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静脉注射帕米膦酸治疗骨纤维异常增殖症:长期疗效及治疗反应预测因素评估

Treatment of fibrous dysplasia of bone with intravenous pamidronate: long-term effectiveness and evaluation of predictors of response to treatment.

作者信息

Chapurlat R D, Hugueny P, Delmas P D, Meunier P J

机构信息

Department of Rheumatology and Bone Diseases and INSERM U403, Pavillon F, Edouard Herriot Hospital, 5 Place d'Arsonval, 69437 Lyon Cedex 03, France.

出版信息

Bone. 2004 Jul;35(1):235-42. doi: 10.1016/j.bone.2004.03.004.

Abstract

Fibrous dysplasia (FD) of bone is a rare but potentially severe bone disease that often entails fractures, deformities, and bone pain. An activating mutation of the alpha subunit of Gs proteins leads to differentiation abnormalities of the osteoblastic lineage, which are responsible for development of fibrous tissue in the medulla and increased osteoclastic activity. This increased bone resorption has been the rationale to use bisphosphonates in our center since 1988. So, we have analyzed the largest series, so far, of patients treated with the bisphosphonate pamidronate and sought predictors of response to treatment. We have treated 58 patients (41 adults and 17 under 18 years of age) with FD in an open study, using intravenous (IV) pamidronate 180 mg every 6 months and calcium and vitamin D supplements, in combination with oral phosphate and calcitriol in patients with FD who also had renal phosphate wasting. Patients were followed up with biannual visits, for an average 50 months, with pain assessment, annual radiographs of affected bones, measurement of biochemical markers of bone turnover, and annual bone mineral density measurements in the case of affected hips. We found that pain intensity significantly decreased with treatment in the 44 patients who had bone pain at baseline, biochemical markers of bone turnover were significantly reduced, and about 50% of patients had improvement of bone lesions on radiographs, evidenced by filling of osteolytic lesions and/or cortex thickening. Bone mineral density was substantially increased in the 12 patients who had hip FD. There was no significant clinical or biological predictor of positive radiographic response to pamidronate treatment. Long-term treatment with pamidronate was safe, in particular among the 12 patients who were followed up for more than 8 years. Despite the lack of a control group, our results suggest that intravenous pamidronate improves radiological aspect in half of the patients with FD, decreases bone turnover, and may decrease pain intensity.

摘要

骨纤维发育不良(FD)是一种罕见但可能严重的骨病,常伴有骨折、畸形和骨痛。Gs蛋白α亚基的激活突变导致成骨细胞系分化异常,这是导致骨髓中纤维组织形成和破骨细胞活性增加的原因。自1988年以来,这种增加的骨吸收一直是我们中心使用双膦酸盐的理论依据。因此,我们分析了迄今为止接受双膦酸盐帕米膦酸治疗的最大系列患者,并寻找治疗反应的预测因素。在一项开放性研究中,我们用FD治疗了58例患者(41例成人和17例18岁以下患者),每6个月静脉注射(IV)帕米膦酸180mg,并补充钙和维生素D,对于同时患有肾性磷酸盐消耗的FD患者,联合口服磷酸盐和骨化三醇。患者每半年随访一次,平均随访50个月,进行疼痛评估、患骨的年度X线片检查、骨转换生化标志物的测量,对于患髋患者进行年度骨密度测量。我们发现,在基线时有骨痛的44例患者中,疼痛强度随着治疗显著降低,骨转换生化标志物显著降低,约50%的患者X线片上骨病变有所改善,表现为溶骨性病变填充和/或皮质增厚。12例患髋FD患者的骨密度显著增加。对于帕米膦酸治疗的阳性X线反应,没有显著的临床或生物学预测因素。长期使用帕米膦酸治疗是安全的,特别是在12例随访超过8年的患者中。尽管缺乏对照组,但我们的结果表明,静脉注射帕米膦酸可使一半的FD患者的影像学表现得到改善,降低骨转换,并可能降低疼痛强度。

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