Literature DB >> 29540582

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

Jean K Mah1, Jia Feng2, Marni B Jacobs2, Tina Duong2, Kate Carroll2, Katy de Valle2, Cara L Carty2, Lauren P Morgenroth2, Michela Guglieri2, Monique M Ryan2, Paula R Clemens2, Mathula Thangarajh2, Richard Webster2, Edward Smith2, Anne M Connolly2, Craig M McDonald2, Peter Karachunski2, Mar Tulinius2, Amy Harper2, Avital Cnaan2, Yi-Wen Chen2.   

Abstract

OBJECTIVES: To investigate motor function associations with age, sex, and D4Z4 repeats among participants with early-onset facioscapulohumeral muscular dystrophy (FSHD) type 1 as defined by weakness onset before 10 years of age.
METHODS: We collected standardized motor assessments, including manual muscle testing (MMT), quantitative muscle testing, functional motor evaluations, and clinical severity scores (CSSs), at 12 Cooperative International Neuromuscular Research Group centers. To measure associations, we used linear regression models adjusted for sex, evaluation age, age at onset of weakness, and D4Z4 repeats.
RESULTS: Among 52 participants (60% female, mean age 22.9 ± 14.7 years), weakness was most pronounced in the shoulder and abdominal musculature. Older enrollment age was associated with greater CSSs (p = 0.003). When adjusted for enrollment age, sex, and D4Z4 repeats, younger age at onset of facial weakness was associated with greater CSSs, slower velocities in timed function tests, and lower MMT scores (p < 0.05).
CONCLUSION: Significant clinical variability was observed in early-onset FSHD. Earlier age at onset of facial weakness was associated with greater disease severity. Longitudinal assessments are needed to determine the rate of disease progression in this population.
© 2018 American Academy of Neurology.

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Year:  2018        PMID: 29540582      PMCID: PMC5894929          DOI: 10.1212/WNL.0000000000005297

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  40 in total

1.  Asymptomatic carriers and gender differences in facioscapulohumeral muscular dystrophy (FSHD).

Authors:  M M O Tonini; M R Passos-Bueno; A Cerqueira; S R Matioli; R Pavanello; M Zatz
Journal:  Neuromuscul Disord       Date:  2004-01       Impact factor: 4.296

2.  A prospective, quantitative study of the natural history of facioscapulohumeral muscular dystrophy (FSHD): implications for therapeutic trials. The FSH-DY Group.

Authors: 
Journal:  Neurology       Date:  1997-01       Impact factor: 9.910

3.  Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2.

Authors:  Richard J L F Lemmers; Jelle J Goeman; Patrick J van der Vliet; Merlijn P van Nieuwenhuizen; Judit Balog; Marianne Vos-Versteeg; Pilar Camano; Maria Antonia Ramos Arroyo; Ivonne Jerico; Mark T Rogers; Daniel G Miller; Meena Upadhyaya; Jan J G M Verschuuren; Adolfo Lopez de Munain Arregui; Baziel G M van Engelen; George W Padberg; Sabrina Sacconi; Rabi Tawil; Stephen J Tapscott; Bert Bakker; Silvère M van der Maarel
Journal:  Hum Mol Genet       Date:  2014-09-25       Impact factor: 6.150

Review 4.  Facioscapulohumeral muscular dystrophy.

Authors:  Sabrina Sacconi; Leonardo Salviati; Claude Desnuelle
Journal:  Biochim Biophys Acta       Date:  2014-05-29

5.  Severe phenotype in infantile facioscapulohumeral muscular dystrophy.

Authors:  Lars Klinge; Michelle Eagle; Irene D Haggerty; Catherine E Roberts; Volker Straub; Kate M Bushby
Journal:  Neuromuscul Disord       Date:  2006-08-24       Impact factor: 4.296

6.  Upper vs lower extremity functional loss in neuromuscular disease.

Authors:  J P Lord; M M Portwood; W M Fowler; J S Lieberman; R Carson
Journal:  Arch Phys Med Rehabil       Date:  1987-01       Impact factor: 3.966

Review 7.  Development of the Performance of the Upper Limb module for Duchenne muscular dystrophy.

Authors:  Anna Mayhew; Elena S Mazzone; Michelle Eagle; Tina Duong; Maria Ash; Valerie Decostre; Marlene Vandenhauwe; Katrijn Klingels; Julaine Florence; Marion Main; Flaviana Bianco; Erik Henrikson; Laurent Servais; Giles Campion; Elizabeth Vroom; Valeria Ricotti; Natalie Goemans; Craig McDonald; Eugenio Mercuri
Journal:  Dev Med Child Neurol       Date:  2013-08-01       Impact factor: 5.449

8.  Muscle MRI findings in facioscapulohumeral muscular dystrophy.

Authors:  Simonetta Gerevini; Marina Scarlato; Lorenzo Maggi; Mariangela Cava; Giandomenico Caliendo; Barbara Pasanisi; Andrea Falini; Stefano Carlo Previtali; Lucia Morandi
Journal:  Eur Radiol       Date:  2015-06-27       Impact factor: 5.315

9.  Individual epigenetic status of the pathogenic D4Z4 macrosatellite correlates with disease in facioscapulohumeral muscular dystrophy.

