Submassive hepatic necrosis distinguishes HBV-associated acute on chronic liver failure from cirrhotic patients with acute decompensation
[Display omitted] Distinguishing between acute on chronic liver failure (ACLF) and decompensated liver cirrhosis is difficult due to a lack of pathological evidence. A prospective single-center study investigated 174 patients undergoing liver transplantation due to acute decompensation of hepatitis...
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creator | Li, Hai Xia, Qiang Zeng, Bo Li, Shu-Ting Liu, Heng Li, Qi Li, Jun Yang, Shu-Yin Dong, Xiao-Jun Gao, Ting Munker, Stefan Liu, Yan Liebe, Roman Xue, Feng Li, Qi-Gen Chen, Xiao-Song Liu, Qiang Zeng, Hui Wang, Ji-Yao Xie, Qing Meng, Qin-Hua Wang, Jie-Fei Mertens, Peter R Lammert, Frank Singer, Manfred V Dooley, Steven Ebert, Matthias P.A Qiu, De-Kai Wang, Tai-Ling Weng, Hong-Lei |
description | [Display omitted]
Distinguishing between acute on chronic liver failure (ACLF) and decompensated liver cirrhosis is difficult due to a lack of pathological evidence.
A prospective single-center study investigated 174 patients undergoing liver transplantation due to acute decompensation of hepatitis B virus (HBV)-associated liver cirrhosis. Two groups were distinguished by the presence or absence of submassive hepatic necrosis (SMHN, defined as necrosis of 15–90% of the entire liver on explant). Core clinical features of ACLF were compared between these groups. Disease severity scoring systems were applied to describe liver function and organ failure. Serum cytokine profile assays, gene expression microarrays and immunohistochemical analyzes were used to study systemic and local inflammatory responses.
SMHN was identified in 69 of 174 patients proven to have cirrhosis by histological means. Characteristic features of SMHN were extensive necrosis along terminal hepatic veins and spanning multiple adjacent cirrhotic nodules accompanied by various degrees of liver progenitor cell-derived regeneration, cholestasis, and ductular bilirubinostasis. Patients with SMHN presented with more severely impaired hepatic function, a higher prevalence of multiple organ failure (as indicated by higher CLIF-SOFA and SOFA scores) and a shorter interval between acute decompensation and liver transplantation than those without SMHN (p |
doi_str_mv | 10.1016/j.jhep.2015.01.029 |
format | Article |
fullrecord | <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_1690212682</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>1_s2_0_S0168827815000604</els_id><sourcerecordid>1690212682</sourcerecordid><originalsourceid>FETCH-LOGICAL-c481t-82717d4966ccea5b523e1b513d5b5c0278ff1695f042cc2acb648a2cbc2192a83</originalsourceid><addsrcrecordid>eNp9kkFv1DAQhS0EokvhD3BAPnJJGDuJm0gIiVZAkSpxKHC1nMmEOGTjxU6K-hP410y0CwcOnDyS3_ukeW-EeK4gV6DMqzEfBzrkGlSVg8pBNw_EThmADEypHoodi-qs1hf1mXiS0ggABTTlY3GmK1Oaum524tft2u5dSv6OJMPc4lHOhDEkn2Tn0-Lnb6tPAyV5ffk1Y2VA7xbqpMN1IRlmiUMMM9smZkTZOz-tkWQfw16ij3EIG3Mj07wk-dMvw8nbEYb9gebEf2F-Kh71bkr07PSeiy_v332-us5uPn34ePX2JsOyVsu2jrroysYYRHJVW-mCVFupouMZgZfte2WaqodSI2qHrSlrp7FFrRrt6uJcvDxyDzH8WCktdu8T0jS5mcKaLJtBK21qzVJ9lG55pEi9PUS_d_HeKrBbBXa0WwV2q8CCslwBm16c-JwsdX8tfzJnweujgHjLO0_RJuRskDofCRfbBf9__pt_7Dh5zt9N3-me0hjWOHN-VtmkLdjb7Qi2G1AV92-gLH4DnI-v8g</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1690212682</pqid></control><display><type>article</type><title>Submassive