Tagliaferro Marzia, Marino Mariapaola, Basile Valerio, Pocino Krizia, Rapaccini Gian Ludovico, Ciasca Gabriele, Basile Umberto, Carnazzo Valeria
Dipartimento di Patologia Clinica, Ospedale Santa Maria Goretti, A.U.S.L. Latina, 04100 Latina, Italy.
Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.
J Pers Med. 2024 Jul 29;14(8):798. doi: 10.3390/jpm14080798.
Chronic liver diseases (CLD) stem from various causes and lead to a gradual progression that ultimately may result in fibrosis and eventually cirrhosis. This process is typically prolonged and asymptomatic, characterized by the complex interplay among various cell types, signaling pathways, extracellular matrix components, and immune responses. With the prevalence of CLD increasing, diagnoses are often delayed, which leads to poor prognoses and in some cases, the need for liver transplants. Consequently, there is an urgent need for the development of novel, non-invasive methods for the diagnosis and monitoring of CLD. In this context, serum biomarkers-safer, repeatable, and more acceptable alternatives to tissue biopsies-are attracting significant research interest, although their clinical implementation is not yet widespread. This review summarizes the latest advancements in serum biomarkers for detecting hepatic fibrogenesis and advocates for concerted efforts to consolidate current knowledge, thereby providing patients with early, effective, and accessible diagnoses that facilitate personalized therapeutic strategies.
慢性肝病(CLD)由多种病因引起,导致病情逐渐进展,最终可能导致纤维化并最终发展为肝硬化。这个过程通常持续时间较长且无症状,其特征是各种细胞类型、信号通路、细胞外基质成分和免疫反应之间复杂的相互作用。随着CLD患病率的增加,诊断往往被延迟,这导致预后不良,在某些情况下还需要进行肝移植。因此,迫切需要开发新的、非侵入性的方法来诊断和监测CLD。在这种背景下,血清生物标志物——比组织活检更安全、可重复且更易接受的替代方法——正吸引着大量的研究兴趣,尽管它们在临床上的应用尚未广泛普及。本综述总结了用于检测肝纤维化的血清生物标志物的最新进展,并倡导共同努力整合现有知识,从而为患者提供早期、有效且可及的诊断,以促进个性化治疗策略的制定。