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用于人类膝关节骨关节炎的临床相关分子生物标志物:系统评价。

Clinically Relevant Molecular Biomarkers for Use in Human Knee Osteoarthritis: A Systematic Review.

机构信息

Faculty of Biology, Medicine and Health, University of Manchester, Manchester, UK.

出版信息

Cartilage. 2021 Dec;13(1_suppl):1511S-1531S. doi: 10.1177/1947603520941239. Epub 2020 Jul 17.

Abstract

OBJECTIVE

Biomarkers in osteoarthritis (OA) could serve as objective clinical indicators for various disease parameters, and act as surrogate endpoints in clinical trials for disease-modifying drugs. The aim of this systematic review was to produce a comprehensive list of candidate molecular biomarkers for knee OA after the 2013 ESCEO review and discern whether any have been studied in sufficient detail for use in clinical settings.

DESIGN

MEDLINE and Embase databases were searched between August 2013 and May 2018 using the keywords "knee osteoarthritis," "osteoarthritis," and "biomarker." Studies were screened by title, abstract, and full text. Human studies on knee OA that were published in the English language were included. Excluded were studies on genetic/imaging/cellular markers, studies on participants with secondary OA, and publications that were review/abstract-only. Study quality and bias were assessed. Statistically significant data regarding the relationship between a biomarker and a disease parameter were extracted.

RESULTS

A total of 80 studies were included in the final review and 89 statistically significant individual molecular biomarkers were identified. C-telopeptide of type II collagen (CTXII) was shown to predict progression of knee OA in urine and serum in multiple studies. Synovial fluid vascular endothelial growth factor concentration was reported by 2 studies to be predictive of knee OA progression.

CONCLUSION

Despite the clear need for biomarkers of OA, the lack of coordination in current research has led to incompatible results. As such, there is yet to be a suitable biomarker to be used in a clinical setting.

摘要

目的

骨关节炎(OA)的生物标志物可作为各种疾病参数的客观临床指标,并可作为疾病修饰药物临床试验中的替代终点。本系统评价的目的是在 2013 年 ESCEO 综述之后生成一份全面的膝关节 OA 候选分子生物标志物清单,并确定是否有任何标志物已经过充分研究,可用于临床环境。

设计

使用“膝关节骨关节炎”、“骨关节炎”和“生物标志物”等关键词,于 2013 年 8 月至 2018 年 5 月在 MEDLINE 和 Embase 数据库中进行搜索。通过标题、摘要和全文筛选研究。纳入了发表在英文期刊上的膝关节 OA 的人类研究。排除了针对遗传/成像/细胞标志物的研究、针对继发性 OA 参与者的研究以及仅为综述/摘要的出版物。评估了研究质量和偏倚。提取了生物标志物与疾病参数之间关系的具有统计学意义的数据。

结果

共有 80 项研究最终纳入综述,确定了 89 个具有统计学意义的单个分子生物标志物。多项研究表明,Ⅱ型胶原 C 端肽(CTXII)在尿液和血清中可预测膝关节 OA 的进展。有 2 项研究报告滑膜液血管内皮生长因子浓度可预测膝关节 OA 的进展。

结论

尽管 OA 的生物标志物明显是必要的,但当前研究缺乏协调,导致结果不一致。因此,目前还没有适合在临床环境中使用的生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/05e9/8808945/325c87ebdcb2/10.1177_1947603520941239-fig1.jpg

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