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血管性肝脏疾病的分子机制:聚焦于血栓形成。

Molecular Mechanisms Underlying Vascular Liver Diseases: Focus on Thrombosis.

机构信息

Hepatology Unit, CEMAD Centro Malattie Dell'Apparato Digerente, Medicina Interna e Gastroenterologia, Fondazione Policlinico Universitario Gemelli IRCCS, 00168 Rome, Italy.

Dipartimento di Medicina e Chirurgia Traslazionale, Università Cattolica del Sacro Cuore, 00168 Rome, Italy.

出版信息

Int J Mol Sci. 2023 Aug 13;24(16):12754. doi: 10.3390/ijms241612754.

Abstract

Vascular liver disorders (VLDs) comprise a wide spectrum of clinical-pathological entities that primarily affect the hepatic vascular system of both cirrhotic and non-cirrhotic patients. VLDs more frequently involve the portal and the hepatic veins, as well as liver sinusoids, resulting in an imbalance of liver homeostasis with serious consequences, such as the development of portal hypertension and liver fibrosis. Surprisingly, many VLDs are characterized by a prothrombotic phenotype. The molecular mechanisms that cause thrombosis in VLD are only partially explained by the alteration in the Virchow's triad (hypercoagulability, blood stasis, and endothelial damage) and nowadays their pathogenesis is incompletely described and understood. Studies about this topic have been hampered by the low incidence of VLDs in the general population and by the absence of suitable animal models. Recently, the role of coagulation imbalance in liver disease has been postulated as one of the main mechanisms linked to fibrogenesis, so a novel interest in vascular alterations of the liver has been renewed. This review provides a detailed analysis of the current knowledge of molecular mechanisms of VLD. We also focus on the promising role of anticoagulation as a strategy to prevent liver complications and to improve the outcome of these patients.

摘要

血管性肝疾病(VLDs)包括广泛的临床病理学实体,主要影响肝硬化和非肝硬化患者的肝血管系统。VLDs 更常累及门脉和肝静脉以及肝窦,导致肝内稳态失衡,产生严重后果,如门静脉高压和肝纤维化的发展。令人惊讶的是,许多 VLDs 的特征是存在血栓形成倾向。VLD 中导致血栓形成的分子机制部分可以用 Virchow 三联征(高凝状态、血液淤滞和内皮损伤)的改变来解释,而目前其发病机制尚未完全描述和理解。由于普通人群中 VLD 的发病率较低,且缺乏合适的动物模型,因此针对这一课题的研究受到了阻碍。最近,人们提出凝血失衡是肝纤维化的主要机制之一,因此对肝脏血管改变的新兴趣重新出现。本综述详细分析了 VLD 的分子机制的现有知识。我们还重点介绍了抗凝治疗作为预防肝并发症和改善这些患者预后的一种有前途的策略的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9135/10454315/9207d80e6b6b/ijms-24-12754-g001.jpg

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