دورية أكاديمية

Ambulatory Duchenne muscular dystrophy children: cross-sectional correlation between function, quantitative muscle ultrasound and MRI.

التفاصيل البيبلوغرافية
العنوان: Ambulatory Duchenne muscular dystrophy children: cross-sectional correlation between function, quantitative muscle ultrasound and MRI.
المؤلفون: Abdulhady H; Department of Physical Medicine, Rheumatology and Rehabilitation, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Sakr HM; Department of Diagnostic and Interventional Radiology and Molecular Imaging, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Elsayed NS; Department of Medical Genetics, Faculty of Medicine, Ain Shams University, Cairo, Egypt., El-Sobky TA; Division of Pediatric Orthopedics, Department of Orthopedic Surgery, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Fahmy N; Neuromuscular Unit, Department of Neuropsychiatry, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Saadawy AM; Department of Diagnostic and Interventional Radiology and Molecular Imaging, Faculty of Medicine, Ain Shams University, Cairo, Egypt., Elsedfy H; Department of Medical Genetics, Faculty of Medicine, Ain Shams University, Cairo, Egypt.
المصدر: Acta myologica : myopathies and cardiomyopathies : official journal of the Mediterranean Society of Myology [Acta Myol] 2022 Mar 31; Vol. 41 (1), pp. 1-14. Date of Electronic Publication: 2022 Mar 31 (Print Publication: 2022).
نوع المنشور: Journal Article
اللغة: English
بيانات الدورية: Publisher: Gaetano Conte Academy Country of Publication: Italy NLM ID: 9811169 Publication Model: eCollection Cited Medium: Internet ISSN: 2532-1900 (Electronic) Linking ISSN: 11282460 NLM ISO Abbreviation: Acta Myol Subsets: MEDLINE
أسماء مطبوعة: Original Publication: Napoli : Gaetano Conte Academy
مواضيع طبية MeSH: Muscular Dystrophy, Duchenne*/diagnostic imaging, Adolescent ; Child ; Child, Preschool ; Cross-Sectional Studies ; Humans ; Magnetic Resonance Imaging/methods ; Male ; Muscle, Skeletal/diagnostic imaging ; Retrospective Studies
مستخلص: Duchenne muscular dystrophy (DMD) is a progressive genetic muscle disease. Quantitative muscle ultrasound (US), muscle MRI, and functional tools are important to delineate characteristics of muscle involvement. We aimed to establish correlations between clinical/functional and above-named imaging tools respecting their diagnostic and prognostic role in DMD children. A cross-sectional retrospective study of 27 steroid-naive, ambulant male children/adolescents with genetically-confirmed DMD (mean age, 8.8 ± 3.3 years). Functional performance was assessed using motor function measure (MFM) which assess standing/transfer (D1), proximal (D2) and distal (D3) motor function, and six-minute walk test (6MWT). Imaging evaluation included quantitative muscle MRI which measured muscle fat content in a specific location of right rectus femoris by mDixon sequence. Quantitative muscle US measured right rectus femoris muscle brightness in standardized US image as an indicator of muscle fat content. We found a highly significant positive correlation between the mean MFM total score and 6MWT (R = 0.537, p = 0.007), and a highly significant negative correlation between fat content by muscle US and MFM total score (R = -0.603, p = 0.006) and its D1 subscore (R =-0.712, p = 0.001), and a significant negative correlation between fat content by US and 6MWT (R = -0.529, p = 0.02), and a significant positive correlation between muscle fat content by mDixon MRI and patient's age (R = 0.617, p = 0.01). Quantitative muscle US correlates significantly with clinical/functional assessment tools as MFM and 6MWT, and augments their role in disease-tracking of DMD. Quantitative muscle US has the potential to act as a substitute to functional assessment tools.
Competing Interests: Conflict of interest statement None of the Authors has any conflict of interest to disclose. No benefits in any form were received or will be received from a commercial party related directly or indirectly to the subject of this article.
(©2022 Gaetano Conte Academy - Mediterranean Society of Myology.)
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فهرسة مساهمة: Keywords: 6-minute walk test; dystrophinopathies; motor function measure; muscle ultrasonography; quantitative magnetic resonance imaging
تواريخ الأحداث: Date Created: 20220425 Date Completed: 20220426 Latest Revision: 20220716
رمز التحديث: 20240628
مُعرف محوري في PubMed: PMC9004336
DOI: 10.36185/2532-1900-063
PMID: 35465338
قاعدة البيانات: MEDLINE
الوصف
تدمد:2532-1900
DOI:10.36185/2532-1900-063