There is an unmet need for high-quality liquid biomarkers that can safely and reproducibly predict the stage of fibrosis and the outcomes of chronic liver disease (CLD). The requirement for such markers has intensified because of the high global prevalence of diseases such as non-alcoholic fatty liver disease (NAFLD). In particular, there is a need for diagnostic and prognostic tools, as well as predictive biomarkers that reflect the efficacy of interventions, as described by the BEST criteria (Biomarkers, EndpointS, and other Tools Resource). This review covers the various liver collagens, their functional role in tissue homeostasis and delineates the common nomenclature for biomarkers based on BEST criteria. It addresses the common confounders affecting serological biomarkers, and describes defined collagen epitope biomarkers that originate from the dynamic processes of extracellular matrix (ECM) remodelling during liver injury.

译文

:对能够安全,可重复地预测纤维化阶段和慢性肝病(CLD)结局的高质量液体生物标志物的需求未得到满足。由于诸如非酒精性脂肪肝疾病(NAFLD)之类的疾病在全球的普遍流行,因此对此类标记物的需求日益增加。特别是,需要一种诊断和预后工具,以及反映干预效果的预测性生物标志物,如BEST标准(生物标志物,EndpointS和其他工具资源)所述。这篇综述涵盖了各种肝脏胶原蛋白,它们在组织体内稳态中的功能作用,并根据BEST标准描述了生物标志物的常用命名法。它解决了影响血清生物标志物的常见混杂因素,并描述了确定的胶原蛋白表位生物标志物,其起源于肝损伤期间细胞外基质(ECM)重塑的动态过程。

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