A-gluthathione S-transferase as an early marker of hepatic ischemia/reperfusion injury after liver resection

Organ dysfunction following liver resection is one of the major postoperative complications of liver surgery. The Pringle maneuver is often applied during liver resection to minimize bleeding, which in turn complicates the postoperative course owing to liver ischemia and reperfusion. Routinely, hepa...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:World journal of surgery 2005-04, Vol.29 (4), p.528-534
Hauptverfasser: CHOUKER, Alexander, MARTIGNONI, André, PETER, Klaus, THIEL, Manfred, SCHAUER, Rolf J, DUGAS, Martin, SCHACHTNER, Thomas, KAUFMANN, Ines, SETZER, Florian, RAU, Horst G, LÖHE, Florian, JAUCH, Karl-W
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 534
container_issue 4
container_start_page 528
container_title World journal of surgery
container_volume 29
creator CHOUKER, Alexander
MARTIGNONI, André
PETER, Klaus
THIEL, Manfred
SCHAUER, Rolf J
DUGAS, Martin
SCHACHTNER, Thomas
KAUFMANN, Ines
SETZER, Florian
RAU, Horst G
LÖHE, Florian
JAUCH, Karl-W
description Organ dysfunction following liver resection is one of the major postoperative complications of liver surgery. The Pringle maneuver is often applied during liver resection to minimize bleeding, which in turn complicates the postoperative course owing to liver ischemia and reperfusion. Routinely, hepatocellular damage is diagnosed by, for example, abnormal aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels and the prothrombin time (PT). The cytosolic liver enzyme α-glutathione S-transferase (α-GST) has recently been shown to have good sensitivity for detecting hepatic injury after acetaminophen poisoning or liver transplantation, but its role in non-transplantation liver surgery has not been assessed. In this prospective randomized clinical study, the diagnostic role of plasma α-GST following warm ischemia and reperfusion is reported. A total of 75 patients who underwent liver resection were randomly assigned to three groups: (1) without Pringle (NPR); (2) with Pringle (PR); (3) with ischemic preconditioning by 10 minutes of ischemia and reperfusion each prior to the Pringle manuever (IPC). The major findings are as follows: (1) ALT, AST, and α-GST increased upon liver manipulation as early as prior to resection, with a rapid return of α-GST values to preoperative levels, whereas ALT and AST further increased on the first postoperative day. (2) In the PR group, α-GST, but not ALT and AST, was significantly elevated compared with that in the NPR group at 15 and 30 minutes and 2 hours after resection/reperfusion. In addition, only levels of α-GST significantly correlated with the Pringle duration. (3) The ischemia/reperfusion-induced early rise in α-GST was completely prevented by ischemic preconditioning. Moreover, only α-GST concentrations (>490 μg L-1) determined early after resection (2 hours) predicted postoperative liver dysfunction (24 hours PT < 60%) with a positive predictive value of 74% and a negative predictive value of 76%. Thus α-GST seems to be a sensitive, predictive marker of ischemia/reperfusion-induced hepatocellular injury and postoperative liver dysfunction.
doi_str_mv 10.1007/s00268-004-7431-3
format Article
fullrecord <record><control><sourceid>proquest_pasca</sourceid><recordid>TN_cdi_proquest_journals_219963389</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>876459461</sourcerecordid><originalsourceid>FETCH-LOGICAL-p579-51e87be1892f4c8c838b0fcf23dcf71c3cb2f7068b9c4a0676bdbbec56eeede73</originalsourceid><addsrcrecordid>eNotj0tLAzEUhYMoWKs_wF0QXMbmMZNklqX4goILux-S9MZJnc6MSUbovzdgN-ceOB_nchC6Z_SJUapWiVIuNaG0IqoSjIgLtGCV4IQLLi7RggpZFc_ENbpJ6UApU5LKBerX5Kufc2dyF8YB8CfJ0QzJQzQJsEnYDBhM7E_4aOI3RDx63MFkcnA4JNfBMZhVhAmin1NpwGE4zPGEjc8F7sNv0QgJXC7hLbrypk9wd75LtHt53m3eyPbj9X2z3pKpVg2pGWhlgemG-8ppp4W21DvPxd55xZxwlntFpbaNqwyVStq9teBqCQB7UGKJHv5rpzj-zJByexjnOJSPLWdNI4XQTYEez5BJzvS-rHYhtVMMZeipZVLXvFZK_AE1vWnR</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>219963389</pqid></control><display><type>article</type><title>A-gluthathione S-transferase as an early marker of hepatic ischemia/reperfusion injury after liver resection</title><source>Wiley Online Library Journals Frontfile Complete</source><source>SpringerLink Journals - AutoHoldings</source><creator>CHOUKER, Alexander ; MARTIGNONI, André ; PETER, Klaus ; THIEL, Manfred ; SCHAUER, Rolf J ; DUGAS, Martin ; SCHACHTNER, Thomas ; KAUFMANN, Ines ; SETZER, Florian ; RAU, Horst G ; LÖHE, Florian ; JAUCH, Karl-W</creator><creatorcontrib>CHOUKER, Alexander ; MARTIGNONI, André ; PETER, Klaus ; THIEL, Manfred ; SCHAUER, Rolf J ; DUGAS, Martin ; SCHACHTNER, Thomas ; KAUFMANN, Ines ; SETZER, Florian ; RAU, Horst G ; LÖHE, Florian ; JAUCH, Karl-W</creatorcontrib><description>Organ dysfunction following liver resection is one of the major postoperative complications of liver surgery. The Pringle maneuver is often applied during liver resection to minimize bleeding, which in turn complicates the postoperative course owing to liver ischemia and reperfusion. Routinely, hepatocellular damage is diagnosed by, for example, abnormal aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels and the prothrombin time (PT). The cytosolic liver enzyme α-glutathione S-transferase (α-GST) has recently been shown to have good sensitivity for detecting hepatic injury after acetaminophen poisoning or liver transplantation, but its role in non-transplantation liver surgery has not been assessed. In this prospective randomized clinical study, the diagnostic role of plasma α-GST following warm ischemia and reperfusion is reported. A total of 75 patients who underwent liver resection were randomly assigned to three groups: (1) without Pringle (NPR); (2) with Pringle (PR); (3) with ischemic preconditioning by 10 minutes of ischemia and reperfusion each prior to the Pringle manuever (IPC). The major findings are as follows: (1) ALT, AST, and α-GST increased upon liver manipulation as early as prior to resection, with a rapid return of α-GST values to preoperative levels, whereas ALT and AST further increased on the first postoperative day. (2) In the PR group, α-GST, but not ALT and AST, was significantly elevated compared with that in the NPR group at 15 and 30 minutes and 2 hours after resection/reperfusion. In addition, only levels of α-GST significantly correlated with the Pringle duration. (3) The ischemia/reperfusion-induced early rise in α-GST was completely prevented by ischemic preconditioning. Moreover, only α-GST concentrations (&gt;490 μg L-1) determined early after resection (2 hours) predicted postoperative liver dysfunction (24 hours PT &lt; 60%) with a positive predictive value of 74% and a negative predictive value of 76%. Thus α-GST seems to be a sensitive, predictive marker of ischemia/reperfusion-induced hepatocellular injury and postoperative liver dysfunction.</description><identifier>ISSN: 0364-2313</identifier><identifier>EISSN: 1432-2323</identifier><identifier>DOI: 10.1007/s00268-004-7431-3</identifier><identifier>CODEN: WJSUDI</identifier><language>eng</language><publisher>New York, NY: Springer</publisher><subject>Biological and medical sciences ; Gastroenterology. Liver. Pancreas. Abdomen ; General aspects ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Medical sciences ; Other diseases. Semiology</subject><ispartof>World journal of surgery, 2005-04, Vol.29 (4), p.528-534</ispartof><rights>2005 INIST-CNRS</rights><rights>Société Internationale de Chirurgie 2005</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27923,27924</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16852577$$DView record in Pascal Francis$$Hfree_for_read</backlink></links><search><creatorcontrib>CHOUKER, Alexander</creatorcontrib><creatorcontrib>MARTIGNONI, André</creatorcontrib><creatorcontrib>PETER, Klaus</creatorcontrib><creatorcontrib>THIEL, Manfred</creatorcontrib><creatorcontrib>SCHAUER, Rolf J</creatorcontrib><creatorcontrib>DUGAS, Martin</creatorcontrib><creatorcontrib>SCHACHTNER, Thomas</creatorcontrib><creatorcontrib>KAUFMANN, Ines</creatorcontrib><creatorcontrib>SETZER, Florian</creatorcontrib><creatorcontrib>RAU, Horst G</creatorcontrib><creatorcontrib>LÖHE, Florian</creatorcontrib><creatorcontrib>JAUCH, Karl-W</creatorcontrib><title>A-gluthathione S-transferase as an early marker of hepatic ischemia/reperfusion injury after liver resection</title><title>World journal of surgery</title><description>Organ dysfunction following liver resection is one of the major postoperative complications of liver surgery. The Pringle maneuver is often applied during liver resection to minimize bleeding, which in turn complicates the postoperative course owing to liver ischemia and reperfusion. Routinely, hepatocellular damage is diagnosed by, for example, abnormal aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels and the prothrombin time (PT). The cytosolic liver enzyme α-glutathione S-transferase (α-GST) has recently been shown to have good sensitivity for detecting hepatic injury after acetaminophen poisoning or liver transplantation, but its role in non-transplantation liver surgery has not been assessed. In this prospective randomized clinical study, the diagnostic role of plasma α-GST following warm ischemia and reperfusion is reported. A total of 75 patients who underwent liver resection were randomly assigned to three groups: (1) without Pringle (NPR); (2) with Pringle (PR); (3) with ischemic preconditioning by 10 minutes of ischemia and reperfusion each prior to the Pringle manuever (IPC). The major findings are as follows: (1) ALT, AST, and α-GST increased upon liver manipulation as early as prior to resection, with a rapid return of α-GST values to preoperative levels, whereas ALT and AST further increased on the first postoperative day. (2) In the PR group, α-GST, but not ALT and AST, was significantly elevated compared with that in the NPR group at 15 and 30 minutes and 2 hours after resection/reperfusion. In addition, only levels of α-GST significantly correlated with the Pringle duration. (3) The ischemia/reperfusion-induced early rise in α-GST was completely prevented by ischemic preconditioning. Moreover, only α-GST concentrations (&gt;490 μg L-1) determined early after resection (2 hours) predicted postoperative liver dysfunction (24 hours PT &lt; 60%) with a positive predictive value of 74% and a negative predictive value of 76%. Thus α-GST seems to be a sensitive, predictive marker of ischemia/reperfusion-induced hepatocellular injury and postoperative liver dysfunction.</description><subject>Biological and medical sciences</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>General aspects</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Medical sciences</subject><subject>Other diseases. Semiology</subject><issn>0364-2313</issn><issn>1432-2323</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNotj0tLAzEUhYMoWKs_wF0QXMbmMZNklqX4goILux-S9MZJnc6MSUbovzdgN-ceOB_nchC6Z_SJUapWiVIuNaG0IqoSjIgLtGCV4IQLLi7RggpZFc_ENbpJ6UApU5LKBerX5Kufc2dyF8YB8CfJ0QzJQzQJsEnYDBhM7E_4aOI3RDx63MFkcnA4JNfBMZhVhAmin1NpwGE4zPGEjc8F7sNv0QgJXC7hLbrypk9wd75LtHt53m3eyPbj9X2z3pKpVg2pGWhlgemG-8ppp4W21DvPxd55xZxwlntFpbaNqwyVStq9teBqCQB7UGKJHv5rpzj-zJByexjnOJSPLWdNI4XQTYEez5BJzvS-rHYhtVMMZeipZVLXvFZK_AE1vWnR</recordid><startdate>20050401</startdate><enddate>20050401</enddate><creator>CHOUKER, Alexander</creator><creator>MARTIGNONI, André</creator><creator>PETER, Klaus</creator><creator>THIEL, Manfred</creator><creator>SCHAUER, Rolf J</creator><creator>DUGAS, Martin</creator><creator>SCHACHTNER, Thomas</creator><creator>KAUFMANN, Ines</creator><creator>SETZER, Florian</creator><creator>RAU, Horst G</creator><creator>LÖHE, Florian</creator><creator>JAUCH, Karl-W</creator><general>Springer</general><general>Springer Nature B.V</general><scope>IQODW</scope><scope>3V.</scope><scope>7QO</scope><scope>7T5</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>H94</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope></search><sort><creationdate>20050401</creationdate><title>A-gluthathione S-transferase as an early marker of hepatic ischemia/reperfusion injury after liver resection</title><author>CHOUKER, Alexander ; MARTIGNONI, André ; PETER, Klaus ; THIEL, Manfred ; SCHAUER, Rolf J ; DUGAS, Martin ; SCHACHTNER, Thomas ; KAUFMANN, Ines ; SETZER, Florian ; RAU, Horst G ; LÖHE, Florian ; JAUCH, Karl-W</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p579-51e87be1892f4c8c838b0fcf23dcf71c3cb2f7068b9c4a0676bdbbec56eeede73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Biological and medical sciences</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>General aspects</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Medical sciences</topic><topic>Other diseases. Semiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>CHOUKER, Alexander</creatorcontrib><creatorcontrib>MARTIGNONI, André</creatorcontrib><creatorcontrib>PETER, Klaus</creatorcontrib><creatorcontrib>THIEL, Manfred</creatorcontrib><creatorcontrib>SCHAUER, Rolf J</creatorcontrib><creatorcontrib>DUGAS, Martin</creatorcontrib><creatorcontrib>SCHACHTNER, Thomas</creatorcontrib><creatorcontrib>KAUFMANN, Ines</creatorcontrib><creatorcontrib>SETZER, Florian</creatorcontrib><creatorcontrib>RAU, Horst G</creatorcontrib><creatorcontrib>LÖHE, Florian</creatorcontrib><creatorcontrib>JAUCH, Karl-W</creatorcontrib><collection>Pascal-Francis</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Immunology