Literature DB >> 33415332

Natural history of Charcot-Marie-Tooth disease type 2A: a large international multicentre study.

Menelaos Pipis1, Shawna M E Feely2, James M Polke1, Mariola Skorupinska1, Laura Perez2, Rosemary R Shy2, Matilde Laura1, Jasper M Morrow1, Isabella Moroni3, Chiara Pisciotta4, Franco Taroni5, Dragan Vujovic6, Thomas E Lloyd7, Gyula Acsadi8, Sabrina W Yum9, Richard A Lewis10, Richard S Finkel11, David N Herrmann12, John W Day13, Jun Li14, Mario Saporta15, Reza Sadjadi16, David Walk17, Joshua Burns18, Francesco Muntoni19, Sindhu Ramchandren20, Rita Horvath21, Nicholas E Johnson22, Stephan Züchner23, Davide Pareyson4, Steven S Scherer6, Alexander M Rossor1, Michael E Shy2, Mary M Reilly1.   

Abstract

Mitofusin-2 (MFN2) is one of two ubiquitously expressed homologous proteins in eukaryote cells, playing a critical role in mitochondrial fusion. Mutations in MFN2 (most commonly autosomal dominant) cause Charcot-Marie-Tooth disease type 2A (CMT2A), the commonest axonal form of CMT, with significant allelic heterogeneity. Previous, moderately-sized, cross sectional genotype-phenotype studies of CMT2A have described the phenotypic spectrum of the disease, but longitudinal natural history studies are lacking. In this large multicentre prospective cohort study of 196 patients with dominant and autosomal recessive CMT2A, we present an in-depth genotype-phenotype study of the baseline characteristics of patients with CMT2A and longitudinal data (1-2 years) to describe the natural history. A childhood onset of autosomal dominant CMT2A is the most predictive marker of significant disease severity and is independent of the disease duration. When compared to adult onset autosomal dominant CMT2A, it is associated with significantly higher rates of use of ankle-foot orthoses, full-time use of wheelchair, dexterity difficulties and also has significantly higher CMT Examination Score (CMTESv2) and CMT Neuropathy Score (CMTNSv2) at initial assessment. Analysis of longitudinal data using the CMTESv2 and its Rasch-weighted counterpart, CMTESv2-R, show that over 1 year, the CMTESv2 increases significantly in autosomal dominant CMT2A (mean change 0.84 ± 2.42; two-tailed paired t-test P = 0.039). Furthermore, over 2 years both the CMTESv2 (mean change 0.97 ± 1.77; two-tailed paired t-test P = 0.003) and the CMTESv2-R (mean change 1.21 ± 2.52; two-tailed paired t-test P = 0.009) increase significantly with respective standardized response means of 0.55 and 0.48. In the paediatric CMT2A population (autosomal dominant and autosomal recessive CMT2A grouped together), the CMT Pediatric Scale increases significantly both over 1 year (mean change 2.24 ± 3.09; two-tailed paired t-test P = 0.009) and over 2 years (mean change 4.00 ± 3.79; two-tailed paired t-test P = 0.031) with respective standardized response means of 0.72 and 1.06. This cross-sectional and longitudinal study of the largest CMT2A cohort reported to date provides guidance for variant interpretation, informs prognosis and also provides natural history data that will guide clinical trial design.
© The Author(s) (2021). Published by Oxford University Press on behalf of the Guarantors of Brain.

Entities:  

Keywords:  Charcot-Marie-Tooth Examination Score v2.0; Charcot-Marie-Tooth disease type 2A; genotype-phenotype correlations; mitofusin-2; standardized response mean

Mesh:

Substances:

Year:  2020        PMID: 33415332      PMCID: PMC7805791          DOI: 10.1093/brain/awaa323

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  69 in total

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