |
_version_ | 1785038866511560704 |
---|---|
author | Zhao, Kanhao Fonzo, Gregory A. Xie, Hua Oathes, Desmond J. Keller, Corey J. Carlisle, Nancy Etkin, Amit Garza-Villarreal, Eduardo A Zhang, Yu |
author_facet | Zhao, Kanhao Fonzo, Gregory A. Xie, Hua Oathes, Desmond J. Keller, Corey J. Carlisle, Nancy Etkin, Amit Garza-Villarreal, Eduardo A Zhang, Yu |
author_sort | Zhao, Kanhao |
collection | PubMed |
description | Cocaine use disorder (CUD) is a prevalent substance abuse disorder, and repetitive transcranial magnetic stimulation (rTMS) has shown potential in reducing cocaine cravings. However, a robust and replicable biomarker for CUD phenotyping is lacking, and the association between CUD brain phenotypes and treatment response remains unclear. Our study successfully established a cross-validated functional connectivity signature for accurate CUD phenotyping, using resting-state functional magnetic resonance imaging from a discovery cohort, and demonstrated its generalizability in an independent replication cohort. We identified phenotyping FCs involving increased connectivity between the visual network and dorsal attention network, and between the frontoparietal control network and ventral attention network, as well as decreased connectivity between the default mode network and limbic network in CUD patients compared to healthy controls. These abnormal connections correlated significantly with other drug use history and cognitive dysfunctions, e.g., non-planning impulsivity. We further confirmed the prognostic potential of the identified discriminative FCs for rTMS treatment response in CUD patients and found that the treatment-predictive FCs mainly involved the frontoparietal control and default mode networks. Our findings provide new insights into the neurobiological mechanisms of CUD and the association between CUD phenotypes and rTMS treatment response, offering promising targets for future therapeutic development. |
format | Online Article Text |
id | pubmed-10168499 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Cold Spring Harbor Laboratory |
record_format | MEDLINE/PubMed |
spelling | pubmed-101684992023-05-10 A generalizable functional connectivity signature characterizes brain dysfunction and links to rTMS treatment response in cocaine use disorder Zhao, Kanhao Fonzo, Gregory A. Xie, Hua Oathes, Desmond J. Keller, Corey J. Carlisle, Nancy Etkin, Amit Garza-Villarreal, Eduardo A Zhang, Yu medRxiv Article Cocaine use disorder (CUD) is a prevalent substance abuse disorder, and repetitive transcranial magnetic stimulation (rTMS) has shown potential in reducing cocaine cravings. However, a robust and replicable biomarker for CUD phenotyping is lacking, and the association between CUD brain phenotypes and treatment response remains unclear. Our study successfully established a cross-validated functional connectivity signature for accurate CUD phenotyping, using resting-state functional magnetic resonance imaging from a discovery cohort, and demonstrated its generalizability in an independent replication cohort. We identified phenotyping FCs involving increased connectivity between the visual network and dorsal attention network, and between the frontoparietal control network and ventral attention network, as well as decreased connectivity between the default mode network and limbic network in CUD patients compared to healthy controls. These abnormal connections correlated significantly with other drug use history and cognitive dysfunctions, e.g., non-planning impulsivity. We further confirmed the prognostic potential of the identified discriminative FCs for rTMS treatment response in CUD patients and found that the treatment-predictive FCs mainly involved the frontoparietal control and default mode networks. Our findings provide new insights into the neurobiological mechanisms of CUD and the association between CUD phenotypes and rTMS treatment response, offering promising targets for future therapeutic development. Cold Spring Harbor Laboratory 2023-05-04 /pmc/articles/PMC10168499/ /pubmed/37162878 http://dx.doi.org/10.1101/2023.04.21.23288948 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator. |
spellingShingle | Article Zhao, Kanhao Fonzo, Gregory A. Xie, Hua Oathes, Desmond J. Keller, Corey J. Carlisle, Nancy Etkin, Amit Garza-Villarreal, Eduardo A Zhang, Yu A generalizable functional connectivity signature characterizes brain dysfunction and links to rTMS treatment response in cocaine use disorder |
title | A generalizable functional connectivity signature characterizes brain dysfunction and links to rTMS treatment response in cocaine use disorder |
title_full | A generalizable functional connectivity signature characterizes brain dysfunction and links to rTMS treatment response in cocaine use disorder |
title_fullStr | A generalizable functional connectivity signature characterizes brain dysfunction and links to rTMS treatment response in cocaine use disorder |
title_full_unstemmed | A generalizable functional connectivity signature characterizes brain dysfunction and links to rTMS treatment response in cocaine use disorder |
title_short | A generalizable functional connectivity signature characterizes brain dysfunction and links to rTMS treatment response in cocaine use disorder |
title_sort | generalizable functional connectivity signature characterizes brain dysfunction and links to rtms treatment response in cocaine use disorder |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10168499/ https://www.ncbi.nlm.nih.gov/pubmed/37162878 http://dx.doi.org/10.1101/2023.04.21.23288948 |
work_keys_str_mv | AT zhaokanhao ageneralizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT fonzogregorya ageneralizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT xiehua ageneralizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT oathesdesmondj ageneralizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT kellercoreyj ageneralizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT carlislenancy ageneralizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT etkinamit ageneralizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT garzavillarrealeduardoa ageneralizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT zhangyu ageneralizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT zhaokanhao generalizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT fonzogregorya generalizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT xiehua generalizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT oathesdesmondj generalizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT kellercoreyj generalizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT carlislenancy generalizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT etkinamit generalizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT garzavillarrealeduardoa generalizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder AT zhangyu generalizablefunctionalconnectivitysignaturecharacterizesbraindysfunctionandlinkstortmstreatmentresponseincocaineusedisorder |