Evidence map›Paper›PMID 36657992›Full record

ArticleNeurology2023

Cutaneous α-Synuclein Signatures in Patients With Multiple System Atrophy and Parkinson Disease.

Christopher Gibbons, Ningshan Wang, Sharika Rajan, Drew Kern, Jose-Alberto Palma, Horacio Kaufmann, Roy Freeman

Erratum issuedOpen access · greenAbstract read
In one paragraph

Article in Neurology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 68 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
68citing papers in PubMed, 2 pooled it
18.7field-weighted citation impact, top 1% of its field
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

68 citing papers in PubMed, 2 syntheses or guidelines pooled it, 91 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Trial
  5. Cutaneous alpha-synuclein deposition informs autonomic function in individuals with early-stage multiple system atrophy.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2026
    Article
  6. Article
  7. Article
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  9. Cutaneous Phosphorylated Alpha-Synuclein in Lewy Body Dementia.Annals of clinical and translational neurology · 2026
    Article
  10. Types of Pain in Multiple System Atrophy.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  11. Article
  12. Article
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  16. Diagnosis and Management of Parkinson Disease in Individuals with Pre-Existing Mood Disorders.International journal of environmental research and public health · 2026
    Review
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  18. Article
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  20. Review

8 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors at 1 institution in 1 country.

Christopher GibbonsFrom the Department of Neurology (C.G., N.W., R.F.), Beth Israel Deaconess Medical Center, Boston, MA; Department of Pathology (S.R.), NIH, Bethesda, MD; Department of Neurology (D.K.), University of Colorado, Aurora, CO; and Department of Neurology (J.-A.P., H.K.), NYU Grossman School of Medicine, New York, NY.
Ningshan WangFrom the Department of Neurology (C.G., N.W., R.F.), Beth Israel Deaconess Medical Center, Boston, MA; Department of Pathology (S.R.), NIH, Bethesda, MD; Department of Neurology (D.K.), University of Colorado, Aurora, CO; and Department of Neurology (J.-A.P., H.K.), NYU Grossman School of Medicine, New York, NY.
Sharika RajanFrom the Department of Neurology (C.G., N.W., R.F.), Beth Israel Deaconess Medical Center, Boston, MA; Department of Pathology (S.R.), NIH, Bethesda, MD; Department of Neurology (D.K.), University of Colorado, Aurora, CO; and Department of Neurology (J.-A.P., H.K.), NYU Grossman School of Medicine, New York, NY.
Drew KernFrom the Department of Neurology (C.G., N.W., R.F.), Beth Israel Deaconess Medical Center, Boston, MA; Department of Pathology (S.R.), NIH, Bethesda, MD; Department of Neurology (D.K.), University of Colorado, Aurora, CO; and Department of Neurology (J.-A.P., H.K.), NYU Grossman School of Medicine, New York, NY.
Jose-Alberto PalmaFrom the Department of Neurology (C.G., N.W., R.F.), Beth Israel Deaconess Medical Center, Boston, MA; Department of Pathology (S.R.), NIH, Bethesda, MD; Department of Neurology (D.K.), University of Colorado, Aurora, CO; and Department of Neurology (J.-A.P., H.K.), NYU Grossman School of Medicine, New York, NY.
Horacio KaufmannFrom the Department of Neurology (C.G., N.W., R.F.), Beth Israel Deaconess Medical Center, Boston, MA; Department of Pathology (S.R.), NIH, Bethesda, MD; Department of Neurology (D.K.), University of Colorado, Aurora, CO; and Department of Neurology (J.-A.P., H.K.), NYU Grossman School of Medicine, New York, NY.
Roy FreemanFrom the Department of Neurology (C.G., N.W., R.F.), Beth Israel Deaconess Medical Center, Boston, MA; Department of Pathology (S.R.), NIH, Bethesda, MD; Department of Neurology (D.K.), University of Colorado, Aurora, CO; and Department of Neurology (J.-A.P., H.K.), NYU Grossman School of Medicine, New York, NY. rfreeman@bidmc.harvard.edu.ORCID 0000-0003-3976-6022
University of Colorado Anschutz Medical Campus · US

Funding

Training CoreU54NS065736 · NINDS · VANDERBILT UNIVERSITY MEDICAL CENTER · PI BIAGGIONI, ITALO · 2009 to 2018
$11.6M
NINDS NIH HHS U54 NS065736
6 · The paper itself

Abstract

BACKGROUND AND

objectivesMultiple system atrophy (MSA) is a progressive neurodegenerative disorder caused by the abnormal accumulation of α-synuclein in the nervous system. Clinical features include autonomic and motor dysfunction, which overlap with those of Parkinson disease (PD), particularly at early disease stages. There is an unmet need for accurate diagnostic and prognostic biomarkers for MSA and, specifically, a critical need to distinguish MSA from other synucleinopathies, particularly PD. The purpose of the study was to develop a unique cutaneous pathologic signature of phosphorylated α-synuclein that could distinguish patients with MSA from patients with PD and healthy controls.

methodsWe studied 31 patients with MSA and 54 patients with PD diagnosed according to current clinical consensus criteria. We also included 24 matched controls. All participants underwent neurologic examinations, autonomic testing, and skin biopsies at 3 locations. The density of intraepidermal, sudomotor, and pilomotor nerve fibers was measured. The deposition of phosphorylated α-synuclein was quantified. Results were compared with clinical rating assessments and autonomic function test results.

resultsPatients with PD had reduced nerve fiber densities compared with patients with MSA ( DISCUSSION: α-synuclein is present in the peripheral autonomic nerves of patients with MSA and when combined with synuclein distribution accurately distinguishes MSA from PD. CLASSIFICATION OF EVIDENCE: This study provides Class II evidence that measurement of phosphorylated α-synuclein in skin biopsies can differentiate patients with MSA from those with PD.

Indexed as

Multiple System AtrophyParkinson Diseasealpha-SynucleinHumansNerve DegenerationSkinalpha-Synuclein

Identifiers

PMID36657992
PMCPMC10103107
OpenAlexW4317469313

What OpenQuestion holds

Textmetadata
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.