Literature DB >> 34937785

Phenotypic Spectrum of Dystrophinopathy Due to Duchenne Muscular Dystrophy Exon 2 Duplications.

Alberto A Zambon1, Megan A Waldrop1, Roxane Alles1, Robert B Weiss1, Sara Conroy1, Melissa Moore-Clingenpeel1, Stefano Previtali1, Kevin M Flanigan2.   

Abstract

BACKGROUND AND OBJECTIVES: To describe the phenotypic spectrum of dystrophinopathy in a large cohort of individuals with DMD exon 2 duplications (Dup2), who may be particularly amenable to therapies directed at restoring expression of either full-length dystrophin or nearly full-length dystrophin through utilization of the DMD exon 5 internal ribosome entry site (IRES).
METHODS: In this retrospective observational study, we analyzed data from large genotype-phenotype databases (the United Dystrophinopathy Project [UDP] and the Italian DMD network) and classified participants into Duchenne muscular dystrophy (DMD), intermediate muscular dystrophy (IMD), or Becker muscular dystrophy (BMD) phenotypes. Log-rank tests for time-to-event variables were used to compare age at loss of ambulation (LOA) in participants with Dup2 vs controls without Dup2 in the UDP database and for comparisons between steroid-treated vs steroid-naive participants with Dup2.
RESULTS: Among 66 participants with Dup2 (UDP = 40, Italy = 26), 61% were classified as DMD, 9% as IMD, and 30% as BMD. Median age at last observation was 15.4 years (interquartile range 8.79-26.0) and 75% had been on corticosteroids for at least 6 months. Age at LOA differed significantly between participants with Dup2 DMD and historical controls without Dup2 DMD (p < 0.001). Valid spirometry was limited but suggested a delay in the typical age-related decline in forced vital capacity and 24 of 55 participants with adequate cardiac data had cardiomyopathy. DISCUSSION: Some patients with Dup2 display a milder disease course than controls without Dup2 DMD, and prolonged ambulation with corticosteroids suggests the potential of IRES activation as a molecular mechanism. As Dup2-targeted therapies reach clinical applications, this information is critical to aid in the interpretation of the efficacy of new treatments.
© 2021 American Academy of Neurology.

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Year:  2021        PMID: 34937785      PMCID: PMC8865888          DOI: 10.1212/WNL.0000000000013246

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


  40 in total

1.  Contemporary cardiac issues in Duchenne muscular dystrophy. Working Group of the National Heart, Lung, and Blood Institute in collaboration with Parent Project Muscular Dystrophy.

Authors:  Elizabeth M McNally; Jonathan R Kaltman; D Woodrow Benson; Charles E Canter; Linda H Cripe; Dongsheng Duan; Jonathan D Finder; William J Groh; Eric P Hoffman; Daniel P Judge; Naomi Kertesz; Kathi Kinnett; Roxanne Kirsch; Joseph M Metzger; Gail D Pearson; Jill A Rafael-Fortney; Subha V Raman; Christopher F Spurney; Shari L Targum; Kathryn R Wagner; Larry W Markham
Journal:  Circulation       Date:  2015-05-05       Impact factor: 29.690

2.  Clinical and mutational characteristics of Duchenne muscular dystrophy patients based on a comprehensive database in South China.

Authors:  Dan-Ni Wang; Zhi-Qiang Wang; Lei Yan; Jin He; Min-Ting Lin; Wan-Jin Chen; Ning Wang
Journal:  Neuromuscul Disord       Date:  2017-02-21       Impact factor: 4.296

Review 3.  The role of IRES trans-acting factors in carcinogenesis.

Authors:  Mame Daro Faye; Martin Holcik
Journal:  Biochim Biophys Acta       Date:  2014-09-23

4.  Duplications in the DMD gene.

Authors:  S J White; A Aartsma-Rus; K M Flanigan; R B Weiss; A L J Kneppers; T Lalic; A A M Janson; H B Ginjaar; M H Breuning; J T den Dunnen
Journal:  Hum Mutat       Date:  2006-09       Impact factor: 4.878

5.  Importance of SPP1 genotype as a covariate in clinical trials in Duchenne muscular dystrophy.

Authors:  Luca Bello; Luisa Piva; Andrea Barp; Antonella Taglia; Esther Picillo; Gessica Vasco; Marika Pane; Stefano C Previtali; Yvan Torrente; Elisabetta Gazzerro; Maria Chiara Motta; Gaetano S Grieco; Sara Napolitano; Francesca Magri; Adele D'Amico; Guja Astrea; Sonia Messina; Maria Sframeli; Gian Luca Vita; Patrizia Boffi; Tiziana Mongini; Alessandra Ferlini; Francesca Gualandi; Gianni Soraru'; Mario Ermani; Giuseppe Vita; Roberta Battini; Enrico Bertini; Giacomo P Comi; Angela Berardinelli; Carlo Minetti; Claudio Bruno; Eugenio Mercuri; Luisa Politano; Corrado Angelini; Eric P Hoffman; Elena Pegoraro
Journal:  Neurology       Date:  2012-06-27       Impact factor: 9.910

