Department of Clinical Immunology and Rheumatology, Sanjay Gandhi Postgraduate Institute of Medical Sciences (SGPGIMS), Rae Bareli Road, Lucknow, Uttar Pradesh, 226014, India.
Rheumatol Int. 2019 Aug;39(8):1431-1438. doi: 10.1007/s00296-019-04344-2. Epub 2019 Jun 15.
Methotrexate (MTX) reduces inflammation by increasing extracellular adenosine levels in rheumatoid arthritis (RA) patients. Adenosine acts via G-protein coupled receptors; ADORA1, ADORA2a, ADORA2b and ADORA3. We studied if baseline expression of whole blood adenosine receptors can predict response to MTX. RA patients [American College of Rheumatology/European-League-Against-Rheumatism (EULAR) 2010 criteria], Disease modifying anti-rheumatic drug (DMARD) naïve with active disease [Disease Activity Score 28 (DAS28) > 3.2] were enrolled. Blood samples were collected at baseline (n = 100) and at 4 months after therapy (n = 50). Patients were treated with MTX monotherapy. Based on EULAR response, patients were categorized into three groups i.e. good, moderate and non-responders. Adenosine receptors gene expression (ADORA1, ADORA2a, ADORA2b and ADORA3) in whole-blood RNA was measured using real-time PCR. HPRT1 was used as housekeeping gene. Receptor expression at baseline was correlated with response to MTX. All values are expressed as median (interquartile range). Hundred patients [87% females; age 40 (18) years]; duration of disease 24 (24.75) months; DAS28 4.7 (1.25) were enrolled. Fifty-one were classified as good, 28 moderate and 21 as non-responders. No expression of ADORA1 and ADORA2b was detected. Significant difference was observed in the expression levels of ADORA3 between good vs non-responder (P = 0.03) and moderate vs non-responder (P = 0.002). On ROC curve analysis, ADORA3 with cut-off value of less than - 0.60 (ΔCt) predicted non-response to MTX treatment (AUC: 0.7, P = 0.006). ADORA3 mRNA levels in whole blood may serve as a biomarker of response to MTX.
甲氨蝶呤(MTX)通过增加类风湿关节炎(RA)患者细胞外腺苷水平来减轻炎症。腺苷通过 G 蛋白偶联受体起作用;ADORA1、ADORA2a、ADORA2b 和 ADORA3。我们研究了全血腺苷受体的基线表达是否可以预测对 MTX 的反应。招募了符合美国风湿病学会/欧洲抗风湿病联盟(EULAR)2010 标准的 RA 患者(DMARD 初治且疾病活跃[DAS28>3.2])。在基线(n=100)和治疗后 4 个月(n=50)采集血样。患者接受 MTX 单药治疗。根据 EULAR 反应,患者分为三组,即良好、中度和无反应者。使用实时 PCR 测量全血 RNA 中的腺苷受体基因表达(ADORA1、ADORA2a、ADORA2b 和 ADORA3)。HPRT1 用作管家基因。基线时的受体表达与 MTX 反应相关。所有值均表示为中位数(四分位距)。100 名患者[87%为女性;年龄 40(18)岁];疾病持续时间 24(24.75)个月;DAS28 4.7(1.25)。51 例被归类为良好,28 例为中度,21 例为无反应。未检测到 ADORA1 和 ADORA2b 的表达。在 ADORA3 的表达水平方面,良好与无反应者之间存在显著差异(P=0.03),中度与无反应者之间也存在显著差异(P=0.002)。在 ROC 曲线分析中,ADORA3 的截断值小于-0.60(ΔCt)可预测 MTX 治疗无反应(AUC:0.7,P=0.006)。全血 ADORA3 mRNA 水平可作为 MTX 反应的生物标志物。