Evidence map›Paper›PMID 40719373›Full record

ReviewAnnals of medicine2025

Autonomic dysfunction in multiple system atrophy: from pathophysiology to clinical manifestations.

Yuqi Luo, Nan Yang, Wanlin Yang, Baoling Chen, Shuzhen Zhu, YihRu Wu, Qing Wang

Abstract readReview
In one paragraph

Review in Annals of medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Article
  2. Small-Conductance CaNeuroscience bulletin · 2026
    Review
  3. Review
  4. Article
  5. Article
  6. Review
  7. Article
  8. 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

7 authors.

Yuqi LuoDepartment of Neurology, Zhujiang Hospital of Southern Medical University, Guangzhou, China.ORCID 0009-0003-4221-009X
Nan YangDepartment of Neurology and Rehabilitation, Zhongshan Hospital of Traditional Chinese Medicine, Zhongshan, China.
Wanlin YangDepartment of Neurology, Zhujiang Hospital of Southern Medical University, Guangzhou, China.
Baoling ChenDepartment of Neurology, Zhujiang Hospital of Southern Medical University, Guangzhou, China.
Shuzhen ZhuDepartment of Neurology, Zhujiang Hospital of Southern Medical University, Guangzhou, China.
YihRu WuDepartment of Neurology, Chang Gung Memorial Hospital Linkou Medical Center and College of Medicine, Chang-Gung University, Taoyuan, Taiwan.
Qing WangDepartment of Neurology, Zhujiang Hospital of Southern Medical University, Guangzhou, China.ORCID 0000-0002-3882-6540

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionMultiple system atrophy (MSA) is a sporadic, fatal, and rapidly progressive neurodegenerative disease of unknown etiology, pathologically characterized by the presence of α-synuclein (α-syn) immunoreactive cytoplasmic inclusions in oligodendrocytes. The deposition of α-synuclein in highly interconnected neuronal networks with different neurochemistry properties in different regions of the cortex, diencephalon, brain stem and spinal cord leads to early onset and extensive autonomic dysfunction in MSA. Mainly affected areas include the hypothalamus, pons, raphe nucleus, locus coeruleus, arcuate nucleus, dorsal vagus nucleus, fuzzy nucleus, the thoracolumbar middle lateral column and Onuf's nucleus of the spinal cord. Clinical manifestations include orthostatic hypotension, incomplete bladder emptying, erectile dysfunction, and constipation. DISCUSSION: In this review, we aim to discuss and summarize the clinicopathological correlation of MSA autonomic dysfunction, and focus on the pathophysiological mechanisms of various autonomic dysfunction, from neural control networks under normal physiological conditions to specific pathological involvement structures in MSA. In addition, we also elaborated on the corresponding clinical manifestations caused by various pathological structures.

conclusionsIn summary, the autonomic dysfunction of MSA involves the comprehensive control of cardiovascular, urinary, reproductive, and gastrointestinal functions by the autonomic nervous network in the central nervous system (CNS). The currently summarized physiology and pathophysiology of MSA have not been fully clarified. Further and deeper studies are needed to elucidate the relationship between pathogenesis and clinical manifestations of MSA.

Indexed as

Autonomic Nervous SystemAutonomic Nervous System DiseasesMultiple System Atrophyalpha-SynucleinHumansHypotension, Orthostaticalpha-Synucleinautonomic dysfunctioncentral autonomic networkclinical manifestationsMultiple system atrophypathophysiology

Identifiers

PMID40719373
PMCPMC11983539

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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.