Alterations in the functional capacity of albumin in patients with decompensated cirrhosis is associated with increased mortality

Albumin concentration is diminished in patients with liver failure. Albumin infusion improves survival of cirrhotic patients with spontaneous bacterial peritonitis, and it is hypothesized that this may be due in part to its detoxifying capabilities. The aim of this study was to perform detailed quan...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Hepatology (Baltimore, Md.) Md.), 2009-08, Vol.50 (2), p.555-564
Hauptverfasser: Jalan, Rajiv, Schnurr, Kerstin, Mookerjee, Rajeshwar P., Sen, Sambit, Cheshire, Lisa, Hodges, Stephen, Muravsky, Vladimir, Williams, Roger, Matthes, Gert, Davies, Nathan A.
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 564
container_issue 2
container_start_page 555
container_title Hepatology (Baltimore, Md.)
container_volume 50
creator Jalan, Rajiv
Schnurr, Kerstin
Mookerjee, Rajeshwar P.
Sen, Sambit
Cheshire, Lisa
Hodges, Stephen
Muravsky, Vladimir
Williams, Roger
Matthes, Gert
Davies, Nathan A.
description Albumin concentration is diminished in patients with liver failure. Albumin infusion improves survival of cirrhotic patients with spontaneous bacterial peritonitis, and it is hypothesized that this may be due in part to its detoxifying capabilities. The aim of this study was to perform detailed quantitative and qualitative assessment of albumin function in patients with cirrhosis. Healthy controls and patients with acute deterioration of cirrhosis requiring hospital admission (n = 34) were included. Albumin function was assessed using affinity of the fatty acid binding sites using a spin label (16 doxyl‐stearate) titration and electron paramagnetic resonance spectroscopy and ischemia‐modified albumin (IMA) was measured. Twenty‐two patients developed acute‐on‐chronic liver failure. Twelve were treated with the Molecular Adsorbents Recirculating System (MARS) and 10 with standard medical therapy. For each parameter measured, the patients' albumin had reduced functional ability, which worsened with disease severity. Fifteen patients died, and IMA, expressed as an albumin ratio (IMAR), was significantly higher in nonsurvivors compared with survivors (P < 0.001; area under the receiver operating curve = 0.8). No change in the patients' albumin function was observed following MARS therapy. A significant negative correlation between IMAR and the fatty acid binding coefficients for sites 1 and 2 (P < 0.001 for both) was observed, indicating possible sites of association on the protein. Conclusion: The results of this study suggests marked dysfunction of albumin function in advanced cirrhosis and provide further evidence for damage to the circulating albumin, which is not reversed by MARS therapy. IMAR correlates with disease severity and may have prognostic use in acute‐on‐chronic liver failure. (HEPATOLOGY 2009;50:555–564.)
