E Medea Scientific Institute, Bosisio Parini, Italy.
Pharmacol Res. 2012 Apr;65(4):472-9. doi: 10.1016/j.phrs.2012.01.006. Epub 2012 Jan 25.
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.
本开放性、单中心的初步研究旨在评估硝酸异山梨酯(一种一氧化氮供体)和布洛芬(一种非甾体抗炎药)联合应用于一组成年型营养不良患者(杜氏肌营养不良症、贝克型肌营养不良症和肢带型肌营养不良症)的安全性和耐受性。共招募了 71 名患者:35 名接受药物联合治疗 12 个月,36 名未接受治疗。通过报告的体征和症状、体格检查、血液检查、心脏和呼吸功能检查来评估安全性和不良事件。还应用了探索性结局测量,如运动功能测量量表。长期联合使用这些药物具有良好的安全性和耐受性。报告的副作用较少且短暂(即头痛和低血压)。此外,探索性结局测量在研究中所有疾病人群中都是可行的,并在 MFM 量表的一个维度上显示出改善的趋势,达到了统计学意义。布洛芬和硝酸异山梨酯的全身给药为评估疗效的临床研究提供了足够的安全边际。