Literature DB >> 28983837

Treatment Advances in Spinal Muscular Atrophy.

Diana Bharucha-Goebel1,2, Petra Kaufmann3.   

Abstract

PURPOSE OF REVIEW: Spinal muscular atrophy (SMA) is a genetic disorder of motor neurons in the anterior horns of the spinal cord and brainstem that results in muscle atrophy and weakness. SMA is an autosomal recessive disease linked to deletions of the SMN1 gene on chromosome 5q. Humans have a duplicate gene (SMN2) whose product can mitigate disease severity, leading to the variability in severity and age of onset of disease, and is therefore a target for drug development. RECENT
FINDINGS: Advances in preclinical and clinical trials have paved the way for novel therapeutic options for SMA patients, including many currently in clinical trials. In 2016, the first treatment for SMA has been approved in the USA, an antisense oligonucleotide that increases full-length protein product derived from SMN2. The approval of a first treatment for SMA and the rapid advances in clinical trials provide the prospect for multiple approaches to disease modification. There are several other promising therapeutics in different stages of development, based on approaches such as neuroprotection, or gene therapy.

Entities:  

Keywords:  Clinical trials; Functional biomarkers; Gene therapy; Natural history; Newborn screening; Spinal muscular atrophy; Standard of care

Mesh:

Year:  2017        PMID: 28983837      PMCID: PMC5678931          DOI: 10.1007/s11910-017-0798-y

Source DB:  PubMed          Journal:  Curr Neurol Neurosci Rep        ISSN: 1528-4042            Impact factor:   5.081


  28 in total

Review 1.  Spinal muscular atrophy: Factors that modulate motor neurone vulnerability.

Authors:  Wen-Yo Tu; Julie E Simpson; J Robin Highley; Paul R Heath
Journal:  Neurobiol Dis       Date:  2017-02-02       Impact factor: 5.996

2.  Safety and efficacy of olesoxime in patients with type 2 or non-ambulatory type 3 spinal muscular atrophy: a randomised, double-blind, placebo-controlled phase 2 trial.

Authors:  Enrico Bertini; Eric Dessaud; Eugenio Mercuri; Francesco Muntoni; Janbernd Kirschner; Carol Reid; Anna Lusakowska; Giacomo P Comi; Jean-Marie Cuisset; Jean-Louis Abitbol; Bruno Scherrer; Patricia Sanwald Ducray; Jeppe Buchbjerg; Eduardo Vianna; W Ludo van der Pol; Carole Vuillerot; Thomas Blaettler; Paulo Fontoura
Journal:  Lancet Neurol       Date:  2017-04-28       Impact factor: 44.182

3.  Improving single injection CSF delivery of AAV9-mediated gene therapy for SMA: a dose-response study in mice and nonhuman primates.

Authors:  Kathrin Meyer; Laura Ferraiuolo; Leah Schmelzer; Lyndsey Braun; Vicki McGovern; Shibi Likhite; Olivia Michels; Alessandra Govoni; Julie Fitzgerald; Pablo Morales; Kevin D Foust; Jerry R Mendell; Arthur H M Burghes; Brian K Kaspar
Journal:  Mol Ther       Date:  2014-10-31       Impact factor: 11.454

4.  Consensus statement for standard of care in spinal muscular atrophy.

Authors:  Ching H Wang; Richard S Finkel; Enrico S Bertini; Mary Schroth; Anita Simonds; Brenda Wong; Annie Aloysius; Leslie Morrison; Marion Main; Thomas O Crawford; Anthony Trela
Journal:  J Child Neurol       Date:  2007-08       Impact factor: 1.987

5.  SMA CARNI-VAL trial part I: double-blind, randomized, placebo-controlled trial of L-carnitine and valproic acid in spinal muscular atrophy.

Authors:  Kathryn J Swoboda; Charles B Scott; Thomas O Crawford; Louise R Simard; Sandra P Reyna; Kristin J Krosschell; Gyula Acsadi; Bakri Elsheik; Mary K Schroth; Guy D'Anjou; Bernard LaSalle; Thomas W Prior; Susan L Sorenson; Jo Anne Maczulski; Mark B Bromberg; Gary M Chan; John T Kissel
Journal:  PLoS One       Date:  2010-08-19       Impact factor: 3.240

6.  Prospective cohort study of spinal muscular atrophy types 2 and 3.

Authors:  Petra Kaufmann; Michael P McDermott; Basil T Darras; Richard S Finkel; Douglas M Sproule; Peter B Kang; Maryam Oskoui; Andrei Constantinescu; Clifton L Gooch; A Reghan Foley; Michele L Yang; Rabi Tawil; Wendy K Chung; William B Martens; Jacqueline Montes; Vanessa Battista; Jessica O'Hagen; Sally Dunaway; Jean Flickinger; Janet Quigley; Susan Riley; Allan M Glanzman; Maryjane Benton; Patricia A Ryan; Mark Punyanitya; Megan J Montgomery; Jonathan Marra; Benjamin Koo; Darryl C De Vivo
Journal:  Neurology       Date:  2012-10-17       Impact factor: 9.910

7.  SMA CARNIVAL TRIAL PART II: a prospective, single-armed trial of L-carnitine and valproic acid in ambulatory children with spinal muscular atrophy.

