Literature DB >> 22402864

Pentoxifylline as a rescue treatment for DMD: a randomized double-blind clinical trial.

D M Escolar1, A Zimmerman, T Bertorini, P R Clemens, A M Connolly, L Mesa, K Gorni, A Kornberg, H Kolski, N Kuntz, Y Nevo, C Tesi-Rocha, K Nagaraju, S Rayavarapu, L P Hache, J E Mayhew, J Florence, F Hu, A Arrieta, E Henricson, R T Leshner, J K Mah.   

Abstract

OBJECTIVE: To determine whether pentoxifylline (PTX) slows the decline of muscle strength and function in ambulatory boys with Duchenne muscular dystrophy (DMD).
METHODS: This was a multicenter, randomized, double-blinded, controlled trial comparing 12 months of daily treatment with PTX or placebo in corticosteroid-treated boys with DMD using a slow-release PTX formulation (~20 mg/kg/day). The primary outcome was the change in mean total quantitative muscle testing (QMT) score. Secondary outcomes included changes in QMT subscales, manual muscle strength, pulmonary function, and timed function tests. Outcomes were compared using Student t tests and a linear mixed-effects model. Adverse events (AEs) were compared using the Fisher exact test.
RESULTS: A total of 64 boys with DMD with a mean age of 9.9 ± 2.9 years were randomly assigned to PTX or placebo in 11 participating Cooperative International Neuromuscular Research Group centers. There was no significant difference between PTX and the placebo group in total QMT scores (p = 0.14) or in most of the secondary outcomes after a 12-month treatment. The use of PTX was associated with mild to moderate gastrointestinal or hematologic AEs.
CONCLUSION: The addition of PTX to corticosteroid-treated boys with DMD at a moderate to late ambulatory stage of disease did not improve or halt the deterioration of muscle strength and function over a 12-month study period. CLASSIFICATION OF EVIDENCE: This study provides Class I evidence that treatment with PTX does not prevent deterioration in muscle function or strength in corticosteroid-treated boys with DMD.

Entities:  

Mesh:

Substances:

Year:  2012        PMID: 22402864      PMCID: PMC3306159          DOI: 10.1212/WNL.0b013e31824c46be

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


  32 in total

1.  Pre-clinical screening of drugs using the mdx mouse.

Authors:  J A Granchelli; C Pollina; M S Hudecki
Journal:  Neuromuscul Disord       Date:  2000-06       Impact factor: 4.296

2.  Liquid formulation of pentoxifylline is a poorly tolerated treatment for duchenne dystrophy.

Authors:  Angela Zimmerman; Paula R Clemens; Carolina Tesi-Rocha; Anne Connolly; Susan T Iannaccone; Nancy Kuntz; Adrienne Arrieta; Lauren Hache; Erik Henricson; Fengming Hu; Jill Mayhew; Diana M Escolar
Journal:  Muscle Nerve       Date:  2011-06-14       Impact factor: 3.217

3.  Duchenne muscular dystrophy: Canadian paediatric neuromuscular physicians survey.

Authors:  Hugh J McMillan; Craig Campbell; Jean K Mah
Journal:  Can J Neurol Sci       Date:  2010-03       Impact factor: 2.104

Review 4.  Molecular treatments in Duchenne muscular dystrophy.

Authors:  Michela Guglieri; Kate Bushby
Journal:  Curr Opin Pharmacol       Date:  2010-04-29       Impact factor: 5.547

Review 5.  Signal transduction in inflammatory processes, current and future therapeutic targets: a mini review.

Authors:  R Witkamp; M Monshouwer
Journal:  Vet Q       Date:  2000-01       Impact factor: 3.320

6.  Elevated plasma levels of transforming growth factor beta1 in patients with muscular dystrophy.

Authors:  M Ishitobi; K Haginoya; Y Zhao; A Ohnuma; J Minato; T Yanagisawa; M Tanabu; M Kikuchi; K Iinuma
Journal:  Neuroreport       Date:  2000-12-18       Impact factor: 1.837

7.  Elevated plasma levels of tissue inhibitors of metalloproteinase-1 and their overexpression in muscle in human and mouse muscular dystrophy.

Authors:  Guilian Sun; Kazuhiro Haginoya; Yoko Chiba; Mitsugu Uematsu; Naomi Hino-Fukuyo; Soichiro Tanaka; Akira Onuma; Kazuie Iinuma; Shigeru Tsuchiya
Journal:  J Neurol Sci       Date:  2010-07-23       Impact factor: 3.181

Review 8.  Pentoxifylline in preterm neonates: a systematic review.

Authors:  Emma Harris; Sven M Schulzke; Sanjay K Patole
Journal:  Paediatr Drugs       Date:  2010-10-01       Impact factor: 3.022

9.  Double-blind placebo-controlled trial of pentoxifylline added to risperidone: effects on aberrant behavior in children with autism.

