Potential clinical biomarkers in rheumatoid arthritis with an omic approach.

Q1 Medicine
Yolima Puentes-Osorio, Pedro Amariles, Miguel Ángel Calleja, Vicente Merino, Juan Camilo Díaz-Coronado, Daniel Taborda
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引用次数: 18

Abstract

Objective: To aid in the selection of the most suitable therapeutic option in patients with diagnosis of rheumatoid arthritis according to the phase of disease, through the review of articles that identify omics biological markers.

Methods: A systematic review in PubMed/Medline databases was performed. We searched articles from August 2014 to September 2019, in English and Spanish, filtered by title and full text; and using the terms "Biomarkers" AND "Rheumatoid arthritis".

Results: This article supplies an exhaustive review from research of objective measurement, omics biomarkers and how disease activity appraise decrease unpredictability in treatment determinations, and finally, economic, and clinical outcomes of treatment options by biomarkers' potential influence. A total of 122 articles were included. Only 92 met the established criteria for review purposes and 17 relevant references about the topic were included as well. Therefore, it was possible to identify 196 potential clinical biomarkers: 22 non-omics, 20 epigenomics, 33 genomics, 21 transcriptomics, 78 proteomics, 4 glycomics, 1 lipidomics and 17 metabolomics.

Conclusion: A biomarker is a measurable indicator of some, biochemical, physiological, or morphological condition; evaluable at a molecular, biochemical, or cellular level. Biomarkers work as indicators of physiological or pathological processes, or as a result of a therapeutic management. In the last five years, new biomarkers have been identified, especially the omics, which are those that proceed from the investigation of genes (genomics), metabolites (metabolomics), and proteins (proteomics). These biomarkers contribute to the physician choosing the best therapeutic option in patients with rheumatoid arthritis.

Abstract Image

Abstract Image

类风湿关节炎的潜在临床生物标志物组学方法。
目的:通过对识别组学生物学标记的文章的回顾,帮助根据疾病阶段诊断为类风湿关节炎的患者选择最合适的治疗方案。方法:系统回顾PubMed/Medline数据库。我们检索了2014年8月至2019年9月的英文和西班牙文文章,按标题和全文过滤;并使用术语“生物标志物”和“类风湿关节炎”。结果:本文从客观测量、组学生物标志物和疾病活动性评估如何减少治疗决定中的不可预测性,以及生物标志物潜在影响的治疗方案的经济和临床结果等方面的研究进行了详尽的综述。共纳入122篇文章。只有92份符合审查目的的既定标准,还包括17份关于该专题的相关参考文献。因此,可以确定196个潜在的临床生物标志物:22个非组学,20个表观基因组学,33个基因组学,21个转录组学,78个蛋白质组学,4个糖组学,1个脂质组学和17个代谢组学。结论:生物标志物是某种生化、生理或形态状况的可测量指标;可在分子、生物化学或细胞水平上评价的生物标志物作为生理或病理过程的指标,或作为治疗管理的结果。在过去的五年中,新的生物标志物被发现,特别是组学,它们是那些从基因(基因组学)、代谢物(代谢组学)和蛋白质(蛋白质组学)的研究中产生的。这些生物标志物有助于医生在类风湿关节炎患者中选择最佳治疗方案。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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