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首页> 外文期刊>The Journal of Bone and Joint Surgery. American Volume >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.
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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.

机译:未成熟股骨头缺血性坏死后伊班膦酸和骨形态发生蛋白2的局部给药:刺激骨形成并减少股骨头畸形的联合疗法。

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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.
机译:背景:在实验和短期临床研究中,双膦酸盐疗法已被证明可保护股骨头坏死。然而,由于抑制了骨重塑,在保留的股骨头内缺乏新的骨形成是一个问题。这项研究的目的是确定由伊班膦酸盐和骨形态发生蛋白2(BMP-2)组成的联合治疗是否可以在不成熟的缺血性骨坏死动物模型中保持股骨头的形状并刺激新的骨形成。方法:通过手术诱导未成熟猪缺血性坏死。研究了四组:正常组,盐溶液治疗,伊班膦酸盐治疗以及伊班膦酸盐和BMP-2疗法(伊班膦酸盐+ BMP-2组)。手术八周后将动物处死。进行了影像学,组织学和组织形态学评估。结果:影像学评估显示,股骨头形状的保存性更好,即伊班膦酸钠+ BMP-2组的平均epi骨商数比生理盐水高54%(CI [95%置信区间]:22%,86%)组。组织学评估显示,伊班膦酸+ BMP-2组的小梁骨比生理盐水组增加。小梁骨体积,厚度和数量以及成骨细胞表面的平均值分别为400%(CI:242%,558%),212%(CI:166%,259%),71%(CI:6)伊班膦酸+ BMP-2组比生理盐水组分别高1%,137%)和2402%(CI:2113%,2693%)。与生理盐水组相比,伊班膦酸+ BMP-2组的破骨细胞数量显着减少(-59%[CI:-75%,-42%])。伊班膦酸盐+ BMP-2组的平均成骨细胞表面价值明显高于伊班膦酸盐组(2567%[CI:2258%,2877%])。伊班膦酸+ BMP-2组的髋关节囊中存在异位骨化。结论:伊班膦酸和BMP-2的组合可在不成熟的缺血性骨坏死动物模型中减少股骨头畸形并刺激骨骼形成。

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