OC的病因、诊断和治疗(D)

P. René van Weeren DVM, PhD, Dipl ECVS
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引用次数: 67

摘要

骨性软骨病(OC)可以定义为关节-骨骺复合体软骨内成骨过程的紊乱。骨化前缘的不规则性导致厚厚的软骨塞,其较深的部分可能因为扩散的营养不足而坏死。在最后阶段,骨软骨碎片可能分离,成为疏松或半疏松的关节内体或关节小鼠。在这个阶段,使用术语骨软骨炎夹层。骨软骨病在大多数温血犬种和赛马场中发病率很高(平均为25%)。性能并不总是受到影响,但马业的损失是巨大的,直接和间接地通过失去育种潜力和受影响动物的市场价值贬值。骨软骨病是一种多因素疾病,其中遗传影响(约占表型的25%)、营养因素、生物力学影响和构象起作用。在生命的最初几个月,这种疾病是非常动态的,此时病变可能自发出现和消退,这表明OC具有二重性,其中最终的临床结果由上述病因和病变引发的修复过程决定。随着年龄的增长,软骨细胞外基质的重塑率降低,在一定年龄后,病变的影像学表现不再有实质性变化。一般来说,1岁以后不会有大的变化。出于这个原因,建议不要在这个年龄之前应用关节镜手术的治疗选择。OC的诊断一直是基于临床和影像学表现,但更先进的成像技术,如磁共振成像和生物标志物的使用可能在未来发挥更重要的作用。生物标记物也可用于预防,以识别有发展OC风险的动物。对这些动物来说,环境条件可以加以控制,以最大限度地降低患OC的风险。遗传标记也可能成为一种工具,但由于OC的复杂特性和环境因素的较大影响,使这一领域难以取得真正的突破。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Etiology, Diagnosis, and Treatment of OC(D)

Osteochondrosis (OC) can be defined as a disturbance of the process of endochondral ossification of the articular-epiphyseal complex. The ensuing irregularities of the ossification front lead to thick cartilage plugs, the deeper parts of which may become necrotic because nutrition by diffusion becomes insufficient. In the final stage osteochondral fragments may detach and become loose or semiloose intraarticular bodies or joint mice. In this stage, the term osteochondritis dissecans is used. Osteochondrosis has a high incidence (on average 25%) in most Warmblood breeds and in the racing breeds. Performance is not always affected, but losses to the equine industry are huge, both directly and indirectly through loss of breeding potential and depreciation of market value of affected animals. Osteochondrosis is a multifactorial disease in which genetic influences (accounting for about 25% of the phenotype), nutritional factors, biomechanical influences, and conformation play a role. The disease is very dynamic during the first months of life when lesions may appear and regress spontaneously, indicating that OC has a dualistic character in which the final clinical outcome is determined by the etiologic factors mentioned above and a repair process incited by the lesions. With increasing age, the remodeling rate of the extracellular matrix of the cartilage decreases and after a certain age no substantial change in the radiographic appearance of lesions is seen anymore. In general, no major change can be expected after 1 year of age. For this reason it is advised not to apply the treatment of choice, which is arthroscopic surgery, before this age. Diagnosis of OC has always been based on clinical and radiographic findings, but more advanced imaging techniques, such as magnetic resonance imaging, and the use of biomarkers may play a more important role in the future. Biomarkers may also be used for prevention to identify animals that are at risk for the development of OC. For these animals, environmental conditions may then be manipulated to maximally reduce the risk of OC. Genetic markers may become a tool too, but the complex character of OC and the relatively big influence of environmental factors make a real breakthrough in this area improbable.

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