Conforti Anita, Chiamulera Christian, Moretti Ugo, Colcera Sonia, Fumagalli Guido, Leone Roberto
Department of Medicine and Public Health, Section of Pharmacology, University of Verona, Italy.
Curr Drug Saf. 2007 Jan;2(1):47-63. doi: 10.2174/157488607779315516.
The musculoskeletal system can be a target organ for adverse drug reactions (ADRs). Drug-induced muscle, bone or connective tissue injuries may be due to, i), primary direct drug action, or, ii), undirected consequence of generalized drug-induced disease. Musculoskeletal ADRs may be only temporarily disabling, such as muscle cramps, as well as in other cases may be serious and life-threatening, such as rhabdomyolysis. In the last few years there has been an increasing awareness of musculoskeletal ADRs. Some recent drug safety issues dealt with serious or uncommon musculoskeletal reactions like rhabdomyolysis associated to statins and tendon rupture associated to fluoroquinolones. In this review, we firstly selected those drug classes having a significantly high percentage of musculoskeletal disorder reports in the WHO adverse drug reaction database, maintained by the Uppsala Monitoring Centre. Secondly, the different musculoskeletal ADRs were closely analyzed through the data obtained from an Italian interregional ADRs spontaneous reporting database. The findings on drugs associated to different musculoskeletal disorders, have been integrated with a review of the epidemiological data available in the literature. For the most involved drugs (HMG-CoA reductase inhibitors, fluoroquinolones, corticosteroids, bisphosphonates, retinoids) the underlying musculoskeletal ADR mechanisms were also reviewed and discussed.
肌肉骨骼系统可能是药物不良反应(ADR)的靶器官。药物引起的肌肉、骨骼或结缔组织损伤可能归因于:i)药物的直接主要作用,或ii)药物引起的全身性疾病的间接后果。肌肉骨骼ADR可能只是暂时致残,如肌肉痉挛,在其他情况下也可能很严重甚至危及生命,如横纹肌溶解。在过去几年中,人们对肌肉骨骼ADR的认识不断提高。最近一些药物安全问题涉及严重或罕见的肌肉骨骼反应,如与他汀类药物相关的横纹肌溶解和与氟喹诺酮类药物相关的肌腱断裂。在本综述中,我们首先从乌普萨拉监测中心维护的世界卫生组织药物不良反应数据库中,挑选出肌肉骨骼疾病报告比例显著较高的药物类别。其次,通过从意大利地区间药物不良反应自发报告数据库获得的数据,对不同的肌肉骨骼ADR进行了仔细分析。关于与不同肌肉骨骼疾病相关药物的研究结果,已结合文献中现有的流行病学数据进行了综合分析。对于涉及最多的药物(HMG-CoA还原酶抑制剂、氟喹诺酮类、皮质类固醇、双膦酸盐、维甲酸),还对其潜在的肌肉骨骼ADR机制进行了综述和讨论。