hepatic necrosis distinguishes HBV-associated acute on chronic liver failure from cirrhotic patients with acute decompensation</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Li, Hai ; Xia, Qiang ; Zeng, Bo ; Li, Shu-Ting ; Liu, Heng ; Li, Qi ; Li, Jun ; Yang, Shu-Yin ; Dong, Xiao-Jun ; Gao, Ting ; Munker, Stefan ; Liu, Yan ; Liebe, Roman ; Xue, Feng ; Li, Qi-Gen ; Chen, Xiao-Song ; Liu, Qiang ; Zeng, Hui ; Wang, Ji-Yao ; Xie, Qing ; Meng, Qin-Hua ; Wang, Jie-Fei ; Mertens, Peter R ; Lammert, Frank ; Singer, Manfred V ; Dooley, Steven ; Ebert, Matthias P.A ; Qiu, De-Kai ; Wang, Tai-Ling ; Weng, Hong-Lei</creator><creatorcontrib>Li, Hai ; Xia, Qiang ; Zeng, Bo ; Li, Shu-Ting ; Liu, Heng ; Li, Qi ; Li, Jun ; Yang, Shu-Yin ; Dong, Xiao-Jun ; Gao, Ting ; Munker, Stefan ; Liu, Yan ; Liebe, Roman ; Xue, Feng ; Li, Qi-Gen ; Chen, Xiao-Song ; Liu, Qiang ; Zeng, Hui ; Wang, Ji-Yao ; Xie, Qing ; Meng, Qin-Hua ; Wang, Jie-Fei ; Mertens, Peter R ; Lammert, Frank ; Singer, Manfred V ; Dooley, Steven ; Ebert, Matthias P.A ; Qiu, De-Kai ; Wang, Tai-Ling ; Weng, Hong-Lei</creatorcontrib><description>[Display omitted]
Distinguishing between acute on chronic liver failure (ACLF) and decompensated liver cirrhosis is difficult due to a lack of pathological evidence.
A prospective single-center study investigated 174 patients undergoing liver transplantation due to acute decompensation of hepatitis B virus (HBV)-associated liver cirrhosis. Two groups were distinguished by the presence or absence of submassive hepatic necrosis (SMHN, defined as necrosis of 15–90% of the entire liver on explant). Core clinical features of ACLF were compared between these groups. Disease severity scoring systems were applied to describe liver function and organ failure. Serum cytokine profile assays, gene expression microarrays and immunohistochemical analyzes were used to study systemic and local inflammatory responses.
SMHN was identified in 69 of 174 patients proven to have cirrhosis by histological means. Characteristic features of SMHN were extensive necrosis along terminal hepatic veins and spanning multiple adjacent cirrhotic nodules accompanied by various degrees of liver progenitor cell-derived regeneration, cholestasis, and ductular bilirubinostasis. Patients with SMHN presented with more severely impaired hepatic function, a higher prevalence of multiple organ failure (as indicated by higher CLIF-SOFA and SOFA scores) and a shorter interval between acute decompensation and liver transplantation than those without SMHN (p<0.01 for all parameters). Further analyzes based on serum cytokine profile assays, gene expression microarrays and immunohistochemical analyzes revealed higher levels of anti-inflammatory cytokines in patients with SMHN.
