Evidence map›Paper›PMID 41318614›Full record

ArticleNPJ Parkinson's disease2025

Mapping the neural and molecular basis underlying fatigue in Parkinson's disease.

Futing Yang, Junyi Shen, Zhiqin Sun, Lingli Tan, Rucheng Yang, Lina Zhu, Yin Mo, Heng Shao, Jianhong Hou, Zanzong Sun and 3 more

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

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

1 citing paper in PubMed.

  1. Article
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

13 authors.

Futing Yang *State Key Laboratory of Primate Biomedical Research, Institute of Primate Translational Medicine, Kunming University of Science and Technology, Kunming, China.
Junyi Shen *Division of Liver Surgery, Department of General Surgery, West China Hospital, Sichuan University, Chengdu, China.
Zhiqin SunDepartment of Emergency and Critical Care Medicine, The First People's Hospital of Chongqing High-tech Zone, Chongqing, China.
Lingli TanChongqing Industry and Trade, Technician College, Chongqing, China.
Rucheng YangDehongzhou Hospital of Traditional Chinese Medicine, Dehong, China.
Lina ZhuRehabilitation Medicine Center and Institute of Rehabilitation Medicine, West China Hospital, Sichuan University, Chengdu, China.
Yin MoDepartment of Radiology, Kunming Medical University, First Affiliated Hospital, Kunming, China.
Heng ShaoDepartment of Geriatrics, The First People's Hospital of Yunnan Province, Kunming, China.
Jianhong HouDepartment of Orthopaedics, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, China.
Zanzong SunDehongzhou Hospital of Traditional Chinese Medicine, Dehong, China. 625112463@qq.com.
Yuan GaoDepartment of Neurology, The First People's Hospital of Yunnan Province, The Affiliated Hospital of Kunming University of Science and Technology, Kunming, China. gy610829@163.com.
Yanbing HouCenter of Gerontology and Geriatrics, West China Hospital, Sichuan University, Chengdu, China. ybhou2019@126.com.
Jiaojian WangState Key Laboratory of Primate Biomedical Research, Institute of Primate Translational Medicine, Kunming University of Science and Technology, Kunming, China. jiaojianwang@uestc.edu.cn.

Funding

The Natural Science Foundation of Yunnan Province 202501AV070005
6 · The paper itself

Abstract

Fatigue is a common and debilitating non-motor symptom in patients with Parkinson's disease (PD). By integrating the activation likelihood estimation (ALE) meta-analysis and activation network mapping (ANM) technique, the brain network underlying fatigue (referred to as "fatigue-related network") in PD was identified, comprising widespread brain regions primarily involving the somatomotor and frontoparietal networks. This network was interpreted through transcriptomic patterns, chemoarchitectures, and behavioral relevance. Fatigue-related genes were predominantly enriched in synaptic and actin filament-related biological processes and showed primary expression in neurons and oligodendrocytes. The fatigue-related network closely corresponded to the spatial distribution of acetylcholine, glutamate, and norepinephrine systems and was primarily linked to motor function. This study defines a distinct brain network substrate underlying fatigue in PD, advancing our understanding of the neurobiological mechanisms and facilitating the development of effective therapies for affected patients.

Identifiers

PMID41318614
PMCPMC12769569

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Registered trials

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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.