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Swallowing dysfunction in patients with nephropathic cystinosis

  • A. E. van Rijssel
  • , S. Knuijt
  • , K. Veys
  • , E. N. Levtchenko
  • , M. C.H. Janssen*
  • *Corresponding author for this work
  • Radboud University Nijmegen
  • KU Leuven

Research output: Contribution to journalArticleAcademicpeer-review

Abstract

Introduction: Nephropathic cystinosis is a rare autosomal recessive lysosomal storage disorder caused by mutations in the CTNS gene. Patients with nephropathic cystinosis suffer not only from renal disease but have also other systemic complications like myopathy and swallowing dysfunction. Dysphagia for solid food is mentioned in patients with cystinosis, but in clinical practice swallowing investigations are only performed when the patient has complaints. The aim of this study was to explore the swallowing function in patients with cystinosis by use of the Test of Mastication and Swallowing Solids (TOMASS), and to compare their performance with patients with myotonic dystrophy type 1 – a neuromuscular disease in which dysphagia for solid food is a known problem. Methods: Twenty adult patients with cystinosis (11 men and 9 women, range 19–51 years)and 10 patients with myotonic dystrophy type 1 (5 men and 5 women, range 20–60 years)were included. All cystinosis patients were treated with cysteamine. Data of the two groups were compared with normative data using independent-samples t-tests. In case the variables were not normally distributed, the non-parametric Mann-Whitney U test was used. Results: There was a significant difference in the number of bites, masticatory cycles, swallows and total time between the normal values and cystinosis patients. The results of the cystinosis patients were comparable to those of the patients with myotonic dystrophy. Discussion and conclusion: Adult patients with cystinosis have significant dysphagia for solid food. Clinicians treating these patients should be aware of this fact. The TOMASS can be performed easily in clinical practice to investigate whether patients with cystinosis have swallowing dysfunction. The swallowing dysfunction can now be diagnosed by use of a non-invasive, very simple, non-harmful test. It can be discussed whether this should be added to the regular care scheme of cystinosis patients in order to regularly follow-up swallowing function.

Original languageEnglish
Pages (from-to)413-415
Number of pages3
JournalMolecular genetics and metabolism
Volume126
Issue number4
DOIs
Publication statusPublished - Apr 2019
Externally publishedYes

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Cystinosis
  • Dysphagia?
  • Nephropathic
  • Swallowing dysfunction

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