The influence of low molecular weight heparin on the expression of osteogenic growth factors in human fracture healing

被引:4
作者
Sarahrudi, Kambiz [1 ]
Kaiser, Georg [1 ]
Thomas, Anita [2 ]
Michel, Mark [1 ]
Wolf, Harald [1 ]
Mousavi, Mehdi [3 ]
Aharinejad, Seyedhossein [2 ]
机构
[1] Med Univ Vienna, Dept Traumatol, Vienna, Austria
[2] Med Univ Vienna, Ctr Anat & Cell Biol, Lab Cardiovasc Res, Vienna, Austria
[3] Danube Hosp Vienna, Dept Traumatol & Sporttraumatol, Vienna, Austria
关键词
IN-VITRO; UNFRACTIONATED HEPARIN; HUMAN OSTEOBLASTS; RAT; ANGIOGENESIS; DALTEPARIN; REPAIR; CELLS; MODEL;
D O I
10.1007/s00264-011-1392-6
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
Anticoagulant therapy with low molecular weight heparins (LMWH) and mechanical compression is considered the gold standard for the prevention of thrombosis. However, evidence exists that LMWHs impair bone metabolism. The aim of this study was therefore to analyse alterations in the expression of M-CSF, VEGF and TGF-1 after treatment with enoxaparin in patients with long bone fracture to investigate the effect of LMWH on human fracture healing. A total of 81 patients with long bone fractures were included in the study and divided into two groups. One group comprised patients who received enoxaparin and the other group, patients who did not receive enoxaparin postoperatively. Growth factor levels were analysed in patients' serum and different groups were retrospectively compared. M-CSF serum concentrations were found to be significantly higher only at 48 weeks after surgery in enoxaparin. Mean overall VEGF serum concentration was higher in patients with enoxaparin. TGF-beta 1 serum concentrations were higher at 48 weeks after surgery in patients with enoxaparin. This is the first comparative systemic measurement of M-CSF, VEGF and TGF-1 serum levels in patients with and without enoxaparin after long bone fracture. Significant differences of the expression of the growth factors after enoxaparin therapy were only observed at week 48 after surgery for M-CSF and TGF-1.
引用
收藏
页码:1095 / 1098
页数:4
相关论文
共 26 条
  • [1] INDOMETHACIN AND ASPIRIN - EFFECT OF NON-STEROIDAL ANTI-INFLAMMATORY AGENTS ON THE RATE OF FRACTURE REPAIR IN THE RAT
    ALLEN, HL
    WASE, A
    BEAR, WT
    [J]. ACTA ORTHOPAEDICA SCANDINAVICA, 1980, 51 (04): : 595 - 600
  • [2] The heparins and cancer: review of clinical trials and biological properties
    Castelli, R
    Porro, F
    Tarsia, P
    [J]. VASCULAR MEDICINE, 2004, 9 (03) : 205 - 213
  • [3] EFFECTS ON FRACTURE-HEALING OF AN ANTAGONIST OF THE VITAMIN-K CYCLE
    DODDS, RA
    CATTERALL, A
    BITENSKY, L
    CHAYEN, J
    [J]. CALCIFIED TISSUE INTERNATIONAL, 1984, 36 (02) : 233 - 238
  • [4] Effects of heparin and low-molecular-weight heparins on bone mechanical properties in rats
    Folwarczna, J
    Janiec, W
    Sliwinski, L
    [J]. THROMBOSIS AND HAEMOSTASIS, 2004, 92 (05) : 940 - 946
  • [5] VEGF couples hypertrophic cartilage remodeling, ossification and angiogenesis during endochondral bone formation
    Gerber, HP
    Vu, TH
    Ryan, AM
    Kowalski, J
    Werb, Z
    Ferrara, N
    [J]. NATURE MEDICINE, 1999, 5 (06) : 623 - 628
  • [6] Hach W, 2002, PHLEBOLOGIE, V31, P56
  • [7] Effect of low molecular weight heparin on fracture healing in a stabilized rat femur fracture model
    Hak, DJ
    Stewart, RL
    Hazelwood, SJ
    [J]. JOURNAL OF ORTHOPAEDIC RESEARCH, 2006, 24 (04) : 645 - 652
  • [8] Effect of low molecular weight heparin (dalteparin) and fondaparinux (Arixtra®) on human osteoblasts in vitro
    Handschin, AE
    Trentz, OA
    Hoerstrup, SP
    Kock, HJ
    Wanner, GA
    Trentz, O
    [J]. BRITISH JOURNAL OF SURGERY, 2005, 92 (02) : 177 - 183
  • [9] Heparin effect on osteoblast-like cells in vitro
    Handschin, AE
    Wanner, GA
    Trentz, OA
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 2004, 93 (01) : 1 - 1
  • [10] Low doses and high doses of heparin have different effects on osteoblast-like Saos-2 cells in vitro
    Hausser, HJ
    Brenner, RE
    [J]. JOURNAL OF CELLULAR BIOCHEMISTRY, 2004, 91 (05) : 1062 - 1073