Alekseeva E I, Shakhbazian I E
Ter Arkh. 1998;70(5):37-41.
To ascertain criteria of aggressive course of juvenile rheumatoid arthritis (JRA) during 6-12 months since the disease onset, to measure the rate of destruction progression, to formulate indications for conduction of early immunosuppressive therapy.
The study included 30 patients (21 girls and 9 boys) aged 4-15 years with classic JRA. 25 children (76.2%) had systemic, 5 children--articular disease (23.8%).
50% and 20% of the examinees got the disease before they reached the age of 5 years and in puberty, respectively. Severe systemic disease in the debute was registered in 83.3% of patients, 16.7% developed primarily articular JRA. For 1 year the disease transformed into generalized and polyarticular in 43.3% and 56.7% of patients, respectively. Its activity reached the third degree in all the patients. IgG levels exceeded the age standards 1.5 times. Articular dysfunction occurred in 100% of the cases. Destruction in the joints was recorded in 37% and 92.5% of patients after 1 and 2 years of the disease, respectively.
Early or in prepuberty, puberty onset of JRA, systemic variants of the debute, debute by classical seropositive RA without systemic symptoms, fast appearance of symmetric, generalized joint lesions, recurrent course with high ESR, C-reactive protein, IgG, growing joint functional insufficiency within the first year of the disease may severe criteria of aggressive course of RA in children.
The presence of the above markers in RA patients is indication for administration of the disease-controlling drugs within the first 12 months before development of anatomic destruction and the patients' invalidation.
确定青少年类风湿关节炎(JRA)发病后6至12个月内侵袭性病程的标准,测量破坏进展速度,制定早期免疫抑制治疗的指征。
本研究纳入了30例年龄在4至15岁的经典型JRA患者(21例女孩和9例男孩)。25例儿童(76.2%)患有全身型,5例儿童患有关节型疾病(23.8%)。
分别有50%和20%的受检者在5岁之前和青春期发病。初发时严重全身型疾病在83.3%的患者中出现,16.7%主要发展为关节型JRA。1年内,分别有43.3%和56.7%的患者疾病转变为全身型和多关节型。所有患者的疾病活动度均达到三级。IgG水平超过年龄标准1.5倍。100%的病例出现关节功能障碍。疾病1年和2年后,分别有37%和92.5%的患者出现关节破坏。
JRA在早期或青春期前、青春期发病,初发为全身型,初发为无全身症状的经典血清阳性类风湿关节炎,快速出现对称性、全身性关节病变,疾病复发时血沉、C反应蛋白、IgG升高,疾病第一年关节功能不全加重,这些可能是儿童类风湿关节炎侵袭性病程的严重标准。
类风湿关节炎患者出现上述标志物,提示在解剖学破坏和患者失能发生前的12个月内给予疾病控制药物。