Evidence map›Paper›PMID 35459232›Full record

ArticleNPJ Parkinson's disease2022

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

Xuyang Wang, Kwangsun Yoo, Huafu Chen, Ting Zou, Hongyu Wang, Qing Gao, Li Meng, Xiaofei Hu, Rong Li

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

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Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

9 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Xuyang Wang *The Clinical Hospital of Chengdu Brain Science Institute, MOE Key Laboratory for Neuroinformation, High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 610054, People's Republic of China.
Kwangsun Yoo *Department of Psychology, Yale University, New Haven, CT, 06520, USA.ORCID http://orcid.org/0000-0002-5213-4575
Huafu ChenThe Clinical Hospital of Chengdu Brain Science Institute, MOE Key Laboratory for Neuroinformation, High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 610054, People's Republic of China. chenhf@uestc.edu.cn.ORCID http://orcid.org/0000-0002-4062-4753
Ting ZouThe Clinical Hospital of Chengdu Brain Science Institute, MOE Key Laboratory for Neuroinformation, High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 610054, People's Republic of China.
Hongyu WangThe Clinical Hospital of Chengdu Brain Science Institute, MOE Key Laboratory for Neuroinformation, High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 610054, People's Republic of China.
Qing GaoSchool of Mathematical Sciences, University of Electronic Science and Technology of China, Chengdu, 610054, People's Republic of China.
Li MengDepartment of Radiology, Xiangya Hospital, Central South University, Changsha, 410008, People's Republic of China. mengli96130@csu.edu.cn.ORCID http://orcid.org/0000-0001-7844-7740
Xiaofei HuDepartment of Radiology, Southwest Hospital, Third Military Medical University, Chongqing, 610054, People's Republic of China. harryzonetmmu@163.com.ORCID http://orcid.org/0000-0001-5376-2779
Rong LiThe Clinical Hospital of Chengdu Brain Science Institute, MOE Key Laboratory for Neuroinformation, High-Field Magnetic Resonance Brain Imaging Key Laboratory of Sichuan Province, School of Life Science and Technology, University of Electronic Science and Technology of China, Chengdu, 610054, People's Republic of China. rongli1120@gmail.com.ORCID http://orcid.org/0000-0001-7266-0241

Funding

Chengdu Science and Technology Bureau 2021-YF05-01211-SNNational Natural Science Foundation of China (National Science Foundation of China) 62036003National Natural Science Foundation of China (National Science Foundation of China) 62173070National Natural Science Foundation of China (National Science Foundation of China) No. 61906034National Natural Science Foundation of China (National Science Foundation of China) No. 82072006
6 · The paper itself

Abstract

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.

Identifiers

PMID35459232
PMCPMC9033778

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.