• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肿瘤坏死因子抑制剂似乎可抑制高安动脉炎的疾病进展并改善其预后;一项基于人群的观察性时间趋势研究。

TNF inhibitors appear to inhibit disease progression and improve outcome in Takayasu arteritis; an observational, population-based time trend study.

作者信息

Gudbrandsson Birgir, Molberg Øyvind, Palm Øyvind

机构信息

Oslo University Hospital, Postboks 4950 Nydalen, 0424, Oslo, Norway.

Department of Rheumatology, Oslo University Hospital - Rikshospitalet, Oslo, Norway.

出版信息

Arthritis Res Ther. 2017 May 18;19(1):99. doi: 10.1186/s13075-017-1316-y.

DOI:10.1186/s13075-017-1316-y
PMID:28521841
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5437509/
Abstract

BACKGROUND

Magnetic resonance imaging (MRI) and computed tomography (CT) angiography have now largely replaced interventional angiography in the diagnoses and follow up of Takayasu arteritis (TAK) but data on the effects of this change of imaging method on diagnostic delay and vascular damage, and detailed data on the effect of different treatment regimens on the accumulation of vascular damage are missing. The aim of this study was to assess time trends in diagnostic delay, therapeutic approaches, arterial lesion accrual, persistent disease activity and remission rates in TAK.

METHODS

The study cohort included all 78 patients from the 1999 - 2012 population-based South-East Norway TAK cohort and 19 patients from a tertiary referral cohort. TAK was classified by the 1990 American College of Rheumatology criteria and/or the 1995 modified Ishikawa diagnostic criteria. Data were retrieved by review of electronic patient journals and imaging data analyses.

RESULTS

Diagnostic delay fell significantly during the study period and the number of lesions at diagnoses fell from three to two. Patients diagnosed from 2000 onwards more often received up-front treatment with disease-modifying antirheumatic drugs (DMARDs) than those diagnosed before 2000 (51% vs 4%; p < 0.01), and they were more often treated with TNF inhibitors during the disease course (44% vs 14%). During the first 2 years after initiation of therapy, 10% (3/32) of TNF-inhibitor-treated patients developed new lesions, compared to 40% (16/40) on DMARD treatment (OR 0.13) and 92% (14/15) on prednisolone monotherapy (OR 0.02). Patients on TNF inhibitors had a higher sustained remission rate than patients on DMARDs (42% vs 20%; p = 0.03). From 2000 onwards, the proportion of patients without new arterial lesions during the first 5 years after diagnosis increased from 29% in the patients diagnosed in 2000-2004, to 39% in 2005-2009 and 59% of patients diagnosed in 2010-2012.

CONCLUSION

Our observational data indicate that more aggressive use of TNF inhibitors and DMARDs improve the outcome in TAK, but damage accrual is a continuous challenge and sustained remission is still relatively rare.

摘要

背景

在大动脉炎(TAK)的诊断和随访中,磁共振成像(MRI)和计算机断层扫描(CT)血管造影现已在很大程度上取代了介入血管造影,但关于这种成像方法的改变对诊断延迟和血管损伤的影响的数据,以及关于不同治疗方案对血管损伤累积影响的详细数据尚缺。本研究的目的是评估TAK患者在诊断延迟、治疗方法、动脉病变累积、持续疾病活动和缓解率方面的时间趋势。

方法

研究队列包括1999年至2012年基于挪威东南部人群的TAK队列中的所有78例患者以及来自三级转诊队列的19例患者。TAK根据1990年美国风湿病学会标准和/或1995年改良的石川诊断标准进行分类。通过查阅电子病历和影像学数据分析获取数据。

结果

在研究期间,诊断延迟显著缩短,诊断时的病变数量从三个降至两个。2000年以后诊断的患者比2000年以前诊断的患者更常接受改善病情抗风湿药物(DMARDs)的初始治疗(51%对4%;p<0.01),并且在病程中接受肿瘤坏死因子(TNF)抑制剂治疗的频率更高(44%对14%)。在开始治疗后的前2年,接受TNF抑制剂治疗的患者中有10%(3/32)出现新病变,而接受DMARD治疗的患者中这一比例为40%(16/40)(比值比[OR]0.13),接受泼尼松龙单药治疗的患者中这一比例为92%(14/15)(OR 0.02)。接受TNF抑制剂治疗的患者持续缓解率高于接受DMARDs治疗的患者(42%对20%;p=0.03)。从2000年起,诊断后前5年无新动脉病变的患者比例从2000 - 2004年诊断的患者中的29%,增加到2005 - 2009年的39%以及2010 - 2012年诊断的患者中的59%。

结论

我们的观察数据表明,更积极地使用TNF抑制剂和DMARDs可改善TAK的预后,但损伤累积仍是一个持续的挑战,持续缓解仍然相对少见。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5027/5437509/a87cf2252f5b/13075_2017_1316_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5027/5437509/bc9b39a9f2d2/13075_2017_1316_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5027/5437509/13b656ce29a4/13075_2017_1316_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5027/5437509/a87cf2252f5b/13075_2017_1316_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5027/5437509/bc9b39a9f2d2/13075_2017_1316_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5027/5437509/13b656ce29a4/13075_2017_1316_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5027/5437509/a87cf2252f5b/13075_2017_1316_Fig3_HTML.jpg

