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Antagonistic network signature of motor function in Parkinson’s disease revealed by connectome-based predictive modeling

Motor impairment is a core clinical feature of Parkinson’s disease (PD). Although the decoupled brain connectivity has been widely reported in previous neuroimaging studies, how the functional connectome is involved in motor dysfunction has not been well elucidated in PD patients. Here we developed...

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Autores principales: Wang, Xuyang, Yoo, Kwangsun, Chen, Huafu, Zou, Ting, Wang, Hongyu, Gao, Qing, Meng, Li, Hu, Xiaofei, Li, Rong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033778/
https://www.ncbi.nlm.nih.gov/pubmed/35459232
http://dx.doi.org/10.1038/s41531-022-00315-w
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author Wang, Xuyang
Yoo, Kwangsun
Chen, Huafu
Zou, Ting
Wang, Hongyu
Gao, Qing
Meng, Li
Hu, Xiaofei
Li, Rong
author_facet Wang, Xuyang
Yoo, Kwangsun
Chen, Huafu
Zou, Ting
Wang, Hongyu
Gao, Qing
Meng, Li
Hu, Xiaofei
Li, Rong
author_sort Wang, Xuyang
collection PubMed
description Motor impairment is a core clinical feature of Parkinson’s disease (PD). Although the decoupled brain connectivity has been widely reported in previous neuroimaging studies, how the functional connectome is involved in motor dysfunction has not been well elucidated in PD patients. Here we developed a distributed brain signature by predicting clinical motor scores of PD patients across multicenter datasets (total n = 236). We decomposed the Pearson’s correlation into accordance and discordance via a temporal discrete procedure, which can capture coupling and anti-coupling respectively. Using different profiles of functional connectivity, we trained candidate predictive models and tested them on independent and heterogeneous PD samples. We showed that the antagonistic model measured by discordance had the best sensitivity and generalizability in all validations and it was dubbed as Parkinson’s antagonistic motor signature (PAMS). The PAMS was dominated by the subcortical, somatomotor, visual, cerebellum, default-mode, and frontoparietal networks, and the motor-visual stream accounted for the most part of predictive weights among network pairs. Additional stage-specific analysis showed that the predicted scores generated from the antagonistic model tended to be higher than the observed scores in the early course of PD, indicating that the functional signature may vary more sensitively with the neurodegenerative process than clinical behaviors. Together, these findings suggest that motor dysfunction of PD is represented as antagonistic interactions within multi-level brain systems. The signature shows great potential in the early motor evaluation and developing new therapeutic approaches for PD in the clinical realm.
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spelling pubmed-90337782022-04-28 Antagonistic network signature of motor function in Parkinson’s disease revealed by connectome-based predictive modeling Wang, Xuyang Yoo, Kwangsun Chen, Huafu Zou, Ting Wang, Hongyu Gao, Qing Meng, Li Hu, Xiaofei Li, Rong NPJ Parkinsons Dis Article Motor impairment is a core clinical feature of Parkinson’s disease (PD). Although the decoupled brain connectivity has been widely reported in previous neuroimaging studies, how the functional connectome is involved in motor dysfunction has not been well elucidated in PD patients. Here we developed a distributed brain signature by predicting clinical motor scores of PD patients across multicenter datasets (total n = 236). We decomposed the Pearson’s correlation into accordance and discordance via a temporal discrete procedure, which can capture coupling and anti-coupling respectively. Using different profiles of functional connectivity, we trained candidate predictive models and tested them on independent and heterogeneous PD samples. We showed that the antagonistic model measured by discordance had the best sensitivity and generalizability in all validations and it was dubbed as Parkinson’s antagonistic motor signature (PAMS). The PAMS was dominated by the subcortical, somatomotor, visual, cerebellum, default-mode, and frontoparietal networks, and the motor-visual stream accounted for the most part of predictive weights among network pairs. Additional stage-specific analysis showed that the predicted scores generated from the antagonistic model tended to be higher than the observed scores in the early course of PD, indicating that the functional signature may vary more sensitively with the neurodegenerative process than clinical behaviors. Together, these findings suggest that motor dysfunction of PD is represented as antagonistic interactions within multi-level brain systems. The signature shows great potential in the early motor evaluation and developing new therapeutic approaches for PD in the clinical realm. Nature Publishing Group UK 2022-04-22 /pmc/articles/PMC9033778/ /pubmed/35459232 http://dx.doi.org/10.1038/s41531-022-00315-w Text en © The Author(s) 2022, corrected publication 2022 https://creativecommons.org/licenses/by/4.0/Open Access This 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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Wang, Xuyang
Yoo, Kwangsun
Chen, Huafu
Zou, Ting
Wang, Hongyu
Gao, Qing
Meng, Li
Hu, Xiaofei
Li, Rong
Antagonistic network signature of motor function in Parkinson’s disease revealed by connectome-based predictive modeling
title Antagonistic network signature of motor function in Parkinson’s disease revealed by connectome-based predictive modeling
title_full Antagonistic network signature of motor function in Parkinson’s disease revealed by connectome-based predictive modeling
title_fullStr Antagonistic network signature of motor function in Parkinson’s disease revealed by connectome-based predictive modeling
title_full_unstemmed Antagonistic network signature of motor function in Parkinson’s disease revealed by connectome-based predictive modeling
title_short Antagonistic network signature of motor function in Parkinson’s disease revealed by connectome-based predictive modeling
title_sort antagonistic network signature of motor function in parkinson’s disease revealed by connectome-based predictive modeling
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9033778/
https://www.ncbi.nlm.nih.gov/pubmed/35459232
http://dx.doi.org/10.1038/s41531-022-00315-w
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