TY - JOUR
T1 - Microvascular Thrombosis and Liver Fibrosis Progression: Mechanisms and Clinical Applications
AU - Airola, Carlo
AU - Pallozzi, Maria
AU - Cerrito, Lucia
AU - Santopaolo, Francesco
AU - Stella, Leonardo
AU - Gasbarrini, Antonio
AU - Ponziani, Francesca Romana
PY - 2023
Y1 - 2023
N2 - Fibrosis is an unavoidable consequence of chronic inflammation. Extracellular matrix deposition by fibroblasts, stimulated by multiple pathways, is the first step in the onset of chronic liver disease, and its propagation promotes liver dysfunction. At the same time, chronic liver disease is characterized by alterations in primary and secondary hemostasis but unlike previously thought, these changes are not associated with an increased risk of bleeding complications. In recent years, the role of coagulation imbalance has been postulated as one of the main mechanisms promoting hepatic fibrogenesis. In this review, we aim to investigate the function of microvascular thrombosis in the progression of liver disease and highlight the molecular and cellular networks linking hemostasis to fibrosis in this context. We analyze the predictive and prognostic role of coagulation products as biomarkers of liver decompensation (ascites, variceal hemorrhage, and hepatic encephalopathy) and liver-related mortality. Finally, we evaluate the current evidence on the application of antiplatelet and anticoagulant therapies for prophylaxis of hepatic decompensation or prevention of the progression of liver fibrosis.
AB - Fibrosis is an unavoidable consequence of chronic inflammation. Extracellular matrix deposition by fibroblasts, stimulated by multiple pathways, is the first step in the onset of chronic liver disease, and its propagation promotes liver dysfunction. At the same time, chronic liver disease is characterized by alterations in primary and secondary hemostasis but unlike previously thought, these changes are not associated with an increased risk of bleeding complications. In recent years, the role of coagulation imbalance has been postulated as one of the main mechanisms promoting hepatic fibrogenesis. In this review, we aim to investigate the function of microvascular thrombosis in the progression of liver disease and highlight the molecular and cellular networks linking hemostasis to fibrosis in this context. We analyze the predictive and prognostic role of coagulation products as biomarkers of liver decompensation (ascites, variceal hemorrhage, and hepatic encephalopathy) and liver-related mortality. Finally, we evaluate the current evidence on the application of antiplatelet and anticoagulant therapies for prophylaxis of hepatic decompensation or prevention of the progression of liver fibrosis.
KW - ADAMTS-13
KW - coagulation
KW - fibrosis
KW - hepatic stellate cells
KW - von Willebrand factor
KW - microthrombosis
KW - parenchymal extinction
KW - platelets
KW - liver cirrhosis
KW - ADAMTS-13
KW - coagulation
KW - fibrosis
KW - hepatic stellate cells
KW - von Willebrand factor
KW - microthrombosis
KW - parenchymal extinction
KW - platelets
KW - liver cirrhosis
UR - http://hdl.handle.net/10807/292378
U2 - 10.3390/cells12131712
DO - 10.3390/cells12131712
M3 - Article
SN - 2073-4409
VL - 12
SP - N/A-N/A
JO - Cells
JF - Cells
ER -