Enzyme replacement therapy and fatigue in adults with Pompe disease

Pompe disease is a hereditary metabolic myopathy, for which enzyme replacement therapy (ERT) has been available since 2006. We investigated whether ERT reduces fatigue in adult patients with Pompe disease. In this prospective international observational survey, we used the Fatigue Severity Scale (FS...

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Veröffentlicht in:Molecular genetics and metabolism 2013-06, Vol.109 (2), p.174-178
Hauptverfasser: Güngör, Deniz, de Vries, Juna M., Brusse, Esther, Kruijshaar, Michelle E., Hop, Wim C.J., Murawska, Magda, van den Berg, Linda E.M., Reuser, Arnold J.J., van Doorn, Pieter A., Hagemans, Marloes L.C., Plug, Iris, van der Ploeg, Ans T.
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Sprache:eng
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Zusammenfassung:Pompe disease is a hereditary metabolic myopathy, for which enzyme replacement therapy (ERT) has been available since 2006. We investigated whether ERT reduces fatigue in adult patients with Pompe disease. In this prospective international observational survey, we used the Fatigue Severity Scale (FSS) to measure fatigue. Repeated measures ANOVA was used to analyze the data over time. In a subgroup of patients, we also evaluated muscle strength using the Medical Research Council Scale, measured pulmonary function as Forced Vital Capacity, and assessed depression using the Hospital Anxiety and Depression Scale. We followed 163 patients for a median period of 4years before ERT and for 3years during ERT. Before ERT, the mean FSS score remained stable at around 5.3 score points; during ERT, scores improved significantly by 0.13 score points per year (p
ISSN:1096-7192
1096-7206
DOI:10.1016/j.ymgme.2013.03.016