Turku PET Centre, Turku University Hospital and University of Turku, Kiinamyllynkatu 4-8, 20521, Turku, Finland.
Eur J Nucl Med Mol Imaging. 2013 Feb;40(3):403-10. doi: 10.1007/s00259-012-2282-x. Epub 2012 Nov 15.
This study evaluated the potential of functional imaging to monitor disease activity and response to treatment with disease-modifying antirheumatic drugs (DMARD) in DMARD-naive patients with early rheumatoid arthritis (RA).
The study involved 17 patients with active RA in whom combination therapy was initiated with methotrexate, sulfasalazine, hydroxychloroquine, and low-dose oral prednisolone. Clinical disease activity was assessed at screening, at baseline and after 2, 4, 8 and 12 weeks of therapy. (18)F-FDG PET/CT of all joints was performed at baseline and after 2 and 4 weeks of therapy.
(18)F-FDG maximum standardized uptake values showed a reduction of 22 ± 13 % in 76 % of patients from baseline to week 2 and a reduction of 29 ± 13 % in 81 % of patients from baseline to week 4. The percentage decrease in (18)F-FDG uptake from baseline to week 2 correlated with clinical outcome, as measured by the disease activity score (DAS-28) at week 12. In addition, changes in C-reactive protein levels and erythrocyte sedimentation rate were positively associated with changes shown by PET.
(18)F-FDG PET/CT findings after 2 and 4 weeks of triple combination oral DMARD therapy correlated with treatment efficacy and clinical outcome in patients with early RA. (18)F-FDG PET/CT may help predict the therapeutic response to novel drug treatments.
本研究评估了功能成像在初诊类风湿关节炎(RA)患者中监测疾病活动度和对疾病修饰抗风湿药物(DMARD)治疗反应的潜力。
本研究纳入了 17 例活动性 RA 患者,这些患者接受了甲氨蝶呤、柳氮磺胺吡啶、羟氯喹和低剂量口服泼尼松龙联合治疗。在筛选时、基线时以及治疗 2、4、8 和 12 周时评估临床疾病活动度。在基线时和治疗 2 周和 4 周时对所有关节进行(18)F-FDG PET/CT 检查。
(18)F-FDG 最大标准化摄取值在基线至第 2 周时,76%的患者降低了 22±13%,在基线至第 4 周时,81%的患者降低了 29±13%。(18)F-FDG 摄取量从基线到第 2 周的百分比下降与第 12 周时的疾病活动评分(DAS-28)的临床结果相关。此外,C 反应蛋白水平和红细胞沉降率的变化与 PET 所示的变化呈正相关。
在接受三联口服 DMARD 治疗 2 周和 4 周后,(18)F-FDG PET/CT 结果与早期 RA 患者的治疗效果和临床结果相关。(18)F-FDG PET/CT 可能有助于预测新型药物治疗的反应。