Authors:  John T Kissel; Charles B Scott; Sandra P Reyna; Thomas O Crawford; Louise R Simard; Kristin J Krosschell; Gyula Acsadi; Bakri Elsheik; Mary K Schroth; Guy D'Anjou; Bernard LaSalle; Thomas W Prior; Susan Sorenson; Jo Anne Maczulski; Mark B Bromberg; Gary M Chan; Kathryn J Swoboda
Journal:  PLoS One       Date:  2011-07-06       Impact factor: 3.240

Review 8.  Emerging therapies and challenges in spinal muscular atrophy.

Authors:  Michelle A Farrar; Susanna B Park; Steve Vucic; Kate A Carey; Bradley J Turner; Thomas H Gillingwater; Kathryn J Swoboda; Matthew C Kiernan
Journal:  Ann Neurol       Date:  2017-02-17       Impact factor: 10.422

9.  Content validity and clinical meaningfulness of the HFMSE in spinal muscular atrophy.

Authors:  Maria C Pera; Giorgia Coratti; Nicola Forcina; Elena S Mazzone; Mariacristina Scoto; Jacqueline Montes; Amy Pasternak; Anna Mayhew; Sonia Messina; Maria Sframeli; Marion Main; Robert Muni Lofra; Tina Duong; Danielle Ramsey; Sally Dunaway; Rachel Salazar; Lavinia Fanelli; Matthew Civitello; Roberto de Sanctis; Laura Antonaci; Leonardo Lapenta; Simona Lucibello; Marika Pane; John Day; Basil T Darras; Darryl C De Vivo; Francesco Muntoni; Richard Finkel; Eugenio Mercuri
Journal:  BMC Neurol       Date:  2017-02-23       Impact factor: 2.474

10.  Patterns of disease progression in type 2 and 3 SMA: Implications for clinical trials.

Authors:  Eugenio Mercuri; Richard Finkel; Jacqueline Montes; Elena S Mazzone; Maria Pia Sormani; Marion Main; Danielle Ramsey; Anna Mayhew; Allan M Glanzman; Sally Dunaway; Rachel Salazar; Amy Pasternak; Janet Quigley; Marika Pane; Maria Carmela Pera; Mariacristina Scoto; Sonia Messina; Maria Sframeli; Gian Luca Vita; Adele D'Amico; Marleen van den Hauwe; Serena Sivo; Nathalie Goemans; Petra Kaufmann; Basil T Darras; Enrico Bertini; Francesco Muntoni; Darryl C De Vivo
Journal:  Neuromuscul Disord       Date:  2015-12-03       Impact factor: 4.296

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  7 in total

Review 1.  Molecular Biomarkers for Spinal Muscular Atrophy: A Systematic Review.

Authors:  Angela Navarrete-Opazo; Sheldon Garrison; Mindy Waite
Journal:  Neurol Clin Pract       Date:  2021-08

2.  Engineering Crystal Packing in RNA-Protein Complexes II: A Historical Perspective from the Structural Studies of the Spliceosome.

Authors:  Adelaine Kwun-Wai Leung; Yasushi Kondo; Daniel A Pomeranz Krummel; Jade Li; Stephen R Price; Anne-Marie M van Roon
Journal:  Crystals (Basel)       Date:  2021-08-15       Impact factor: 2.589

Review 3.  Biomarkers and the Development of a Personalized Medicine Approach in Spinal Muscular Atrophy.

Authors:  Didu S T Kariyawasam; Arlene D'Silva; Cindy Lin; Monique M Ryan; Michelle A Farrar
Journal:  Front Neurol       Date:  2019-08-19       Impact factor: 4.003

4.  Inhibition of myostatin prevents microgravity-induced loss of skeletal muscle mass and strength.

Authors:  Rosamund C Smith; Martin S Cramer; Pamela J Mitchell; Jonathan Lucchesi; Alicia M Ortega; Eric W Livingston; Darryl Ballard; Ling Zhang; Jeff Hanson; Kenneth Barton; Shawn Berens; Kelly M Credille; Ted A Bateman; Virginia L Ferguson; Yanfei L Ma; Louis S Stodieck
Journal:  PLoS One       Date:  2020-04-21       Impact factor: 3.240

5.  Economic burden of spinal muscular atrophy: an analysis of claims data.

Authors:  Lisa Belter; Rosángel Cruz; Sierra Kulas; Emily McGinnis; Omar Dabbous; Jill Jarecki
Journal:  J Mark Access Health Policy       Date:  2020-11-08

Review 6.  RNA-Targeted Therapies and Amyotrophic Lateral Sclerosis.

Authors:  Stéphane Mathis; Gwendal Le Masson
Journal:  Biomedicines       Date:  2018-01-15

7.  TorsinB overexpression prevents abnormal twisting in DYT1 dystonia mouse models.

Authors:  Jay Li; Chun-Chi Liang; Samuel S Pappas; William T Dauer
Journal:  Elife       Date:  2020-03-23       Impact factor: 8.140

  7 in total

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