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Pathological Features of Mitochondrial Ultrastructure Predict Susceptibility to Post-TIPS Hepatic Encephalopathy

BACKGROUND: Post-TIPS hepatic encephalopathy (PSE) is a complex process involving numerous risk factors; the root cause is unclear, but an elevation of blood ammonia due to portosystemic shunt and metabolic disorders in hepatocytes has been proposed as an important risk factor. AIMS: The aim of this...

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Autores principales: Li, Hong-bin, Yue, Zhen-dong, Zhao, Hong-wei, Wang, Lei, Fan, Zhen-hua, He, Fu-liang, Dong, Xiao-qun, Liu, Fu-quan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069695/
https://www.ncbi.nlm.nih.gov/pubmed/30079331
http://dx.doi.org/10.1155/2018/4671590
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author Li, Hong-bin
Yue, Zhen-dong
Zhao, Hong-wei
Wang, Lei
Fan, Zhen-hua
He, Fu-liang
Dong, Xiao-qun
Liu, Fu-quan
author_facet Li, Hong-bin
Yue, Zhen-dong
Zhao, Hong-wei
Wang, Lei
Fan, Zhen-hua
He, Fu-liang
Dong, Xiao-qun
Liu, Fu-quan
author_sort Li, Hong-bin
collection PubMed
description BACKGROUND: Post-TIPS hepatic encephalopathy (PSE) is a complex process involving numerous risk factors; the root cause is unclear, but an elevation of blood ammonia due to portosystemic shunt and metabolic disorders in hepatocytes has been proposed as an important risk factor. AIMS: The aim of this study was to investigate the impact of pathological features of mitochondrial ultrastructure on PSE via transjugular liver biopsy at TIPS implantation. METHODS: We evaluated the pathological damage of mitochondrial ultrastructure on recruited patients by the Flameng classification system. A score ≤2 (no or low damage) was defined as group A, and a score >2 (high damage level) was defined as group B; routine follow-up was required at 1 and 2 years; the incidence of PSE and multiple clinical data were recorded. RESULTS: A total of 78 cases in group A and 42 in group B completed the study. The incidence of PSE after 1 and 2 years in group B (35.7% and 45.2%, respectively) was significantly higher than that in group A (16.7% and 24.4%, respectively); the 1- and 2-year OR (95% CI) were 2.778 (1.166-6.615) and 2.565 (1.155-5.696), respectively, for groups A and B. Importantly, group B had worse incidence of PSE than group A [P=0.014, hazard ratio (95%CI): 2.172 (1.190-4.678)]. CONCLUSION: Aggressive damage to mitochondrial ultrastructure in liver shunt predicts susceptibility to PSE. The registration number is NCT02540382.
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spelling pubmed-60696952018-08-05 Pathological Features of Mitochondrial Ultrastructure Predict Susceptibility to Post-TIPS Hepatic Encephalopathy Li, Hong-bin Yue, Zhen-dong Zhao, Hong-wei Wang, Lei Fan, Zhen-hua He, Fu-liang Dong, Xiao-qun Liu, Fu-quan Can J Gastroenterol Hepatol Clinical Study BACKGROUND: Post-TIPS hepatic encephalopathy (PSE) is a complex process involving numerous risk factors; the root cause is unclear, but an elevation of blood ammonia due to portosystemic shunt and metabolic disorders in hepatocytes has been proposed as an important risk factor. AIMS: The aim of this study was to investigate the impact of pathological features of mitochondrial ultrastructure on PSE via transjugular liver biopsy at TIPS implantation. METHODS: We evaluated the pathological damage of mitochondrial ultrastructure on recruited patients by the Flameng classification system. A score ≤2 (no or low damage) was defined as group A, and a score >2 (high damage level) was defined as group B; routine follow-up was required at 1 and 2 years; the incidence of PSE and multiple clinical data were recorded. RESULTS: A total of 78 cases in group A and 42 in group B completed the study. The incidence of PSE after 1 and 2 years in group B (35.7% and 45.2%, respectively) was significantly higher than that in group A (16.7% and 24.4%, respectively); the 1- and 2-year OR (95% CI) were 2.778 (1.166-6.615) and 2.565 (1.155-5.696), respectively, for groups A and B. Importantly, group B had worse incidence of PSE than group A [P=0.014, hazard ratio (95%CI): 2.172 (1.190-4.678)]. CONCLUSION: Aggressive damage to mitochondrial ultrastructure in liver shunt predicts susceptibility to PSE. The registration number is NCT02540382. Hindawi 2018-07-16 /pmc/articles/PMC6069695/ /pubmed/30079331 http://dx.doi.org/10.1155/2018/4671590 Text en Copyright © 2018 Hong-bin Li et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Study
Li, Hong-bin
Yue, Zhen-dong
Zhao, Hong-wei
Wang, Lei
Fan, Zhen-hua
He, Fu-liang
Dong, Xiao-qun
Liu, Fu-quan
Pathological Features of Mitochondrial Ultrastructure Predict Susceptibility to Post-TIPS Hepatic Encephalopathy
title Pathological Features of Mitochondrial Ultrastructure Predict Susceptibility to Post-TIPS Hepatic Encephalopathy
title_full Pathological Features of Mitochondrial Ultrastructure Predict Susceptibility to Post-TIPS Hepatic Encephalopathy
title_fullStr Pathological Features of Mitochondrial Ultrastructure Predict Susceptibility to Post-TIPS Hepatic Encephalopathy
title_full_unstemmed Pathological Features of Mitochondrial Ultrastructure Predict Susceptibility to Post-TIPS Hepatic Encephalopathy
title_short Pathological Features of Mitochondrial Ultrastructure Predict Susceptibility to Post-TIPS Hepatic Encephalopathy
title_sort pathological features of mitochondrial ultrastructure predict susceptibility to post-tips hepatic encephalopathy
topic Clinical Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6069695/
https://www.ncbi.nlm.nih.gov/pubmed/30079331
http://dx.doi.org/10.1155/2018/4671590
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