相似文献

1
TNF inhibitors appear to inhibit disease progression and improve outcome in Takayasu arteritis; an observational, population-based time trend study.肿瘤坏死因子抑制剂似乎可抑制高安动脉炎的疾病进展并改善其预后;一项基于人群的观察性时间趋势研究。
Arthritis Res Ther. 2017 May 18;19(1):99. doi: 10.1186/s13075-017-1316-y.
2
Serial analysis of clinical and imaging indices reveals prolonged efficacy of TNF-α and IL-6 receptor targeted therapies in refractory Takayasu arteritis.临床和影像学指标的连续分析显示,TNF-α 和 IL-6 受体靶向治疗在难治性大动脉炎中具有持久疗效。
Clin Exp Rheumatol. 2014 May-Jun;32(3 Suppl 82):S11-8. Epub 2013 Sep 30.
3
Efficacy of Biological-Targeted Treatments in Takayasu Arteritis: Multicenter, Retrospective Study of 49 Patients.生物靶向治疗在多发性大动脉炎中的疗效:49 例患者的多中心回顾性研究。
Circulation. 2015 Nov 3;132(18):1693-700. doi: 10.1161/CIRCULATIONAHA.114.014321. Epub 2015 Sep 9.
4
Long-term outcome of 251 patients with Takayasu arteritis on combination immunosuppressant therapy: Single centre experience from a large tertiary care teaching hospital in Southern India.251 例 Takayasu 动脉炎患者联合免疫抑制剂治疗的长期预后:来自印度南部一家大型三级教学医院的单中心经验。
Semin Arthritis Rheum. 2018 Apr;47(5):718-726. doi: 10.1016/j.semarthrit.2017.09.014. Epub 2017 Sep 30.
5
Tumor necrosis factor inhibitors in patients with Takayasu arteritis: experience from a referral center with long-term followup.大动脉炎患者的肿瘤坏死因子抑制剂:来自一家有长期随访的转诊中心的经验。
Arthritis Care Res (Hoboken). 2012 Jul;64(7):1079-83. doi: 10.1002/acr.21636.
6
Management of Takayasu arteritis.高安动脉炎的管理
Best Pract Res Clin Rheumatol. 2023 Mar;37(1):101826. doi: 10.1016/j.berh.2023.101826. Epub 2023 May 26.
7
Takayasu arteritis: a cohort of Italian patients and recent pathogenetic and therapeutic advances.Takayasu 动脉炎:意大利患者队列及近期发病机制和治疗进展。
Clin Exp Med. 2021 Feb;21(1):49-62. doi: 10.1007/s10238-020-00668-7. Epub 2020 Oct 7.
8
Childhood Takayasu arteritis: disease course and response to therapy.儿童 Takayasu 动脉炎:疾病过程和治疗反应。
Arthritis Res Ther. 2017 Nov 22;19(1):255. doi: 10.1186/s13075-017-1452-4.
9
Childhood-onset Takayasu arteritis: A 15-year experience from a tertiary referral center.儿童期发病的大动脉炎:来自三级转诊中心的15年经验。
Int J Rheum Dis. 2019 Jan;22(1):132-139. doi: 10.1111/1756-185X.13425. Epub 2018 Nov 5.
10
Infantile Takayasu: clinical features and long-term outcome.婴儿型多发性大动脉炎:临床特征与长期预后。
Rheumatology (Oxford). 2023 Sep 1;62(9):3126-3132. doi: 10.1093/rheumatology/keac691.

引用本文的文献

1
Dendritic cell heterogeneity and its role in connective tissue diseases.树突状细胞的异质性及其在结缔组织疾病中的作用。
Inflamm Regen. 2025 Jul 28;45(1):24. doi: 10.1186/s41232-025-00388-z.
2
Biologic therapies for the treatment of large vessel vasculitis: A systematic review and meta-analysis.用于治疗大血管血管炎的生物疗法:一项系统评价和荟萃分析。
PLoS One. 2025 Mar 10;20(3):e0314566. doi: 10.1371/journal.pone.0314566. eCollection 2025.
3
Assessment of damage in Takayasu's arteritis.高安动脉炎的损伤评估。

