Literature DB >> 20544930

A standardized clinical evaluation of patients affected by facioscapulohumeral muscular dystrophy: The FSHD clinical score.

Costanza Lamperti1, Greta Fabbri, Liliana Vercelli, Roberto D'Amico, Roberto Frusciante, Emanuela Bonifazi, Chiara Fiorillo, Carlo Borsato, Michelangelo Cao, Maura Servida, Francesca Greco, Rita Di Leo, Leda Volpi, Claudia Manzoli, Paola Cudia, Ebe Pastorello, Leopoldo Ricciardi, Gabriele Siciliano, Giuliana Galluzzi, Carmelo Rodolico, Lucio Santoro, Giuliano Tomelleri, Corrado Angelini, Enzo Ricci, Laura Palmucci, Maurizio Moggio, Rossella Tupler.   

Abstract

To define numerically the clinical severity of facioscapulohumeral muscular dystrophy (FSHD), we developed a protocol that quantifies muscle weakness by combining the functional evaluation of six muscle groups affected in this disease. To validate reproducibility of the protocol, 69 patients were recruited. Each patient was evaluated by at least five neurologists, and an FSHD severity score was given by each examiner. The degree of agreement among clinicians' evaluations was measured by kappa-statistics. Nineteen subjects received a score between 0 and 1, 9 had a score between 2 and 4, 20 received a score between 5 and 10, and 8 had a score between 11 and 15. Of the 13 subjects with D4Z4 alleles within the normal range (ranging from 10 to 150 repeats), 12 obtained a score of 0 and only 1 had a score of 1. Kappa-statistics showed a very high concordance for all muscle groups. We developed a simple, reliable, easily used tool to define the clinical expression of FSHD. Longitudinal studies will assess its sensitivity and utility in measuring changes for widespread use.

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Year:  2010        PMID: 20544930     DOI: 10.1002/mus.21671

Source DB:  PubMed          Journal:  Muscle Nerve        ISSN: 0148-639X            Impact factor:   3.217


  50 in total

1.  Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy.

Authors:  Rianne J M Goselink; Karlien Mul; Caroline R van Kernebeek; Richard J L F Lemmers; Silvère M van der Maarel; Tim H A Schreuder; Corrie E Erasmus; George W Padberg; Jeffrey M Statland; Nicol C Voermans; Baziel G M van Engelen
Journal:  Neurology       Date:  2018-12-19       Impact factor: 9.910

2.  A new double-trouble phenotype: fascioscapulohumeral muscular dystrophy ameliorates hereditary spastic paraparesis due to spastin mutation.

Authors:  Marina Scarlato; Arturo Nuara; Simonetta Gerevini; Sara Benedetti; Paolo Rossi; Maurizio Ferrari; Stefano Carlo Previtali
Journal:  J Neurol       Date:  2014-12-16       Impact factor: 4.849

3.  Reachable workspace reflects dynamometer-measured upper extremity strength in facioscapulohumeral muscular dystrophy.

Authors:  Jay J Han; Evan De Bie; Alina Nicorici; Richard T Abresch; Ruzena Bajcsy; Gregorij Kurillo
Journal:  Muscle Nerve       Date:  2015-06-19       Impact factor: 3.217

4.  MRI as outcome measure in facioscapulohumeral muscular dystrophy: 1-year follow-up of 45 patients.

Authors:  Grete Andersen; Julia R Dahlqvist; Christoffer R Vissing; Karen Heje; Carsten Thomsen; John Vissing
Journal:  J Neurol       Date:  2016-12-20       Impact factor: 4.849

5.  Adding quantitative muscle MRI to the FSHD clinical trial toolbox.

Authors:  Karlien Mul; Sanne C C Vincenten; Nicol C Voermans; Richard J L F Lemmers; Patrick J van der Vliet; Silvère M van der Maarel; George W Padberg; Corinne G C Horlings; Baziel G M van Engelen
Journal:  Neurology       Date:  2017-10-13       Impact factor: 9.910

6.  An instrumented timed up and go in facioscapulohumeral muscular dystrophy.

Authors:  Jessie Huisinga; Adam Bruetsch; Ayla Mccalley; Melissa Currence; Laura Herbelin; Omar Jawdat; Mamatha Pasnoor; Mazen Dimachkie; Richard Barohn; Jeffrey Statland
Journal:  Muscle Nerve       Date:  2017-10-06       Impact factor: 3.217

7.  Longitudinal study of upper extremity reachable workspace in fascioscapulohumeral muscular dystrophy.

Authors:  Maya N Hatch; Kiin Kim; Gregorij Kurillo; Alina Nicorici; Craig M McDonald; Jay J Han
Journal:  Neuromuscul Disord       Date:  2019-05-23       Impact factor: 4.296

8.  High-intensity interval training in facioscapulohumeral muscular dystrophy type 1: a randomized clinical trial.

Authors:  Grete Andersen; Karen Heje; Astrid Emile Buch; John Vissing
Journal:  J Neurol       Date:  2017-05-03       Impact factor: 4.849

9.  A multinational study on motor function in early-onset FSHD.

Authors:  Jean K Mah; Jia Feng; Marni B Jacobs; Tina Duong; Kate Carroll; Katy de Valle; Cara L Carty; Lauren P Morgenroth; Michela Guglieri; Monique M Ryan; Paula R Clemens; Mathula Thangarajh; Richard Webster; Edward Smith; Anne M Connolly; Craig M McDonald; Peter Karachunski; Mar Tulinius; Amy Harper; Avital Cnaan; Yi-Wen Chen
Journal:  Neurology       Date:  2018-03-14       Impact factor: 9.910

10.  Facioscapulohumeral muscular dystrophy functional composite outcome measure.

Authors:  Katy Eichinger; Chad Heatwole; Stanley Iyadurai; Wendy King; Lindsay Baker; Susanne Heininger; Amy Bartlett; Nuran Dilek; William B Martens; Michael Mcdermott; John T Kissel; Rabi Tawil; Jeffrey M Statland
Journal:  Muscle Nerve       Date:  2018-01-30       Impact factor: 3.217

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