Cargando…
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...
Autores principales: | , , , , , , , |
---|---|
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 |
_version_ | 1783343548747218944 |
---|---|
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. |
format | Online Article Text |
id | pubmed-6069695 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT lihongbin pathologicalfeaturesofmitochondrialultrastructurepredictsusceptibilitytoposttipshepaticencephalopathy AT yuezhendong pathologicalfeaturesofmitochondrialultrastructurepredictsusceptibilitytoposttipshepaticencephalopathy AT zhaohongwei pathologicalfeaturesofmitochondrialultrastructurepredictsusceptibilitytoposttipshepaticencephalopathy AT wanglei pathologicalfeaturesofmitochondrialultrastructurepredictsusceptibilitytoposttipshepaticencephalopathy AT fanzhenhua pathologicalfeaturesofmitochondrialultrastructurepredictsusceptibilitytoposttipshepaticencephalopathy AT hefuliang pathologicalfeaturesofmitochondrialultrastructurepredictsusceptibilitytoposttipshepaticencephalopathy AT dongxiaoqun pathologicalfeaturesofmitochondrialultrastructurepredictsusceptibilitytoposttipshepaticencephalopathy AT liufuquan pathologicalfeaturesofmitochondrialultrastructurepredictsusceptibilitytoposttipshepaticencephalopathy |