doi_str_mv 10.1002/hep.22913
format Article
fullrecord <record><control><sourceid>proquest_cross</sourceid><recordid>TN_cdi_proquest_miscellaneous_67550755</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>67550755</sourcerecordid><originalsourceid>FETCH-LOGICAL-c3883-1c187210159577f623cc74b62e0bf03e51143509a177bb2a3cdd688ee08dbdea3</originalsourceid><addsrcrecordid>eNp10M-L1TAQB_AgivtcPfgPSC4KHrqbH22THpdldYUFPei5TNMpL5I2NZOyvKP_udn3HnoSEkKGT2bIl7G3UlxJIdT1HtcrpTqpn7GdbJSptG7Ec7YTyoiqlLsL9oropxCiq5V9yS5k19ZKmnrHft-EjAmyjwtxv_C8Rz5ti3sqQOAOVnA-H3icOIRhmwspay0PcMnEH33e8xFdnFdcCDKO3PmU9pF8aUcciKLzx_qR-sUlBCrXOaYMobR-zV5MEAjfnM9L9uPT3ffb--rh6-cvtzcPldPW6ko6aY2SQjZdY8zUKu2cqYdWoRgmobGRsi6_7kAaMwwKtBvH1lpEYcdhRNCX7MOp75rirw0p97MnhyHAgnGjvjVNI8ou8OMJuhSJEk79mvwM6dBL0T_l3Ze8-2Pexb47N92GGcd_8hxwAe_PAMhBmBIsztNfV4yVtpbFXZ_cow94-P_E_v7u22n0H0JhmWo</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>67550755</pqid></control><display><type>article</type><title>Alterations in the functional capacity of albumin in patients with decompensated cirrhosis is associated with increased mortality</title><source>MEDLINE</source><source>Wiley Online Library Journals Frontfile Complete</source><source>EZB-FREE-00999 freely available EZB journals</source><creator>Jalan, Rajiv ; Schnurr, Kerstin ; Mookerjee, Rajeshwar P. ; Sen, Sambit ; Cheshire, Lisa ; Hodges, Stephen ; Muravsky, Vladimir ; Williams, Roger ; Matthes, Gert ; Davies, Nathan A.</creator><creatorcontrib>Jalan, Rajiv ; Schnurr, Kerstin ; Mookerjee, Rajeshwar P. ; Sen, Sambit ; Cheshire, Lisa ; Hodges, Stephen ; Muravsky, Vladimir ; Williams, Roger ; Matthes, Gert ; Davies, Nathan A.</creatorcontrib><description>Albumin concentration is diminished in patients with liver failure. Albumin infusion improves survival of cirrhotic patients with spontaneous bacterial peritonitis, and it is hypothesized that this may be due in part to its detoxifying capabilities. The aim of this study was to perform detailed quantitative and qualitative assessment of albumin function in patients with cirrhosis. Healthy controls and patients with acute deterioration of cirrhosis requiring hospital admission (n = 34) were included. Albumin function was assessed using affinity of the fatty acid binding sites using a spin label (16 doxyl‐stearate) titration and electron paramagnetic resonance spectroscopy and ischemia‐modified albumin (IMA) was measured. Twenty‐two patients developed acute‐on‐chronic liver failure. Twelve were treated with the Molecular Adsorbents Recirculating System (MARS) and 10 with standard medical therapy. For each parameter measured, the patients' albumin had reduced functional ability, which worsened with disease severity. Fifteen patients died, and IMA, expressed as an albumin ratio (IMAR), was significantly higher in nonsurvivors compared with survivors (P &lt; 0.001; area under the receiver operating curve = 0.8). No change in the patients' albumin function was observed following MARS therapy. A significant negative correlation between IMAR and the fatty acid binding coefficients for sites 1 and 2 (P &lt; 0.001 for both) was observed, indicating possible sites of association on the protein. Conclusion: The results of this study suggests marked dysfunction of albumin function in advanced cirrhosis and provide further evidence for damage to the circulating albumin, which is not reversed by MARS therapy. IMAR correlates with disease severity and may have prognostic use in acute‐on‐chronic liver failure. (HEPATOLOGY 2009;50:555–564.)