Gladman D D, Farewell V T
University of Toronto, Ontario, Canada.
Arthritis Rheum. 1995 Jun;38(6):845-50. doi: 10.1002/art.1780380619.
To identify HLA markers for the development of severe disease in psoriatic arthritis (PsA).
Patients with PsA who were followed up prospectively over a 14-year period were included. Clinical and laboratory assessments of both active inflammation and clinical damage were performed at 6-month intervals according to a standard protocol, which also included serologic HLA typing for class I and II antigens. Progression of damage was defined as transition into higher damage states, defined by the number of damaged joints. Both univariate and multivariate models were developed to identify predictors for progression of damage.
Univariate analysis revealed that the HLA antigens B27, B39, and DQw3 were associated with disease progression, while HLA-DR7 was "protective." The best multivariate model identified the HLA antigens B27, when DR7 was present, and DQw3, when DR7 was not present, as predicting disease progression across all transitions, while HLA-B39 was associated with progression in early disease. The addition of these HLA indicators to a model containing clinical variables resulted in a significant improvement in fit.
The HLA antigens associated with PsA, B27 and B39, are risk factors for disease progression, as is the HLA class II antigen DQw3. In combination with clinical measures of disease, these HLA variables are the dominant predictors of progression.
确定与银屑病关节炎(PsA)严重疾病发展相关的人类白细胞抗原(HLA)标志物。
纳入在14年期间进行前瞻性随访的PsA患者。按照标准方案每6个月进行一次关于活动性炎症和临床损伤的临床及实验室评估,其中还包括对I类和II类抗原进行血清学HLA分型。损伤进展定义为转变为更高的损伤状态,根据受损关节数量来界定。构建单变量和多变量模型以确定损伤进展的预测因素。
单变量分析显示,HLA抗原B27、B39和DQw3与疾病进展相关,而HLA-DR7具有“保护作用”。最佳多变量模型确定,当存在DR7时,HLA抗原B27以及当不存在DR7时HLA抗原DQw3可预测所有转变阶段的疾病进展,而HLA-B39与早期疾病进展相关。将这些HLA指标添加到包含临床变量的模型中,拟合度有显著改善。
与PsA相关的HLA抗原B27和B39以及HLA II类抗原DQw3是疾病进展的危险因素。与疾病的临床指标相结合,这些HLA变量是进展的主要预测因素。