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Late-onset Pompe disease (LOPD) in Belgium: clinical characteristics and outcome measures.
Vanherpe, P; Fieuws, S; D'Hondt, A; Bleyenheuft, C; Demaerel, P; De Bleecker, J; Van den Bergh, P; Baets, J; Remiche, G; Verhoeven, K; Delstanche, S; Toussaint, M; Buyse, B; Van Damme, P; Depuydt, C E; Claeys, K G.
Afiliación
  • Vanherpe P; Department of Neurology, Neuromuscular Reference Centre, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.
  • Fieuws S; KU Leuven - University of Leuven, Interuniversity Institute for Biostatistics and Statistical Bioinformatics, Leuven, Belgium.
  • D'Hondt A; Department of Neurology, Neuromuscular Reference Centre, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.
  • Bleyenheuft C; Sciensano, Brussels, Belgium.
  • Demaerel P; Department of Radiology, University Hospitals Leuven, Leuven, Belgium.
  • De Bleecker J; Department of Neurology, Neuromuscular Reference Centre, University Hospital Gent, Gent, Belgium.
  • Van den Bergh P; Department of Neurology, Neuromuscular Reference Centre, University Hospital Saint-Luc, Brussels, Belgium.
  • Baets J; Department of Neurology, Neuromuscular Reference Centre, University Hospital Antwerpen, Antwerpen, Belgium.
  • Remiche G; Department of Neurology, Neuromuscular Reference Centre, University Hospital Erasme, Université Libre de Bruxelles, Brussels, Belgium.
  • Verhoeven K; Department of Neurology, AZ Sint-Jan Brugge, Brugge, Belgium.
  • Delstanche S; Department of Neurology, Neuromuscular Reference Centre of Liège, CHU Liège, Liège, Belgium.
  • Toussaint M; Department of Rehabilitation, Centre for Home Mechanical Ventilation and Neuromuscular Reference Centre, Rehabilitation Hospital Inkendaal, Brussels, Belgium.
  • Buyse B; Department of Pulmonology, Leuven University Centre for Sleep and Wake Disorders, University Hospitals Leuven, Leuven, Belgium.
  • Van Damme P; Department of Neurology, Neuromuscular Reference Centre, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.
  • Depuydt CE; VIB, Center for Brain & Disease Research, Laboratory of Neurobiology, Leuven, Belgium.
  • Claeys KG; Department of Neurosciences - Experimental Neurology, Laboratory for Muscle Diseases and Neuropathies, KU Leuven, Leuven, Belgium.
Orphanet J Rare Dis ; 15(1): 83, 2020 04 05.
Article en En | MEDLINE | ID: mdl-32248831
BACKGROUND: Late-onset Pompe disease (LOPD) is a rare, hereditary, progressive disorder that is usually characterized by limb-girdle muscle weakness and/or respiratory insufficiency. LOPD is caused by mutations in the acid alpha-glucosidase (GAA) gene and treated with enzyme replacement therapy (ERT). METHODS: We studied the clinical, brain imaging, and genetic features of the Belgian cohort of late-onset Pompe disease patients (N = 52), and explored the sensitivity of different outcome measures, during a longitudinal period of 7 years (2010-2017), including the activity limitations ActivLim score, 6 min walking distance (6MWD), 10 m walk test (10MWT), MRC sum score, and forced vital capacity (FVC) sitting/supine. RESULTS: In Belgium, we calculated an LOPD prevalence of 3.9 per million. Mean age at onset of 52 LOPD patients was 28.9 years (SD: 15.8 y), ranging from 7 months to 68 years. Seventy-five percent (N = 39) of the patients initially presented with limb-girdle weakness, whereas in 13% (N = 7) respiratory symptoms were the only initial symptom. Non-invasive ventilation (NIV) was started in 37% (N = 19), at a mean age of 49.5 years (SD: 11.9 y), with a mean duration of 15 years (SD: 10.2 y) after symptom onset. Brain imaging revealed abnormalities in 25% (N = 8) of the patients, with the presence of small cerebral aneurysm(s) in two patients and a vertebrobasilar dolichoectasia in another two. Mean diagnostic delay was 12.9 years. All patients were compound heterozygotes with the most prevalent mutation being c.-32-13 T > G in 96%. We identified two novel mutations in GAA: c.1610_1611delA and c.186dup11. For the 6MWD, MRC sum score, FVC sitting and FVC supine, we measured a significant decrease over time (p = 0.0002, p = 0.0001, p = 0.0077, p = 0.0151), which was not revealed with the ActivLim score and 10MWT (p > 0.05). CONCLUSIONS: Awareness on LOPD should even be further increased because of the long diagnostic delay. The 6MWD, but not the ActivLim score, is a sensitive outcome measure to follow up LOPD patients.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo II Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Límite: Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Asunto principal: Enfermedad del Almacenamiento de Glucógeno Tipo II Tipo de estudio: Diagnostic_studies / Prognostic_studies / Risk_factors_studies Aspecto: Patient_preference Límite: Humans / Middle aged País/Región como asunto: Europa Idioma: En Revista: Orphanet J Rare Dis Asunto de la revista: MEDICINA Año: 2020 Tipo del documento: Article País de afiliación: Bélgica Pais de publicación: Reino Unido