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从生化标志物到骨关节炎的分子内型:已验证生物标志物的综述。

From biochemical markers to molecular endotypes of osteoarthritis: a review on validated biomarkers.

机构信息

ImmunoScience, Nordic Bioscience A/S, Herlev, Denmark.

Department of Biomedical Sciences, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.

出版信息

Expert Rev Mol Diagn. 2024 Jan-Feb;24(1-2):23-38. doi: 10.1080/14737159.2024.2315282. Epub 2024 Feb 14.

DOI:10.1080/14737159.2024.2315282
PMID:38353446
Abstract

INTRODUCTION

Osteoarthritis (OA) affects over 500 million people worldwide. OA patients are symptomatically treated, and current therapies exhibit marginal efficacy and frequently carry safety-risks associated with chronic use. No disease-modifying therapies have been approved to date leaving surgical joint replacement as a last resort. To enable effective patient care and successful drug development there is an urgent need to uncover the pathobiological drivers of OA and how these translate into disease endotypes. Endotypes provide a more precise and mechanistic definition of disease subgroups than observable phenotypes, and a panel of tissue- and pathology-specific biochemical markers may uncover treatable endotypes of OA.

AREAS COVERED

We have searched PubMed for full-text articles written in English to provide an in-depth narrative review of a panel of validated biochemical markers utilized for endotyping of OA and their association to key OA pathologies.

EXPERT OPINION

As utilized in IMI-APPROACH and validated in OAI-FNIH, a panel of biochemical markers may uncover disease subgroups and facilitate the enrichment of treatable molecular endotypes for recruitment in therapeutic clinical trials. Understanding the link between biochemical markers and patient-reported outcomes and treatable endotypes that may respond to given therapies will pave the way for new drug development in OA.

摘要

简介

骨关节炎(OA)影响着全球超过 5 亿人。OA 患者接受对症治疗,目前的治疗方法疗效有限,且经常伴有与长期使用相关的安全风险。迄今为止,尚无批准的疾病修正疗法,因此手术关节置换成为最后手段。为了实现有效的患者护理和成功的药物开发,迫切需要揭示 OA 的病理生物学驱动因素以及这些因素如何转化为疾病内型。内型比可观察的表型提供了更精确和更具机制的疾病亚组定义,一组组织和病理特异性生化标志物可能揭示 OA 的可治疗内型。

涵盖领域

我们已在 PubMed 上搜索了全文英文文章,以深入叙述性综述用于 OA 内型鉴定的一组经过验证的生化标志物及其与 OA 主要病理的关联。

专家意见

正如在 IMI-APPROACH 中使用并在 OAI-FNIH 中验证的那样,一组生化标志物可揭示疾病亚组,并有助于为治疗性临床试验招募可治疗的分子内型。了解生化标志物与患者报告的结果之间的联系以及可能对特定治疗有反应的可治疗内型,将为 OA 的新药开发铺平道路。

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