Effect of transverse tibial bone transport on expression of serum angiogenesis-related growth factors_Chinese Journal of Reparative and Reconstructive Surgery

Authors：

OU Shuanji , XU Changpeng , LI Guitao , SUN Hongtao , YANG Yang , LU Hanyu , LI Wenjun ,  QI Yong

Department of Joint Orthopaedics, Guangdong Second Provincial General Hospital, Guangzhou Guangdong, 510317, P.R.China;

Corresponding?author：

QI Yong, Email: yongqi1979@163.com

Keywords：

Transverse tibial bone transport; diabetic foot; angiogenesis-related growth factor

DOI：

10.7507/1002-1892.201906130

Video：

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Objective To investigate the effect of transverse tibial bone transport on the expression of angiogenesis-related growth factors in the serum of diabetic foot patients.Methods Between January 2018 and December 2018, 10 patients who suffered from diabetes mellitus accompanied with Wagner stage 4 diabetic foot underwent transverse tibial bone transport. There were 5 males and 5 females with an average age of 59.2 years (range, 51-70 years). The duration of diabetes was 2-60 months, with an average of 24.2 months. The duration of diabetic foot was 30-120 days, with an average of 54.1 days. Peripheral venous blood was taken at 1 day before operation and at 1, 4, 11, 18, 28, and 35 days after operation. The serum was centrifuged and subjected to ELISA test to detect the expression levels of serum vascular endothelial growth factor (VEGF), basic fibroblast growth factor (bFGF), epidermal growth factor (EGF), and platelet-derived growth factor (PDGF).Results The levels of serum VEGF, bFGF, and EGF increased rapidly at 11 days after operation, and the expression levels of the factors at 11, 18, 28, and 35 days were significantly higher than those before operation (P<0.05). The expression level of PDGF increased suddenly at 18 days after operation, and the expression level of PDGF at 18, 28, and 35 days was significantly higher than that before operation (P<0.05).Conclusion Transverse tibial bone transport for the treatment of diabetic foot can significantly increase the expression of serum angiogenesis-related growth factors in early stage, which may be the mechanism of promoting the healing of diabetic foot wounds.

Citation： OU Shuanji, XU Changpeng, LI Guitao, SUN Hongtao, YANG Yang, LU Hanyu, LI Wenjun, QI Yong. Effect of transverse tibial bone transport on expression of serum angiogenesis-related growth factors. Chinese Journal of Reparative and Reconstructive Surgery, 2020, 34(1): 98-101. doi: 10.7507/1002-1892.201906130 Copy

1.	歐栓機, 齊勇, 孫鴻濤, 等. 經皮微創脛骨截骨橫向骨搬移術治療糖尿病足. 中國矯形外科雜志, 2018, 26(15): 1385-1389.
2.	花奇凱, 秦泗河, 趙良軍, 等. Ilizarov 技術脛骨橫向骨搬移術治療糖尿病足. 中國矯形外科雜志, 2017, 25(4): 303-307.
3.	王斌, 劉偉, 霍永新, 等. 股-股動脈旁路移植聯合脛骨橫向骨搬移術治療下肢動脈硬化閉塞癥或合并糖尿病足. 中國修復重建外科雜志, 2018, 32(12): 1576-1580.
4.	鎮普祥, 陳炎, 高偉, 等. 應用 Ilizarov 技術脛骨橫向骨搬移術治療合并全身性炎癥反應綜合征的重度糖尿病足. 中國修復重建外科雜志, 2018, 32(10): 1261-1266.
5.	Brem H, Tomic-Canic M. Cellular and molecular basis of wound healing in diabetes. J Clin Invest, 2007, 117(5): 1219-1222.
6.	Tsang MW, Wong WK, Hung CS, et al. Human epidermal growth factor enhances healing of diabetic foot ulcers. Diabetes Care, 2003, 26(6): 1856-1861.
7.	Ilizarov GA. The tension-stress effect on the genesis and growth of tissues: Part Ⅱ. The influence of the rate and frequency of distraction. Clin Orthop Relat Res, 1989, (239): 263-285.
8.	Ilizarov GA. The tension-stress effect on the genesis and growth of tissues. The influence of stability of fixation and soft-tissue preservation. Clin Orthop Relat Res, 1989, (238): 249-281.
9.	Rafehi H, El-Osta A, Karagiannis TC. Epigenetic mechanisms in the pathogenesis of diabetic foot ulcers. J Diabetes Complications, 2012, 26(6): 554-561.
10.	Stefanini MO, Wu FT, Mac GF, et al. A compartment model of VEGF distribution in blood, healthy and diseased tissues. BMC Syst Biol, 2008, 2: 77.
11.	Maione AG, Brudno Y, Stojadinovic O, et al. Three-dimensional human tissue models that incorporate diabetic foot ulcer-derived fibroblasts mimic in vivo features of chronic wounds. Tissue Eng Part C Methods, 2015, 21(5): 499-508.
12.	Przybylski M. A review of the current research on the role of bFGF and VEGF in angiogenesis. J Wound Care, 2009, 18(12): 516-519.
13.	Tiaka EK, Papanas N, Manolakis AC, et al. Epidermal growth factor in the treatment of diabetic foot ulcers: an update. Perspect Vasc Surg Endovasc Ther, 2012, 24(1): 37-44.
14.	Tuyet HL, Nguyen Quynh TT, Vo Hoang Minh H, et al. The efficacy and safety of epidermal growth factor in treatment of diabetic foot ulcers: the preliminary results. Int Wound J, 2009, 6(2): 159-166.
15.	Barrientos S, Brem H, Stojadinovic O, et al. Clinical application of growth factors and cytokines in wound healing. Wound Repair Regen, 2014, 22(5): 569-578.
16.	Shah JM, Omar E, Pai DR, et al. Cellular events and biomarkers of wound healing. Indian J Plast Surg, 2012, 45(2): 220-228.
17.	Bai Y, Bai L, Zhou J, et al. Sequential delivery of VEGF, FGF-2 and PDGF from the polymeric system enhance HUVECs angiogenesis in vitro and CAM angiogenesis. Cell Immunol, 2018, 323: 19-32.
18.	Quinn TP, Schlueter M, Soifer SJ, et al. Cyclic mechanical stretch induces VEGF and FGF-2 expression in pulmonary vascular smooth muscle cells. Am J Physiol Lung Cell Mol Physiol, 2002, 282(5): L897-903.
19.	Choi SM, Lee KM, Kim HJ, et al. Effects of structurally stabilized EGF and bFGF on wound healing in type Ⅰ and type Ⅱ diabetic mice. Acta Biomater, 2018, 66: 325-334.
20.	Virakul S, Heutz JW, Dalm VA, et al. Basic FGF and PDGF-BB synergistically stimulate hyaluronan and IL-6 production by orbital fibroblasts. Mol Cell Endocrinol, 2016, 433: 94-104.

