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类风湿因子阳性与接受甲氨蝶呤治疗的类风湿关节炎患者关节破坏增加以及外周血中基质金属蛋白酶9和组织蛋白酶K基因表达上调有关。

Rheumatoid factor positivity is associated with increased joint destruction and upregulation of matrix metalloproteinase 9 and cathepsin k gene expression in the peripheral blood in rheumatoid arthritic patients treated with methotrexate.

作者信息

Tchetina Elena V, Demidova Natalia V, Karateev Dmitry E, Nasonov Eugeny L

机构信息

Clinical Immunology Department, Nasonova Research Institute of Rheumatology, Russian Academy of Medical Sciences, Kashirskoye Shosse 34A, Moscow 115522, Russia.

Early Rheumatoid Arthritis Department, Nasonova Research Institute of Rheumatology, Russian Academy of Medical Sciences, Moscow 115522, Russia.

出版信息

Int J Rheumatol. 2013;2013:457876. doi: 10.1155/2013/457876. Epub 2013 Nov 14.

Abstract

We evaluated changes in gene expression of mTOR, p21, caspase-3, ULK1, TNF α , matrix metalloproteinase (MMP)-9, and cathepsin K in the whole blood of rheumatoid arthritic (RA) patients treated with methotrexate (MTX) in relation to their rheumatoid factor status, clinical, immunological, and radiological parameters, and therapeutic response after a 24-month follow-up. The study group consisted of 35 control subjects and 33 RA patients without previous history of MTX treatment. Gene expression was measured using real-time RT-PCR. Decreased disease activity in patients at the end of the study was associated with significant downregulation of TNF α expression. Downregulation of mTOR was observed in seronegative patients, while no significant changes in the expression of p21, ULK1, or caspase-3 were noted in any RA patients at the end of the study. The increase in erosion numbers observed in the seropositive patients at the end of the follow-up was accompanied by upregulation of MMP-9 and cathepsin K, while seronegative patients demonstrated an absence of significant changes in MMP-9 and cathepsin K expression and no increase in the erosion score. Our results suggest that increased expression of MMP-9 and cathepsin K genes in the peripheral blood might indicate higher bone tissue destruction activity in RA patients treated with methotrexate. The clinical study registration number is 0120.0810610.

摘要

我们评估了甲氨蝶呤(MTX)治疗的类风湿性关节炎(RA)患者全血中mTOR、p21、caspase-3、ULK1、TNFα、基质金属蛋白酶(MMP)-9和组织蛋白酶K的基因表达变化,这些变化与患者的类风湿因子状态、临床、免疫学和放射学参数以及24个月随访后的治疗反应相关。研究组由35名对照受试者和33名无MTX治疗史的RA患者组成。使用实时RT-PCR测量基因表达。研究结束时患者疾病活动度降低与TNFα表达显著下调相关。在血清阴性患者中观察到mTOR下调,而在研究结束时,任何RA患者的p21、ULK1或caspase-3表达均未发现显著变化。随访结束时血清阳性患者中观察到的侵蚀数量增加伴随着MMP-9和组织蛋白酶K的上调,而血清阴性患者的MMP-9和组织蛋白酶K表达无显著变化,侵蚀评分也未增加。我们的结果表明,外周血中MMP-9和组织蛋白酶K基因表达增加可能表明接受甲氨蝶呤治疗的RA患者骨组织破坏活性更高。临床研究注册号为0120.0810610。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f5ee/3848347/32a5accfa917/IJR2013-457876.001.jpg

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