本文引用的文献

1
Prevalence, Incidence, and Disease Characteristics of Takayasu Arteritis by Ethnic Background: Data From a Large, Population-Based Cohort Resident in Southern Norway.不同种族背景的高安动脉炎的患病率、发病率及疾病特征:来自挪威南部一个大型人群队列的数据
Arthritis Care Res (Hoboken). 2017 Feb;69(2):278-285. doi: 10.1002/acr.22931. Epub 2016 Dec 31.
2
Takayasu arteritis in southern Sweden.瑞典南部的高安动脉炎。
J Rheumatol. 2015 May;42(5):853-8. doi: 10.3899/jrheum.140843. Epub 2015 Mar 15.
3
Tumor necrosis factor inhibitors in patients with Takayasu arteritis: experience from a referral center with long-term followup.
Rheumatology (Oxford). 2025 Feb 1;64(2):682-689. doi: 10.1093/rheumatology/keae333.
4
Diagnostic delays in systemic vasculitides.系统性血管炎的诊断延误。
Rheumatol Int. 2024 Jun;44(6):1003-1011. doi: 10.1007/s00296-024-05582-9. Epub 2024 Apr 8.
5
Effectiveness and safety of adalimumab compared with leflunomide in patients with Takayasu arteritis: a retrospective cohort study.阿达木单抗与来氟米特治疗大动脉炎患者的疗效和安全性:一项回顾性队列研究。
RMD Open. 2024 Mar 4;10(1):e003992. doi: 10.1136/rmdopen-2023-003992.
6
A Rare Case of Takayasu Arteritis Presenting as Pericarditis with Effusion.1例表现为心包炎伴积液的罕见高安动脉炎病例
Case Rep Rheumatol. 2023 Aug 24;2023:6044765. doi: 10.1155/2023/6044765. eCollection 2023.
7
Successful pregnancies in a patient with Takayasu arteritis and antiphospholipid syndrome, maintained on infliximab corticosteroid-free regimen: case-based review.他克莫司联合糖皮质激素治疗大动脉炎伴抗磷脂抗体综合征一例并文献复习
Rheumatol Int. 2024 Jul;44(7):1359-1367. doi: 10.1007/s00296-023-05440-0. Epub 2023 Sep 1.
8
Clinical observations on infliximab treatment of infantile onset Takayasu arteritis.英夫利昔单抗治疗儿童起病的多发性大动脉炎的临床观察。
Pediatr Rheumatol Online J. 2022 Aug 4;20(1):61. doi: 10.1186/s12969-022-00708-4.
9
Giant cell arteritis versus Takayasu's Arteritis: Two sides of the same coin?巨细胞动脉炎与高安动脉炎:同一硬币的两面?
Saudi J Ophthalmol. 2022 Apr 18;35(3):198-203. doi: 10.4103/SJOPT.SJOPT_152_21. eCollection 2021 Jul-Sep.
10
An Update on Childhood-Onset Takayasu Arteritis.儿童期发病的大动脉炎最新进展
Front Pediatr. 2022 Apr 13;10:872313. doi: 10.3389/fped.2022.872313. eCollection 2022.
大动脉炎患者的肿瘤坏死因子抑制剂:来自一家有长期随访的转诊中心的经验。
Arthritis Care Res (Hoboken). 2012 Jul;64(7):1079-83. doi: 10.1002/acr.21636.
4
Improved prognosis of Takayasu arteritis over the past decade--comprehensive analysis of 106 patients.过去十年 Takayasu 动脉炎的预后改善——106 例患者的综合分析。
Circ J. 2012;76(4):1004-11. doi: 10.1253/circj.cj-11-1108. Epub 2012 Feb 2.
5
Efficacy and tolerance of infliximab in refractory Takayasu arteritis: French multicentre study.英夫利昔单抗治疗难治性多发性大动脉炎的疗效和耐受性:法国多中心研究。
Rheumatology (Oxford). 2012 May;51(5):882-6. doi: 10.1093/rheumatology/ker380. Epub 2012 Jan 5.
6
Anti TNF-α in refractory Takayasu's arteritis: cases series and review of the literature.抗 TNF-α 治疗难治性多发性大动脉炎:病例系列及文献复习。
Autoimmun Rev. 2012 Jul;11(9):678-84. doi: 10.1016/j.autrev.2011.11.025. Epub 2011 Dec 4.
7
Assessment of disease activity and progression in Takayasu's arteritis.大动脉炎疾病活动度和进展的评估。
Clin Exp Rheumatol. 2011 Jan-Feb;29(1 Suppl 64):S86-91. Epub 2011 May 11.
8
A population-based study of Takayasu´s arteritis in eastern Denmark.丹麦东部基于人群的 Takayasu 动脉炎研究。
Clin Exp Rheumatol. 2011 Jan-Feb;29(1 Suppl 64):S40-2. Epub 2011 May 11.
9
Takayasu's arteritis progression on anti-TNF biologics: a case series.Takayasu 动脉炎在抗 TNF 生物制剂治疗下的进展:一项病例系列研究。
Clin Rheumatol. 2011 May;30(5):703-6. doi: 10.1007/s10067-010-1658-1. Epub 2011 Jan 11.
10
Takayasu arteritis: assessment of response to medical therapy based on clinical activity criteria and imaging techniques.Takayasu 动脉炎:基于临床活动标准和影像学技术评估对药物治疗的反应。
Rheumatol Int. 2012 Mar;32(3):703-9. doi: 10.1007/s00296-010-1694-9. Epub 2010 Dec 9.