Evidence map›Paper›PMID 33816659›Full record

ReviewMovement disorders clinical practice2021

Laboratory-Supported Multiple System Atrophy beyond Autonomic Function Testing and Imaging: A Systematic Review by the MoDiMSA Study Group.

Iva Stankovic, Alessandra Fanciulli, Vladimir S Kostic, Florian Krismer, Wassilios G Meissner, Jose Alberto Palma, Jalesh N Panicker, Klaus Seppi, Gregor K Wenning, MoDiMSA Study Group

Open access · bronzeAbstract readReview
In one paragraph

Review in Movement disorders clinical practice, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
1.1field-weighted citation impact, top 20% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 15 citations in OpenAlex.

  1. The Movement Disorder Society Criteria for the Diagnosis of Multiple System Atrophy.Movement disorders : official journal of the Movement Disorder Society · 2022
    Pooled it
  2. Heart rate variability provides prognostic value in multiple system atrophy.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Review
  7. Multiple system atrophy.Practical neurology · 2023
    Review
  8. A case of Lewy body disease and anaplastic astrocytoma presenting with atypical parkinsonism.Neuropathology : official journal of the Japanese Society of Neuropathology · 2022
    Article
  9. Multiple system atrophy.Nature reviews. Disease primers · 2022
    Review
  10. Different phenoconversion pathways in pure autonomic failure with versus without Lewy bodies.Clinical autonomic research : official journal of the Clinical Autonomic Research Society · 2021
    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

10 authors at 5 institutions in 6 countries.

Iva StankovicNeurology Clinic, Clinical Center of Serbia, School of Medicine University of Belgrade Belgrade Serbia.
Alessandra FanciulliDepartment of Neurology Medical University of Innsbruck Innsbruck Austria.ORCID https://orcid.org/0000-0002-2854-4179
Vladimir S KosticNeurology Clinic, Clinical Center of Serbia, School of Medicine University of Belgrade Belgrade Serbia.
Florian KrismerDepartment of Neurology Medical University of Innsbruck Innsbruck Austria.ORCID https://orcid.org/0000-0002-4493-5073
Wassilios G MeissnerDepartment of Neurology for Neurodegenerative Diseases, French Reference Center for MSA University Hospital Bordeaux Bordeaux France.ORCID https://orcid.org/0000-0003-2172-7527
Jose Alberto PalmaDepartment of Neurology, Dysautonomia Center, Langone Medical Center New York University School of Medicine New York New York USA.ORCID https://orcid.org/0000-0002-1345-6774
Jalesh N PanickerUCL Institute of Neurology London United Kingdom.
Klaus SeppiDepartment of Neurology Medical University of Innsbruck Innsbruck Austria.
Gregor K WenningDepartment of Neurology Medical University of Innsbruck Innsbruck Austria.
MoDiMSA Study Group
Innsbruck Medical University · ATUniversity of Belgrade · RSCentre National de la Recherche Scientifique · FRNational Hospital for Neurology and Neurosurgery · GBNYU Langone Health · US

Funding

Genetic characterization of atypical parkinsonismZIANS003154 · NINDS · NATIONAL INSTITUTE OF NEUROLOGICAL DISORDERS AND STROKE · PI SCHOLZ, SONJA · 2016 to 2025
$15.4M
Intramural NIH HHS ZIA NS003154
6 · The paper itself

Abstract

backgroundNeuroimaging has been used to support a diagnosis of possible multiple system atrophy (MSA). Only blood pressure changes upon standing are included in the second consensus criteria but other autonomic function tests (AFT) are also useful to diagnose widespread and progressive autonomic failure typical of MSA. Additional diagnostic tools are of interest to improve accuracy of MSA diagnosis.

objectivesTo assess the utility of diagnostic tools beyond brain imaging and AFT in enhancing a laboratory-supported diagnosis of MSA to support the upcoming revision of the consensus criteria.

methodsThe International Parkinson and Movement Disorders Society MSA Study Group (MoDiMSA) performed a systematic review of original papers on biomarkers, sleep studies, genetic, neuroendocrine, neurophysiological, neuropsychological and other tests including olfactory testing and acute levodopa challenge test published before August 2019.

resultsEvaluation of history of levodopa responsiveness and olfaction is useful in patients in whom MSA-parkinsonian subtype is suspected. Neuropsychological testing is useful to exclude dementia at time of diagnosis. Applicability of sphincter EMG is limited. When MSA-cerebellar subtype is suspected, a screening for the common causes of adult-onset progressive ataxia is useful, including spinocerebellar ataxias in selected patients. Diagnosing stridor and REM sleep behavior disorder is useful in both MSA subtypes. However, none of these tools are validated in large longitudinal cohorts of postmortem confirmed MSA cases.

conclusionsDespite limited evidence, additional laboratory work-up of patients with possible MSA beyond imaging and AFT should be considered to optimize the clinical diagnostic accuracy.

Indexed as

diagnostic testsmultiple system atrophy

Identifiers

PMID33816659
PMCPMC8015918
OpenAlexW3127587701

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.