• 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

类风湿关节炎持续关节损伤的生化标志物——当前和未来的应用、局限性和机遇。

Biochemical markers of ongoing joint damage in rheumatoid arthritis--current and future applications, limitations and opportunities.

机构信息

Nordic Bioscience, Herlev Hovedgade 207, DK-2730 Herlev, Denmark.

出版信息

Arthritis Res Ther. 2011 Apr 28;13(2):215. doi: 10.1186/ar3280.

DOI:10.1186/ar3280
PMID:21539724
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3132026/
Abstract

Rheumatoid arthritis (RA) is a chronic systemic autoimmune disease associated with potentially debilitating joint inflammation, as well as altered skeletal bone metabolism and co-morbid conditions. Early diagnosis and aggressive treatment to control disease activity offers the highest likelihood of preserving function and preventing disability. Joint inflammation is characterized by synovitis, osteitis, and/or peri-articular osteopenia, often accompanied by development of subchondral bone erosions, as well as progressive joint space narrowing. Biochemical markers of joint cartilage and bone degradation may enable timely detection and assessment of ongoing joint damage, and their use in facilitating treatment strategies is under investigation. Early detection of joint damage may be assisted by the characterization of biochemical markers that identify patients whose joint damage is progressing rapidly and who are thus most in need of aggressive treatment, and that, alone or in combination, identify those individuals who are likely to respond best to a potential treatment, both in terms of limiting joint damage and relieving symptoms. The aims of this review are to describe currently available biochemical markers of joint metabolism in relation to the pathobiology of joint damage and systemic bone loss in RA; to assess the limitations of, and need for additional, novel biochemical markers in RA and other rheumatic diseases, and the strategies used for assay development; and to examine the feasibility of advancement of personalized health care using biochemical markers to select therapeutic agents to which a patient is most likely to respond.

摘要

类风湿关节炎(RA)是一种慢性系统性自身免疫性疾病,与潜在的使人衰弱的关节炎症、骨骼代谢改变以及合并症有关。早期诊断和积极治疗以控制疾病活动度,是最大程度保留功能和预防残疾的关键。关节炎症的特征是滑膜炎、骨炎和/或关节周围骨质疏松症,常伴有软骨下骨侵蚀的发展,以及关节间隙的进行性狭窄。关节软骨和骨降解的生化标志物可实现对持续关节损伤的及时检测和评估,其在治疗策略中的应用正在研究中。通过对识别关节损伤进展迅速的患者的生化标志物的特征化,可能有助于早期发现关节损伤,这些患者最需要积极治疗,单独或联合使用这些标志物可以识别出那些对潜在治疗最有可能有良好反应的个体,既可以限制关节损伤,又可以缓解症状。本综述的目的是描述目前可用于评估 RA 中关节代谢以及关节损伤和全身骨质流失的生化标志物;评估 RA 和其他风湿性疾病中现有和新的生化标志物的局限性和需求,以及用于检测方法开发的策略;并探讨使用生化标志物选择患者最可能有反应的治疗药物来推进个性化医疗的可行性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/ac0bcd881073/ar3280-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/96a8ebf1382b/ar3280-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/3b10eaf69ff9/ar3280-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/2d13403265d9/ar3280-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/153abc6c7deb/ar3280-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/237001b0cd04/ar3280-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/ac0bcd881073/ar3280-6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/96a8ebf1382b/ar3280-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/3b10eaf69ff9/ar3280-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/2d13403265d9/ar3280-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/153abc6c7deb/ar3280-4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/237001b0cd04/ar3280-5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5a3d/3132026/ac0bcd881073/ar3280-6.jpg