SMHN is a critical histological feature of HBV-associated ACLF. Identification of a characteristic pathological feature strongly supports that ACLF is a separate entity in end-stage liver disease.</description><identifier>ISSN: 0168-8278</identifier><identifier>EISSN: 1600-0641</identifier><identifier>DOI: 10.1016/j.jhep.2015.01.029</identifier><identifier>PMID: 25646889</identifier><language>eng</language><publisher>Netherlands: Elsevier B.V</publisher><subject>Acute decompensation ; Acute-on-chronic liver failure ; Acute-On-Chronic Liver Failure - diagnosis ; Acute-On-Chronic Liver Failure - surgery ; Cirrhosis ; Diagnosis, Differential ; Disease Progression ; Female ; Follow-Up Studies ; Gastroenterology and Hepatology ; HBV ; Hepatitis B Antibodies - immunology ; Hepatitis B virus - immunology ; Humans ; Liver - pathology ; Liver Cirrhosis - diagnosis ; Liver histology ; Liver Transplantation ; Male ; Middle Aged ; Necrosis - diagnosis ; Prognosis ; Prospective Studies ; Severity of Illness Index ; Submassive hepatic necrosis</subject><ispartof>Journal of hepatology, 2015-07, Vol.63 (1), p.50-59</ispartof><rights>European Association for the Study of the Liver</rights><rights>2015 European Association for the Study of the Liver</rights><rights>Copyright © 2015 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c481t-82717d4966ccea5b523e1b513d5b5c0278ff1695f042cc2acb648a2cbc2192a83</citedby><cites>FETCH-LOGICAL-c481t-82717d4966ccea5b523e1b513d5b5c0278ff1695f042cc2acb648a2cbc2192a83</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0168827815000604$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,776,780,3537,27901,27902,65534</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/25646889$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Li, Hai</creatorcontrib><creatorcontrib>Xia, Qiang</creatorcontrib><creatorcontrib>Zeng, Bo</creatorcontrib><creatorcontrib>Li, Shu-Ting</creatorcontrib><creatorcontrib>Liu, Heng</creatorcontrib><creatorcontrib>Li, Qi</creatorcontrib><creatorcontrib>Li, Jun</creatorcontrib><creatorcontrib>Yang, Shu-Yin</creatorcontrib><creatorcontrib>Dong, Xiao-Jun</creatorcontrib><creatorcontrib>Gao, Ting</creatorcontrib><creatorcontrib>Munker, Stefan</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Liebe, Roman</creatorcontrib><creatorcontrib>Xue, Feng</creatorcontrib><creatorcontrib>Li, Qi-Gen</creatorcontrib><creatorcontrib>Chen, Xiao-Song</creatorcontrib><creatorcontrib>Liu, Qiang</creatorcontrib><creatorcontrib>Zeng, Hui</creatorcontrib><creatorcontrib>Wang, Ji-Yao</creatorcontrib><creatorcontrib>Xie, Qing</creatorcontrib><creatorcontrib>Meng, Qin-Hua</creatorcontrib><creatorcontrib>Wang, Jie-Fei</creatorcontrib><creatorcontrib>Mertens, Peter R</creatorcontrib><creatorcontrib>Lammert, Frank</creatorcontrib><creatorcontrib>Singer, Manfred V</creatorcontrib><creatorcontrib>Dooley, Steven</creatorcontrib><creatorcontrib>Ebert, Matthias P.A</creatorcontrib><creatorcontrib>Qiu, De-Kai</creatorcontrib><creatorcontrib>Wang, Tai-Ling</creatorcontrib><creatorcontrib>Weng, Hong-Lei</creatorcontrib><title>Submassive hepatic necrosis distinguishes HBV-associated acute on chronic liver failure from cirrhotic patients with acute decompensation</title><title>Journal of hepatology</title><addtitle>J Hepatol</addtitle><description>[Display omitted]
Distinguishing between acute on chronic liver failure (ACLF) and decompensated liver cirrhosis is difficult due to a lack of pathological evidence.
A prospective single-center study investigated 174 patients undergoing liver transplantation due to acute decompensation of hepatitis B virus (HBV)-associated liver cirrhosis. Two groups were distinguished by the presence or absence of submassive hepatic necrosis (SMHN, defined as necrosis of 15–90% of the entire liver on explant). Core clinical features of ACLF were compared between these groups. Disease severity scoring systems were applied to describe liver function and organ failure. Serum cytokine profile assays, gene expression microarrays and immunohistochemical analyzes were used to study systemic and local inflammatory responses.
