Evidence map›Paper›PMID 39267719›Full record

ArticleFrontiers in aging neuroscience2024

Comparison of spontaneous brain activity in distinguishing parkinsonian variant of multiple system atrophy from Parkinson's disease at an early stage.

Shichan Wang, Yi Xiao, Yanbing Hou, Chunyu Li, Lingyu Zhang, Ruwei Ou, Qianqian Wei, Junyu Lin, Tianmi Yang, Ningning Che and 4 more

Abstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. The role of neuro-imaging in multiple system atrophy.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
  2. Review
  3. Review
  4. Review
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

14 authors.

Shichan Wang *Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Yi Xiao *Laboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Yanbing HouNational Clinical Research Center for Geriatrics (WCH), West China Hospital, Sichuan University, Chengdu, China.
Chunyu LiLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Lingyu ZhangLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Ruwei OuLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Qianqian WeiLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Junyu LinLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Tianmi YangLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Ningning CheLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Qirui JiangLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Xiaoting ZhengLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Jiyong LiuLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.
Huifang ShangLaboratory of Neurodegenerative Disorders, National Clinical Research Center for Geriatrics, West China Hospital, Department of Neurology, Sichuan University, Chengdu, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The overlapping clinical manifestations in parkinsonian variant of multiple system atrophy (MSA-P) and Parkinson's Disease (PD) can complicate clinical diagnostic accuracy, particularly in the early stage. The study aims to uncover the patterns of brain function in the initial phase of the two conditions. Methods: We recruited 24 MSA-P patients, 34 PD patients and 27 healthy controls (HC). Voxel-wise fractional amplitude of low-frequency fluctuation (fALFF) was compared to characterize regional brain function, followed by seed-based functional connectivity (FC) analysis. Receiver operating characteristic (ROC) analyses were used to examine the diagnostic accuracy of fALFF. Results: Compared to HC, decreased fALFF was observed in the bilateral basal ganglia (BG) of MSA-P patients, while decreased fALFF was identified in the left BG of PD patients. Additionally, elevated fALFF was found in the superior cerebellum for MSA-P patients and the temporo-occipital cortex for PD patients. Furthermore, PD patients exhibited increased FC in the cortico-striatal loop compared to MSA-P patients. The fALFF of the left caudate distinguished MSA-P from HC with an area under the curve (AUC) of 0.838 ( Conclusion: Our findings indicated common and distinct abnormalities in spontaneous brain activity within BG, cerebellum, and cortices in early-stage MSA-P and PD patients. PD patients employed more compensatory mechanisms than MSA-P patients. Furthermore, fALFF may aid in early differentiation between MSA-P and PD.

Indexed as

early-stagefractional amplitude of low-frequency fluctuationmultiple system atrophyParkinson’s diseaseresting-state functional magnetic resonance imaging

Identifiers

PMID39267719
PMCPMC11390528

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.