</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.22913</identifier><identifier>PMID: 19642174</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Albumins - metabolism ; Binding Sites ; Biological and medical sciences ; Case-Control Studies ; Electron Spin Resonance Spectroscopy ; F2-Isoprostanes - blood ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; Ischemia - metabolism ; Liver Cirrhosis - complications ; Liver Cirrhosis - metabolism ; Liver Cirrhosis - mortality ; Liver Failure, Acute - etiology ; Liver Failure, Acute - metabolism ; Liver Failure, Acute - mortality ; Liver Failure, Acute - therapy ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Malondialdehyde - blood ; Medical sciences ; Middle Aged ; Other diseases. Semiology ; Oxidative Stress ; Renal Dialysis</subject><ispartof>Hepatology (Baltimore, Md.), 2009-08, Vol.50 (2), p.555-564</ispartof><rights>Copyright © 2009 American Association for the Study of Liver Diseases</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3883-1c187210159577f623cc74b62e0bf03e51143509a177bb2a3cdd688ee08dbdea3</citedby><cites>FETCH-LOGICAL-c3883-1c187210159577f623cc74b62e0bf03e51143509a177bb2a3cdd688ee08dbdea3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fhep.22913$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhep.22913$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,27907,27908,45557,45558</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=21781841$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/19642174$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Jalan, Rajiv</creatorcontrib><creatorcontrib>Schnurr, Kerstin</creatorcontrib><creatorcontrib>Mookerjee, Rajeshwar P.</creatorcontrib><creatorcontrib>Sen, Sambit</creatorcontrib><creatorcontrib>Cheshire, Lisa</creatorcontrib><creatorcontrib>Hodges, Stephen</creatorcontrib><creatorcontrib>Muravsky, Vladimir</creatorcontrib><creatorcontrib>Williams, Roger</creatorcontrib><creatorcontrib>Matthes, Gert</creatorcontrib><creatorcontrib>Davies, Nathan A.</creatorcontrib><title>Alterations in the functional capacity of albumin in patients with decompensated cirrhosis is associated with increased mortality</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>Albumin concentration is diminished in patients with liver failure. Albumin infusion improves survival of cirrhotic patients with spontaneous bacterial peritonitis, and it is hypothesized that this may be due in part to its detoxifying capabilities. The aim of this study was to perform detailed quantitative and qualitative assessment of albumin function in patients with cirrhosis. Healthy controls and patients with acute deterioration of cirrhosis requiring hospital admission (n = 34) were included. Albumin function was assessed using affinity of the fatty acid binding sites using a spin label (16 doxyl‐stearate) titration and electron paramagnetic resonance spectroscopy and ischemia‐modified albumin (IMA) was measured. Twenty‐two patients developed acute‐on‐chronic liver failure. Twelve were treated with the Molecular Adsorbents Recirculating System (MARS) and 10 with standard medical therapy. For each parameter measured, the patients' albumin had reduced functional ability, which worsened with disease severity. Fifteen patients died, and IMA, expressed as an albumin ratio (IMAR), was significantly higher in nonsurvivors compared with survivors (P &lt; 0.001; area under the receiver operating curve = 0.8). No change in the patients' albumin function was observed following MARS therapy. A significant negative correlation between IMAR and the fatty acid binding coefficients for sites 1 and 2 (P &lt; 0.001 for both) was observed, indicating possible sites of association on the protein. Conclusion: The results of this study suggests marked dysfunction of albumin function in advanced cirrhosis and provide further evidence for damage to the circulating albumin, which is not reversed by MARS therapy. IMAR correlates with disease severity and may have prognostic use in acute‐on‐chronic liver failure. (HEPATOLOGY 2009;50:555–564.)