SMHN was identified in 69 of 174 patients proven to have cirrhosis by histological means. Characteristic features of SMHN were extensive necrosis along terminal hepatic veins and spanning multiple adjacent cirrhotic nodules accompanied by various degrees of liver progenitor cell-derived regeneration, cholestasis, and ductular bilirubinostasis. Patients with SMHN presented with more severely impaired hepatic function, a higher prevalence of multiple organ failure (as indicated by higher CLIF-SOFA and SOFA scores) and a shorter interval between acute decompensation and liver transplantation than those without SMHN (p<0.01 for all parameters). Further analyzes based on serum cytokine profile assays, gene expression microarrays and immunohistochemical analyzes revealed higher levels of anti-inflammatory cytokines in patients with SMHN.
SMHN is a critical histological feature of HBV-associated ACLF. Identification of a characteristic pathological feature strongly supports that ACLF is a separate entity in end-stage liver disease.</description><subject>Acute decompensation</subject><subject>Acute-on-chronic liver failure</subject><subject>Acute-On-Chronic Liver Failure - diagnosis</subject><subject>Acute-On-Chronic Liver Failure - surgery</subject><subject>Cirrhosis</subject><subject>Diagnosis, Differential</subject><subject>Disease Progression</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastroenterology and Hepatology</subject><subject>HBV</subject><subject>Hepatitis B Antibodies - immunology</subject><subject>Hepatitis B virus - immunology</subject><subject>Humans</subject><subject>Liver - pathology</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver histology</subject><subject>Liver Transplantation</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Necrosis - diagnosis</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Severity of Illness Index</subject><subject>Submassive hepatic necrosis</subject><issn>0168-8278</issn><issn>1600-0641</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kkFv1DAQhS0EokvhD3BAPnJJGDuJm0gIiVZAkSpxKHC1nMmEOGTjxU6K-hP410y0CwcOnDyS3_ukeW-EeK4gV6DMqzEfBzrkGlSVg8pBNw_EThmADEypHoodi-qs1hf1mXiS0ggABTTlY3GmK1Oaum524tft2u5dSv6OJMPc4lHOhDEkn2Tn0-Lnb6tPAyV5ffk1Y2VA7xbqpMN1IRlmiUMMM9smZkTZOz-tkWQfw16ij3EIG3Mj07wk-dMvw8nbEYb9gebEf2F-Kh71bkr07PSeiy_v332-us5uPn34ePX2JsOyVsu2jrroysYYRHJVW-mCVFupouMZgZfte2WaqodSI2qHrSlrp7FFrRrt6uJcvDxyDzH8WCktdu8T0jS5mcKaLJtBK21qzVJ9lG55pEi9PUS_d_HeKrBbBXa0WwV2q8CCslwBm16c-JwsdX8tfzJnweujgHjLO0_RJuRskDofCRfbBf9__pt_7Dh5zt9N3-me0hjWOHN-VtmkLdjb7Qi2G1AV92-gLH4DnI-v8g</recordid><startdate>20150701</startdate><enddate>20150701</enddate><creator>Li, Hai</creator><creator>Xia, Qiang</creator><creator>Zeng, Bo</creator><creator>Li, Shu-Ting</creator><creator>Liu, Heng</creator><creator>Li, Qi</creator><creator>Li, Jun</creator><creator>Yang, Shu-Yin</creator><creator>Dong, Xiao-Jun</creator><creator>Gao, Ting</creator><creator>Munker, Stefan</creator><creator>Liu, Yan</creator><creator>Liebe, Roman</creator><creator>Xue, Feng</creator><creator>Li, Qi-Gen</creator><creator>Chen, Xiao-Song</creator><creator>Liu, Qiang</creator><creator>Zeng, Hui</creator><creator>Wang, Ji-Yao</creator><creator>Xie, Qing</creator><creator>Meng, Qin-Hua</creator><creator>Wang, Jie-Fei</creator><creator>Mertens, Peter R</creator><creator>Lammert, Frank</creator><creator>Singer, Manfred V</creator><creator>Dooley, Steven</creator><creator>Ebert, Matthias