Frisbie D D, Al-Sobayil F, Billinghurst R C, Kawcak C E, McIlwraith C W
Orthopaedic Research Center, Colorado State University, 300 West Drake, Fort Collins, CO 80523, United States.
Osteoarthritis Cartilage. 2008 Oct;16(10):1196-204. doi: 10.1016/j.joca.2008.03.008. Epub 2008 Apr 28.
To discriminate between changes in biomarkers with exercise compared to changes in biomarkers with osteoarthritis (OA) in exercising horses.
Sixteen, 2-year-old horses were randomly assigned either to an exercise-alone (n=8) or OA-affected (also exercised) (n=8) group. All horses had both mid-carpal joints arthroscoped and OA induced in one mid-carpal joint in the OA-affected joints of OA-affected horses. Two weeks after surgery all horses commenced a strenuous exercise program on a high-speed treadmill. Clinical outcomes and synovial fluid and serum biomarkers, were evaluated weekly. Synovial and serum biomarkers evaluated were epitope CS846 (CS846), epitope CPII (CPII), glycosaminoglycans (GAGs), epitope Col CEQ (Col CEQ) (a marker of type II collagen degradation), type I and II collagen degradation fragments (C1,2C), osteocalcin, C-terminal of bone type I collagen (CTX1), type I collagen (Col I) and (synovial fluid only of cartilage) prostaglandin E2 (PGE2) levels. Horses were euthanized at day 91 and their joints assessed grossly, histopathologically, and histochemically.
Exercise induced a significant increase in synovial fluid CS846, CPII, GAG, Col CEQ, C1,2C, osteocalcin and Col I concentrations. There was a significant increase in synovial fluid CS846, CPII, Col CEQ, C1,2C, osteocalcin, Col I and PGE2 concentrations in OA-affected joints compared to exercise-alone joints. The concentration of serum CS846, CPII, GAG, osteocalcin, C1,2C and Col I increased with exercise. For each of these biomarkers there was also a statistically significant increase in serum biomarker levels in OA-affected horses compared to exercise-alone horses.
Six synovial fluid and serum biomarkers were useful in separating early experimental OA from exercise alone but synovial fluid CTX1 and serum Col CEQ and CTX1 were not.
区分运动马体内生物标志物的变化与骨关节炎(OA)马体内生物标志物的变化。
16匹2岁马被随机分为单纯运动组(n = 8)和OA患病(也运动)组(n = 8)。所有马匹均接受腕中关节关节镜检查,并在OA患病马的OA患病关节中的一个腕中关节诱导产生OA。术后两周,所有马匹开始在高速跑步机上进行高强度运动计划。每周评估临床结果以及滑液和血清生物标志物。评估的滑液和血清生物标志物包括表位CS846(CS846)、表位CPII(CPII)、糖胺聚糖(GAGs)、表位Col CEQ(Col CEQ)(II型胶原降解标志物)、I型和II型胶原降解片段(C1,2C)、骨钙素、骨I型胶原C端(CTX1)、I型胶原(Col I)以及(仅滑液中的软骨)前列腺素E2(PGE2)水平。在第91天对马匹实施安乐死,并对其关节进行大体、组织病理学和组织化学评估。
运动导致滑液中CS846、CPII、GAG、Col CEQ、C1,2C、骨钙素和Col I浓度显著增加。与单纯运动关节相比,OA患病关节中滑液CS846、CPII、Col CEQ、C1,2C、骨钙素、Col I和PGE2浓度显著增加。血清CS846、CPII、GAG、骨钙素、C1,2C和Col I浓度随运动增加。与单纯运动的马相比,OA患病马的这些生物标志物血清水平也有统计学意义的显著增加。
六种滑液和血清生物标志物有助于区分早期实验性OA与单纯运动,但滑液CTX1以及血清Col CEQ和CTX1则无此作用。