Natural history of respiratory muscle strength in spinal muscular atrophy: a prospective national cohort study
Veldhoen, Esther S.; Wijngaarde, Camiel A.; Hulzebos, Erik H.J.; Wösten-van Asperen, Roelie M.; Wadman, Renske I.; van Eijk, Ruben P.A.; Asselman, Fay Lynn; Stam, Marloes; Otto, Louise A.M.; Cuppen, Inge; Scheijmans, Feline E.V.; den Oudenrijn, Laura P.Verweij van; Bartels, Bart; Gaytant, Michael A.; van der Ent, Cornelis K.; van der Pol, W. Ludo
(2022) Orphanet Journal of Rare Diseases, volume 17, issue 1, pp. 1 - 11
(Article)
Abstract
BACKGROUND: Respiratory complications are the most important cause of morbidity and mortality in spinal muscular atrophy (SMA). Respiratory muscle weakness results in impaired cough, recurrent respiratory tract infections and eventually can cause respiratory failure. We assessed longitudinal patterns of respiratory muscle strength in a national cohort of treatment-naïve children and
... read more
adults with SMA, hypothesizing a continued decline throughout life. METHODS: We measured maximal expiratory and inspiratory pressure (PE max and PI max), Sniff Nasal inspiratory pressure (SNIP), peak expiratory flow (PEF), and peak cough flow (PCF) in treatment-naïve patients with SMA. We used mixed-models to analyze natural history patterns. RESULTS: We included 2172 measurements of respiratory muscle function from 80 treatment-naïve patients with SMA types 1c-3b. All outcomes were lower in the more severe phenotypes. Significant differences in PEF were present between SMA types from early ages onwards. PEF decline was linear (1-2%/year). PEF reached values below 80% during early childhood in types 1c-2, and during adolescence in type 3a. PE max and PI max were severely lowered in most patients throughout life, with PE max values abnormally low (i.e. < 80 cmH 2O) in virtually all patients. The PE max/PI max ratio was < 1 throughout life in all SMA types, indicating that expiratory muscles were most affected. All but SMA type 3b patients had a lowered PCF. Patients with types 2b and 3a had PCF levels between 160 and 270 L/min, those with type 2a around 160 L/min and patients with type 1c well below 160 L/min. Finally, SNIP was low in nearly all patients, most pronounced in more severely affected patients. CONCLUSIONS: There are clear differences in respiratory muscle strength and its progressive decline between SMA types. We observed lower outcomes in more severe SMA types. Particularly PEF may be a suitable outcome measure for the follow-up of respiratory strength in patients with SMA. PEF declines in a rather linear pattern in all SMA types, with clear differences at baseline. These natural history data may serve as a reference for longer-term treatment efficacy assessments.
show less
Download/Full Text
Keywords: Child, Preschool, Cohort Studies, Cough, Humans, Muscle Strength/physiology, Muscular Atrophy, Spinal, Prospective Studies, Respiratory Insufficiency, Respiratory Muscles, Spinal muscular atrophy, Neuromuscular, Lung function, Respiratory muscle strength, Natural history, Research Support, Non-U.S. Gov't, Journal Article
ISSN: 1750-1172
Publisher: BioMed Central
Note: Funding Information: We thank all patients with SMA who have been participating in our ongoing study and the Dutch organization for Neuromuscular Diseases (Spierziekten Nederland) for their continuing support of our research. Funding Information: Our work was financially supported by the Prinses Beatrix Spierfonds (WAR 08-24, 13-07, and 14-26) and stichting Spieren voor Spieren. Publisher Copyright: © 2022, The Author(s).
(Peer reviewed)