Epidemiology, Genetics and Atherosclerosis Research Group on Systemic Inflammatory Diseases, Rheumatology Division, IFIMAV, Santander, Spain.
Clin Exp Rheumatol. 2014 Mar-Apr;32(2):218-24. Epub 2013 Dec 16.
To determine whether circulating gelsolin (GSN) levels in patients with ankylosing spondylitis (AS) undergoing TNF-α antagonist-infliximab-therapy are altered compared with controls and to establish whether disease activity, systemic inflammation and metabolic syndrome are potential determinants of circulating GSN levels in these patients.
We assessed GSN serum concentrations in a series of 30 non-diabetic AS patients without cardiovascular (CV) disease undergoing TNF-α antagonist-infliximab therapy and 48 matched controls. GSN levels were measured immediately before and after an infliximab infusion. Correlations of GSN serum levels with disease activity, systemic inflammation and metabolic syndrome were assessed. Potential changes in GSN concentration following an infusion of anti-TNF-α monoclonal antibody-infliximab were also analysed.
Although at the time of the study AS patients undergoing anti-TNF-α therapy had adequate control of the disease (mean BASDAI 2.94), they showed lower GSN serum levels than healthy controls (mean±SD: 38660.42±23624.6 ng/ml versus 68975.43±31246.79 ng/ml; p<0.0001). When AS patients were stratified according to sex, we observed that GSN levels were significantly lower in men than in women (p=0.032). However, no differences in GSN levels according to the specific clinical features of the disease were seen. No association was found between GSN concentration and adipokines or biomarkers of endothelial cell activation. However, correlation between basal GSN levels and insulin resistance was observed. A single infliximab infusion did not lead to significant changes in GSN levels.
GSN concentration is reduced in AS patients undergoing periodical anti-TNF-α therapy and low disease activity. Potential association with some metabolic syndrome features seems to exist.
确定接受 TNF-α 拮抗剂英夫利昔单抗治疗的强直性脊柱炎(AS)患者循环中的凝胶蛋白(GSN)水平是否与对照组相比发生改变,并确定疾病活动度、全身炎症和代谢综合征是否为这些患者循环 GSN 水平的潜在决定因素。
我们评估了一系列 30 名无糖尿病的接受 TNF-α 拮抗剂英夫利昔单抗治疗的 AS 患者和 48 名匹配对照者的 GSN 血清浓度。在英夫利昔单抗输注前后测量 GSN 水平。评估 GSN 血清水平与疾病活动度、全身炎症和代谢综合征的相关性。还分析了抗 TNF-α 单克隆抗体英夫利昔单抗输注后 GSN 浓度的潜在变化。
尽管在研究时,接受抗 TNF-α 治疗的 AS 患者对疾病有足够的控制(平均 BASDAI 为 2.94),但他们的 GSN 血清水平低于健康对照组(平均值±标准差:38660.42±23624.6 ng/ml 与 68975.43±31246.79 ng/ml;p<0.0001)。当 AS 患者按性别分层时,我们观察到男性的 GSN 水平明显低于女性(p=0.032)。然而,在疾病的具体临床特征方面,GSN 水平没有差异。GSN 浓度与脂肪因子或内皮细胞激活的生物标志物之间没有关联。然而,观察到基础 GSN 水平与胰岛素抵抗之间存在相关性。单次英夫利昔单抗输注不会导致 GSN 水平的显著变化。
接受周期性抗 TNF-α 治疗且疾病活动度低的 AS 患者 GSN 浓度降低。与某些代谢综合征特征存在潜在关联。