Literature DB >> 25612243

Clinical phenotypes as predictors of the outcome of skipping around DMD exon 45.

Andrew R Findlay1, Nicolas Wein, Yuuki Kaminoh, Laura E Taylor, Diane M Dunn, Jerry R Mendell, Wendy M King, Alan Pestronk, Julaine M Florence, Katherine D Mathews, Richard S Finkel, Kathryn J Swoboda, Michael T Howard, John W Day, Craig McDonald, Aurélie Nicolas, Elisabeth Le Rumeur, Robert B Weiss, Kevin M Flanigan.   

Abstract

OBJECTIVE: Exon-skipping therapies aim to convert Duchenne muscular dystrophy (DMD) into less severe Becker muscular dystrophy (BMD) by altering pre-mRNA splicing to restore an open reading frame, allowing translation of an internally deleted and partially functional dystrophin protein. The most common single exon deletion-exon 45 (Δ45)-may theoretically be treated by skipping of either flanking exon (44 or 46). We sought to predict the impact of these by assessing the clinical severity in dystrophinopathy patients.
METHODS: Phenotypic data including clinical diagnosis, age at wheelchair use, age at loss of ambulation, and presence of cardiomyopathy were analyzed from 41 dystrophinopathy patients containing equivalent in-frame deletions.
RESULTS: As expected, deletions of either exons 45 to 47 (Δ45-47) or exons 45 to 48 (Δ45-48) result in BMD in 97% (36 of 37) of subjects. Unexpectedly, deletion of exons 45 to 46 (Δ45-46) is associated with the more severe DMD phenotype in 4 of 4 subjects despite an in-frame transcript. Notably, no patients with a deletion of exons 44 to 45 (Δ44-45) were found within the United Dystrophinopathy Project database, and this mutation has only been reported twice before, which suggests an ascertainment bias attributable to a very mild phenotype.
INTERPRETATION: The observation that Δ45-46 patients have typical DMD suggests that the conformation of the resultant protein may result in protein instability or altered binding of critical partners. We conclude that in DMD patients with Δ45, skipping of exon 44 and multiexon skipping of exons 46 and 47 (or exons 46-48) are better potential therapies than skipping of exon 46 alone.
© 2015 American Neurological Association.

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Year:  2015        PMID: 25612243      PMCID: PMC4376581          DOI: 10.1002/ana.24365

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  31 in total

1.  Systemic administration of PRO051 in Duchenne's muscular dystrophy.

Authors:  Nathalie M Goemans; Mar Tulinius; Johanna T van den Akker; Brigitte E Burm; Peter F Ekhart; Niki Heuvelmans; Tjadine Holling; Anneke A Janson; Gerard J Platenburg; Jessica A Sipkens; J M Ad Sitsen; Annemieke Aartsma-Rus; Gert-Jan B van Ommen; Gunnar Buyse; Niklas Darin; Jan J Verschuuren; Giles V Campion; Sjef J de Kimpe; Judith C van Deutekom
Journal:  N Engl J Med       Date:  2011-03-23       Impact factor: 91.245

2.  Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center.

Authors:  Yasuhiro Takeshima; Mariko Yagi; Yo Okizuka; Hiroyuki Awano; Zhujun Zhang; Yumiko Yamauchi; Hisahide Nishio; Masafumi Matsuo
Journal:  J Hum Genet       Date:  2010-05-20       Impact factor: 3.172

3.  Engineering multiple U7snRNA constructs to induce single and multiexon-skipping for Duchenne muscular dystrophy.

Authors:  Aurélie Goyenvalle; Jordan Wright; Arran Babbs; Vivienne Wilkins; Luis Garcia; Kay E Davies
Journal:  Mol Ther       Date:  2012-02-21       Impact factor: 11.454

4.  Exon skipping and dystrophin restoration in patients with Duchenne muscular dystrophy after systemic phosphorodiamidate morpholino oligomer treatment: an open-label, phase 2, dose-escalation study.

