Pullerits Rille, d'Elia Helena Forsblad, Tarkowski Andrej, Carlsten Hans
Department of Rheumatology and Inflammation Research, University of Gothenburg, Gothenburg, Sweden.
Rheumatology (Oxford). 2009 Jul;48(7):785-90. doi: 10.1093/rheumatology/kep079. Epub 2009 May 4.
The aim of the study was to prospectively investigate the effects of HRT on serum soluble receptor for advanced glycation end product (sRAGE) levels in RA patients and to determine whether sRAGE production is related to bone/cartilage metabolism.
Eighty-eight post-menopausal RA patients were randomized to receive vitamin D3 and calcium supplementation with or without HRT (oestradiol plus noretisterone acetate). The levels of total sRAGE in sera were measured before, 1 and 2 years after treatment initiation. Potential associations between sRAGE levels, bone/cartilage metabolic markers and BMD were investigated.
Patients receiving HRT displayed significantly decreased levels of serum sRAGE at 1 and 2 years as compared with levels at study entry. The increase in serum oestradiol was associated with the decline in sRAGE levels. Importantly, sRAGE levels at baseline significantly correlated with bone/cartilage turnover markers including C-terminal propeptide of type I procollagen, carboxyterminal telopeptide of type I collagen and cartilage oligomeric matrix protein, and the decrease of sRAGE levels paralleled with diminished concentration of these molecules. BMD in hip and femoral neck and progression of Larsen score at 1 year were associated with baseline sRAGE levels. The decline in sRAGE levels significantly correlated with an increase in total BMD following 2 years of treatment in patients receiving HRT but not in the control group.
Our findings suggest that HRT decreases the levels of endogenous sRAGE in post-menopausal RA patients implicating its role in sRAGE regulation. In addition, serum sRAGE was associated with BMD and markers of bone/cartilage metabolism. These data suggest that sRAGE is involved directly or indirectly in bone metabolism. Trial registration. Current Controlled Trials, ISRCTN46523456, http://www.controlled-trials.com/isrctn/search.html?srch=ISRCTN46523456.
本研究旨在前瞻性调查激素替代疗法(HRT)对类风湿关节炎(RA)患者血清晚期糖基化终末产物可溶性受体(sRAGE)水平的影响,并确定sRAGE的产生是否与骨/软骨代谢相关。
88名绝经后RA患者被随机分为接受维生素D3和钙补充剂,同时接受或不接受HRT(雌二醇加醋酸炔诺酮)。在治疗开始前、治疗1年和2年后测量血清中总sRAGE的水平。研究sRAGE水平、骨/软骨代谢标志物和骨密度(BMD)之间的潜在关联。
与研究开始时的水平相比,接受HRT的患者在1年和2年时血清sRAGE水平显著降低。血清雌二醇的增加与sRAGE水平的下降相关。重要的是,基线时sRAGE水平与骨/软骨转换标志物显著相关,包括I型前胶原C端前肽、I型胶原羧基末端肽和软骨寡聚基质蛋白,sRAGE水平的降低与这些分子浓度的降低平行。髋部和股骨颈的骨密度以及1年时Larsen评分的进展与基线sRAGE水平相关。接受HRT的患者在治疗2年后sRAGE水平的下降与总骨密度的增加显著相关,但对照组未观察到这种相关性。
我们的研究结果表明,HRT可降低绝经后RA患者内源性sRAGE的水平,提示其在sRAGE调节中的作用。此外,血清sRAGE与骨密度和骨/软骨代谢标志物相关。这些数据表明,sRAGE直接或间接参与骨代谢。试验注册。当前对照试验,ISRCTN46523456,http://www.controlled-trials.com/isrctn/search.html?srch=ISRCTN46523456 。