Histomorphometric description of allograft bone remodeling and union in a canine segmental femoral defect model: a comparison of rhBMP-2, cancellous bone graft, and absorbable collagen sponge

被引:51
作者
Zabka, AG
Pluhar, GE
Edwards, RB
Manley, PA
Hayashi, K
Heiner, JP
Kalscheur, VL
Seeherman, HJ
Markel, MD
机构
[1] Univ Wisconsin, Sch Vet Med, Dept Med Sci, Comparat Orthopaed Res Lab, Madison, WI 53706 USA
[2] Univ Wisconsin, Sch Med, Div Orthopaed Surg, Madison, WI 53706 USA
[3] Genet Inst Inc, Andover, MA 01810 USA
关键词
D O I
10.1016/S0736-0266(00)90003-2
中图分类号
R826.8 [整形外科学]; R782.2 [口腔颌面部整形外科学]; R726.2 [小儿整形外科学]; R62 [整形外科学(修复外科学)];
学科分类号
摘要
The purpose of this study was to determine the effect of recombinant human bone morphogenetic protein type 2 (rhBMP-2) on the histomorphometry of femoral allograft-host bone union and allograft remodeling. A 6 cm mid-diaphyseal femoral defect was created and filled with an allograft stabilized with an interlocking nail in 21 dogs. Dogs were randomly divided into three equal groups and the allograft-host bone junctions and the mid-diaphyses of the allografts were treated with either an absorbable collagen sponge (ACS) loaded with rhBMP-2 (BMP group), an autogenous cancellous bone graft (CBG group), or ACS loaded with buffer solution (ACS group). All dogs received daily tetracycline until sacrifice at 24 weeks to label new bone formation. Histomorphometric analyses on sections of proximal and distal allograft-host bone junctions and the mid-diaphyseal portion of allografts were performed using fluorescent and regular light microscopy. Analyses of the host bone and junctions between allograft and host bone revealed significantly greater new bone formation and larger osteon radii in the BMP group compared to CBG and ACS groups and contralateral intact bone. Porosity in CBG and ACS groups was significantly higher than in the BMP group, which had similar values to intact bone. In transverse sections of allografts. the largest pore diameters were present in the CBG group. Based on all parameters measured, significantly higher bone turnover occurred in the outer cortical area of the allograft in all groups as compared to the inner cortical and mid-cortical al eas. New bone formation and osteon radius/osteon width in allografts were similar for all three groups. Higher porosity and larger pore diameters in the CBG and ACS groups suggested higher bone resorption vel sus formation in these groups compared to the BMP group. The results of this study reveal more balanced allograft bone resorption and bone formation in the BMP group, with greater resorptive activity in the CBG and ACS groups. However, neither rbBMP-2 nor autogenous bone graft increased allograft incorporation when compared to the negative control (ACS group). (C) Orthopaedic Research Society. Published by Elsevier Science Ltd. All rights reserved.
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页码:318 / 327
页数:10
相关论文
共 57 条
  • [1] AHO AJ, 1991, LIMB SALVAGE MAJOR R, P17
  • [2] FRACTURES OF ALLOGRAFTS - FREQUENCY, TREATMENT, AND END-RESULTS
    BERREY, BH
    LORD, CF
    GEBHARDT, MC
    MANKIN, HJ
    [J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1990, 72A (06) : 825 - 833
  • [3] IMMUNOLOCALIZATION AND EXPRESSION OF BONE MORPHOGENETIC PROTEIN-2 AND PROTEIN-4 IN FRACTURE-HEALING
    BOSTROM, MPG
    LANE, JM
    BERBERIAN, WS
    MISSRI, AAE
    TOMIN, E
    WEILAND, A
    DOTY, SB
    GLASER, D
    ROSEN, VM
    [J]. JOURNAL OF ORTHOPAEDIC RESEARCH, 1995, 13 (03) : 357 - 367
  • [4] BOUXSEIN ML, 1999, T ORTHOP RES SOC
  • [5] DELLOYE C, 1988, ARCH ORTHOP TRAUM SU, V107, P31
  • [6] DELLOYE C, 1992, CLIN ORTHOP RELAT R, V282, P273
  • [7] DELLOYE C, 1991, LIMB SALVAGE MAJOR R, P9
  • [8] AUTOGENOUS CORTICAL BONE-GRAFTS IN THE RECONSTRUCTION OF SEGMENTAL SKELETAL DEFECTS
    ENNEKING, WF
    EADY, JL
    BURCHARDT, H
    [J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1980, 62 (07) : 1039 - 1058
  • [9] OBSERVATIONS ON MASSIVE RETRIEVED HUMAN ALLOGRAFTS
    ENNEKING, WF
    MINDELL, ER
    [J]. JOURNAL OF BONE AND JOINT SURGERY-AMERICAN VOLUME, 1991, 73A (08) : 1123 - 1142
  • [10] Fischgrund JS, 1997, J SPINAL DISORD, V10, P467