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AI-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: COORDINATE-MDD consortium design and rationale
BACKGROUND: Efforts to develop neuroimaging-based biomarkers in major depressive disorder (MDD), at the individual level, have been limited to date. As diagnostic criteria are currently symptom-based, MDD is conceptualized as a disorder rather than a disease with a known etiology; further, neural me...
Autores principales: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869598/ https://www.ncbi.nlm.nih.gov/pubmed/36690972 http://dx.doi.org/10.1186/s12888-022-04509-7 |
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author | Fu, Cynthia H. Y. Erus, Guray Fan, Yong Antoniades, Mathilde Arnone, Danilo Arnott, Stephen R. Chen, Taolin Choi, Ki Sueng Fatt, Cherise Chin Frey, Benicio N. Frokjaer, Vibe G. Ganz, Melanie Garcia, Jose Godlewska, Beata R. Hassel, Stefanie Ho, Keith McIntosh, Andrew M. Qin, Kun Rotzinger, Susan Sacchet, Matthew D. Savitz, Jonathan Shou, Haochang Singh, Ashish Stolicyn, Aleks Strigo, Irina Strother, Stephen C. Tosun, Duygu Victor, Teresa A. Wei, Dongtao Wise, Toby Woodham, Rachel D. Zahn, Roland Anderson, Ian M. Deakin, J. F. William Dunlop, Boadie W. Elliott, Rebecca Gong, Qiyong Gotlib, Ian H. Harmer, Catherine J. Kennedy, Sidney H. Knudsen, Gitte M. Mayberg, Helen S. Paulus, Martin P. Qiu, Jiang Trivedi, Madhukar H. Whalley, Heather C. Yan, Chao-Gan Young, Allan H. Davatzikos, Christos |
author_facet | Fu, Cynthia H. Y. Erus, Guray Fan, Yong Antoniades, Mathilde Arnone, Danilo Arnott, Stephen R. Chen, Taolin Choi, Ki Sueng Fatt, Cherise Chin Frey, Benicio N. Frokjaer, Vibe G. Ganz, Melanie Garcia, Jose Godlewska, Beata R. Hassel, Stefanie Ho, Keith McIntosh, Andrew M. Qin, Kun Rotzinger, Susan Sacchet, Matthew D. Savitz, Jonathan Shou, Haochang Singh, Ashish Stolicyn, Aleks Strigo, Irina Strother, Stephen C. Tosun, Duygu Victor, Teresa A. Wei, Dongtao Wise, Toby Woodham, Rachel D. Zahn, Roland Anderson, Ian M. Deakin, J. F. William Dunlop, Boadie W. Elliott, Rebecca Gong, Qiyong Gotlib, Ian H. Harmer, Catherine J. Kennedy, Sidney H. Knudsen, Gitte M. Mayberg, Helen S. Paulus, Martin P. Qiu, Jiang Trivedi, Madhukar H. Whalley, Heather C. Yan, Chao-Gan Young, Allan H. Davatzikos, Christos |
author_sort | Fu, Cynthia H. Y. |
collection | PubMed |
description | BACKGROUND: Efforts to develop neuroimaging-based biomarkers in major depressive disorder (MDD), at the individual level, have been limited to date. As diagnostic criteria are currently symptom-based, MDD is conceptualized as a disorder rather than a disease with a known etiology; further, neural measures are often confounded by medication status and heterogeneous symptom states. METHODS: We describe a consortium to quantify neuroanatomical and neurofunctional heterogeneity via the dimensions of novel multivariate coordinate system (COORDINATE-MDD). Utilizing imaging harmonization and machine learning methods in a large cohort of medication-free, deeply phenotyped MDD participants, patterns of brain alteration are defined in replicable and neurobiologically-based dimensions and offer the potential to predict treatment response at the individual level. International datasets are being shared from multi-ethnic community populations, first episode and recurrent MDD, which are medication-free, in a current depressive episode with prospective longitudinal treatment outcomes and in remission. Neuroimaging data consist of de-identified, individual, structural MRI and resting-state functional MRI with additional positron emission tomography (PET) data at specific sites. State-of-the-art analytic methods include automated image processing for extraction of anatomical and functional imaging variables, statistical harmonization of imaging variables to account for site and scanner variations, and semi-supervised machine learning methods that identify dominant patterns associated with MDD from neural structure and function in healthy participants. RESULTS: We are applying an iterative process by defining the neural dimensions that characterise deeply phenotyped samples and then testing the dimensions in novel samples to assess specificity and reliability. Crucially, we aim to use machine learning methods to identify novel predictors of treatment response based on prospective longitudinal treatment outcome data, and we can externally validate the dimensions in fully independent sites. CONCLUSION: We describe the consortium, imaging protocols and analytics using preliminary results. Our findings thus far demonstrate how datasets across many sites can be harmonized and constructively pooled to enable execution of this large-scale project. |
format | Online Article Text |