Abstracts</collection><collection>Health &amp; Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><jtitle>World journal of surgery</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>CHOUKER, Alexander</au><au>MARTIGNONI, André</au><au>PETER, Klaus</au><au>THIEL, Manfred</au><au>SCHAUER, Rolf J</au><au>DUGAS, Martin</au><au>SCHACHTNER, Thomas</au><au>KAUFMANN, Ines</au><au>SETZER, Florian</au><au>RAU, Horst G</au><au>LÖHE, Florian</au><au>JAUCH, Karl-W</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>A-gluthathione S-transferase as an early marker of hepatic ischemia/reperfusion injury after liver resection</atitle><jtitle>World journal of surgery</jtitle><date>2005-04-01</date><risdate>2005</risdate><volume>29</volume><issue>4</issue><spage>528</spage><epage>534</epage><pages>528-534</pages><issn>0364-2313</issn><eissn>1432-2323</eissn><coden>WJSUDI</coden><abstract>Organ dysfunction following liver resection is one of the major postoperative complications of liver surgery. The Pringle maneuver is often applied during liver resection to minimize bleeding, which in turn complicates the postoperative course owing to liver ischemia and reperfusion. Routinely, hepatocellular damage is diagnosed by, for example, abnormal aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels and the prothrombin time (PT). The cytosolic liver enzyme α-glutathione S-transferase (α-GST) has recently been shown to have good sensitivity for detecting hepatic injury after acetaminophen poisoning or liver transplantation, but its role in non-transplantation liver surgery has not been assessed. In this prospective randomized clinical study, the diagnostic role of plasma α-GST following warm ischemia and reperfusion is reported. A total of 75 patients who underwent liver resection were randomly assigned to three groups: (1) without Pringle (NPR); (2) with Pringle (PR); (3) with ischemic preconditioning by 10 minutes of ischemia and reperfusion each prior to the Pringle manuever (IPC). The major findings are as follows: (1) ALT, AST, and α-GST increased upon liver manipulation as early as prior to resection, with a rapid return of α-GST values to preoperative levels, whereas ALT and AST further increased on the first postoperative day. (2) In the PR group, α-GST, but not ALT and AST, was significantly elevated compared with that in the NPR group at 15 and 30 minutes and 2 hours after resection/reperfusion. In addition, only levels of α-GST significantly correlated with the Pringle duration. (3) The ischemia/reperfusion-induced early rise in α-GST was completely prevented by ischemic preconditioning. Moreover, only α-GST concentrations (&gt;490 μg L-1) determined early after resection (2 hours) predicted postoperative liver dysfunction (24 hours PT &lt; 60%) with a positive predictive value of 74% and a negative predictive value of 76%. Thus α-GST seems to be a sensitive, predictive marker of ischemia/reperfusion-induced hepatocellular injury and postoperative liver dysfunction.</abstract><cop>New York, NY</cop><pub>Springer</pub><doi>10.1007/s00268-004-7431-3</doi><tpages>7</tpages></addata></record>
fulltext fulltext
identifier ISSN: 0364-2313
ispartof World journal of surgery, 2005-04, Vol.29 (4), p.528-534
issn 0364-2313
1432-2323
language eng
recordid cdi_proquest_journals_219963389
source Wiley Online Library Journals Frontfile Complete; SpringerLink Journals - AutoHoldings
subjects Biological and medical sciences
Gastroenterology. Liver. Pancreas. Abdomen
General aspects
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Medical sciences
Other diseases. Semiology
title A-gluthathione S-transferase as an early marker of hepatic ischemia/reperfusion injury after liver resection
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-11T00%3A37%3A43IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pasca&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=A-gluthathione%20S-transferase%20as%20an%20early%20marker%20of%20hepatic%20ischemia/reperfusion%20injury%20after%20liver%20resection&rft.jtitle=World%20journal%20of%20surgery&rft.au=CHOUKER,%20Alexander&rft.date=2005-04-01&rft.volume=29&rft.issue=4&rft.spage=528&rft.epage=534&rft.pages=528-534&rft.issn=0364-2313&rft.eissn=1432-2323&rft.coden=WJSUDI&rft_id=info:doi/10.1007/s00268-004-7431-3&rft_dat=%3Cproquest_pasca%3E876459461%3C/proquest_pasca%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=219963389&rft_id=info:pmid/&rfr_iscdi=true