Literature DB >> 22306844

Nitric oxide donor and non steroidal anti inflammatory drugs as a therapy for muscular dystrophies: evidence from a safety study with pilot efficacy measures in adult dystrophic patients.

Maria Grazia D'Angelo1, Sandra Gandossini, Filippo Martinelli Boneschi, Clara Sciorati, Sara Bonato, Erika Brighina, Giacomo Pietro Comi, Anna Carla Turconi, Francesca Magri, Giuseppe Stefanoni, Silvia Brunelli, Nereo Bresolin, Dario Cattaneo, Emilio Clementi.   

Abstract

This open-label, single centre pilot study was designed to evaluate safety and tolerability of the combination of the drugs isosorbide dinitrate, a nitric oxide donor, and ibuprofen, a non steroid anti-inflammatory drug, in a cohort of adult dystrophic patients (Duchenne, Becker and Limb-Girdle Muscular Dystrophy). Seventy-one patients were recruited: 35, treated with the drug combination for 12 months, and 36 untreated. Safety and adverse events were assessed by reported signs and symptoms, physical examinations, blood tests, cardiac and respiratory function tests. Exploratory outcomes measure, such as the motor function measure scale, were also applied. Good safety and tolerability profiles of the long-term co-administration of the drugs were demonstrated. Few and transient side effects (i.e. headache and low blood pressure) were reported. Additionally, exploratory outcomes measures were feasible in all the disease population studied and evidenced a trend towards amelioration that reached statistical significance in one dimension of the MFM scale. Systemic administration of ibuprofen and isosorbide dinitrate provides an adequate safety margin for clinical studies aimed at assessing efficacy.
Copyright © 2012 Elsevier Ltd. All rights reserved.

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Year:  2012        PMID: 22306844     DOI: 10.1016/j.phrs.2012.01.006

Source DB:  PubMed          Journal:  Pharmacol Res        ISSN: 1043-6618            Impact factor:   7.658


  21 in total

Review 1.  Fat deposition and accumulation in the damaged and inflamed skeletal muscle: cellular and molecular players.

Authors:  Clara Sciorati; Emilio Clementi; Angelo A Manfredi; Patrizia Rovere-Querini
Journal:  Cell Mol Life Sci       Date:  2015-02-18       Impact factor: 9.261

2.  Delayed bone regeneration is linked to chronic inflammation in murine muscular dystrophy.

Authors:  Rana Abou-Khalil; Frank Yang; Marie Mortreux; Shirley Lieu; Yan-Yiu Yu; Maud Wurmser; Catia Pereira; Frédéric Relaix; Theodore Miclau; Ralph S Marcucio; Céline Colnot
Journal:  J Bone Miner Res       Date:  2014-02       Impact factor: 6.741

Review 3.  Emerging drugs for Duchenne muscular dystrophy.

Authors:  Vinod Malik; Louise R Rodino-Klapac; Jerry R Mendell
Journal:  Expert Opin Emerg Drugs       Date:  2012-06       Impact factor: 4.191

4.  Requirement of inducible nitric oxide synthase for skeletal muscle regeneration after acute damage.

Authors:  Elena Rigamonti; Thierry Touvier; Emilio Clementi; Angelo A Manfredi; Silvia Brunelli; Patrizia Rovere-Querini
Journal:  J Immunol       Date:  2013-01-18       Impact factor: 5.422

Review 5.  Ongoing therapeutic trials and outcome measures for Duchenne muscular dystrophy.

Authors:  Alessandra Govoni; Francesca Magri; Simona Brajkovic; Chiara Zanetta; Irene Faravelli; Stefania Corti; Nereo Bresolin; Giacomo P Comi
Journal:  Cell Mol Life Sci       Date:  2013-06-18       Impact factor: 9.261

6.  Age-related loss of nitric oxide synthase in skeletal muscle causes reductions in calpain S-nitrosylation that increase myofibril degradation and sarcopenia.

Authors:  Giuseppina Samengo; Anna Avik; Brian Fedor; Daniel Whittaker; Kyu H Myung; Michelle Wehling-Henricks; James G Tidball
Journal:  Aging Cell       Date:  2012-10-04       Impact factor: 9.304

Review 7.  Nitric oxide in myogenesis and therapeutic muscle repair.

Authors:  Clara De Palma; Emilio Clementi
Journal:  Mol Neurobiol       Date:  2012-07-22       Impact factor: 5.590

Review 8.  Pre-clinical drug tests in the mdx mouse as a model of dystrophinopathies: an overview.

Authors:  Annamaria De Luca
Journal:  Acta Myol       Date:  2012-05

9.  Treatment with a nitric oxide-donating NSAID alleviates functional muscle ischemia in the mouse model of Duchenne muscular dystrophy.

Authors:  Gail D Thomas; Jianfeng Ye; Claudio De Nardi; Angela Monopoli; Ennio Ongini; Ronald G Victor
Journal:  PLoS One       Date:  2012-11-05       Impact factor: 3.240

10.  Autophagy as a new therapeutic target in Duchenne muscular dystrophy.

Authors:  C De Palma; F Morisi; S Cheli; S Pambianco; V Cappello; M Vezzoli; P Rovere-Querini; M Moggio; M Ripolone; M Francolini; M Sandri; E Clementi
Journal:  Cell Death Dis       Date:  2012-11-15       Impact factor: 8.469

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