Evidence map›Paper›PMID 41140054›Full record

ArticleEuropean journal of neurology2025

Causes of Death and Comorbidities in Adult Patients With Late-Onset Pompe Disease: A French Pompe Registry Retrospective Study.

Diana Maria Chitimus, Céline Tard, Maxime Fournier, Françoise Bouhour, Anthony Béhin, Emmanuelle Salort-Campana, Emmeline Lagrange, Anne-Laure Kaminsky, Armelle Magot, Stéphane Beltran and 17 more

Abstract read
In one paragraph

Article in European journal of neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

27 authors.

Diana Maria ChitimusRaymond Poincaré University Hospital, APHP, Garches, France.ORCID 0000-0003-3241-2782
Céline TardNord-Est-Ile-de-France, Neuromuscular Reference Center, FHU PHENIX; Inserm, Paris, France.
Maxime FournierDepartment of Neurology, CHU Caen, Caen, France.
Françoise BouhourService D'electroneuromyographie et Pathologies Neuromusculaires, Hospices Civils de Lyon, Lyon, France.
Anthony BéhinNord-Est-Ile-de-France, Neuromuscular Reference Center, FHU PHENIX, APHP, Paris, France.
Emmanuelle Salort-CampanaCentre de Référence Des, Maladies Neuromusculaires, Hôpital Timone Adultes, Assistance Publique, Hôpitaux de Marseille, PACA, Marseille, France.
Emmeline LagrangeDepartment of Neurology, Grenoble University Hospital, Grenoble, France.
Anne-Laure KaminskyService de Neurologie, Centre Référent Des Maladies Neuromusculaires Rares, CHU de Saint Etienne, Saint-Etienne, France.
Armelle MagotCentre de Référence Des, Maladies Neuromusculaires, AOC, CHU Hôtel Dieu, Nantes, France.ORCID 0000-0002-7589-1421
Stéphane BeltranCentre SLA, Service de Neurologie, CHU Bretonneau, Tours, France.
Jean-Baptiste NouryNeurology Department, Neuromuscular Center, CHRU Cavale Blanche, Brest, France.
Laurent MagyService de Neurologie, Centre de référence Des Maladies Neuromusculaires, Hôpital Dupuytren, CHU de Limoges, Limoges, France.
Guilhem SoléNeuromuscular Reference Center, Bordeaux University, Bordeaux, France.
Dimitri RenardDepartment of Neurology, CHU Nimes, University of Montpellier, Montpellier, Nimes, France.
Marco SpinazziNeuromuscular Reference Center, Department of Neurology, University Hospital, Angers, France.
Florence DemurgerService de Génétique, CHBA, Vannes, France.
Pascal CintasDepartement de Neurologie, Hopital Purpan, CHU, Toulouse, France.
Aleksandra Nadaj-PaklezaNord-Est-Ile-de-France, Neuromuscular Reference Center, FHU PHENIX, ERN EURO-NMD, Paris, France.
Joelle Deibener-KaminskyService de Médecine Interne et Immunologie Clinique, CHU Nancy Brabois, Vandœuvre-lès-Nancy, France.
Guillaume BassezCentre de référence Des Maladies Neuromusculaires Nord/Est/Ile de France, Institut de Myologie, Hôpital Pitié-Salpêtrière, Assistance Publique Des Hôpitaux de Paris, Paris, France.
Nadjib TaouaghNeurology Department, Raymond Poincare University Hospital, Garches, France.
Azzedine ArrassiNord-Est-Ile-de-France, Neuromuscular Reference Center, FHU PHENIX, APHP, Paris, France.
Claire LefeuvreNord-Est-Ile-de-France Neuromuscular, Reference Center, FHU, PHENIX, Garches, France.
Sharam AttarianCentre de Référence Des, Maladies Neuromusculaires, Hôpital Timone Adultes, Assistance Publique, Hôpitaux de Marseille, PACA, Marseille, France.ORCID 0000-0002-7211-4694
Dalil HamrounCentre Hospitalo-Universitaire de Montpellier, Montpellier, France.ORCID 0000-0002-4853-8227
Pascal LaforêtNeurology Department, Raymond Poincaré University Hospital, Garches, France.ORCID 0000-0002-4489-4718
for French Pompe study group

Funding

Sanofi Genzyme
6 · The paper itself

Abstract

BACKGROUND AND

objectivesMortality in Late-Onset Pompe Disease (LOPD) has been associated with the rapid progression of respiratory and motor impairment. However, an in-depth approach to the exact causes of death in these patients is still lacking.

methodsIn this retrospective cohort study, we analyzed the cause of death and the comorbidities of all deceased patients from the French Late-Onset Pompe Disease registry.

resultsBy the time of the last extraction, 60 patients diagnosed with LOPD and monitored were registered as deceased in the French national registry, out of a total of 260 patients included. The median age of death was 70.5 years, while the median age of diagnosis was 58 years. The causes of death were divided into disease-related, accounting for 46.6% of deaths, and non-disease-related, comprising 28.3% of total deaths. Fifteen patients (25%) died of an unknown cause. The most frequent etiology of disease-related death was respiratory failure (n = 14), while for the non-disease-related group, malignant neoplasm was the most common (n = 8). Patients in the non-disease-related death group had significantly higher forced vital capacity (FVC) values compared to those in the disease-related death group (54.7% vs. 38%). Treatment-wise, the median period elapsed from diagnosis to ERT introduction was higher in the disease-related group. DISCUSSION: This is the first study to focus on the specific causes of death of LOPD patients. The majority of the LOPD deaths in the French registry were attributed to respiratory failure and malignant neoplasms.

Indexed as

Cause of DeathGlycogen Storage Disease Type IIAgedAge of OnsetComorbidityFemaleFranceHumansMaleMiddle AgedNeoplasmsRegistriesRespiratory InsufficiencyRetrospective StudiesFrench registrylate‐onset Pompe diseasemetabolic myopathymortalityrespiratory failure

Identifiers

PMID41140054
PMCPMC12554947

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