P.A</creator><creator>Qiu, De-Kai</creator><creator>Wang, Tai-Ling</creator><creator>Weng, Hong-Lei</creator><general>Elsevier B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>20150701</creationdate><title>Submassive hepatic necrosis distinguishes HBV-associated acute on chronic liver failure from cirrhotic patients with acute decompensation</title><author>Li, Hai ; Xia, Qiang ; Zeng, Bo ; Li, Shu-Ting ; Liu, Heng ; Li, Qi ; Li, Jun ; Yang, Shu-Yin ; Dong, Xiao-Jun ; Gao, Ting ; Munker, Stefan ; Liu, Yan ; Liebe, Roman ; Xue, Feng ; Li, Qi-Gen ; Chen, Xiao-Song ; Liu, Qiang ; Zeng, Hui ; Wang, Ji-Yao ; Xie, Qing ; Meng, Qin-Hua ; Wang, Jie-Fei ; Mertens, Peter R ; Lammert, Frank ; Singer, Manfred V ; Dooley, Steven ; Ebert, Matthias P.A ; Qiu, De-Kai ; Wang, Tai-Ling ; Weng, Hong-Lei</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c481t-82717d4966ccea5b523e1b513d5b5c0278ff1695f042cc2acb648a2cbc2192a83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Acute decompensation</topic><topic>Acute-on-chronic liver failure</topic><topic>Acute-On-Chronic Liver Failure - diagnosis</topic><topic>Acute-On-Chronic Liver Failure - surgery</topic><topic>Cirrhosis</topic><topic>Diagnosis, Differential</topic><topic>Disease Progression</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gastroenterology and Hepatology</topic><topic>HBV</topic><topic>Hepatitis B Antibodies - immunology</topic><topic>Hepatitis B virus - immunology</topic><topic>Humans</topic><topic>Liver - pathology</topic><topic>Liver Cirrhosis - diagnosis</topic><topic>Liver histology</topic><topic>Liver Transplantation</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Necrosis - diagnosis</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Severity of Illness Index</topic><topic>Submassive hepatic necrosis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Li, Hai</creatorcontrib><creatorcontrib>Xia, Qiang</creatorcontrib><creatorcontrib>Zeng, Bo</creatorcontrib><creatorcontrib>Li, Shu-Ting</creatorcontrib><creatorcontrib>Liu, Heng</creatorcontrib><creatorcontrib>Li, Qi</creatorcontrib><creatorcontrib>Li, Jun</creatorcontrib><creatorcontrib>Yang, Shu-Yin</creatorcontrib><creatorcontrib>Dong, Xiao-Jun</creatorcontrib><creatorcontrib>Gao, Ting</creatorcontrib><creatorcontrib>Munker, Stefan</creatorcontrib><creatorcontrib>Liu, Yan</creatorcontrib><creatorcontrib>Liebe, Roman</creatorcontrib><creatorcontrib>Xue, Feng</creatorcontrib><creatorcontrib>Li, Qi-Gen</creatorcontrib><creatorcontrib>Chen, Xiao-Song</creatorcontrib><creatorcontrib>Liu, Qiang</creatorcontrib><creatorcontrib>Zeng, Hui</creatorcontrib><creatorcontrib>Wang, Ji-Yao</creatorcontrib><creatorcontrib>Xie, Qing</creatorcontrib><creatorcontrib>Meng, Qin-Hua</creatorcontrib><creatorcontrib>Wang, Jie-Fei</creatorcontrib><creatorcontrib>Mertens, Peter R</creatorcontrib><creatorcontrib>Lammert, Frank</creatorcontrib><creatorcontrib>Singer, Manfred V</creatorcontrib><creatorcontrib>Dooley, Steven</creatorcontrib><creatorcontrib>Ebert, Matthias P.A</creatorcontrib><creatorcontrib>Qiu, De-Kai</creatorcontrib><creatorcontrib>Wang, Tai-Ling</creatorcontrib><creatorcontrib>Weng, Hong-Lei</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Li, Hai</au><au>Xia, Qiang</au><au>Zeng, Bo</au><au>Li, Shu-Ting</au><au>Liu, Heng</au><au>Li, Qi</au><au>Li, Jun</au><au>Yang, Shu-Yin</au><au>Dong, Xiao-Jun</au><au>Gao, Ting</au><au>Munker, Stefan</au><au>Liu, Yan</au><au>Liebe, Roman</au><au>Xue, Feng</au><au>Li, Qi-Gen</au><au>Chen, Xiao-Song</au><au>Liu, Qiang</au><au>Zeng, Hui</au><au>Wang, Ji-Yao</au><au>Xie, Qing</au><au>Meng, Qin-Hua</au><au>Wang, Jie-Fei</au><au>Mertens, Peter