1. 歐栓機, 齊勇, 孫鴻濤, 等. 經皮微創脛骨截骨橫向骨搬移術治療糖尿病足. 中國矯形外科雜志, 2018, 26(15): 1385-1389.
2. 花奇凱, 秦泗河, 趙良軍, 等. Ilizarov 技術脛骨橫向骨搬移術治療糖尿病足. 中國矯形外科雜志, 2017, 25(4): 303-307.
3. 王斌, 劉偉, 霍永新, 等. 股-股動脈旁路移植聯合脛骨橫向骨搬移術治療下肢動脈硬化閉塞癥或合并糖尿病足. 中國修復重建外科雜志, 2018, 32(12): 1576-1580.
4. 鎮普祥, 陳炎, 高偉, 等. 應用 Ilizarov 技術脛骨橫向骨搬移術治療合并全身性炎癥反應綜合征的重度糖尿病足. 中國修復重建外科雜志, 2018, 32(10): 1261-1266.
5. Brem H, Tomic-Canic M. Cellular and molecular basis of wound healing in diabetes. J Clin Invest, 2007, 117(5): 1219-1222.
6. Tsang MW, Wong WK, Hung CS, et al. Human epidermal growth factor enhances healing of diabetic foot ulcers. Diabetes Care, 2003, 26(6): 1856-1861.
7. Ilizarov GA. The tension-stress effect on the genesis and growth of tissues: Part Ⅱ. The influence of the rate and frequency of distraction. Clin Orthop Relat Res, 1989, (239): 263-285.
8. Ilizarov GA. The tension-stress effect on the genesis and growth of tissues. The influence of stability of fixation and soft-tissue preservation. Clin Orthop Relat Res, 1989, (238): 249-281.
9. Rafehi H, El-Osta A, Karagiannis TC. Epigenetic mechanisms in the pathogenesis of diabetic foot ulcers. J Diabetes Complications, 2012, 26(6): 554-561.
10. Stefanini MO, Wu FT, Mac GF, et al. A compartment model of VEGF distribution in blood, healthy and diseased tissues. BMC Syst Biol, 2008, 2: 77.
11. Maione AG, Brudno Y, Stojadinovic O, et al. Three-dimensional human tissue models that incorporate diabetic foot ulcer-derived fibroblasts mimic in vivo features of chronic wounds. Tissue Eng Part C Methods, 2015, 21(5): 499-508.
12. Przybylski M. A review of the current research on the role of bFGF and VEGF in angiogenesis. J Wound Care, 2009, 18(12): 516-519.
13. Tiaka EK, Papanas N, Manolakis AC, et al. Epidermal growth factor in the treatment of diabetic foot ulcers: an update. Perspect Vasc Surg Endovasc Ther, 2012, 24(1): 37-44.
14. Tuyet HL, Nguyen Quynh TT, Vo Hoang Minh H, et al. The efficacy and safety of epidermal growth factor in treatment of diabetic foot ulcers: the preliminary results. Int Wound J, 2009, 6(2): 159-166.
15. Barrientos S, Brem H, Stojadinovic O, et al. Clinical application of growth factors and cytokines in wound healing. Wound Repair Regen, 2014, 22(5): 569-578.
16. Shah JM, Omar E, Pai DR, et al. Cellular events and biomarkers of wound healing. Indian J Plast Surg, 2012, 45(2): 220-228.
17. Bai Y, Bai L, Zhou J, et al. Sequential delivery of VEGF, FGF-2 and PDGF from the polymeric system enhance HUVECs angiogenesis in vitro and CAM angiogenesis. Cell Immunol, 2018, 323: 19-32.
18. Quinn TP, Schlueter M, Soifer SJ, et al. Cyclic mechanical stretch induces VEGF and FGF-2 expression in pulmonary vascular smooth muscle cells. Am J Physiol Lung Cell Mol Physiol, 2002, 282(5): L897-903.
19. Choi SM, Lee KM, Kim HJ, et al. Effects of structurally stabilized EGF and bFGF on wound healing in type Ⅰ and type Ⅱ diabetic mice. Acta Biomater, 2018, 66: 325-334.
20. Virakul S, Heutz JW, Dalm VA, et al. Basic FGF and PDGF-BB synergistically stimulate hyaluronan and IL-6 production by orbital fibroblasts. Mol Cell Endocrinol, 2016, 433: 94-104.

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