Authors:  Sebahattin Cirak; Virginia Arechavala-Gomeza; Michela Guglieri; Lucy Feng; Silvia Torelli; Karen Anthony; Stephen Abbs; Maria Elena Garralda; John Bourke; Dominic J Wells; George Dickson; Matthew J A Wood; Steve D Wilton; Volker Straub; Ryszard Kole; Stephen B Shrewsbury; Caroline Sewry; Jennifer E Morgan; Kate Bushby; Francesco Muntoni
Journal:  Lancet       Date:  2011-07-23       Impact factor: 79.321

5.  Assessment of the feasibility of exon 45-55 multiexon skipping for Duchenne muscular dystrophy.

Authors:  Laura van Vliet; Christa L de Winter; Judith C T van Deutekom; Gert-Jan B van Ommen; Annemieke Aartsma-Rus
Journal:  BMC Med Genet       Date:  2008-12-01       Impact factor: 2.103

6.  Differential stabilities of alternative exon-skipped rod motifs of dystrophin.

Authors:  Chris Ruszczak; Ahmed Mirza; Nick Menhart
Journal:  Biochim Biophys Acta       Date:  2009-03-12

7.  Mutational spectrum of DMD mutations in dystrophinopathy patients: application of modern diagnostic techniques to a large cohort.

Authors:  Kevin M Flanigan; Diane M Dunn; Andrew von Niederhausern; Payam Soltanzadeh; Eduard Gappmaier; Michael T Howard; Jacinda B Sampson; Jerry R Mendell; Cheryl Wall; Wendy M King; Alan Pestronk; Julaine M Florence; Anne M Connolly; Katherine D Mathews; Carrie M Stephan; Karla S Laubenthal; Brenda L Wong; Paula J Morehart; Amy Meyer; Richard S Finkel; Carsten G Bonnemann; Livija Medne; John W Day; Joline C Dalton; Marcia K Margolis; Veronica J Hinton; Robert B Weiss
Journal:  Hum Mutat       Date:  2009-12       Impact factor: 4.878

8.  Genotype-phenotype analysis in 2,405 patients with a dystrophinopathy using the UMD-DMD database: a model of nationwide knowledgebase.

Authors:  Sylvie Tuffery-Giraud; Christophe Béroud; France Leturcq; Rabah Ben Yaou; Dalil Hamroun; Laurence Michel-Calemard; Marie-Pierre Moizard; Rafaëlle Bernard; Mireille Cossée; Pierre Boisseau; Martine Blayau; Isabelle Creveaux; Anne Guiochon-Mantel; Bérengère de Martinville; Christophe Philippe; Nicole Monnier; Eric Bieth; Philippe Khau Van Kien; François-Olivier Desmet; Véronique Humbertclaude; Jean-Claude Kaplan; Jamel Chelly; Mireille Claustres
Journal:  Hum Mutat       Date:  2009-06       Impact factor: 4.878

9.  MLPA analysis/complete sequencing of the DMD gene in a group of Bulgarian Duchenne/Becker muscular dystrophy patients.

Authors:  Albena Todorova; Tihomir Todorov; Bilyana Georgieva; Michaela Lukova; Velina Guergueltcheva; Ivo Kremensky; Vanyo Mitev
Journal:  Neuromuscul Disord       Date:  2008-07-23       Impact factor: 4.296

10.  Variable phenotype of del45-55 Becker patients correlated with nNOSμ mislocalization and RYR1 hypernitrosylation.

Authors:  Christel Gentil; France Leturcq; Rabah Ben Yaou; Jean-Claude Kaplan; Pascal Laforet; Isabelle Pénisson-Besnier; Caroline Espil-Taris; Thomas Voit; Luis Garcia; France Piétri-Rouxel
Journal:  Hum Mol Genet       Date:  2012-05-15       Impact factor: 6.150

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  17 in total

1.  Effective regeneration of dystrophic muscle using autologous iPSC-derived progenitors with CRISPR-Cas9 mediated precise correction.