R</au><au>Lammert, Frank</au><au>Singer, Manfred V</au><au>Dooley, Steven</au><au>Ebert, Matthias P.A</au><au>Qiu, De-Kai</au><au>Wang, Tai-Ling</au><au>Weng, Hong-Lei</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Submassive hepatic necrosis distinguishes HBV-associated acute on chronic liver failure from cirrhotic patients with acute decompensation</atitle><jtitle>Journal of hepatology</jtitle><addtitle>J Hepatol</addtitle><date>2015-07-01</date><risdate>2015</risdate><volume>63</volume><issue>1</issue><spage>50</spage><epage>59</epage><pages>50-59</pages><issn>0168-8278</issn><eissn>1600-0641</eissn><abstract>[Display omitted]
Distinguishing between acute on chronic liver failure (ACLF) and decompensated liver cirrhosis is difficult due to a lack of pathological evidence.
A prospective single-center study investigated 174 patients undergoing liver transplantation due to acute decompensation of hepatitis B virus (HBV)-associated liver cirrhosis. Two groups were distinguished by the presence or absence of submassive hepatic necrosis (SMHN, defined as necrosis of 15–90% of the entire liver on explant). Core clinical features of ACLF were compared between these groups. Disease severity scoring systems were applied to describe liver function and organ failure. Serum cytokine profile assays, gene expression microarrays and immunohistochemical analyzes were used to study systemic and local inflammatory responses.
SMHN was identified in 69 of 174 patients proven to have cirrhosis by histological means. Characteristic features of SMHN were extensive necrosis along terminal hepatic veins and spanning multiple adjacent cirrhotic nodules accompanied by various degrees of liver progenitor cell-derived regeneration, cholestasis, and ductular bilirubinostasis. Patients with SMHN presented with more severely impaired hepatic function, a higher prevalence of multiple organ failure (as indicated by higher CLIF-SOFA and SOFA scores) and a shorter interval between acute decompensation and liver transplantation than those without SMHN (p<0.01 for all parameters). Further analyzes based on serum cytokine profile assays, gene expression microarrays and immunohistochemical analyzes revealed higher levels of anti-inflammatory cytokines in patients with SMHN.
SMHN is a critical histological feature of HBV-associated ACLF. Identification of a characteristic pathological feature strongly supports that ACLF is a separate entity in end-stage liver disease.</abstract><cop>Netherlands</cop><pub>Elsevier B.V</pub><pmid>25646889</pmid><doi>10.1016/j.jhep.2015.01.029</doi><tpages>10</tpages></addata></record> |
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subjects | Acute decompensation Acute-on-chronic liver failure Acute-On-Chronic Liver Failure - diagnosis Acute-On-Chronic Liver Failure - surgery Cirrhosis Diagnosis, Differential Disease Progression Female Follow-Up Studies Gastroenterology and Hepatology HBV Hepatitis B Antibodies - immunology Hepatitis B virus - immunology Humans Liver - pathology Liver Cirrhosis - diagnosis Liver histology Liver Transplantation Male Middle Aged Necrosis - diagnosis Prognosis Prospective Studies Severity of Illness Index Submassive hepatic necrosis |
title | Submassive hepatic necrosis distinguishes HBV-associated acute on chronic liver failure from cirrhotic patients with acute decompensation |
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