Chen Hsiang-Cheng, Shah Svati H, Li Yi-Ju, Stabler Thomas V, Jordan Joanne M, Kraus Virginia Byers
Duke University Medical Center, Durham, North Carolina 27710, USA.
Arthritis Rheum. 2008 Dec;58(12):3854-64. doi: 10.1002/art.24319.
Extensive joint hypermobility, lower serum cartilage oligomeric matrix protein (COMP) levels, and early-onset osteoarthritis (OA) are phenotypes of inherited pseudoachondroplasia and multiple epiphyseal dysplasia. However, few studies have evaluated the association between articular hypermobility and primary OA. We undertook the present study to evaluate this association and to test the hypothesis that COMP levels are associated with hypermobility in patients with OA and individuals without OA.
Two separate cohorts were available for analysis, the CARRIAGE (CARolinas Region Interaction of Aging Genes and Environment) extended family and a subset of the GOGO (Genetics of Generalized Osteoarthritis) sibpair cohort. In the CARRIAGE family, we performed hand and knee examinations and hypermobility evaluations (Beighton criteria) and obtained sera for measurement of COMP and hyaluronan (HA). Data on COMP and HA levels and extensive joint radiographic and hypermobility data were also available for the GOGO cohort.
The prevalence of hypermobility was 13% in the CARRIAGE family and 5% in the GOGO cohort. In the CARRIAGE family, hypermobility was associated with a significantly reduced prevalence of hand (especially proximal interphalangeal joint) and knee OA and lower mean serum COMP levels, both in the total cohort and in non-hand-OA subgroups. These results were further validated in the GOGO subsets without radiographic OA, in which hypermobility was also associated with a significantly reduced mean serum COMP level (P < 0.0001 adjusted for age). Serum HA levels did not differ in relation to hypermobility in either cohort.
The present results indicate that there is an inverse relationship between hypermobility and hand and knee OA, and that hypermobility is associated with lower serum COMP levels. Genetic variations of the COMP gene may account for some subgroups of benign joint hypermobility.
广泛的关节过度活动、较低的血清软骨寡聚基质蛋白(COMP)水平以及早发性骨关节炎(OA)是遗传性假性软骨发育不全和多发性骨骺发育不良的表型。然而,很少有研究评估关节过度活动与原发性OA之间的关联。我们进行了本研究以评估这种关联,并检验COMP水平与OA患者及非OA个体的关节过度活动相关的假设。
有两个独立的队列可供分析,即CARRIAGE(卡罗来纳州衰老基因与环境相互作用)扩展家族和GOGO(全身性骨关节炎遗传学)同胞对队列的一个子集。在CARRIAGE家族中,我们对手部和膝部进行了检查和关节过度活动评估(Beighton标准),并采集血清以测量COMP和透明质酸(HA)。GOGO队列也有关于COMP和HA水平以及广泛的关节影像学和关节过度活动数据。
CARRIAGE家族中关节过度活动的患病率为13%,GOGO队列中为5%。在CARRIAGE家族中,无论是在整个队列还是非手部OA亚组中,关节过度活动都与手部(尤其是近端指间关节)和膝部OA的患病率显著降低以及平均血清COMP水平降低相关。这些结果在无影像学OA的GOGO子集中得到进一步验证,其中关节过度活动也与平均血清COMP水平显著降低相关(年龄校正后P<0.0001)。在两个队列中,血清HA水平与关节过度活动均无差异。
目前的结果表明,关节过度活动与手部和膝部OA之间存在负相关,并且关节过度活动与较低的血清COMP水平相关。COMP基因的遗传变异可能解释了良性关节过度活动的一些亚组。