Świerkot Jerzy, Gruszecka Katarzyna, Matuszewska Agnieszka, Wiland Piotr
Department of Rheumatology and Internal Medicine, Wroclaw Medical University, Wrocław, Poland.
Department of Pharmacology, Wroclaw Medical University, Wrocław, Poland.
Arch Immunol Ther Exp (Warsz). 2015 Oct;63(5):397-404. doi: 10.1007/s00005-015-0338-x. Epub 2015 Apr 3.
Proinflammatory cytokines and growth factors, which regulate mutual interactions between immune system cells and bone tissue cells, play a major role in the formation of bone changes in rheumatoid arthritis (RA). The aim of the work was to assess serum concentration of osteoprotegerin (OPG), RANKL, Dkk-1 and sclerostin in RA patients compared to a control group and to analyze changes of these concentrations during methotrexate (MTX) therapy. Patients enrolled in the study were 30 women of Caucasian origin aged 30-74 years with RA. Patients with active form of the disease were administered recommended doses of MTX for at least 6 months. The study group was divided into subgroup I-patients with improvement; and subgroup II-patients with no improvement. The control group consisted of 12 healthy women in the age of 41-73. Before MTX therapy, RA patients had higher levels of RANKL (644.97 ± 477.13 vs. 255.19 ± 130.26 pmol/l), lower values of OPG/RANKL (0.01 ± 0.0101 vs. 0.02 ± 0.0078) and higher levels of Dkk-1 protein (1821.32 ± 1060.28 vs. 548.52 ± 36.35 pg/ml) compared to the control group. In the analyzed group of patients (all patients receiving MTX regardless of responder non responder status) after 6 months of therapy, a statistically significant increase in the ratio of OPG/RANKL was found (0.0118 ± 0.0102 vs. 0.0141 ± 0.0118; p = 0.02). The index value of OPG/RANKL differed significantly depending on the resultant effect of treatment (0.01702 ± 0.01274 in the subgroup of improvement vs. 0.00675 ± 0.00289 in the subgroup without improvement). The difference in the mean concentrations of Dkk-1 before and after treatment with MTX between subgroups I and II was statistically significant (p = 0.002). In subgroup I, mean concentration of Dkk-1 decreased after 6 months of treatment with MTX (2054.72 ± 1004.74 vs. 1831.70 ± 851.70 pg/ml); while in subgroup II, the mean concentration of Dkk-1 increased (1214.48 ± 738.32 vs. 2275.01 ± 1385.23 pg/ml). There were no statistically significant changes in the mean concentrations of sclerostin before and after treatment with MTX (in whole group treatment with MTX, in subgroup I, and in subgroup II). The results confirm the presence of disorders of bone metabolism in patients with RA. Treatment with MTX affects the value of the ratio of OPG/RANKL and concentration of Dkk-1.
促炎细胞因子和生长因子调节免疫系统细胞与骨组织细胞之间的相互作用,在类风湿关节炎(RA)的骨改变形成中起主要作用。本研究的目的是评估与对照组相比,RA患者血清骨保护素(OPG)、核因子κB受体活化因子配体(RANKL)、 Dickkopf-1(Dkk-1)和硬化蛋白的浓度,并分析甲氨蝶呤(MTX)治疗期间这些浓度的变化。纳入研究的患者为30名年龄在30 - 74岁的白种女性RA患者。疾病处于活动期的患者接受推荐剂量的MTX治疗至少6个月。研究组分为亚组I(病情改善的患者)和亚组II(病情未改善的患者)。对照组由12名年龄在41 - 73岁的健康女性组成。在MTX治疗前,RA患者的RANKL水平较高(644.97±477.13 vs. 255.19±130.26 pmol/L),OPG/RANKL值较低(0.01±0.0101 vs. 0.02±0.0078),Dkk-1蛋白水平较高(1821.32±1060.28 vs. 548.52±36.35 pg/mL),与对照组相比差异有统计学意义。在分析的患者组(所有接受MTX治疗的患者,无论是否有反应)治疗6个月后,发现OPG/RANKL比值有统计学意义的升高(0.0118±0.0102 vs. 0.0141±0.0118;p = 0.02)。OPG/RANKL的指数值因治疗结果不同而有显著差异(改善亚组为0.01702±0.01274,未改善亚组为0.00675±0.00289)。亚组I和亚组II在MTX治疗前后Dkk-1平均浓度的差异有统计学意义(p = 0.002)。在亚组I中,MTX治疗6个月后Dkk-1的平均浓度降低(2054.72±1004.74 vs. 1831.70±851.70 pg/mL);而在亚组II中,Dkk-1的平均浓度升高(1214.48±738.3