Cargando…

Liver stiffness and thrombin generation in compensated cirrhosis

BACKGROUND: Decompensated cirrhosis is associated with coagulation abnormalities that can increase the risk of thrombosis and bleeding. It is unclear precisely when these abnormalities arise and whether they are exacerbated as compensated cirrhosis progresses. Transient elastography using FibroScan...

Descripción completa

Detalles Bibliográficos
Autores principales: Dillon, Audrey, Egan, Karl, Kevane, Barry, Galvin, Zita, Maguire, Patricia, Ní Áinle, Fionnuala, Stewart, Stephen
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462746/
https://www.ncbi.nlm.nih.gov/pubmed/31011714
http://dx.doi.org/10.1002/rth2.12173
_version_ 1783410631562493952
author Dillon, Audrey
Egan, Karl
Kevane, Barry
Galvin, Zita
Maguire, Patricia
Ní Áinle, Fionnuala
Stewart, Stephen
author_facet Dillon, Audrey
Egan, Karl
Kevane, Barry
Galvin, Zita
Maguire, Patricia
Ní Áinle, Fionnuala
Stewart, Stephen
author_sort Dillon, Audrey
collection PubMed
description BACKGROUND: Decompensated cirrhosis is associated with coagulation abnormalities that can increase the risk of thrombosis and bleeding. It is unclear precisely when these abnormalities arise and whether they are exacerbated as compensated cirrhosis progresses. Transient elastography using FibroScan generates liver stiffness measurements (LSM) that associate with portal hypertension, clinical outcomes and provides prognostic information at an earlier stage than traditional liver function scores eg, MELD score. OBJECTIVE: To characterize thrombin generation in patients with compensated cirrhosis and to determine whether parameters of coagulation change throughout compensated cirrhosis, staged using LSM. PATIENTS/METHODS: Blood samples were collected from well‐compensated cirrhotic patients n = 61, All Child Pugh A stage) attending the Mater Misericordiae University Hospital, Ireland. Comprehensive clinical staging of liver disease, including LSM, was performed. Tissue Factor‐stimulated thrombin generation was measured by calibrated automated thrombography. RESULTS: Using LSM to stage well‐compensated cirrhotic patients, we demonstrate a significant decrease in the rate of propagation, the rate of attenuation, and total thrombin generation as LSM increase. LSM correlated with endogenous thrombin potential, peak thrombin generation, the rate of propagation, and the rate of attenuation. This association between thrombin generation and LSM was still evident in sub‐analyses excluding patients with ongoing alcohol use, active HCV infection, or a history of decompensation. In contrast, there was no significant correlation between thrombin generation, prothrombin times, Child‐Pugh scores, or MELD scores. CONCLUSION: Liver stiffness measurements identify differences in parameters of thrombin generation within a cohort of compensated cirrhotic patients before changes in clotting times occur.
format Online
Article
Text
id pubmed-6462746
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher John Wiley and Sons Inc.
record_format MEDLINE/PubMed
spelling pubmed-64627462019-04-22 Liver stiffness and thrombin generation in compensated cirrhosis Dillon, Audrey Egan, Karl Kevane, Barry Galvin, Zita Maguire, Patricia Ní Áinle, Fionnuala Stewart, Stephen Res Pract Thromb Haemost Original Articles: Haemostasis BACKGROUND: Decompensated cirrhosis is associated with coagulation abnormalities that can increase the risk of thrombosis and bleeding. It is unclear precisely when these abnormalities arise and whether they are exacerbated as compensated cirrhosis progresses. Transient elastography using FibroScan generates liver stiffness measurements (LSM) that associate with portal hypertension, clinical outcomes and provides prognostic information at an earlier stage than traditional liver function scores eg, MELD score. OBJECTIVE: To characterize thrombin generation in patients with compensated cirrhosis and to determine whether parameters of coagulation change throughout compensated cirrhosis, staged using LSM. PATIENTS/METHODS: Blood samples were collected from well‐compensated cirrhotic patients n = 61, All Child Pugh A stage) attending the Mater Misericordiae University Hospital, Ireland. Comprehensive clinical staging of liver disease, including LSM, was performed. Tissue Factor‐stimulated thrombin generation was measured by calibrated automated thrombography. RESULTS: Using LSM to stage well‐compensated cirrhotic patients, we demonstrate a significant decrease in the rate of propagation, the rate of attenuation, and total thrombin generation as LSM increase. LSM correlated with endogenous thrombin potential, peak thrombin generation, the rate of propagation, and the rate of attenuation. This association between thrombin generation and LSM was still evident in sub‐analyses excluding patients with ongoing alcohol use, active HCV infection, or a history of decompensation. In contrast, there was no significant correlation between thrombin generation, prothrombin times, Child‐Pugh scores, or MELD scores. CONCLUSION: Liver stiffness measurements identify differences in parameters of thrombin generation within a cohort of compensated cirrhotic patients before changes in clotting times occur. John Wiley and Sons Inc. 2019-01-28 /pmc/articles/PMC6462746/ /pubmed/31011714 http://dx.doi.org/10.1002/rth2.12173 Text en © 2019 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals, Inc on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles: Haemostasis
Dillon, Audrey
Egan, Karl
Kevane, Barry
Galvin, Zita
Maguire, Patricia
Ní Áinle, Fionnuala
Stewart, Stephen
Liver stiffness and thrombin generation in compensated cirrhosis
title Liver stiffness and thrombin generation in compensated cirrhosis
title_full Liver stiffness and thrombin generation in compensated cirrhosis
title_fullStr Liver stiffness and thrombin generation in compensated cirrhosis
title_full_unstemmed Liver stiffness and thrombin generation in compensated cirrhosis
title_short Liver stiffness and thrombin generation in compensated cirrhosis
title_sort liver stiffness and thrombin generation in compensated cirrhosis
topic Original Articles: Haemostasis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6462746/
https://www.ncbi.nlm.nih.gov/pubmed/31011714
http://dx.doi.org/10.1002/rth2.12173
work_keys_str_mv AT dillonaudrey liverstiffnessandthrombingenerationincompensatedcirrhosis
AT egankarl liverstiffnessandthrombingenerationincompensatedcirrhosis
AT kevanebarry liverstiffnessandthrombingenerationincompensatedcirrhosis
AT galvinzita liverstiffnessandthrombingenerationincompensatedcirrhosis
AT maguirepatricia liverstiffnessandthrombingenerationincompensatedcirrhosis
AT niainlefionnuala liverstiffnessandthrombingenerationincompensatedcirrhosis
AT stewartstephen liverstiffnessandthrombingenerationincompensatedcirrhosis