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

被引:36
作者
D'Angelo, Maria Grazia [1 ]
Gandossini, Sandra [1 ]
Boneschi, Filippo Martinelli [2 ,3 ]
Sciorati, Clara [2 ,3 ]
Bonato, Sara [1 ]
Brighina, Erika [1 ]
Comi, Giacomo Pietro [4 ]
Turconi, Anna Carla [1 ]
Magri, Francesca [4 ]
Stefanoni, Giuseppe [1 ]
Brunelli, Silvia [5 ]
Bresolin, Nereo [1 ,4 ]
Cattaneo, Dario [6 ]
Clementi, Emilio [1 ,6 ]
机构
[1] E Medea Sci Inst, Bosisio Parini, Italy
[2] Ist Sci San Raffaele, Div Regenerat Med, I-20132 Milan, Italy
[3] Ist Sci San Raffaele, Div Neurosci, I-20132 Milan, Italy
[4] Univ Milan, Dept Neurol Sci, IRCCS Ca Granda Fdn Osped Maggiore Policlin, Dino Ferrari Ctr, I-20122 Milan, Italy
[5] Univ Milano Bicocca, Dept Expt Med, Monza, Italy
[6] Univ Milan, Clin Pharmacol Unit, CNR Neurosci Inst, Dept Clin Sci,Univ Hosp Luigi Sacco, Milan, Italy
关键词
Muscular dystrophies; Pharmacological treatment; Nitric oxide donor; Anti-inflammatory drug; Safety; NONSTEROIDAL ANTIINFLAMMATORY DRUGS; MUSCLE SATELLITE CELLS; MOTOR FUNCTION MEASURE; MITOCHONDRIAL BIOGENESIS; DOUBLE-BLIND; CYCLIC-GMP; TRIAL; DEFICIENCY; PREDNISONE; IBUPROFEN;
D O I
10.1016/j.phrs.2012.01.006
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
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. (c) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:472 / 479
页数:8
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