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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Veröffentlicht in:Journal of hepatology 2015-07, Vol.63 (1), p.50-59
Hauptverfasser: 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
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container_issue 1
container_start_page 50
container_title Journal of hepatology
container_volume 63
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
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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&lt;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. 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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&lt;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&lt;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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