Association between changes in pulmonary function and in patient reported outcomes during enzyme therapy of adult patients with late-onset Pompe disease

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Abstract

Pompe disease is a rare, progressive, and metabolic myopathy. Reduced pulmonary function is one of the main problems seen in adult patients with late-onset Pompe disease (LOPD). We aimed to explore the association between changes over time in pulmonary function and in patient-reported outcome measures (PROMs), in these patients treated with enzyme replacement therapy (ERT). This is a post hoc analysis of two cohort studies. Pulmonary function was assessed as forced vital capacity in the upright position (FVCup). As PROMs, we assessed the physical component summary score (PCS) of the Medical Outcome Study 36-item Short-Form Health Survey (SF-36) and daily life activities (Rasch-Built Pompe-Specific Activity [R-PACT] scale). We fitted Bayesian multivariate mixed-effects models. In the models of PROMs, we assumed a linear association with FVCup, and adjusted for time (nonlinear), sex, and age and disease duration at the start of ERT. One hundred and one patients were eligible for analysis. PCS and R-PAct were positively associated with FVCup, while their relation with time was nonlinear (initial increase then decrease). A 1%-point increase in FVCup is expected to increase PCS by 0.14 points (95% Credible Interval: [0.09;0.19]) and R-PACT by 0.41 points [0.33;0.49] at the same time point. In the first year of ERT, we expect a change of PCS and R-PAct scores by +0.42 and +0.80 points, and in the 5th year of +0.16 and +0.45, respectively. We conclude that the physical domain of quality of life and daily life activities improve when FVCup increases during ERT.

Original languageEnglish
Pages (from-to)595-604
Number of pages10
JournalJournal of Inherited Metabolic Disease
Volume46
Issue number4
Early online date26 Mar 2023
DOIs
Publication statusPublished - Jul 2023

Bibliographical note

Funding Information:
Nadine A. M. E. van der Beek received grants from ZonMW (Veni grant; project no. 09150161910230) and funding from Sanofi‐Genzyme for consultation, presentations, support for attending meetings and/or travel, and participation on data safety monitoring board or advisory board.

Funding Information:
This study was supported by Sanofi‐Genzyme; ZonMW‐The Netherlands Organization for Health Research and Development (projects 152001005, 80‐83600‐98‐13007, and 05‐09‐2007); Prinses Beatrix Spierfonds (projects OP07‐08, W. OR13‐21, and W.OR15‐10); TKI—Health Holland (project LSHM16008); SSWO‐Sophia Children's Hospital Foundation (project 687). Several of the authors of this publication are members of the European Reference Networks for Hereditary Metabolic Disorders (Metab‐ERN) and/or for Rare Neuromuscular Diseases (EURO‐NMD) and/or of the Netherlands Neuromuscular Center (NL‐NMD).

Publisher Copyright:
© 2023 The Authors. Journal of Inherited Metabolic Disease published by John Wiley & Sons Ltd on behalf of SSIEM.

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