Literature DB >> 33723284

Low dystrophin variability between muscles and stable expression over time in Becker muscular dystrophy using capillary Western immunoassay.

Z Koeks1, A A Janson2, C Beekman2, M Signorelli3, H A van Duyvenvoorde4,5, J C van den Bergen1, M T Hooijmans6, I Alleman7, I M Hegeman1, J J G M Verschuuren1,5, J C V Deutekom2, P Spitali8,5, N A Datson2, E H Niks9,10.   

Abstract

Becker muscular dystrophy (BMD) is the milder allelic variant of Duchenne muscular dystrophy, with higher dystrophin levels. To anticipate on results of interventions targeting dystrophin expression it is important to know the natural variation of dystrophin expression between different muscles and over time. Dystrophin was quantified using capillary Western immunoassay (Wes) in the anterior tibial (TA) muscle of 37 BMD patients. Variability was studied using two samples from the same TA biopsy site in nine patients, assessing nine longitudinal TA biopsies, and eight simultaneously obtained vastus lateralis (VL) muscle biopsies. Measurements were performed in duplicate with two primary antibodies. Baseline dystrophin levels were correlated to longitudinal muscle strength and functional outcomes. Results showed low technical variability and high precision for both antibodies. Dystrophin TA levels ranged from 4.8 to 97.7%, remained stable over a 3-5 year period, and did not correlate with changes in longitudinal muscle function. Dystrophin levels were comparable between TA and VL muscles. Intra-muscle biopsy variability was low (5.2% and 11.4% of the total variability of the two antibodies). These observations are relevant for the design of clinical trials targeting dystrophin production, and may urge the need for other biomarkers or surrogate endpoints.

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Year:  2021        PMID: 33723284      PMCID: PMC7971009          DOI: 10.1038/s41598-021-84863-w

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  27 in total

Review 1.  Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and neuromuscular, rehabilitation, endocrine, and gastrointestinal and nutritional management.

Authors:  David J Birnkrant; Katharine Bushby; Carla M Bann; Susan D Apkon; Angela Blackwell; David Brumbaugh; Laura E Case; Paula R Clemens; Stasia Hadjiyannakis; Shree Pandya; Natalie Street; Jean Tomezsko; Kathryn R Wagner; Leanne M Ward; David R Weber
Journal:  Lancet Neurol       Date:  2018-02-03       Impact factor: 44.182

2.  Revertant fibres and dystrophin traces in Duchenne muscular dystrophy: implication for clinical trials.

Authors:  Virginia Arechavala-Gomeza; Maria Kinali; Lucy Feng; Michela Guglieri; Geraldine Edge; Marion Main; David Hunt; Jan Lehovsky; Volker Straub; Kate Bushby; Caroline A Sewry; Jennifer E Morgan; Francesco Muntoni
Journal:  Neuromuscul Disord       Date:  2010-04-14       Impact factor: 4.296

3.  Muscle biopsies in clinical trials for Duchenne muscular dystrophy - Patients' and caregivers' perspective.

Authors:  Ingrid E C Verhaart; Alex Johnson; Sejal Thakrar; Elizabeth Vroom; Fernanda De Angelis; Francesco Muntoni; Annemieke M Aartsma-Rus; Erik H Niks
Journal:  Neuromuscul Disord       Date:  2019-06-12       Impact factor: 4.296

4.  Dystrophin as a diagnostic marker in Duchenne and Becker muscular dystrophy. Correlation of immunofluorescence and western blot.

Authors:  T Voit; P Stuettgen; M Cremer; H H Goebel
Journal:  Neuropediatrics       Date:  1991-08       Impact factor: 1.947

Review 5.  Muscular dystrophy: new challenges and review of the current clinical trials.

Authors:  Eugenio Mercuri; Francesco Muntoni
Journal:  Curr Opin Pediatr       Date:  2013-12       Impact factor: 2.856

6.  An explanation for the phenotypic differences between patients bearing partial deletions of the DMD locus.

Authors:  A P Monaco; C J Bertelson; S Liechti-Gallati; H Moser; L M Kunkel
Journal:  Genomics       Date:  1988-01       Impact factor: 5.736

7.  Exploring the molecular basis for variability among patients with Becker muscular dystrophy: dystrophin gene and protein studies.

Authors:  A H Beggs; E P Hoffman; J R Snyder; K Arahata; L Specht; F Shapiro; C Angelini; H Sugita; L M Kunkel
Journal:  Am J Hum Genet       Date:  1991-07       Impact factor: 11.025

Review 8.  Muscular dystrophies.

Authors:  Eugenio Mercuri; Francesco Muntoni
Journal:  Lancet       Date:  2013-03-09       Impact factor: 79.321

9.  Report of a TREAT-NMD/World Duchenne Organisation Meeting on Dystrophin Quantification Methodology.

Authors:  Annemieke Aartsma-Rus; Jennifer Morgan; Pallavi Lonkar; Hendrik Neubert; Jane Owens; Michael Binks; Marisol Montolio; Rahul Phadke; Nicole Datson; Judith Van Deutekom; Glenn E Morris; V Ashutosh Rao; Eric P Hoffman; Francesco Muntoni; Virginia Arechavala-Gomeza
Journal:  J Neuromuscul Dis       Date:  2019

10.  Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.

Authors:  G P Comi; A Prelle; N Bresolin; M Moggio; A Bardoni; A Gallanti; G Vita; A Toscano; M T Ferro; A Bordoni
Journal:  Brain       Date:  1994-02       Impact factor: 13.501

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  4 in total

1.  High-Throughput Digital Image Analysis Reveals Distinct Patterns of Dystrophin Expression in Dystrophinopathy Patients.

Authors:  Silvia Torelli; Domenic Scaglioni; Valentina Sardone; Matthew J Ellis; Joana Domingos; Adam Jones; Lucy Feng; Darren Chambers; Deborah M Eastwood; France Leturcq; Rabah Ben Yaou; Andoni Urtizberea; Pascal Sabouraud; Christine Barnerias; Tanya Stojkovic; Enzo Ricci; Maud Beuvin; Gisele Bonne; Caroline A Sewry; Tracey Willis; Richa Kulshrestha; Giorgio Tasca; Rahul Phadke; Jennifer E Morgan; Francesco Muntoni
Journal:  J Neuropathol Exp Neurol       Date:  2021-10-26       Impact factor: 3.685

2.  Automated immunofluorescence analysis for sensitive and precise dystrophin quantification in muscle biopsies.

Authors:  Tatyana A Vetter; Stefan Nicolau; Adrienne J Bradley; Emma C Frair; Kevin M Flanigan
Journal:  Neuropathol Appl Neurobiol       Date:  2021-12-28       Impact factor: 6.250

3.  Combining Protein Expression and Molecular Data Improves Mutation Characterization of Dystrophinopathies.

Authors:  Gisela Gaina; Rolf H A M Vossen; Emilia Manole; Doina Anca Plesca; Elena Ionica
Journal:  Front Neurol       Date:  2021-12-07       Impact factor: 4.003

Review 4.  Changes in Myonuclear Number During Postnatal Growth - Implications for AAV Gene Therapy for Muscular Dystrophy.

Authors:  Jennifer Morgan; Francesco Muntoni
Journal:  J Neuromuscul Dis       Date:  2021
  4 in total

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