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小动物研究中系统性受损的骨折愈合:骨折修复模型的综述。

Systemically impaired fracture healing in small animal research: A review of fracture repair models.

机构信息

Keenan Research Centre for Biomedical Science, St. Michael's Hospital - Unity Health Toronto, University of Toronto, Toronto, Ontario, Canada.

Department of Surgery, Division of Orthopaedic Surgery, University of Western Ontario, London, Ontario, Canada.

出版信息

J Orthop Res. 2021 Jul;39(7):1359-1367. doi: 10.1002/jor.25003. Epub 2021 Feb 24.

DOI:10.1002/jor.25003
PMID:33580554
Abstract

Fracture healing is a complex process requiring mechanical stability, an osteoconductive matrix, and osteoinductive and osteogenic biology. This intricate process is easily disrupted by various patient factors such as chronic disease and lifestyle. As the medical complexity and age of patients with fractures continue to increase, the importance of developing relevant experimental models is becoming paramount in preclinical research. The objective of this review is to describe the most common small animal models of systemically impaired fracture healing used in the orthopedic literature including osteoporosis, diabetes mellitus, smoking, alcohol use, obesity, and ageing. This review will provide orthopedic researchers with a summary of current models of systemically impaired fracture healing used in small animals and present an overview of the methods of induction for each condition.

摘要

骨折愈合是一个复杂的过程,需要机械稳定性、骨传导基质以及成骨和诱导生物学。这个复杂的过程很容易被各种患者因素破坏,如慢性病和生活方式。随着骨折患者的医疗复杂性和年龄不断增加,开发相关实验模型在临床前研究中变得至关重要。本综述的目的是描述骨科文献中常用的系统受损骨折愈合的常见小动物模型,包括骨质疏松症、糖尿病、吸烟、饮酒、肥胖和衰老。本综述将为骨科研究人员提供一个总结目前用于小动物的系统受损骨折愈合模型,并概述每种情况下的诱导方法。

相似文献

1
Systemically impaired fracture healing in small animal research: A review of fracture repair models.小动物研究中系统性受损的骨折愈合:骨折修复模型的综述。
J Orthop Res. 2021 Jul;39(7):1359-1367. doi: 10.1002/jor.25003. Epub 2021 Feb 24.
2
Smoking and alcohol drinking and risk of non-union or delayed union after fractures: A protocol for systematic review and dose-response meta-analysis.吸烟、饮酒与骨折后骨不连或延迟愈合的风险:一项系统评价与剂量反应荟萃分析方案
Medicine (Baltimore). 2020 Jan;99(5):e18744. doi: 10.1097/MD.0000000000018744.
3
Recent developments in the biology of fracture repair.骨折修复生物学的最新进展。
J Am Acad Orthop Surg. 2008 Nov;16(11):619-25. doi: 10.5435/00124635-200811000-00001.
4
The Pathobiology of Diabetes Mellitus in Bone Metabolism, Fracture Healing, and Complications.糖尿病在骨代谢、骨折愈合及并发症中的病理生物学
Am J Orthop (Belle Mead NJ). 2015 Oct;44(10):453-7.
5
[The Biological Knife I--Fracture Healing and Patient-Dependent Influencing Factors].[生物手术刀I——骨折愈合及患者相关影响因素]
Z Orthop Unfall. 2015 Aug;153(4):433-40. doi: 10.1055/s-0035-1546139. Epub 2015 Jun 29.
6
Fracture healing in osteoporotic bone.骨质疏松性骨的骨折愈合
Injury. 2016 Jun;47 Suppl 2:S21-6. doi: 10.1016/S0020-1383(16)47004-X.
7
Bicortical fixation of medial malleolar fractures: a review of 23 cases at risk for complicated bone healing.内踝骨折的双皮质固定:23例有复杂骨愈合风险病例的回顾
J Foot Ankle Surg. 2012 Jan-Feb;51(1):39-44. doi: 10.1053/j.jfas.2011.09.007.
8
Cigarette smoking increases complications following fracture: a systematic review.吸烟增加骨折后的并发症:系统评价。
J Bone Joint Surg Am. 2014 Apr 16;96(8):674-81. doi: 10.2106/JBJS.M.00081.
9
Animal models for fracture treatment in osteoporosis.骨质疏松症骨折治疗的动物模型
Osteoporos Int. 2005 Mar;16 Suppl 2:S129-38. doi: 10.1007/s00198-005-1859-7. Epub 2005 Mar 5.
10
The challenges of promoting osteogenesis in segmental bone defects and osteoporosis.促进节段性骨缺损和成骨不全症中骨生成的挑战。 (注:原文中osteoporosis一般指骨质疏松症,这里可能是osteogenesis imperfecta的误写,按照正确的osteogenesis imperfecta翻译为成骨不全症,如果原文无误则按照骨质疏松症翻译,译文可改为:促进节段性骨缺损和骨质疏松症中骨生成的挑战。)
J Orthop Res. 2018 Jun;36(6):1559-1572. doi: 10.1002/jor.23845. Epub 2018 Mar 6.

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Machine-learning-based approach for nonunion prediction following osteoporotic vertebral fractures.
基于机器学习的骨质疏松性椎体骨折后不愈合预测方法。
Eur Spine J. 2023 Nov;32(11):3788-3796. doi: 10.1007/s00586-022-07431-4. Epub 2022 Oct 21.
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Pulsed Electro-Magnetic Field (PEMF) Effect on Bone Healing in Animal Models: A Review of Its Efficacy Related to Different Type of Damage.脉冲电磁场(PEMF)对动物模型骨愈合的影响:关于其与不同类型损伤相关疗效的综述
Biology (Basel). 2022 Mar 5;11(3):402. doi: 10.3390/biology11030402.