Spectrum of Clinical Features in X-Linked Myotubular Myopathy Carriers: An International Questionnaire Study. (3rd August 2021)
- Record Type:
- Journal Article
- Title:
- Spectrum of Clinical Features in X-Linked Myotubular Myopathy Carriers: An International Questionnaire Study. (3rd August 2021)
- Main Title:
- Spectrum of Clinical Features in X-Linked Myotubular Myopathy Carriers
- Authors:
- Reumers, Stacha F.I.
Braun, Frederik
Spillane, Jennifer E.
Böhm, Johann
Pennings, Maartje
Schouten, Meyke
van der Kooi, Anneke J.
Foley, A. Reghan
Bönnemann, Carsten G.
Kamsteeg, Erik-jan
Erasmus, Corrie E.
Schara-Schmidt, Ulrike
Jungbluth, Heinz
Voermans, Nicol C. - Abstract:
- Abstract : Objective: To characterize the spectrum of clinical features in a cohort of X-linked myotubular myopathy (XL-MTM) carriers, including prevalence, genetic features, clinical symptoms, and signs, as well as associated disease burden. Methods: We performed a cross-sectional online questionnaire study among XL-MTM carriers. Participants were recruited from patient associations, medical centers, and registries in the United Kingdom, Germany, and the Netherlands. We used a custom-made questionnaire, the Checklist Individual Strength (CIS), the Frenchay Activities Index (FAI), the Short Form 12 (SF-12) health survey, and the McGill Pain Questionnaire. Carriers were classified as manifesting or nonmanifesting on the basis of self-reported ambulation and muscle weakness. Results: The prevalence of manifesting carriers in this study population (n = 76) was 51%, subdivided into mild (independent ambulation, 39%), moderate (assisted ambulation, 9%), and severe (wheelchair dependent, 3%) phenotypes. In addition to muscle weakness, manifesting carriers frequently reported fatigue (70%) and exercise intolerance (49%). Manifesting carriers scored higher on the overall CIS ( p = 0.001), the fatigue subscale ( p < 0.001), and least severe pain subscale ( p = 0.005) than nonmanifesting carriers. They scored lower on the FAI ( p = 0.005) and the physical component of the SF-12 health survey ( p < 0.001). Conclusions: The prevalence of manifesting XL-MTM carriers may be higher thanAbstract : Objective: To characterize the spectrum of clinical features in a cohort of X-linked myotubular myopathy (XL-MTM) carriers, including prevalence, genetic features, clinical symptoms, and signs, as well as associated disease burden. Methods: We performed a cross-sectional online questionnaire study among XL-MTM carriers. Participants were recruited from patient associations, medical centers, and registries in the United Kingdom, Germany, and the Netherlands. We used a custom-made questionnaire, the Checklist Individual Strength (CIS), the Frenchay Activities Index (FAI), the Short Form 12 (SF-12) health survey, and the McGill Pain Questionnaire. Carriers were classified as manifesting or nonmanifesting on the basis of self-reported ambulation and muscle weakness. Results: The prevalence of manifesting carriers in this study population (n = 76) was 51%, subdivided into mild (independent ambulation, 39%), moderate (assisted ambulation, 9%), and severe (wheelchair dependent, 3%) phenotypes. In addition to muscle weakness, manifesting carriers frequently reported fatigue (70%) and exercise intolerance (49%). Manifesting carriers scored higher on the overall CIS ( p = 0.001), the fatigue subscale ( p < 0.001), and least severe pain subscale ( p = 0.005) than nonmanifesting carriers. They scored lower on the FAI ( p = 0.005) and the physical component of the SF-12 health survey ( p < 0.001). Conclusions: The prevalence of manifesting XL-MTM carriers may be higher than currently assumed, most having a mild phenotype and a wide variety of symptoms. Manifesting carriers are particularly affected by fatigue, limitations of daily activities, pain, and reduced quality of life. Our findings should increase awareness and provide useful information for health care providers and future clinical trials. … (more)
- Is Part Of:
- Neurology. Volume 97:Number 5(2021)
- Journal:
- Neurology
- Issue:
- Volume 97:Number 5(2021)
- Issue Display:
- Volume 97, Issue 5 (2021)
- Year:
- 2021
- Volume:
- 97
- Issue:
- 5
- Issue Sort Value:
- 2021-0097-0005-0000
- Page Start:
- Page End:
- Publication Date:
- 2021-08-03
- Subjects:
- Neurology -- Periodicals
Neurology -- Periodicals
Neurologie -- Périodiques
616.8 - Journal URLs:
- http://www.mdconsult.com/public/search?search_type=journal&j_sort=pub_date&j_issn=0028-3878 ↗
http://www.mdconsult.com/about/journallist/192093418-5/about0nz0.html ↗
http://www.neurology.org ↗
http://journals.lww.com ↗ - DOI:
- 10.1212/WNL.0000000000012236 ↗
- Languages:
- English
- ISSNs:
- 0028-3878
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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