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Natural history of lung function in spinal muscular atrophy

BACKGROUND: Respiratory muscle weakness is an important feature of spinal muscular atrophy (SMA). Progressive lung function decline is the most important cause of mortality and morbidity in patients. The natural history of lung function in SMA has, however, not been studied in much detail. RESULTS:...

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Autores principales: Wijngaarde, Camiel A., Veldhoen, Esther S., van Eijk, Ruben P. A., Stam, Marloes, Otto, Louise A. M., Asselman, Fay-Lynn, Wösten-van Asperen, Roelie M., Hulzebos, Erik H. J., Verweij-van den Oudenrijn, Laura P., Bartels, Bart, Cuppen, Inge, Wadman, Renske I., van den Berg, Leonard H., van der Ent, Cornelis K., van der Pol, W. Ludo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149916/
https://www.ncbi.nlm.nih.gov/pubmed/32276635
http://dx.doi.org/10.1186/s13023-020-01367-y
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author Wijngaarde, Camiel A.
Veldhoen, Esther S.
van Eijk, Ruben P. A.
Stam, Marloes
Otto, Louise A. M.
Asselman, Fay-Lynn
Wösten-van Asperen, Roelie M.
Hulzebos, Erik H. J.
Verweij-van den Oudenrijn, Laura P.
Bartels, Bart
Cuppen, Inge
Wadman, Renske I.
van den Berg, Leonard H.
van der Ent, Cornelis K.
van der Pol, W. Ludo
author_facet Wijngaarde, Camiel A.
Veldhoen, Esther S.
van Eijk, Ruben P. A.
Stam, Marloes
Otto, Louise A. M.
Asselman, Fay-Lynn
Wösten-van Asperen, Roelie M.
Hulzebos, Erik H. J.
Verweij-van den Oudenrijn, Laura P.
Bartels, Bart
Cuppen, Inge
Wadman, Renske I.
van den Berg, Leonard H.
van der Ent, Cornelis K.
van der Pol, W. Ludo
author_sort Wijngaarde, Camiel A.
collection PubMed
description BACKGROUND: Respiratory muscle weakness is an important feature of spinal muscular atrophy (SMA). Progressive lung function decline is the most important cause of mortality and morbidity in patients. The natural history of lung function in SMA has, however, not been studied in much detail. RESULTS: We analysed 2098 measurements of lung function from 170 treatment-naïve patients with SMA types 1c–4, aged 4–74 years. All patients are participating in an ongoing population-based prevalence cohort study. We measured Forced Expiratory Volume in 1 s (FEV(1)), Forced Vital Capacity (FVC), and Vital Capacity (VC). Longitudinal patterns of lung function were analysed using linear mixed-effects and non-linear models. Additionally, we also assessed postural effects on results of FEV(1) and FVC tests. In early-onset SMA types (1c–3a), we observed a progressive decline of lung function at younger ages with relative stabilisation during adulthood. Estimated baseline values were significantly lower in more severely affected patients: %FEV(1) ranged from 42% in SMA type 1c to 100% in type 3b, %FVC 50 to 109%, and %VC 44 to 96%. Average annual decline rates also differed significantly between SMA types, ranging from − 0.1% to − 1.4% for FEV(1), − 0.2% to − 1.4% for FVC, and + 0.2% to − 1.7% for VC. In contrast to SMA types 1c–3a, we found normal values for all outcomes in later-onset SMA types 3b and 4 throughout life, although with some exceptions and based on limited available data. Finally, we found no important differences in FVC or FEV(1) values measured in either sitting or supine position. CONCLUSIONS: Our data illustrate the longitudinal course of lung function in patients with SMA, which is characterised by a progressive decline in childhood and stabilisation in early adulthood. The data do not support an additional benefit of measuring FEV(1) or FVC in both sitting and supine position. These data may serve as a reference to assess longer-term outcomes in clinical trials.
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spelling pubmed-71499162020-04-19 Natural history of lung function in spinal muscular atrophy Wijngaarde, Camiel A. Veldhoen, Esther S. van Eijk, Ruben P. A. Stam, Marloes Otto, Louise A. M. Asselman, Fay-Lynn Wösten-van Asperen, Roelie M. Hulzebos, Erik H. J. Verweij-van den Oudenrijn, Laura P. Bartels, Bart Cuppen, Inge Wadman, Renske I. van den Berg, Leonard H. van der Ent, Cornelis K. van der Pol, W. Ludo Orphanet J Rare Dis Research BACKGROUND: Respiratory muscle weakness is an important feature of spinal muscular atrophy (SMA). Progressive lung function decline is the most important cause of mortality and morbidity in patients. The natural history of lung function in SMA has, however, not been studied in much detail. RESULTS: We analysed 2098 measurements of lung function from 170 treatment-naïve patients with SMA types 1c–4, aged 4–74 years. All patients are participating in an ongoing population-based prevalence cohort study. We measured Forced Expiratory Volume in 1 s (FEV(1)), Forced Vital Capacity (FVC), and Vital Capacity (VC). Longitudinal patterns of lung function were analysed using linear mixed-effects and non-linear models. Additionally, we also assessed postural effects on results of FEV(1) and FVC tests. In early-onset SMA types (1c–3a), we observed a progressive decline of lung function at younger ages with relative stabilisation during adulthood. Estimated baseline values were significantly lower in more severely affected patients: %FEV(1) ranged from 42% in SMA type 1c to 100% in type 3b, %FVC 50 to 109%, and %VC 44 to 96%. Average annual decline rates also differed significantly between SMA types, ranging from − 0.1% to − 1.4% for FEV(1), − 0.2% to − 1.4% for FVC, and + 0.2% to − 1.7% for VC. In contrast to SMA types 1c–3a, we found normal values for all outcomes in later-onset SMA types 3b and 4 throughout life, although with some exceptions and based on limited available data. Finally, we found no important differences in FVC or FEV(1) values measured in either sitting or supine position. CONCLUSIONS: Our data illustrate the longitudinal course of lung function in patients with SMA, which is characterised by a progressive decline in childhood and stabilisation in early adulthood. The data do not support an additional benefit of measuring FEV(1) or FVC in both sitting and supine position. These data may serve as a reference to assess longer-term outcomes in clinical trials. BioMed Central 2020-04-10 /pmc/articles/PMC7149916/ /pubmed/32276635 http://dx.doi.org/10.1186/s13023-020-01367-y Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Wijngaarde, Camiel A.
Veldhoen, Esther S.
van Eijk, Ruben P. A.
Stam, Marloes
Otto, Louise A. M.
Asselman, Fay-Lynn
Wösten-van Asperen, Roelie M.
Hulzebos, Erik H. J.
Verweij-van den Oudenrijn, Laura P.
Bartels, Bart
Cuppen, Inge
Wadman, Renske I.
van den Berg, Leonard H.
van der Ent, Cornelis K.
van der Pol, W. Ludo
Natural history of lung function in spinal muscular atrophy
title Natural history of lung function in spinal muscular atrophy
title_full Natural history of lung function in spinal muscular atrophy
title_fullStr Natural history of lung function in spinal muscular atrophy
title_full_unstemmed Natural history of lung function in spinal muscular atrophy
title_short Natural history of lung function in spinal muscular atrophy
title_sort natural history of lung function in spinal muscular atrophy
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7149916/
https://www.ncbi.nlm.nih.gov/pubmed/32276635
http://dx.doi.org/10.1186/s13023-020-01367-y
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