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联合使用三种口服抗风湿药物治疗早期类风湿关节炎患者后,18F-FDG PET/CT 评估与疾病活动度和炎症标志物的相关性。

Correlation of 18F-FDG PET/CT assessments with disease activity and markers of inflammation in patients with early rheumatoid arthritis following the initiation of combination therapy with triple oral antirheumatic drugs.

机构信息

Turku PET Centre, Turku University Hospital and University of Turku, Kiinamyllynkatu 4-8, 20521, Turku, Finland.

出版信息

Eur J Nucl Med Mol Imaging. 2013 Feb;40(3):403-10. doi: 10.1007/s00259-012-2282-x. Epub 2012 Nov 15.

Abstract

PURPOSE

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).

METHODS

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.

RESULTS

(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.

CONCLUSION

(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.

摘要

目的

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。

方法

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。

结果

(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。

结论

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。

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