Literature DB >> 25085517

Selected items from the Charcot-Marie-Tooth (CMT) Neuropathy Score and secondary clinical outcome measures serve as sensitive clinical markers of disease severity in CMT1A patients.

Manoj Mannil1, Alessandra Solari2, Andreas Leha3, Ana L Pelayo-Negro4, José Berciano4, Beate Schlotter-Weigel5, Maggie C Walter5, Bernd Rautenstrauss6, Tuuli J Schnizer1, Angelo Schenone7, Pavel Seeman8, Chandini Kadian9, Olivia Schreiber5, Natalia G Angarita5, Gian Maria Fabrizi10, Franco Gemignani11, Luca Padua12, Lucio Santoro13, Aldo Quattrone14, Giuseppe Vita15, Daniela Calabrese16, Peter Young17, Matilde Laurà18, Jana Haberlová8, Radim Mazanec8, Walter Paulus19, Tim Beissbarth3, Michael E Shy20, Mary M Reilly18, Davide Pareyson21, Michael W Sereda22.   

Abstract

This study evaluates primary and secondary clinical outcome measures in Charcot-Marie-Tooth disease type 1A (CMT1A) with regard to their contribution towards discrimination of disease severity. The nine components of the composite Charcot-Marie-Tooth disease Neuropathy Score and six additional secondary clinical outcome measures were assessed in 479 adult patients with genetically proven CMT1A and 126 healthy controls. Using hierarchical clustering, we identified four significant clusters of patients according to clinical severity. We then tested the impact of each of the CMTNS components and of the secondary clinical parameters with regard to their power to differentiate these four clusters. The CMTNS components ulnar sensory nerve action potential (SNAP), pin sensibility, vibration and strength of arms did not increase the discriminant value of the remaining five CMTNS components (Ulnar compound motor action potential [CMAP], leg motor symptoms, arm motor symptoms, leg strength and sensory symptoms). However, three of the six additional clinical outcome measures - the 10m-timed walking test (T10MW), 9 hole-peg test (9HPT), and foot dorsal flexion dynamometry - further improved discrimination between severely and mildly affected patients. From these findings, we identified three different composite measures as score hypotheses and compared their discriminant power with that of the CMTNS. A composite of eight components CMAP, Motor symptoms legs, Motor symptoms arms, Strength of Legs, Sensory symptoms), displayed the strongest power to discriminate between the clusters. As a conclusion, five items from the CMTNS and three secondary clinical outcome measures improve the clinical assessment of patients with CMT1A significantly and are beneficial for upcoming clinical and therapeutic trials.
Copyright © 2014 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CMT1A; CMTNS; Charcot-Marie-Tooth; HMSN; Score generation; Secondary clinical outcome measures

Mesh:

Substances:

Year:  2014        PMID: 25085517     DOI: 10.1016/j.nmd.2014.06.431

Source DB:  PubMed          Journal:  Neuromuscul Disord        ISSN: 0960-8966            Impact factor:   4.296


  10 in total

1.  Binocular low-contrast letter acuity and the symbol digit modalities test improve the ability of the Multiple Sclerosis Functional Composite to predict disease in pediatric multiple sclerosis.

Authors:  Amy T Waldman; Salim Chahin; Amy M Lavery; Geraldine Liu; Brenda L Banwell; Grant T Liu; Laura J Balcer
Journal:  Mult Scler Relat Disord       Date:  2016-08-26       Impact factor: 4.339

2.  Candidate imaging biomarkers for PMP22-related inherited neuropathies.

Authors:  Alison R Roth; Jun Li; Richard D Dortch
Journal:  Ann Clin Transl Neurol       Date:  2022-06-03       Impact factor: 5.430

Review 3.  A brief review of recent Charcot-Marie-Tooth research and priorities.

Authors:  Sean Ekins; Nadia K Litterman; Renée J G Arnold; Robert W Burgess; Joel S Freundlich; Steven J Gray; Joseph J Higgins; Brett Langley; Dianna E Willis; Lucia Notterpek; David Pleasure; Michael W Sereda; Allison Moore
Journal:  F1000Res       Date:  2015-02-26

4.  A meta-analysis of randomized double-blind clinical trials in CMT1A to assess the change from baseline in CMTNS and ONLS scales after one year of treatment.

Authors:  Jonas Mandel; Viviane Bertrand; Philippe Lehert; Shahram Attarian; Laurent Magy; Joëlle Micallef; Ilya Chumakov; Catherine Scart-Grès; Mickael Guedj; Daniel Cohen
Journal:  Orphanet J Rare Dis       Date:  2015-06-13       Impact factor: 4.123

Review 5.  Management of Charcot-Marie-Tooth disease: improving long-term care with a multidisciplinary approach.

Authors:  Donald McCorquodale; Evan M Pucillo; Nicholas E Johnson
Journal:  J Multidiscip Healthc       Date:  2016-01-19

6.  A Rasch Analysis of the Charcot-Marie-Tooth Neuropathy Score (CMTNS) in a Cohort of Charcot-Marie-Tooth Type 1A Patients.

Authors:  Wenjia Wang; Mickaël Guedj; Viviane Bertrand; Julie Foucquier; Elisabeth Jouve; Daniel Commenges; Cécile Proust-Lima; Niall P Murphy; Olivier Blin; Laurent Magy; Daniel Cohen; Shahram Attarian
Journal:  PLoS One       Date:  2017-01-17       Impact factor: 3.240

7.  Clinical and metabolic consequences of L-serine supplementation in hereditary sensory and autonomic neuropathy type 1C.

Authors:  Mari Auranen; Jussi Toppila; Saranya Suriyanarayanan; Museer A Lone; Anders Paetau; Henna Tyynismaa; Thorsten Hornemann; Emil Ylikallio
Journal:  Cold Spring Harb Mol Case Stud       Date:  2017-11-21

8.  Case series: Childhood Charcot-Marie-Tooth: Predominance of axonal subtype.

Authors:  Apirada Thongsing; Theeraphong Pho-Iam; Chanin Limwongse; Surachai Likasitwattanakul; Oranee Sanmaneechai
Journal:  eNeurologicalSci       Date:  2019-07-25

9.  AAV2/9-mediated silencing of PMP22 prevents the development of pathological features in a rat model of Charcot-Marie-Tooth disease 1 A.

Authors:  Benoit Gautier; Helene Hajjar; Sylvia Soares; Jade Berthelot; Marie Deck; Scarlette Abbou; Graham Campbell; Maria Ceprian; Sergio Gonzalez; Claire-Maëlle Fovet; Vlad Schütza; Antoine Jouvenel; Cyril Rivat; Michel Zerah; Virginie François; Caroline Le Guiner; Patrick Aubourg; Robert Fledrich; Nicolas Tricaud
Journal:  Nat Commun       Date:  2021-04-21       Impact factor: 14.919

Review 10.  Ascorbic acid for the treatment of Charcot-Marie-Tooth disease.

Authors:  Burkhard Gess; Jonathan Baets; Peter De Jonghe; Mary M Reilly; Davide Pareyson; Peter Young
Journal:  Cochrane Database Syst Rev       Date:  2015-12-11
  10 in total

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