Authors:  Shahin Akhondzadeh; Jalil Fallah; Mohammad-Reza Mohammadi; Reza Imani; Mohammad Mohammadi; Bahman Salehi; Ahmad Ghanizadeh; Maedeh Raznahan; Soodeh Mohebbi-Rasa; Shams-Ali Rezazadeh; Saeedeh Forghani
Journal:  Prog Neuropsychopharmacol Biol Psychiatry       Date:  2009-09-20       Impact factor: 5.067

Review 10.  Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management.

Authors:  Katharine Bushby; Richard Finkel; David J Birnkrant; Laura E Case; Paula R Clemens; Linda Cripe; Ajay Kaul; Kathi Kinnett; Craig McDonald; Shree Pandya; James Poysky; Frederic Shapiro; Jean Tomezsko; Carolyn Constantin
Journal:  Lancet Neurol       Date:  2009-11-27       Impact factor: 44.182

View more
  16 in total

1.  Selective serotonin reuptake inhibitors ameliorate MEGF10 myopathy.

Authors:  Madhurima Saha; Skylar A Rizzo; Manashwi Ramanathan; Rylie M Hightower; Katherine E Santostefano; Naohiro Terada; Richard S Finkel; Jonathan S Berg; Nizar Chahin; Christina A Pacak; Richard E Wagner; Matthew S Alexander; Isabelle Draper; Peter B Kang
Journal:  Hum Mol Genet       Date:  2019-07-15       Impact factor: 6.150

2.  Dystrophin hydrophobic regions in the pathogenesis of Duchenne and Becker muscular dystrophies.

Authors:  Yingyin Liang; Songlin Chen; Jianzong Zhu; Xiangxue Zhou; Chen Yang; Lu Yao; Cheng Zhang
Journal:  Bosn J Basic Med Sci       Date:  2015-05-20       Impact factor: 3.363

3.  Electrical impedance myography for assessment of Duchenne muscular dystrophy.

Authors:  Seward B Rutkove; Kush Kapur; Craig M Zaidman; Jim S Wu; Amy Pasternak; Lavanya Madabusi; Sung Yim; Adam Pacheck; Heather Szelag; Tim Harrington; Basil T Darras
Journal:  Ann Neurol       Date:  2017-05-04       Impact factor: 10.422

Review 4.  Antioxidants to prevent respiratory decline in people with Duchenne muscular dystrophy and progressive respiratory decline.

Authors:  Luis Garegnani; Martin Hyland; Pablo Roson Rodriguez; Camila Micaela E Escobar Liquitay; Juan Va Franco
Journal:  Cochrane Database Syst Rev       Date:  2021-11-08

Review 5.  Antioxidants to prevent respiratory decline in people with Duchenne muscular dystrophy and progressive respiratory decline.

Authors:  Luis Garegnani; Martin Hyland; Pablo Roson Rodriguez; Camila Micaela Escobar Liquitay; Juan Va Franco
Journal:  Cochrane Database Syst Rev       Date:  2021-12-01

Review 6.  Immune-mediated pathology in Duchenne muscular dystrophy.

Authors:  Amy S Rosenberg; Montserrat Puig; Kanneboyina Nagaraju; Eric P Hoffman; S Armando Villalta; V Ashutosh Rao; Lalage M Wakefield; Janet Woodcock
Journal:  Sci Transl Med       Date:  2015-08-05       Impact factor: 17.956

Review 7.  Current and Emerging Therapies for Duchenne Muscular Dystrophy.

Authors:  Megan Crone; Jean K Mah
Journal:  Curr Treat Options Neurol       Date:  2018-06-23       Impact factor: 3.598

8.  Pharmacological therapeutics targeting the secondary defects and downstream pathology of Duchenne muscular dystrophy.

Authors:  Janelle M Spinazzola; Louis M Kunkel
Journal:  Expert Opin Orphan Drugs       Date:  2016-10-18       Impact factor: 0.694

9.  Autophagy is Impaired in the Tibialis Anterior of Dystrophin Null Mice.

Authors:  Pietro Spitali; Paolo Grumati; Monika Hiller; Martina Chrisam; Annemieke Aartsma-Rus; Paolo Bonaldo
Journal:  PLoS Curr       Date:  2013-11-22

10.  Efficacy and safety evaluation of pentoxifylline associated with other antioxidants in medical treatment of Peyronie's disease: a case-control study.

Authors:  Gianni Paulis; Davide Barletta; Paolo Turchi; Antonio Vitarelli; Giuseppe Dachille; Andrea Fabiani; Romano Gennaro
Journal:  Res Rep Urol       Date:  2015-12-31
View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.