Authors:  Takako I Jones; Oliver D King; Charis L Himeda; Sachiko Homma; Jennifer C J Chen; Mary Lou Beermann; Chi Yan; Charles P Emerson; Jeffrey B Miller; Kathryn R Wagner; Peter L Jones
Journal:  Clin Epigenetics       Date:  2015-03-29       Impact factor: 6.551

10.  Upper girdle imaging in facioscapulohumeral muscular dystrophy.

Authors:  Giorgio Tasca; Mauro Monforte; Elisabetta Iannaccone; Francesco Laschena; Pierfrancesco Ottaviani; Emanuele Leoncini; Stefania Boccia; Giuliana Galluzzi; Marco Pelliccioni; Marcella Masciullo; Roberto Frusciante; Eugenio Mercuri; Enzo Ricci
Journal:  PLoS One       Date:  2014-06-16       Impact factor: 3.240

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  7 in total

Review 1.  Facioscapulohumeral Muscular Dystrophy: Update on Pathogenesis and Future Treatments.

Authors:  Johanna Hamel; Rabi Tawil
Journal:  Neurotherapeutics       Date:  2018-10       Impact factor: 7.620

2.  Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy.

Authors:  Lucia Ruggiero; Fabiano Mele; Fiore Manganelli; Dario Bruzzese; Giulia Ricci; Liliana Vercelli; Monica Govi; Antonio Vallarola; Silvia Tripodi; Luisa Villa; Antonio Di Muzio; Marina Scarlato; Elisabetta Bucci; Giovanni Antonini; Lorenzo Maggi; Carmelo Rodolico; Giuliano Tomelleri; Massimiliano Filosto; Stefano Previtali; Corrado Angelini; Angela Berardinelli; Elena Pegoraro; Maurizio Moggio; Tiziana Mongini; Gabriele Siciliano; Lucio Santoro; Rossella Tupler
Journal:  JAMA Netw Open       Date:  2020-05-01

3.  Multi-Omics Identifies Circulating miRNA and Protein Biomarkers for Facioscapulohumeral Dystrophy.

Authors:  Christopher R Heier; Aiping Zhang; Nhu Y Nguyen; Christopher B Tully; Aswini Panigrahi; Heather Gordish-Dressman; Sachchida Nand Pandey; Michela Guglieri; Monique M Ryan; Paula R Clemens; Mathula Thangarajh; Richard Webster; Edward C Smith; Anne M Connolly; Craig M McDonald; Peter Karachunski; Mar Tulinius; Amy Harper; Jean K Mah; Alyson A Fiorillo; Yi-Wen Chen
Journal:  J Pers Med       Date:  2020-11-19

4.  Prevalence and disease progression of genetically-confirmed facioscapulohumeral muscular dystrophy type 1 (FSHD1) in China between 2001 and 2020: a nationwide population-based study.

Authors:  Zhiqiang Wang; Liangliang Qiu; Minting Lin; Long Chen; Fuze Zheng; Lin Lin; Feng Lin; Zhixian Ye; Xiaodan Lin; Junjie He; Lili Wang; Xin Lin; Qifang He; Wanjin Chen; Yi Lin; Ying Fu; Ning Wang
Journal:  Lancet Reg Health West Pac       Date:  2021-11-22

5.  Natural History of Facioscapulohumeral Dystrophy in Children: A 2-Year Follow-up.

Authors:  Jildou N Dijkstra; Rianne J M Goselink; Nens van Alfen; Imelda J M de Groot; Maaike Pelsma; Nienke van der Stoep; Thomas Theelen; Baziel G M van Engelen; Nicol C Voermans; Corrie E Erasmus
Journal:  Neurology       Date:  2021-10-21       Impact factor: 9.910

Review 6.  Early-Onset Infantile Facioscapulohumeral Muscular Dystrophy: A Timely Review.

Authors:  Tai-Heng Chen; Yan-Zhang Wu; Yung-Hao Tseng
Journal:  Int J Mol Sci       Date:  2020-10-21       Impact factor: 5.923

7.  A 5-year clinical follow-up study from the Italian National Registry for FSHD.

Authors:  Liliana Vercelli; Fabiano Mele; Lucia Ruggiero; Francesco Sera; Silvia Tripodi; Giulia Ricci; Antonio Vallarola; Luisa Villa; Monica Govi; Louise Maranda; Antonio Di Muzio; Marina Scarlato; Elisabetta Bucci; Lorenzo Maggi; Carmelo Rodolico; Maurizio Moggio; Massimiliano Filosto; Giovanni Antonini; Stefano Previtali; Corrado Angelini; Angela Berardinelli; Elena Pegoraro; Gabriele Siciliano; Giuliano Tomelleri; Lucio Santoro; Tiziana Mongini; Rossella Tupler
Journal:  J Neurol       Date:  2020-08-19       Impact factor: 4.849

  7 in total

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