6.  Concordant utrophin upregulation in phenotypically discordant DMD/BMD brothers.

Authors:  Mariz Vainzof; Leticia Feitosa; Marta Canovas; Danielle Ayub-Guerrieri; Rita de Cássia M Pavanello; Mayana Zatz
Journal:  Neuromuscul Disord       Date:  2016-01-25       Impact factor: 4.296

7.  Nonsense mutation-associated Becker muscular dystrophy: interplay between exon definition and splicing regulatory elements within the DMD gene.

Authors:  Kevin M Flanigan; Diane M Dunn; Andrew von Niederhausern; Payam Soltanzadeh; Michael T Howard; Jacinda B Sampson; Kathryn J Swoboda; Mark B Bromberg; Jerry R Mendell; Laura E Taylor; Christine B Anderson; Alan Pestronk; Julaine M Florence; Anne M Connolly; Katherine D Mathews; Brenda Wong; Richard S Finkel; Carsten G Bonnemann; John W Day; Craig McDonald; Robert B Weiss
Journal:  Hum Mutat       Date:  2011-03       Impact factor: 4.878

8.  Low-level dystrophin expression attenuating the dystrophinopathy phenotype.

Authors:  Megan A Waldrop; Felecia Gumienny; Saleh El Husayni; Diane E Frank; Robert B Weiss; Kevin M Flanigan
Journal:  Neuromuscul Disord       Date:  2017-11-23       Impact factor: 3.538

9.  Genetic analysis of 1051 Chinese families with Duchenne/Becker Muscular Dystrophy.

Authors:  Xiangdong Kong; Xingjian Zhong; Lina Liu; Siying Cui; Yuxia Yang; Lingrong Kong
Journal:  BMC Med Genet       Date:  2019-08-14       Impact factor: 2.103

10.  The Genetic Landscape of Dystrophin Mutations in Italy: A Nationwide Study.

Authors:  Marcella Neri; Rachele Rossi; Cecilia Trabanelli; Antonio Mauro; Rita Selvatici; Maria Sofia Falzarano; Noemi Spedicato; Alice Margutti; Paola Rimessi; Fernanda Fortunato; Marina Fabris; Francesca Gualandi; Giacomo Comi; Silvana Tedeschi; Manuela Seia; Chiara Fiorillo; Monica Traverso; Claudio Bruno; Emiliano Giardina; Maria Rosaria Piemontese; Giuseppe Merla; Milena Cau; Monica Marica; Carmela Scuderi; Eugenia Borgione; Alessandra Tessa; Guia Astrea; Filippo Maria Santorelli; Luciano Merlini; Marina Mora; Pia Bernasconi; Sara Gibertini; Valeria Sansone; Tiziana Mongini; Angela Berardinelli; Antonella Pini; Rocco Liguori; Massimiliano Filosto; Sonia Messina; Gianluca Vita; Antonio Toscano; Giuseppe Vita; Marika Pane; Serenella Servidei; Elena Pegoraro; Luca Bello; Lorena Travaglini; Enrico Bertini; Adele D'Amico; Manuela Ergoli; Luisa Politano; Annalaura Torella; Vincenzo Nigro; Eugenio Mercuri; Alessandra Ferlini
Journal:  Front Genet       Date:  2020-03-03       Impact factor: 4.599

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  2 in total

1.  The 2022 On-site Padua Days on Muscle and Mobility Medicine hosts the University of Florida Institute of Myology and the Wellstone Center, March 30 - April 3, 2022 at the University of Padua and Thermae of Euganean Hills, Padua, Italy: The collection of abstracts.

Authors:  H Lee Sweeney; Stefano Masiero; Ugo Carraro
Journal:  Eur J Transl Myol       Date:  2022-03-10

2.  Systemic delivery of an AAV9 exon-skipping vector significantly improves or prevents features of Duchenne muscular dystrophy in the Dup2 mouse.

Authors:  Nicolas Wein; Tatyana A Vetter; Adeline Vulin; Tabatha R Simmons; Emma C Frair; Adrienne J Bradley; Liubov V Gushchina; Camila F Almeida; Nianyuan Huang; Daniel Lesman; Dhanarajan Rajakumar; Robert B Weiss; Kevin M Flanigan
Journal:  Mol Ther Methods Clin Dev       Date:  2022-07-11       Impact factor: 5.849

  2 in total

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