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Addressing multi‐site functional MRI heterogeneity through dual‐expert collaborative learning for brain disease identification
Several studies employ multi‐site rs‐fMRI data for major depressive disorder (MDD) identification, with a specific site as the to‐be‐analyzed target domain and other site(s) as the source domain. But they usually suffer from significant inter‐site heterogeneity caused by the use of different scanner...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley & Sons, Inc.
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318248/ https://www.ncbi.nlm.nih.gov/pubmed/37227019 http://dx.doi.org/10.1002/hbm.26343 |
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author | Fang, Yuqi Potter, Guy G. Wu, Di Zhu, Hongtu Liu, Mingxia |
author_facet | Fang, Yuqi Potter, Guy G. Wu, Di Zhu, Hongtu Liu, Mingxia |
author_sort | Fang, Yuqi |
collection | PubMed |
description | Several studies employ multi‐site rs‐fMRI data for major depressive disorder (MDD) identification, with a specific site as the to‐be‐analyzed target domain and other site(s) as the source domain. But they usually suffer from significant inter‐site heterogeneity caused by the use of different scanners and/or scanning protocols and fail to build generalizable models that can well adapt to multiple target domains. In this article, we propose a dual‐expert fMRI harmonization (DFH) framework for automated MDD diagnosis. Our DFH is designed to simultaneously exploit data from a single labeled source domain/site and two unlabeled target domains for mitigating data distribution differences across domains. Specifically, the DFH consists of a domain‐generic student model and two domain‐specific teacher/expert models that are jointly trained to perform knowledge distillation through a deep collaborative learning module. A student model with strong generalizability is finally derived, which can be well adapted to unseen target domains and analysis of other brain diseases. To the best of our knowledge, this is among the first attempts to investigate multi‐target fMRI harmonization for MDD diagnosis. Comprehensive experiments on 836 subjects with rs‐fMRI data from 3 different sites show the superiority of our method. The discriminative brain functional connectivities identified by our method could be regarded as potential biomarkers for fMRI‐related MDD diagnosis. |
format | Online Article Text |
id | pubmed-10318248 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | John Wiley & Sons, Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-103182482023-07-05 Addressing multi‐site functional MRI heterogeneity through dual‐expert collaborative learning for brain disease identification Fang, Yuqi Potter, Guy G. Wu, Di Zhu, Hongtu Liu, Mingxia Hum Brain Mapp Research Articles Several studies employ multi‐site rs‐fMRI data for major depressive disorder (MDD) identification, with a specific site as the to‐be‐analyzed target domain and other site(s) as the source domain. But they usually suffer from significant inter‐site heterogeneity caused by the use of different scanners and/or scanning protocols and fail to build generalizable models that can well adapt to multiple target domains. In this article, we propose a dual‐expert fMRI harmonization (DFH) framework for automated MDD diagnosis. Our DFH is designed to simultaneously exploit data from a single labeled source domain/site and two unlabeled target domains for mitigating data distribution differences across domains. Specifically, the DFH consists of a domain‐generic student model and two domain‐specific teacher/expert models that are jointly trained to perform knowledge distillation through a deep collaborative learning module. A student model with strong generalizability is finally derived, which can be well adapted to unseen target domains and analysis of other brain diseases. To the best of our knowledge, this is among the first attempts to investigate multi‐target fMRI harmonization for MDD diagnosis. Comprehensive experiments on 836 subjects with rs‐fMRI data from 3 different sites show the superiority of our method. The discriminative brain functional connectivities identified by our method could be regarded as potential biomarkers for fMRI‐related MDD diagnosis. John Wiley & Sons, Inc. 2023-05-25 /pmc/articles/PMC10318248/ /pubmed/37227019 http://dx.doi.org/10.1002/hbm.26343 Text en © 2023 The Authors. Human Brain Mapping published by Wiley Periodicals LLC. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Research Articles Fang, Yuqi Potter, Guy G. Wu, Di Zhu, Hongtu Liu, Mingxia Addressing multi‐site functional MRI heterogeneity through dual‐expert collaborative learning for brain disease identification |
title | Addressing multi‐site functional MRI heterogeneity through dual‐expert collaborative learning for brain disease identification |
title_full | Addressing multi‐site functional MRI heterogeneity through dual‐expert collaborative learning for brain disease identification |
title_fullStr | Addressing multi‐site functional MRI heterogeneity through dual‐expert collaborative learning for brain disease identification |
title_full_unstemmed | Addressing multi‐site functional MRI heterogeneity through dual‐expert collaborative learning for brain disease identification |
title_short | Addressing multi‐site functional MRI heterogeneity through dual‐expert collaborative learning for brain disease identification |
title_sort | addressing multi‐site functional mri heterogeneity through dual‐expert collaborative learning for brain disease identification |
topic | Research Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10318248/ https://www.ncbi.nlm.nih.gov/pubmed/37227019 http://dx.doi.org/10.1002/hbm.26343 |
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