Effect of anti-tumor necrosis factor α treatment on radiographic progression in patient with ankylosing spondylitis: A systematic review and meta-analysis.

IF 1.9 4区 医学 Q3 RHEUMATOLOGY Modern Rheumatology Pub Date : 2019-05-01 Epub Date: 2019-01-03 DOI:10.1080/14397595.2018.1525017
He-Xiang Zong, Sheng-Qian Xu, Hui Tong, Xin-Rong Wang, Mei-Juan Pan, Yu-Zhu Teng
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引用次数: 26

Abstract

Background: Efficacy of anti-tumor necrosis factor (anti-TNF)α treatment in patient with active ankylosing spondylitis (AS) had been proved by many clinical studies. Inflammation and new bone formation in spine were two pivotal aspects in AS. TNF α inhibitor could eliminate inflammation including clinical and laboratory inflammatory manifestation. Paradoxical results whether TNF α antagonist could delay radiographic progression in AS were often been reported simultaneously.

Objectives: To review the literature about the effect of TNF α inhibitor on radiographic progression and disease activity in patient with AS.

Methods: We conducted a comprehensive search including Medline, EMBASE and the Cochrane Library from 1 January 2000 to 15 August 2017. Two reviewers independently supplemented with hand searching for the reference lists of inclusion. All trials focusing on radiographic progression or disease activity in patients with AS treated with anti-TNF α agents. Primary outcomes were modified Stokes AS Spinal Score (mSASSS), as well as Bath AS disease activity index (BASDAI) and Bath AS functional index (BASFI). Two reviewers independently selected studies and analyzed data. Methodological quality was assessed using the Newcastle-Ottawa scale (NOS). We pooled effects recorded on different scales as Standardized mean differences (SMDs) with 95% confidence intervals (CIs) using random-effects models.

Results: We included 14 studies of low to moderate risk of bias with 3,186 patients, compared with control group, there was no effect of mSASSS changes (SMD = -0.12, 95% CI: -1.17-0.93, p value = .82, I2 = 95%) and follow-up (SMD = 0.03, 95% CI: 0.21-0.26, p value = .82, I2 = 36%) estimation in anti-TNF α group. However anti-TNF α agent treatment led to remarkable improvements on both Bath AS disease activity index (BASDAI) (SMD = 1.06, 95% CI: 0.22-1.89, p value = .01, I2 = 96%) and Bath AS functional index (BASFI) (SMD = 0.93, 95% CI: 0.24-1.92, p value = .01, I2 = 97%) scores at 12 weeks.

Conclusion: Our meta-analysis found no significant effect on delaying radiographic progression in AS treated with TNF α inhibitor, although TNF α inhibitor could do improve significantly disease activity and physical function in AS.

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抗肿瘤坏死因子α治疗对强直性脊柱炎患者影像学进展的影响:系统回顾和荟萃分析。
背景:抗肿瘤坏死因子(anti-TNF)α治疗活动性强直性脊柱炎(AS)的疗效已被大量临床研究证实。炎症和脊柱新骨形成是AS的两个关键方面。TNF α抑制剂可消除炎症,包括临床和实验室炎症表现。TNF α拮抗剂是否能延缓AS的影像学进展常常同时被报道。目的:回顾有关肿瘤坏死因子α抑制剂对AS患者影像学进展和疾病活动性影响的文献。方法:我们从2000年1月1日至2017年8月15日对Medline、EMBASE和Cochrane图书馆进行了全面的检索。两名审稿人独立地用手搜索纳入的参考文献列表。所有的试验集中于用抗tnf α药物治疗的AS患者的影像学进展或疾病活动性。主要结局为改良Stokes AS脊柱评分(mSASSS)、Bath AS疾病活动指数(BASDAI)和Bath AS功能指数(BASFI)。两位审稿人独立选择研究并分析数据。采用纽卡斯尔-渥太华量表(NOS)评估方法学质量。我们使用随机效应模型将不同量表上记录的效应汇总为95%置信区间的标准化平均差异(SMDs)。结果:纳入14项低至中等偏倚风险的研究,共纳入3186例患者,与对照组相比,mSASSS变化无影响(SMD = -0.12, 95% CI: -1.17-0.93, p值=。82年,I2 = 95%)和后续(SMD = 0.03, 95%置信区间CI: 0.21 - -0.26, p值=。82, I2 = 36%)。但抗肿瘤坏死因子α药物治疗可显著改善两组患者的basas疾病活动指数(BASDAI) (SMD = 1.06, 95% CI: 0.22-1.89, p值=。1.01, I2 = 96%), Bath AS功能指数(BASFI) (SMD = 0.93, 95% CI: 0.24-1.92, p值=。01, I2 = 97%)在12周的评分。结论:我们的荟萃分析发现,尽管TNF α抑制剂可以显著改善AS患者的疾病活动性和身体功能,但TNF α抑制剂对延迟AS患者影像学进展没有显著影响。
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来源期刊
Modern Rheumatology
Modern Rheumatology RHEUMATOLOGY-
CiteScore
4.90
自引率
9.10%
发文量
146
审稿时长
1.5 months
期刊介绍: Modern Rheumatology publishes original papers in English on research pertinent to rheumatology and associated areas such as pathology, physiology, clinical immunology, microbiology, biochemistry, experimental animal models, pharmacology, and orthopedic surgery. Occasional reviews of topics which may be of wide interest to the readership will be accepted. In addition, concise papers of special scientific importance that represent definitive and original studies will be considered. Modern Rheumatology is currently indexed in Science Citation Index Expanded (SciSearch), Journal Citation Reports/Science Edition, PubMed/Medline, SCOPUS, EMBASE, Chemical Abstracts Service (CAS), Google Scholar, EBSCO, CSA, Academic OneFile, Current Abstracts, Elsevier Biobase, Gale, Health Reference Center Academic, OCLC, SCImago, Summon by Serial Solutions
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