Nociceptive pain in late-onset Pompe disease: prevalence, distribution, and clinical correlates.

Authors

Stephan Wenninger, Marcela Arndt, Daniel H Mendelsohn, Corinna Wirner-Piotrowski, Marko Mijic, Natalia Garcia-Angarita, Kristina Gutschmidt, Christoph Schmidt, Lisa Winkler, Dieter Gläser, Karl Christian Knop, Matthias Spranger, Frank Klawonn, Lea Eileen Brauner, Benedikt Schoser

Published in

Journal of neurology. Volume 273. Issue 9. Aug 25, 2026. Epub Aug 25, 2026.

Abstract

Nociceptive pain is often recognized as a relevant symptom in late-onset Pompe disease (LOPD), yet its prevalence, distribution, and underlying determinants remain insufficiently characterized. We aimed to systematically assess nociceptive pain in LOPD and to explore its relationship with muscle function, structural muscle alterations, and potential modifiers.
In this multicenter cross-sectional study, 42 patients with LOPD and 61 disease controls (IBM, FSHD, SMA3) were evaluated. Pain was assessed using validated questionnaires and pain drawings. Motor function tests, pressure pain thresholds, muscle ultrasound, laboratory parameters, and genetic polymorphisms (ACE, ACTN3) were obtained. Associations between pain and clinical, structural, and biological variables were analyzed.
Chronic nociceptive musculoskeletal pain was highly prevalent, particularly in LOPD (83.3%) compared to disease controls (p=0.005). However, pain reported on the assessment day was significantly lower in LOPD (30.9%, p<0.001) and SMA3 (25%, p=0.016). No significant associations were found between pain and muscle strength, motor function tests, ultrasound-detected muscle alterations, ACTN3 and ACE, and laboratory parameters.
Musculoskeletal pain is highly prevalent in LOPD but remains dissociated from objective measures of motor impairment, structural changes of muscle tissue, or genetic modifiers. The significant discrepancy between chronic pain history and acute pain reporting particularly in LOPD and SMA3 suggests that pain represents an independent clinical domain that is not fully captured by single-point assessments. Clinical management should focus on individualized pain assessment, as standard functional tests and snapshot pain assessments do not adequately reflect the patient's pain burden.

PMID:
42640334
Bibliographic data and abstract were imported from PubMed on 26 Aug 2026.

Read full publication at:
Please sign in to see all details.

Stats

1-terrible, 9-excellent. How would you rate this publication? Sign in in to submit your rating.

Post a comment

You need to be signed in to post comments. You can sign in here.

Comments

There are no comments yet.