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局部应用伊班膦酸盐和骨形态发生蛋白-2 治疗未成年股骨头缺血性坏死:一种刺激骨形成和减少股骨头畸形的联合治疗方法。

Local administration of ibandronate and bone morphogenetic protein-2 after ischemic osteonecrosis of the immature femoral head: a combined therapy that stimulates bone formation and decreases femoral head deformity.

机构信息

Center for Excellence in Hip Disorders, Texas Scottish Rite Hospital for Children, 2222 Welborn Street, Dallas, TX 75219, USA.

出版信息

J Bone Joint Surg Am. 2011 May 18;93(10):905-13. doi: 10.2106/JBJS.J.00716.

Abstract

BACKGROUND

Bisphosphonate therapy has been shown to preserve the osteonecrotic femoral head in experimental and short-term clinical studies. However, a lack of new bone formation within the preserved femoral head due to the inhibition of bone remodeling is a concern. The purpose of this investigation was to determine if combined therapy consisting of ibandronate and bone morphogenetic protein-2 (BMP-2) can preserve the shape of the femoral head and stimulate new bone formation in an immature animal model of ischemic osteonecrosis.

METHODS

Ischemic osteonecrosis was surgically induced in immature pigs. Four groups were studied: normal, treated with saline solution, treated with ibandronate, and treated with both ibandronate and BMP-2 (the ibandronate + BMP-2 group). The animals were killed eight weeks after surgery. Radiographic, histological, and histomorphometric assessments were performed.

RESULTS

Radiographic assessment showed better preservation of the femoral head shape-i.e., a 54% (CI [95% confidence interval]: 22%, 86%) higher mean epiphyseal quotient-in the ibandronate + BMP-2 group than in the saline group. Histological assessment showed increased trabecular bone in the ibandronate + BMP-2 group as compared with that in the saline group. The mean values for trabecular bone volume, thickness, and number and for osteoblast surface were an average of 400% (CI: 242%, 558%), 212% (CI: 166%, 259%), 71% (CI: 6%, 137%), and 2402% (CI: 2113%, 2693%) higher, respectively, in the ibandronate + BMP-2 group than in the saline group. The osteoclast number was significantly reduced in the ibandronate + BMP-2 group compared with that in the saline group (-59% [CI: -75%, -42%]). The mean osteoblast surface value in the ibandronate + BMP-2 group was significantly higher (2567% [CI: 2258%, 2877%]) than that in the ibandronate group. Heterotopic ossifications were present in the capsule of the hip joint in the ibandronate + BMP-2 group.

CONCLUSIONS

A combination of ibandronate and BMP-2 decreased femoral head deformity while stimulating bone formation in an immature animal model of ischemic osteonecrosis.

摘要

背景

在实验和短期临床研究中,双膦酸盐治疗已被证明可保留骨坏死的股骨头。然而,由于骨重塑的抑制,保留下的股骨头内缺乏新骨形成是一个问题。本研究的目的是确定包含伊班膦酸盐和骨形态发生蛋白-2(BMP-2)的联合治疗是否可以在缺血性骨坏死的未成年动物模型中保持股骨头的形状并刺激新骨形成。

方法

通过手术在未成年猪中诱导缺血性骨坏死。研究了 4 组:正常组、生理盐水处理组、伊班膦酸盐处理组和伊班膦酸盐+BMP-2 处理组(伊班膦酸盐+BMP-2 组)。手术后 8 周处死动物。进行放射学、组织学和组织形态计量学评估。

结果

放射学评估显示,伊班膦酸盐+BMP-2 组比生理盐水组更好地保留了股骨头的形状,即骺板指数平均高出 54%(95%置信区间:22%,86%)。组织学评估显示,伊班膦酸盐+BMP-2 组的小梁骨增加。与生理盐水组相比,伊班膦酸盐+BMP-2 组的小梁骨体积、厚度、数量和成骨细胞表面的平均值分别平均高出 400%(95%置信区间:242%,558%)、212%(95%置信区间:166%,259%)、71%(95%置信区间:6%,137%)和 2402%(95%置信区间:2113%,2693%)。伊班膦酸盐+BMP-2 组的破骨细胞数量明显低于生理盐水组(-59%[95%置信区间:-75%,-42%])。伊班膦酸盐+BMP-2 组的成骨细胞表面值明显高于伊班膦酸盐组(2567%[95%置信区间:2258%,2877%])。伊班膦酸盐+BMP-2 组的髋关节囊内有异位骨形成。

结论

在缺血性骨坏死的未成年动物模型中,伊班膦酸盐和 BMP-2 的联合使用减少了股骨头畸形,同时刺激了骨形成。

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