Authors:  Mackenzie Hagan; Muhammad Ashraf; Il-Man Kim; Neal L Weintraub; Yaoliang Tang
Journal:  Med Hypotheses       Date:  2017-11-23       Impact factor: 1.538

Review 2.  Dystrophin and the two related genetic diseases, Duchenne and Becker muscular dystrophies.

Authors:  Elisabeth Le Rumeur
Journal:  Bosn J Basic Med Sci       Date:  2015-07-20       Impact factor: 3.363

Review 3.  Duchenne muscular dystrophy animal models for high-throughput drug discovery and precision medicine.

Authors:  Nalinda B Wasala; Shi-Jie Chen; Dongsheng Duan
Journal:  Expert Opin Drug Discov       Date:  2020-01-30       Impact factor: 6.098

4.  Cardiac Phenotype-Genotype Associations in DMD/BMD: A Meta-Analysis and Systematic Review.

Authors:  Huan Zhou; Manli Fu; Bing Mao; Li Yuan
Journal:  Pediatr Cardiol       Date:  2020-10-09       Impact factor: 1.655

5.  Dystrophin's central domain forms a complex filament that becomes disorganized by in-frame deletions.

Authors:  Olivier Delalande; Anne-Elisabeth Molza; Raphael Dos Santos Morais; Angélique Chéron; Émeline Pollet; Céline Raguenes-Nicol; Christophe Tascon; Emmanuel Giudice; Marine Guilbaud; Aurélie Nicolas; Arnaud Bondon; France Leturcq; Nicolas Férey; Marc Baaden; Javier Perez; Pierre Roblin; France Piétri-Rouxel; Jean-François Hubert; Mirjam Czjzek; Elisabeth Le Rumeur
Journal:  J Biol Chem       Date:  2018-03-13       Impact factor: 5.157

6.  Genotype-phenotype correlation in Becker muscular dystrophy in Chinese patients.

Authors:  Ruiyi Yuan; Junfei Yi; Zhiying Xie; Yimeng Zheng; Miao Han; Yue Hou; Zhaoxia Wang; Yun Yuan
Journal:  J Hum Genet       Date:  2018-07-05       Impact factor: 3.172

7.  Correction of Three Prominent Mutations in Mouse and Human Models of Duchenne Muscular Dystrophy by Single-Cut Genome Editing.

Authors:  Yi-Li Min; Francesco Chemello; Hui Li; Cristina Rodriguez-Caycedo; Efrain Sanchez-Ortiz; Alex A Mireault; John R McAnally; John M Shelton; Yu Zhang; Rhonda Bassel-Duby; Eric N Olson
Journal:  Mol Ther       Date:  2020-05-30       Impact factor: 11.454

8.  piggyBac transposons expressing full-length human dystrophin enable genetic correction of dystrophic mesoangioblasts.

Authors:  Mariana Loperfido; Susan Jarmin; Sumitava Dastidar; Mario Di Matteo; Ilaria Perini; Marc Moore; Nisha Nair; Ermira Samara-Kuko; Takis Athanasopoulos; Francesco Saverio Tedesco; George Dickson; Maurilio Sampaolesi; Thierry VandenDriessche; Marinee K Chuah
Journal:  Nucleic Acids Res       Date:  2015-12-17       Impact factor: 16.971

9.  In vitro stability of therapeutically relevant, internally truncated dystrophins.

Authors:  Jackie L McCourt; Katrina K Rhett; Michele A Jaeger; Joseph J Belanto; Dana M Talsness; James M Ervasti
Journal:  Skelet Muscle       Date:  2015-04-28       Impact factor: 4.912

10.  Cardiac Myoediting Attenuates Cardiac Abnormalities in Human and Mouse Models of Duchenne Muscular Dystrophy.

Authors:  Ayhan Atmanli; Andreas C Chai; Miao Cui; Zhaoning Wang; Takahiko Nishiyama; Rhonda Bassel-Duby; Eric N Olson
Journal:  Circ Res       Date:  2021-08-10       Impact factor: 23.213

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