Brantus J F, Meunier P J
Department of Rheumatology and Bone Diseases, Edouard Herriot Hospital, Lyon, France.
Clin Orthop Relat Res. 1998 Jan(346):117-20.
There is no known effective therapy for fibrodysplasia ossificans progressiva. Ethane-1-hydroxy-1-diphosphonate has been studied because of its inhibitory effect on bone mineralization and its potential to impair the rapid ossification process observed after acute episodes of fibrodysplasia ossificans progressiva. In an open study, the effects of intravenously administered ethane-1-hydroxy-1-diphosphonate and oral corticosteroids in the treatment of fibrodysplasia ossificans progressiva was evaluated. Thirty-one fibrodysplasia ossificans progressiva attacks were observed in seven patients during the mean followup of 6 years. In 29 attacks, the authors observed a rapid diminution of local inflammation, swelling, and pain during the first 7 days of treatment. However, despite the ethane-1-hydroxy-1-diphosphonate treatment, 10 new ossifications were observed, causing severe deterioration of joint mobility in all affected patients. In 21 attacks, no new ectopic ossification appeared. The radiologic pattern of preexisting ossifications did not change during the treatment. There are no data in the literature describing the percentage of acute episodes leading to an ossification. The results suggest the possibility that intravenous administration of ethane-1-hydroxy-1-diphosphonate and oral steroids may be helpful for the treatment of fibrodysplasia ossificans progressiva, but more control data on the spontaneous resolution of early flareups are needed.
进行性骨化性纤维发育不良目前尚无已知的有效治疗方法。1-羟基-1-二膦酸乙烷因其对骨矿化的抑制作用以及对进行性骨化性纤维发育不良急性发作后快速骨化过程的潜在影响而受到研究。在一项开放性研究中,评估了静脉注射1-羟基-1-二膦酸乙烷和口服皮质类固醇治疗进行性骨化性纤维发育不良的效果。在平均6年的随访期间,7名患者共出现31次进行性骨化性纤维发育不良发作。在29次发作中,作者观察到在治疗的前7天局部炎症、肿胀和疼痛迅速减轻。然而,尽管使用了1-羟基-1-二膦酸乙烷治疗,仍观察到10处新的骨化,导致所有受影响患者的关节活动度严重恶化。在21次发作中,未出现新的异位骨化。治疗期间,原有骨化的放射学表现未发生变化。文献中没有描述导致骨化的急性发作百分比的数据。结果表明,静脉注射1-羟基-1-二膦酸乙烷和口服类固醇可能有助于治疗进行性骨化性纤维发育不良,但需要更多关于早期发作自发缓解的对照数据。