</description><subject>Adult</subject><subject>Albumins - metabolism</subject><subject>Binding Sites</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Electron Spin Resonance Spectroscopy</subject><subject>F2-Isoprostanes - blood</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>Ischemia - metabolism</subject><subject>Liver Cirrhosis - complications</subject><subject>Liver Cirrhosis - metabolism</subject><subject>Liver Cirrhosis - mortality</subject><subject>Liver Failure, Acute - etiology</subject><subject>Liver Failure, Acute - metabolism</subject><subject>Liver Failure, Acute - mortality</subject><subject>Liver Failure, Acute - therapy</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Malondialdehyde - blood</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Other diseases. Semiology</subject><subject>Oxidative Stress</subject><subject>Renal Dialysis</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2009</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp10M-L1TAQB_AgivtcPfgPSC4KHrqbH22THpdldYUFPei5TNMpL5I2NZOyvKP_udn3HnoSEkKGT2bIl7G3UlxJIdT1HtcrpTqpn7GdbJSptG7Ec7YTyoiqlLsL9oropxCiq5V9yS5k19ZKmnrHft-EjAmyjwtxv_C8Rz5ti3sqQOAOVnA-H3icOIRhmwspay0PcMnEH33e8xFdnFdcCDKO3PmU9pF8aUcciKLzx_qR-sUlBCrXOaYMobR-zV5MEAjfnM9L9uPT3ffb--rh6-cvtzcPldPW6ko6aY2SQjZdY8zUKu2cqYdWoRgmobGRsi6_7kAaMwwKtBvH1lpEYcdhRNCX7MOp75rirw0p97MnhyHAgnGjvjVNI8ou8OMJuhSJEk79mvwM6dBL0T_l3Ze8-2Pexb47N92GGcd_8hxwAe_PAMhBmBIsztNfV4yVtpbFXZ_cow94-P_E_v7u22n0H0JhmWo</recordid><startdate>200908</startdate><enddate>200908</enddate><creator>Jalan, Rajiv</creator><creator>Schnurr, Kerstin</creator><creator>Mookerjee, Rajeshwar P.</creator><creator>Sen, Sambit</creator><creator>Cheshire, Lisa</creator><creator>Hodges, Stephen</creator><creator>Muravsky, Vladimir</creator><creator>Williams, Roger</creator><creator>Matthes, Gert</creator><creator>Davies, Nathan A.</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><scope>IQODW</scope><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>200908</creationdate><title>Alterations in the functional capacity of albumin in patients with decompensated cirrhosis is associated with increased mortality</title><author>Jalan, Rajiv ; Schnurr, Kerstin ; Mookerjee, Rajeshwar P. ; Sen, Sambit ; Cheshire, Lisa ; Hodges, Stephen ; Muravsky, Vladimir ; Williams, Roger ; Matthes, Gert ; Davies, Nathan A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3883-1c187210159577f623cc74b62e0bf03e51143509a177bb2a3cdd688ee08dbdea3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2009</creationdate><topic>Adult</topic><topic>Albumins - metabolism</topic><topic>Binding Sites</topic><topic>Biological and medical sciences</topic><topic>Case-Control Studies</topic><topic>Electron Spin Resonance Spectroscopy</topic><topic>F2-Isoprostanes - blood</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>Ischemia - metabolism</topic><topic>Liver Cirrhosis - complications</topic><topic>Liver Cirrhosis - metabolism</topic><topic>Liver Cirrhosis - mortality</topic><topic>Liver Failure, Acute - etiology</topic><topic>Liver Failure, Acute - metabolism</topic><topic>Liver Failure, Acute - mortality</topic><topic>Liver Failure, Acute - therapy</topic><topic>Liver. Biliary tract. Portal circulation. Exocrine pancreas</topic><topic>Male</topic><topic>Malondialdehyde - blood</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Other diseases. Semiology</topic><topic>Oxidative Stress</topic><topic>Renal Dialysis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Jalan, Rajiv</creatorcontrib><creatorcontrib>Schnurr, Kerstin</creatorcontrib><creatorcontrib>Mookerjee, Rajeshwar P.</creatorcontrib><creatorcontrib>Sen, Sambit</creatorcontrib><creatorcontrib>Cheshire, Lisa</creatorcontrib><creatorcontrib>Hodges, Stephen</creatorcontrib><creatorcontrib>Muravsky, Vladimir</creatorcontrib><creatorcontrib>Williams, Roger</creatorcontrib><creatorcontrib>Matthes, Gert</creatorcontrib><creatorcontrib>Davies, Nathan A.</creatorcontrib><collection>Pascal-Francis</collection><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>Hepatology (Baltimore, Md.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Jalan, Rajiv</au><au>Schnurr, Kerstin</au><au>Mookerjee, Rajeshwar P.