Pattrick M, Manhire A, Ward A M, Doherty M
Rheumatology Unit, City Hospital, Nottingham.
Ann Rheum Dis. 1989 Jun;48(6):470-5. doi: 10.1136/ard.48.6.470.
HLA-A, B and alpha 1-antitrypsin phenotypes were studied in 90 unrelated patients with established nodal generalised osteoarthritis (OA). Compared with standard reference populations, independently increased frequency of the HLA-A1B8 and MZ alpha 1-antitrypsin phenotypes were observed (27% v 11.5%, relative risk 2.79, and 12% v 3.6%, relative risk 3.73 respectively). These associations related to developed of nodal generalised OA rather than to severity as judged by the summated radiographic scores for hand OA. Ten patients had marked subchondral radiographic erosions and were further classified as erosive OA; these patients had an increased frequency of the MS alpha 1-antitrypsin phenotype (30% v 9%) and higher radiographic OA scores corrected for presence of erosions. This first report of two independent genetic markers in nodal generalised OA is of interest in relation to the increasingly recognised inflammatory component of the osteoarthritis process.
对90例确诊为结节性全身性骨关节炎(OA)的非亲属患者进行了HLA - A、B和α1 - 抗胰蛋白酶表型研究。与标准参考人群相比,观察到HLA - A1B8和MZα1 - 抗胰蛋白酶表型频率独立增加(分别为27%对11.5%,相对风险2.79;以及12%对3.6%,相对风险3.73)。这些关联与结节性全身性OA的发生有关,而非与手部OA的综合放射学评分所判断的严重程度有关。10例患者有明显的软骨下放射学侵蚀,被进一步分类为侵蚀性OA;这些患者MSα1 - 抗胰蛋白酶表型频率增加(30%对9%),且校正侵蚀存在后的放射学OA评分更高。结节性全身性OA中两个独立遗传标志物的这一首次报告,对于骨关节炎进程中日益被认识到的炎症成分而言具有重要意义。