相似文献

1
Biochemical markers of ongoing joint damage in rheumatoid arthritis--current and future applications, limitations and opportunities.类风湿关节炎持续关节损伤的生化标志物——当前和未来的应用、局限性和机遇。
Arthritis Res Ther. 2011 Apr 28;13(2):215. doi: 10.1186/ar3280.
2
Osteitis and synovitis, but not bone erosion, is associated with proteoglycan loss and microstructure damage in the cartilage of patients with rheumatoid arthritis.骨炎和滑膜炎与类风湿关节炎患者软骨中蛋白聚糖丢失和微观结构损伤有关,但不伴骨侵蚀。
Ann Rheum Dis. 2014 Jun;73(6):1101-6. doi: 10.1136/annrheumdis-2012-202850. Epub 2013 Apr 26.
3
The clinical features of rheumatoid arthritis.类风湿关节炎的临床特征。
Eur J Radiol. 1998 May;27 Suppl 1:S18-24. doi: 10.1016/s0720-048x(98)00038-2.
4
The interplay between inflammation and metabolism in rheumatoid arthritis.类风湿关节炎中炎症与代谢的相互作用。
Cell Death Dis. 2015 Sep 17;6(9):e1887. doi: 10.1038/cddis.2015.246.
5
Biochemical markers of joint tissue turnover in early rheumatoid arthritis.早期类风湿关节炎关节组织更新的生化标志物
Clin Exp Rheumatol. 2003 Sep-Oct;21(5 Suppl 31):S54-8.
6
Noninvasive techniques for assessing skeletal changes in inflammatory arthritis: bone biomarkers.评估炎症性关节炎骨骼变化的非侵入性技术:骨生物标志物
Curr Opin Rheumatol. 2004 Jul;16(4):428-34. doi: 10.1097/01.moo.0000127830.72761.00.
7
Clinical significance of cartilage biomarkers for monitoring structural joint damage in rheumatoid arthritis patients treated with anti-TNF therapy.抗 TNF 治疗类风湿关节炎患者结构关节损伤监测中软骨生物标志物的临床意义。
PLoS One. 2012;7(5):e37447. doi: 10.1371/journal.pone.0037447. Epub 2012 May 21.
8
Towards a stratified targeted approach with biologic treatments in rheumatoid arthritis: role of synovial pathobiology.迈向类风湿关节炎生物治疗的分层靶向方法:滑膜病理生物学的作用
Curr Pharm Des. 2015;21(17):2216-24. doi: 10.2174/1381612821666150310145758.
9
Core management principles in rheumatoid arthritis to help guide managed care professionals.类风湿关节炎的核心管理原则,以帮助指导管理式医疗专业人员。
J Manag Care Pharm. 2011 Nov-Dec;17(9 Suppl B):S03-8.
10
Cartilage and bone damage in rheumatoid arthritis.类风湿关节炎中的软骨和骨损伤。
Reumatologia. 2018;56(2):111-120. doi: 10.5114/reum.2018.75523. Epub 2018 May 9.

引用本文的文献

1
Fibroblast Activation Protein (FAP)-Mediated Cleavage of Type III Collagen Reveals Serum Biomarker Potential in Non-Small Cell Lung Cancer and Spondyloarthritis.成纤维细胞活化蛋白(FAP)介导的III型胶原蛋白裂解揭示了非小细胞肺癌和脊柱关节炎中的血清生物标志物潜力。
Biomedicines. 2024 Feb 29;12(3):545. doi: 10.3390/biomedicines12030545.
2
Osteopontin, osteoprotegerin and musculoskeletal ultrasound findings in first-degree relatives of rheumatoid arthritis: potential markers of preclinical disease.骨桥蛋白、护骨素和肌肉骨骼超声在类风湿关节炎一级亲属中的发现:临床前疾病的潜在标志物。
BMC Musculoskelet Disord. 2024 Mar 5;25(1):195. doi: 10.1186/s12891-024-07291-7.
3