</au><au>Sen, Sambit</au><au>Cheshire, Lisa</au><au>Hodges, Stephen</au><au>Muravsky, Vladimir</au><au>Williams, Roger</au><au>Matthes, Gert</au><au>Davies, Nathan A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Alterations in the functional capacity of albumin in patients with decompensated cirrhosis is associated with increased mortality</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>2009-08</date><risdate>2009</risdate><volume>50</volume><issue>2</issue><spage>555</spage><epage>564</epage><pages>555-564</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>Albumin concentration is diminished in patients with liver failure. Albumin infusion improves survival of cirrhotic patients with spontaneous bacterial peritonitis, and it is hypothesized that this may be due in part to its detoxifying capabilities. The aim of this study was to perform detailed quantitative and qualitative assessment of albumin function in patients with cirrhosis. Healthy controls and patients with acute deterioration of cirrhosis requiring hospital admission (n = 34) were included. Albumin function was assessed using affinity of the fatty acid binding sites using a spin label (16 doxyl‐stearate) titration and electron paramagnetic resonance spectroscopy and ischemia‐modified albumin (IMA) was measured. Twenty‐two patients developed acute‐on‐chronic liver failure. Twelve were treated with the Molecular Adsorbents Recirculating System (MARS) and 10 with standard medical therapy. For each parameter measured, the patients' albumin had reduced functional ability, which worsened with disease severity. Fifteen patients died, and IMA, expressed as an albumin ratio (IMAR), was significantly higher in nonsurvivors compared with survivors (P &lt; 0.001; area under the receiver operating curve = 0.8). No change in the patients' albumin function was observed following MARS therapy. A significant negative correlation between IMAR and the fatty acid binding coefficients for sites 1 and 2 (P &lt; 0.001 for both) was observed, indicating possible sites of association on the protein. Conclusion: The results of this study suggests marked dysfunction of albumin function in advanced cirrhosis and provide further evidence for damage to the circulating albumin, which is not reversed by MARS therapy. IMAR correlates with disease severity and may have prognostic use in acute‐on‐chronic liver failure. (HEPATOLOGY 2009;50:555–564.)</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>19642174</pmid><doi>10.1002/hep.22913</doi><tpages>10</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0270-9139
ispartof Hepatology (Baltimore, Md.), 2009-08, Vol.50 (2), p.555-564
issn 0270-9139
1527-3350
language eng
recordid cdi_proquest_miscellaneous_67550755
source MEDLINE; Wiley Online Library Journals Frontfile Complete; EZB-FREE-00999 freely available EZB journals
subjects Adult
Albumins - metabolism
Binding Sites
Biological and medical sciences
Case-Control Studies
Electron Spin Resonance Spectroscopy
F2-Isoprostanes - blood
Female
Gastroenterology. Liver. Pancreas. Abdomen
Humans
Ischemia - metabolism
Liver Cirrhosis - complications
Liver Cirrhosis - metabolism
Liver Cirrhosis - mortality
Liver Failure, Acute - etiology
Liver Failure, Acute - metabolism
Liver Failure, Acute - mortality
Liver Failure, Acute - therapy
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Malondialdehyde - blood
Medical sciences
Middle Aged
Other diseases. Semiology
Oxidative Stress
Renal Dialysis
title Alterations in the functional capacity of albumin in patients with decompensated cirrhosis is associated with increased mortality
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-17T05%3A13%3A05IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_cross&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Alterations%20in%20the%20functional%20capacity%20of%20albumin%20in%20patients%20with%20decompensated%20cirrhosis%20is%20associated%20with%20increased%20mortality&rft.jtitle=Hepatology%20(Baltimore,%20Md.)&rft.au=Jalan,%20Rajiv&rft.date=2009-08&rft.volume=50&rft.issue=2&rft.spage=555&rft.epage=564&rft.pages=555-564&rft.issn=0270-9139&rft.eissn=1527-3350&rft.coden=HPTLD9&rft_id=info:doi/10.1002/hep.22913&rft_dat=%3Cproquest_cross%3E67550755%3C/proquest_cross%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=67550755&rft_id=info:pmid/19642174&rfr_iscdi=true