Semra Fırat, Şükran Erten, Serdar Can Güven, Sezen Tutar, Yüksel Maraş, Salim Neşelioğlu, Selçuk Akan, Ahmet Kor, Berkan Armağan, Kevser Orhan, İsmail Doğan, Orhan Küçükşahin, Özcan Erel
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引用次数: 0
Abstract
Objective: Aim of this study is to compare the thiol/disulfide variables before treatment, at the 3rd and 6th months of biologic treatment in patients with axSpA.
Materials & methods: Consecutive patients with axial spondyloarthritis to whom biologic treatment was initiated in our clinic were enrolled upon consent. Demographics, clinical characteristics, laboratory parameters and treatment agents were collected. Disease activity scores and thiol-disulfide balance parameters were recorded at baseline and 3rd, 6th months of treatment. Statistical analyses were performed in all patients and in subgroups of ankylosing spondylitis and non-radiographic axial spondyloarthritis patients.
Results: In all patients, total thiol levels were significantly increased at 6th month in comparison to baseline values (470.5 ± 74.7 vs 491.9 ± 69.6, p = 0.047). Native thiol levels were increased at 6th month close to significance (438.9 ± 70.4 vs 458.8 ± 63.7, p = 0.060). Moderately strong negative correlations were observed between native thiol levels and disease activity parameters (BASDAI: p = 0,019; ASDAS-CRP: p = 0,035; ASDAS-ESR: p = 0,030), and between total thiol levels and disease activity parameters (BASDAI: p = 0,031; ASDAS-CRP: p = 0,020; ASDAS-ESR: p = 0,026) at 6th month evaluation.
Discussion & conclusions: Our results demonstrated oxidative stress reducing effect of biologics in axSpA patients parallel to suppression of disease activity at 6th month of the treatment.
目的:本研究的目的是比较axSpA患者治疗前、生物治疗第3个月和第6个月的硫醇/二硫变量。材料与方法:经同意,连续入组在我诊所接受生物治疗的轴性脊柱炎患者。收集人口统计学、临床特征、实验室参数和治疗药物。在基线和治疗第3、6个月时记录疾病活动度评分和硫醇-二硫平衡参数。对所有患者以及强直性脊柱炎和非影像学中轴性脊柱炎患者亚组进行统计分析。结果:与基线值相比,所有患者在第6个月时总硫醇水平均显著升高(470.5±74.7 vs 491.9±69.6,p = 0.047)。6个月时天然硫醇水平升高接近显著性(438.9±70.4 vs 458.8±63.7,p = 0.060)。在天然硫醇水平和疾病活动参数之间观察到中等强的负相关(BASDAI: p = 0,019;ASDAS-CRP: p = 0.035;ASDAS-ESR: p = 0.030),总硫醇水平与疾病活动参数之间(BASDAI: p = 0.031;ASDAS-CRP: p = 0.020;ASDAS-ESR: p = 0.026)。讨论与结论:我们的研究结果表明,在治疗第6个月时,生物制剂对axSpA患者的氧化应激降低作用与抑制疾病活动平行。
期刊介绍:
The journal Immunopharmacology and Immunotoxicology is devoted to pre-clinical and clinical drug discovery and development targeting the immune system. Research related to the immunoregulatory effects of various compounds, including small-molecule drugs and biologics, on immunocompetent cells and immune responses, as well as the immunotoxicity exerted by xenobiotics and drugs. Only research that describe the mechanisms of specific compounds (not extracts) is of interest to the journal.
The journal will prioritise preclinical and clinical studies on immunotherapy of disorders such as chronic inflammation, allergy, autoimmunity, cancer etc. The effects of small-drugs, vaccines and biologics against central immunological targets as well as cell-based therapy, including dendritic cell therapy, T cell adoptive transfer and stem cell therapy, are topics of particular interest. Publications pointing towards potential new drug targets within the immune system or novel technology for immunopharmacological drug development are also welcome.
With an immunoscience focus on drug development, immunotherapy and toxicology, the journal will cover areas such as infection, allergy, inflammation, tumor immunology, degenerative disorders, immunodeficiencies, neurology, atherosclerosis and more.
Immunopharmacology and Immunotoxicology will accept original manuscripts, brief communications, commentaries, mini-reviews, reviews, clinical trials and clinical cases, on the condition that the results reported are based on original, clinical, or basic research that has not been published elsewhere in any journal in any language (except in abstract form relating to paper communicated to scientific meetings and symposiums).