本文引用的文献

1
Enzyme-linked immunosorbent assay (ELISAs) for metalloproteinase derived type II collagen neoepitope, CIIM--increased serum CIIM in subjects with severe radiographic osteoarthritis.酶联免疫吸附试验(ELISA)检测金属蛋白酶解 II 型胶原新表位(CIIM):严重放射学骨关节炎患者血清 CIIM 升高。
Clin Biochem. 2011 Apr;44(5-6):423-9. doi: 10.1016/j.clinbiochem.2011.01.001. Epub 2011 Jan 9.
2
Humanized anti-interleukin-6-receptor antibody (tocilizumab) monotherapy is more effective in slowing radiographic progression in patients with rheumatoid arthritis at high baseline risk for structural damage evaluated with levels of biomarkers, radiography, and BMI: data from the SAMURAI study.人源化抗白细胞介素-6 受体抗体(托珠单抗)单药治疗在类风湿关节炎患者中更有效,可以减缓影像学进展,这些患者在基线时具有高水平的生物标志物、影像学和 BMI 评估的结构性损伤风险:来自 SAMURAI 研究的数据。
Mod Rheumatol. 2011 Feb;21(1):10-5. doi: 10.1007/s10165-010-0325-3. Epub 2010 Jun 24.
3
Biochemical markers and FokI and TaqI vitamin D receptor genes polymorphism in rheumatoid arthritis.
类风湿关节炎的生化标志物及 FokI 和 TaqI 维生素 D 受体基因多态性。
BMC Med Genomics. 2023 Oct 19;16(1):252. doi: 10.1186/s12920-023-01668-8.
4
Low-Grade Inflammatory Mediators and Metalloproteinases Yield Synchronous and Delayed Responses to Mechanical Joint Loading.低水平炎症介质和金属蛋白酶对机械关节负荷产生同步和延迟反应。
Cartilage. 2024 Dec;15(4):417-427. doi: 10.1177/19476035231193089. Epub 2023 Aug 24.
5
Biomarkers (mRNAs and non-coding RNAs) for the diagnosis and prognosis of rheumatoid arthritis.用于类风湿关节炎诊断和预后的生物标志物(mRNA 和非编码 RNA)。
Front Immunol. 2023 Feb 1;14:1087925. doi: 10.3389/fimmu.2023.1087925. eCollection 2023.
6
The current state of the osteoarthritis drug development pipeline: a comprehensive narrative review of the present challenges and future opportunities.骨关节炎药物研发进展的现状:对当前挑战与未来机遇的全面叙述性综述
Ther Adv Musculoskelet Dis. 2022 Dec 7;14:1759720X221085952. doi: 10.1177/1759720X221085952. eCollection 2022.
7
Collagen Type III as a Possible Blood Biomarker of Fibrosis in Equine Endometrium.III型胶原蛋白作为马子宫内膜纤维化潜在血液生物标志物
Animals (Basel). 2022 Jul 21;12(14):1854. doi: 10.3390/ani12141854.
8
Relationship of serum copper and HLADR4 tissue typing to disease activity and severity in patients with rheumatoid arthritis: A cross sectional study.血清铜及人类白细胞抗原DR4组织分型与类风湿关节炎患者疾病活动度和严重程度的关系:一项横断面研究
Ann Med Surg (Lond). 2021 Dec 24;73:103193. doi: 10.1016/j.amsu.2021.103193. eCollection 2022 Jan.
9
Post-Traumatic Osteoarthritis Assessment in Emerging and Advanced Pre-Clinical Meniscus Repair Strategies: A Review.新兴和先进临床前半月板修复策略中的创伤后骨关节炎评估:综述
Front Bioeng Biotechnol. 2021 Dec 22;9:787330. doi: 10.3389/fbioe.2021.787330. eCollection 2021.
10
Serological assessment of collagen fragments and tumor fibrosis may guide immune checkpoint inhibitor therapy.胶原片段和肿瘤纤维化的血清学评估可能指导免疫检查点抑制剂治疗。
J Exp Clin Cancer Res. 2021 Oct 16;40(1):326. doi: 10.1186/s13046-021-02133-z.
Novel combinations of Post-Translational Modification (PTM) neo-epitopes provide tissue-specific biochemical markers--are they the cause or the consequence of the disease?新型翻译后修饰(PTM)新表位组合提供组织特异性生化标志物——它们是疾病的原因还是后果?
Clin Biochem. 2010 Jul;43(10-11):793-804. doi: 10.1016/j.clinbiochem.2010.03.015. Epub 2010 Apr 8.
4
Increased sclerostin serum levels associated with bone formation and resorption markers in patients with immobilization-induced bone loss.固定性骨丢失患者的血清硬骨素水平升高与骨形成和骨吸收标志物相关。
J Clin Endocrinol Metab. 2010 May;95(5):2248-53. doi: 10.1210/jc.2010-0067. Epub 2010 Mar 19.
5
Biomarkers in early rheumatoid arthritis: longitudinal associations with inflammation and joint destruction measured by magnetic resonance imaging and conventional radiographs.早期类风湿关节炎的生物标志物:通过磁共振成像和常规 X 射线测量的炎症和关节破坏的纵向关联。
Ann Rheum Dis. 2010 May;69(5):845-50. doi: 10.1136/ard.2009.122325. Epub 2010 Mar 16.
6
Application of biochemical markers in development of drugs for treatment of osteoarthritis.生化标志物在治疗骨关节炎药物开发中的应用。
Biomarkers. 2010 Feb;15(1):1-19. doi: 10.3109/13547500903295873.
7
Rapid and sustained improvement in bone and cartilage turnover markers with the anti-interleukin-6 receptor inhibitor tocilizumab plus methotrexate in rheumatoid arthritis patients with an inadequate response to methotrexate: results from a substudy of the multicenter double-blind, placebo-controlled trial of tocilizumab in inadequate responders to methotrexate alone.在对甲氨蝶呤反应不足的类风湿关节炎患者中,抗白细胞介素-6受体抑制剂托珠单抗联合甲氨蝶呤可使骨和软骨转换标志物迅速且持续改善:来自托珠单抗针对单用甲氨蝶呤反应不足者的多中心双盲、安慰剂对照试验的一项子研究结果
Arthritis Rheum. 2010 Jan;62(1):33-43. doi: 10.1002/art.25053.
8
Updated consensus statement on biological agents for the treatment of rheumatic diseases, 2009.《2009年风湿性疾病生物制剂治疗更新共识声明》
Ann Rheum Dis. 2010 Jan;69 Suppl 1:i2-29. doi: 10.1136/ard.2009.123885.
9
Should biochemical markers of bone turnover be considered standard practice for safety pharmacology?骨转换生化标志物是否应被视为安全药理学的标准实践?
Biomarkers. 2010 May;15(3):195-204. doi: 10.3109/13547500903434519.
10
Erythrocyte sedimentation rate, C-reactive protein level, and serum amyloid a protein for patient selection and monitoring of anti-tumor necrosis factor treatment in ankylosing spondylitis.红细胞沉降率、C反应蛋白水平及血清淀粉样蛋白A在强直性脊柱炎患者选择及抗肿瘤坏死因子治疗监测中的应用
Arthritis Rheum. 2009 Nov 15;61(11):1484-90. doi: 10.1002/art.24838.