id | pubmed-9869598 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-98695982023-01-24 AI-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: COORDINATE-MDD consortium design and rationale Fu, Cynthia H. Y. Erus, Guray Fan, Yong Antoniades, Mathilde Arnone, Danilo Arnott, Stephen R. Chen, Taolin Choi, Ki Sueng Fatt, Cherise Chin Frey, Benicio N. Frokjaer, Vibe G. Ganz, Melanie Garcia, Jose Godlewska, Beata R. Hassel, Stefanie Ho, Keith McIntosh, Andrew M. Qin, Kun Rotzinger, Susan Sacchet, Matthew D. Savitz, Jonathan Shou, Haochang Singh, Ashish Stolicyn, Aleks Strigo, Irina Strother, Stephen C. Tosun, Duygu Victor, Teresa A. Wei, Dongtao Wise, Toby Woodham, Rachel D. Zahn, Roland Anderson, Ian M. Deakin, J. F. William Dunlop, Boadie W. Elliott, Rebecca Gong, Qiyong Gotlib, Ian H. Harmer, Catherine J. Kennedy, Sidney H. Knudsen, Gitte M. Mayberg, Helen S. Paulus, Martin P. Qiu, Jiang Trivedi, Madhukar H. Whalley, Heather C. Yan, Chao-Gan Young, Allan H. Davatzikos, Christos BMC Psychiatry Research BACKGROUND: Efforts to develop neuroimaging-based biomarkers in major depressive disorder (MDD), at the individual level, have been limited to date. As diagnostic criteria are currently symptom-based, MDD is conceptualized as a disorder rather than a disease with a known etiology; further, neural measures are often confounded by medication status and heterogeneous symptom states. METHODS: We describe a consortium to quantify neuroanatomical and neurofunctional heterogeneity via the dimensions of novel multivariate coordinate system (COORDINATE-MDD). Utilizing imaging harmonization and machine learning methods in a large cohort of medication-free, deeply phenotyped MDD participants, patterns of brain alteration are defined in replicable and neurobiologically-based dimensions and offer the potential to predict treatment response at the individual level. International datasets are being shared from multi-ethnic community populations, first episode and recurrent MDD, which are medication-free, in a current depressive episode with prospective longitudinal treatment outcomes and in remission. Neuroimaging data consist of de-identified, individual, structural MRI and resting-state functional MRI with additional positron emission tomography (PET) data at specific sites. State-of-the-art analytic methods include automated image processing for extraction of anatomical and functional imaging variables, statistical harmonization of imaging variables to account for site and scanner variations, and semi-supervised machine learning methods that identify dominant patterns associated with MDD from neural structure and function in healthy participants. RESULTS: We are applying an iterative process by defining the neural dimensions that characterise deeply phenotyped samples and then testing the dimensions in novel samples to assess specificity and reliability. Crucially, we aim to use machine learning methods to identify novel predictors of treatment response based on prospective longitudinal treatment outcome data, and we can externally validate the dimensions in fully independent sites. CONCLUSION: We describe the consortium, imaging protocols and analytics using preliminary results. Our findings thus far demonstrate how datasets across many sites can be harmonized and constructively pooled to enable execution of this large-scale project. BioMed Central 2023-01-23 /pmc/articles/PMC9869598/ /pubmed/36690972 http://dx.doi.org/10.1186/s12888-022-04509-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Fu, Cynthia H. Y. Erus, Guray Fan, Yong Antoniades, Mathilde Arnone, Danilo Arnott, Stephen R. Chen, Taolin Choi, Ki Sueng Fatt, Cherise Chin Frey, Benicio N. Frokjaer, Vibe G. Ganz, Melanie Garcia, Jose Godlewska, Beata R. Hassel, Stefanie Ho, Keith McIntosh, Andrew M. Qin, Kun Rotzinger, Susan Sacchet, Matthew D. Savitz, Jonathan Shou, Haochang Singh, Ashish Stolicyn, Aleks Strigo, Irina Strother, Stephen C. Tosun, Duygu Victor, Teresa A. Wei, Dongtao Wise, Toby Woodham, Rachel D. Zahn, Roland Anderson, Ian M. Deakin, J. F. William Dunlop, Boadie W. Elliott, Rebecca Gong, Qiyong Gotlib, Ian H. Harmer, Catherine J. Kennedy, Sidney H. Knudsen, Gitte M. Mayberg, Helen S. Paulus, Martin P. Qiu, Jiang Trivedi, Madhukar H. Whalley, Heather C. Yan, Chao-Gan Young, Allan H. Davatzikos, Christos AI-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: COORDINATE-MDD consortium design and rationale |
title | AI-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: COORDINATE-MDD consortium design and rationale |
title_full | AI-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: COORDINATE-MDD consortium design and rationale |
title_fullStr | AI-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: COORDINATE-MDD consortium design and rationale |
title_full_unstemmed | AI-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: COORDINATE-MDD consortium design and rationale |
title_short | AI-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: COORDINATE-MDD consortium design and rationale |
title_sort | ai-based dimensional neuroimaging system for characterizing heterogeneity in brain structure and function in major depressive disorder: coordinate-mdd consortium design and rationale |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9869598/ https://www.ncbi.nlm.nih.gov/pubmed/36690972 http://dx.doi.org/10.1186/s12888-022-04509-7 |
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