Evidence map›Paper›PMID 39109844›Full record

ArticleEuropean journal of neurology2024

Bulbar muscle impairment in patients with late onset Pompe disease: Insight from the French Pompe registry.

Emilie Retailleau, Claire Lefeuvre, Marie De Antonio, Françoise Bouhour, Celine Tard, Emmanuelle Salort-Campana, Emmeline Lagrange, Anthony Béhin, Guilhem Solé, Jean-Baptiste Noury and 17 more

Abstract read
In one paragraph

Article in European journal of neurology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

  1. Article
  2. Article
  3. 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

27 authors.

Emilie RetailleauNeurology Department, Raymond Poincaré University Hospital, Assistance Publique des Hopitaux de Paris, Garches, France.ORCID 0009-0000-8908-544X
Claire LefeuvreNeurology Department, Raymond Poincaré University Hospital, Assistance Publique des Hopitaux de Paris, Garches, France.
Marie De AntonioBiostatistics Unit, Direction de la Recherche Clinique et de l'Innovation, Clermont-Ferrand University Hospital, Clermont-Ferrand, France.
Françoise BouhourService d'Electroneuromyographie et Pathologies Neuromusculaires, Hospices Civils de Lyon, Hospices Civils de Lyon, Lyon, France.
Celine TardNord-Est-Ile-de-France Neuromuscular Reference Center, Fédération Hospitalo Universitaire PHENIX, Garches, France.
Emmanuelle Salort-CampanaCentre de Référence des Maladies Neuromusculaires, Hôpital Timone Adultes, Assistance Publique Hôpitaux de Marseille, Marseille, France.
Emmeline LagrangeDepartment of Neurology, Grenoble University Hospital, Grenoble, France.ORCID 0000-0002-9844-0762
Anthony BéhinNord-Est-Ile-de-France Neuromuscular Reference Center, Fédération Hospitalo Universitaire PHENIX, Garches, France.
Guilhem SoléNeuromuscular Reference Center, Bordeaux University Hospital (Pellegrin), University of Bordeaux, Bordeaux, France.
Jean-Baptiste NouryInstitut National de la Santé et de la Recherche Médicale, Lymphocytes B Autoimmunité et Immunothérapie, Unité Mixte de Recherche 1227, Centre de Référence des Maladies Neuromusculaires Atlantique Occitanie Caraibes, CHRU de Brest, Brest, France.
Sabrina SacconiPeripheral Nervous System and Muscle Department, Université Cote d'Azur, CHU de Nice, Nice, France.
Armelle MagotCentre de Référence des Maladies Neuromusculaires Atlantique Occitanie Caraibes, CHU de Nantes, Filnemus, European Neuro Muscular Diseases, Nantes, France.ORCID 0000-0002-7589-1421
Aleksandra Nadaj PaklezaNord-Est-Ile-de-France Neuromuscular Reference Center, Fédération Hospitalo Universitaire PHENIX, Garches, France.
David OrlikowskiNord-Est-Ile-de-France Neuromuscular Reference Center, Fédération Hospitalo Universitaire PHENIX, Garches, France.
Stéphane BeltranAmyotrophic Lateral Sclerosis Center, François Rabelais University, Tours, France.ORCID 0000-0003-4718-0902
Marco SpinazziNeuromuscular Reference Center, Department of Neurology, University Hospital, Angers, France.
Pascal CintasDépartement de Neurologie, CHU Toulouse, Hôpital Purpan, Toulouse, France.
Maxime FournierDepartment of Neurology, CHU Caen, Normandie, France.
Fatma BouibedeCHR d'Orléans, Internal Medicine Department, Orléans, France.
Hélène PrigentInstitut National de la Santé et de la Recherche Médicale, Université Versailles Saint Quentin en Yvelines, Paris Saclay, Versailles, France.
Guillaume NicolasNeurology Department, Raymond Poincaré University Hospital, Assistance Publique des Hopitaux de Paris, Garches, France.
Nadjib TaouaghNeurology Department, Raymond Poincaré University Hospital, Assistance Publique des Hopitaux de Paris, Garches, France.
Taissir El GuizaniNeurology Department, Raymond Poincaré University Hospital, Assistance Publique des Hopitaux de Paris, Garches, France.
Shahram AttarianCentre de Référence des Maladies Neuromusculaires, Hôpital Timone Adultes, Assistance Publique Hôpitaux de Marseille, Marseille, France.
Azzeddine ArrassiNord-Est-Ile-de-France Neuromuscular Reference Center, Fédération Hospitalo Universitaire PHENIX, Garches, France.
Dalil HamrounCentre Hospitalo-Universitaire de Montpellier, Hôpital Arnaud-de-Villeneuve, Montpellier, France.
Pascal LaforêtNeurology Department, Raymond Poincaré University Hospital, Assistance Publique des Hopitaux de Paris, Garches, France.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

background and purposeLate onset Pompe disease (LOPD) is a rare neuromuscular disorder caused by a deficit in acid alpha-glucosidase. Macroglossia and swallowing disorders have already been reported, but no study has focused yet on its frequency and functional impact on patients' daily life.

methodsWe reviewed 100 adult LOPD patients followed in 17 hospitals in France included in the French national Pompe disease registry. The Swallowing Quality of Life Questionnaire and the Sydney Swallow Questionnaire were completed by patients, and a specialist carried out a medical examination focused on swallowing and assigned a Salassa score to each patient. Respiratory and motor functions were also recorded. Subgroup analysis compared patients with and without swallowing difficulties based on Salassa score.

resultsThirty-two percent of patients presented with swallowing difficulties, often mild but sometimes severe enough to require percutaneous endoscopic gastrostomy (1%). Daily dysphagia was reported for 20% of our patients and aspirations for 18%; 9.5% were unable to eat away from home. Macroglossia was described in 18% of our patients, and 11% had lingual atrophy. Only 15% of patients presenting with swallowing disorders were followed by a speech therapist. Swallowing difficulties were significantly associated with macroglossia (p = 0.015), longer duration of illness (p = 0.032), and a lower body mass index (p = 0.047).

conclusionsSwallowing difficulties in LOPD are common and have significant functional impact. Increased awareness by physicians of these symptoms with systematic examination of the tongue and questions about swallowing can lead to appropriate multidisciplinary care with a speech therapist and dietitian if needed.

Indexed as

Deglutition DisordersGlycogen Storage Disease Type IIRegistriesAdultAgedFemaleFranceHumansMaleMiddle AgedQuality of LifeSurveys and QuestionnairesdysphagiaFrench Pompe registryglycogenosis type IIlate onset Pompe diseasemacroglossia

Identifiers

PMID39109844
PMCPMC11414798

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Registered trials

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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.