Bone graft versus BMP-7 in a critical size defect -: Cranioplasty in a growing infant model

被引:61
作者
Springer, ING
Açil, Y
Kuchenbecker, S
Bolte, H
Warnke, PH
Abboud, M
Wiltfang, J
Terheyden, H
机构
[1] Univ Kiel, Dept Oral & Maxillofacial Surg, D-24105 Kiel, Germany
[2] Univ Kiel, Dept Diagnost Radiol, D-24105 Kiel, Germany
[3] Bone & Joint Res Unit, Dept Oral Surg, D-53111 Bonn, Germany
关键词
bone regeneration; BMP; bone graft; infant; cranioplasty;
D O I
10.1016/j.bone.2005.05.010
中图分类号
R5 [内科学];
学科分类号
1002 [临床医学]; 100201 [内科学];
摘要
Little data are available as regards to the action of bone morphogenetic protein-7 (rhBMP-7) in growing organisms. We put forward two hypotheses: Firstly, that regeneration of calvarial defects with autologous bone grafts would result in equivalent volume and shape as compared to calvaria regenerated with BMP-7. Secondly, that cranial development would remain undisturbed in infant individuals. A one-sided defect of the parietal bone (2 x 4 cm) including the coronal suture was generated in 2-month-old minipigs (n = 17). Group 1: no further treatment (n 5); group 2: particulated iliac bone graft (n = 6); group 3: rhBMP-7-composite (500 mu g/g collagen + Carboxymethylcellulose, n = 6). After the experimental period (4 months) with fluorochrome labeling, examination was performed by computed-tomography and non-decalcified histology. Group 1: major bony gaps remained, proving that defects of critical size were generated. Group 2: minor bony gaps remained, the bone volume was significantly reduced on the treated as compared to untreated sides (P = 0.028). Group 3: bony continuity was seen in all cases and no significant difference of bone volumes of treated versus untreated sides (P = 0.075) was found. Skull diameters increased by 16.4% but the physiological centrifugal cranial expansion remained undisturbed. Our first hypothesis was contradicted: contrary to our former assumption, bone induction by rhBMP-7 was superior to particulated bone transplants. In this growing model, calvaria approaching normal volume and shape were observed. However, only the quantity not the quality of bone regenerates was different. Our second hypothesis was confirmed: disruption of further cranial development was not seen after bone transplantation or rhBMP-7 implantation. (c) 2005 Elsevier Inc. All rights reserved.
引用
收藏
页码:563 / 569
页数:7
相关论文
共 27 条
[1]
Effects of bone morphogenetic protein-7 stimulation on osteoblasts cultured on different biomaterials [J].
Açil, Y ;
Springer, ING ;
Broek, V ;
Terheyden, H ;
Jepsen, S .
JOURNAL OF CELLULAR BIOCHEMISTRY, 2002, 86 (01) :90-98
[2]
Bone autografting of the calvaria and craniofacial skeleton: Historical background, surgical results in a series of 15 patients, and review of the literature [J].
Artico, M ;
Ferrante, L ;
Pastore, FS ;
Ramundo, EO ;
Cantarelli, D ;
Scopelliti, D ;
Iannetti, G .
SURGICAL NEUROLOGY, 2003, 60 (01) :71-79
[3]
AXHAUSEN G, 1909, LANGENBECKS ARCH KLI, V88, P23
[4]
Boyne PJ, 1997, INT J PERIODONT REST, V17, P10
[5]
Friedlaender GE, 2001, J BONE JOINT SURG AM, V83A, pS160
[6]
Osteogenic activity of OP-1 bone morphogenetic protein (BMP-7) in a human fibular defect [J].
Geesink, RGT ;
Hoefnagels, NHM ;
Bulstra, SK .
JOURNAL OF BONE AND JOINT SURGERY-BRITISH VOLUME, 1999, 81B (04) :710-718
[7]
LONG-TERM EFFECTS OF TISSUE EXPANSION ON CRANIAL AND SKELETAL BONE-DEVELOPMENT IN NEONATAL MINIATURE SWINE - CLINICAL FINDINGS AND HISTOMORPHOMETRIC CORRELATES [J].
MOELLEKEN, BRW ;
MATHES, SJ ;
CANN, CE ;
SIMMONS, DJ ;
GHAFOORI, G .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1990, 86 (05) :825-834
[8]
OP-1 CDNA ENCODES AN OSTEOGENIC PROTEIN IN THE TGF-BETA FAMILY [J].
OZKAYNAK, E ;
RUEGER, DC ;
DRIER, EA ;
CORBETT, C ;
RIDGE, RJ ;
SAMPATH, TK ;
OPPERMANN, H .
EMBO JOURNAL, 1990, 9 (07) :2085-2093
[9]
Complete regeneration of bone in the baboon by recombinant human osteogenic protein-1 (hOP-1, bone morphogenetic protein-7) [J].
Ripamonti, U ;
VandenHeever, B ;
Sampath, TK ;
Tucker, MM ;
Rueger, DC ;
Reddi, AH .
GROWTH FACTORS, 1996, 13 (3-4) :273-&
[10]
Tissue morphogenesis and regeneration by bone morphogenetic proteins [J].
Ripamonti, U ;
Duneas, N .
PLASTIC AND RECONSTRUCTIVE SURGERY, 1998, 101 (01) :227-239