Evidence map›Paper›PMID 41054890›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2026

Stridor Is an Independent Risk Factor for Mortality and Disease Progression in Patients with Multiple System Atrophy.

Pauline Dodet, Cecile Proust-Lima, Federico Sirna, David Bendetowicz, Giulia Lazzeri, Rachel Debs, Anna Delamarre, Margaux Dunoyer, Margherita Fabbri, Claire Georges and 9 more

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

19 authors.

Pauline DodetSorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.ORCID https://orcid.org/0000-0002-7078-8345
Cecile Proust-LimaInserm, Bordeaux Population Health Research Center, U1219, University of Bordeaux, Bordeaux, France.
Federico SirnaInserm, Bordeaux Population Health Research Center, U1219, University of Bordeaux, Bordeaux, France.
David BendetowiczCHU Bordeaux, Service de Neurologie des Maladies Neurodégénératives, IMNc, CRMR AMS, NS-Park/FCRIN Network, Toulouse, France.
Giulia LazzeriCentro Parkinson e Parkinsonismi, ASST G. Pini-CTO, Milan, Italy.
Rachel DebsSleep Unit, Department of Neurology, National Competence Centre for Orphan Diseases, Narcolepsy-Rare Hypersomnias, Pierre-Paul Riquet/Purpan University Hospital, Toulouse, France.
Anna DelamarreCHU Bordeaux, Service de Neurologie des Maladies Neurodégénératives, IMNc, CRMR AMS, NS-Park/FCRIN Network, Toulouse, France.
Margaux DunoyerMSA French Reference Center, Pitié-Salpêtrière Hospital, AP-HP, Paris, France.
Margherita FabbriMSA French Reference Center, University Hospital Toulouse, Toulouse, France.ORCID https://orcid.org/0000-0001-7250-592X
Claire GeorgesMSA French Reference Center, University Hospital Toulouse, Toulouse, France.ORCID https://orcid.org/0000-0001-9969-3246
Imad GhorayebInstitut de Neurosciences Cognitives et Intégratives d'Aquitaine, UMR 5287, Université de Bordeaux, Bordeaux, France.
David GrabliSorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.
Cécile LondnerSleep Unit, National Reference Centre for Orphan Diseases, Narcolepsy and Rare Hypersomnias, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
Anne Pavy-Le TraonMSA French Reference Center, University Hospital Toulouse, Toulouse, France.
Maxime PatoutSleep Unit, National Reference Centre for Orphan Diseases, Narcolepsy and Rare Hypersomnias, Pitié-Salpêtrière hospital, AP-HP, Paris, France.
Olivier RascolMSA French Reference Center, University Hospital Toulouse, Toulouse, France.ORCID https://orcid.org/0000-0002-1410-6397
Isabelle ArnulfSorbonne Université, Paris Brain Institute, Inserm, CNRS, Paris, France.ORCID https://orcid.org/0000-0002-2240-2516
Alexandra Foubert-SamierInserm, Bordeaux Population Health Research Center, U1219, University of Bordeaux, Bordeaux, France.
Wassilios G MeissnerCHU Bordeaux, Service de Neurologie des Maladies Neurodégénératives, IMNc, CRMR AMS, NS-Park/FCRIN Network, Toulouse, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

aimStridor and sleep apnea syndrome (SAS) are common in multiple system atrophy (MSA). Retrospective cohort studies have yielded conflicting results regarding the consequences of stridor and SAS on the disease course. This study aimed to assess the prognostic significance of stridor and SAS, as well as the potential survival benefits of continuous positive airway pressure (CPAP) therapy.

methodRetrospective data from 232 participants with MSA (mean age 65 years old, 51% male) from the three sites of the French Reference Center for MSA were analyzed. Patients underwent video-polysomnography to confirm the presence of stridor and SAS (AHI >15). Survival analyses adjusted for disease progression, age, sex, MSA subtype, and time since symptom onset were conducted using a joint modeling approach. Disease progression was quantified by the repeated assessments of a six-item composite score and the total Unified MSA Rating Scale I + II.

resultsStridor was independently associated with an increased risk of mortality (hazard ratio [HR] = 2.44 [1.41;4.22]), even after adjusting for disease progression. Stridor was also linked to more severe disease progression over time. In contrast, SAS did not independently predict mortality or disease progression. CPAP therapy initiation was associated with a substantial reduction in mortality risk after adjusting for center and AHI (HR = 0.40 [0.19;0.85], P = 0.017). DISCUSSION: Stridor is a critical prognostic factor in MSA, associated with higher mortality and worse disease progression, whereas SAS alone is not associated with a change in mortality. Patients undergoing CPAP therapy have a much better survival among those with stridor. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

Multiple System AtrophyRespiratory SoundsSleep Apnea SyndromesAgedContinuous Positive Airway PressureDisease ProgressionFemaleHumansMaleMiddle AgedPolysomnographyPrognosisRetrospective StudiesRisk Factorsmultiple system atrophysleepstridor

Identifiers

PMID41054890
PMCPMC12882046

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.