Mastication in Patients with Spinal Muscular Atrophy Types 2 and 3 is Characterized by Abnormal Efficiency, Reduced Endurance, and Fatigue

A. M.B. van der Heul, R. P.A. van Eijk, R. I. Wadman, F. Asselman, I. Cuppen, R. A.J. Nievelstein, E. Gerrits, W. L. van der Pol*, L. van den Engel-Hoek

*Corresponding author for this work

Research output: Contribution to journalReview articlepeer-review

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Abstract

Mastication problems can have a negative impact on the intake of food and quality of life. This cross-sectional study characterizes mastication problems using clinical and instrumental assessments in patients with spinal muscular atrophy (SMA) types 2 and 3 with self-reported bulbar problems. We included 27 patients (aged 13–67 years), 18 with SMA type 2 and 9 patients with SMA type 3 (of whom three were still ambulant) and applied a questionnaire, clinical mastication tests (TOMASS and 6-min mastication test), and muscle ultrasound of the mastication muscles. Non-ambulant patients demonstrated inefficient mastication as reflected by median z scores for masticatory cycles (z = 1.8), number of swallows (z = 4.3) and time needed to finish the cracker (z = 3.4), and limited endurance of continuous mastication as demonstrated by the median z scores of the 6-min mastication test (z = − 1.5). Patients reported increased fatigue directly after the 6-min mastication test as well as 5 min after completing the test (p < 0.001; p = 0.003). Reduced maximal mouth opening was associated with mastication problems (p < 0.001). Muscle ultrasound of the mastication muscles showed an abnormal muscle structure in 90% of both ambulant and non-ambulant patients. This study aims to understand the nature and underlying mechanisms of mastication problems in patients with SMA types 2 and 3 with reported bulbar problems.

Original languageEnglish
Pages (from-to)715-723
Number of pages9
JournalDysphagia
Volume37
Issue number4
DOIs
Publication statusPublished - Aug 2022

Keywords

  • Deglutition
  • Deglutition disorders
  • Mastication
  • Oral motor function
  • Spinal muscular atrophy
  • Survival motor neuron gene

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