Hepatitis G virus co‐infection in liver transplantation recipients with chronic hepatitis C and nonviral chronic liver disease
Hepatitis G virus (HGV) is a newly described RNA virus that is parenterally transmitted and has been found frequently in patients with chronic hepatitis C infection. To determine the impact of hepatitis G virus co‐infection on morbidity and mortality following liver transplantation, we measured HGV...
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Veröffentlicht in: | Hepatology (Baltimore, Md.) Md.), 1997-05, Vol.25 (5), p.1271-1275 |
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description | Hepatitis G virus (HGV) is a newly described RNA virus that is parenterally transmitted and has been found frequently in patients with chronic hepatitis C infection. To determine the impact of hepatitis G virus co‐infection on morbidity and mortality following liver transplantation, we measured HGV RNA by polymerase chain reaction in pre and posttransplantation sera from a cohort of patients transplanted for chronic hepatitis C and a control group of patients transplanted for nonviral causes who were negative for hepatitis C virus (HCV) RNA in serum. The overall prevalence rate of HGV RNA in transplanted patients with chronic hepatitis C was 20.7%. HGV infection was present before transplantation in 13% while it appeared to have been acquired at the time of transplantation in 7.4%. Mean serum alanine aminotransferase activity, hepatic histological activity, and patient and graft survival were similar between HGV‐positive and HGV‐negative patients. The prevalence rate of HGV RNA in transplanted controls was 64% (P < .01) with a significantly higher rate of acquisition of HGV infection following transplantation (53%, P < .001) when compared with patients with chronic hepatitis C. Mean serum alanine aminotransferase activity was significantly lower in the control patients with HGV infection alone following transplantation than in patients co‐infected with hepatitis C (37 ± 9 vs. 70 ± 33 U/L, P < .01). Thus, HGV is frequently found in transplantation patients co‐infected with hepatitis C although it appears to have minimal clinical impact. In patients transplanted for nonviral causes of end‐stage liver disease, a high rate of hepatitis G acquisition at the time of transplantation may occur but does not appear to predispose to chronic hepatitis. |
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To determine the impact of hepatitis G virus co‐infection on morbidity and mortality following liver transplantation, we measured HGV RNA by polymerase chain reaction in pre and posttransplantation sera from a cohort of patients transplanted for chronic hepatitis C and a control group of patients transplanted for nonviral causes who were negative for hepatitis C virus (HCV) RNA in serum. The overall prevalence rate of HGV RNA in transplanted patients with chronic hepatitis C was 20.7%. HGV infection was present before transplantation in 13% while it appeared to have been acquired at the time of transplantation in 7.4%. Mean serum alanine aminotransferase activity, hepatic histological activity, and patient and graft survival were similar between HGV‐positive and HGV‐negative patients. The prevalence rate of HGV RNA in transplanted controls was 64% (P < .01) with a significantly higher rate of acquisition of HGV infection following transplantation (53%, P < .001) when compared with patients with chronic hepatitis C. Mean serum alanine aminotransferase activity was significantly lower in the control patients with HGV infection alone following transplantation than in patients co‐infected with hepatitis C (37 ± 9 vs. 70 ± 33 U/L, P < .01). Thus, HGV is frequently found in transplantation patients co‐infected with hepatitis C although it appears to have minimal clinical impact. In patients transplanted for nonviral causes of end‐stage liver disease, a high rate of hepatitis G acquisition at the time of transplantation may occur but does not appear to predispose to chronic hepatitis.</description><identifier>ISSN: 0270-9139</identifier><identifier>EISSN: 1527-3350</identifier><identifier>DOI: 10.1002/hep.510250536</identifier><identifier>PMID: 9141451</identifier><identifier>CODEN: HPTLD9</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Biological and medical sciences ; Chronic Disease ; Female ; Flaviviridae - isolation & purification ; Hepatitis C - mortality ; Hepatitis C - virology ; Hepatitis, Viral, Human - mortality ; Hepatitis, Viral, Human - virology ; Human viral diseases ; Humans ; Infectious diseases ; Liver Diseases - mortality ; Liver Diseases - surgery ; Liver Diseases - virology ; Liver Transplantation - adverse effects ; Male ; Medical sciences ; Middle Aged ; RNA, Viral - blood ; Survival Analysis ; Viral diseases ; Viral hepatitis</subject><ispartof>Hepatology (Baltimore, Md.), 1997-05, Vol.25 (5), p.1271-1275</ispartof><rights>Copyright © 1997 by the American Association for the Study of Liver Diseases</rights><rights>1997 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4046-a476beeb0072110287fdb0adeb2a8f10a29248483b91db95f5be0b6aa1b2c0743</citedby></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.510250536$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fhep.510250536$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2660242$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9141451$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fried, M W</creatorcontrib><creatorcontrib>Khudyakov, Y E</creatorcontrib><creatorcontrib>Smallwood, G A</creatorcontrib><creatorcontrib>Cong, M</creatorcontrib><creatorcontrib>Nichols, B</creatorcontrib><creatorcontrib>Diaz, E</creatorcontrib><creatorcontrib>Siefert, P</creatorcontrib><creatorcontrib>Gutekunst, K</creatorcontrib><creatorcontrib>Gordon, R D</creatorcontrib><creatorcontrib>Boyer, T D</creatorcontrib><creatorcontrib>Fields, H A</creatorcontrib><title>Hepatitis G virus co‐infection in liver transplantation recipients with chronic hepatitis C and nonviral chronic liver disease</title><title>Hepatology (Baltimore, Md.)</title><addtitle>Hepatology</addtitle><description>Hepatitis G virus (HGV) is a newly described RNA virus that is parenterally transmitted and has been found frequently in patients with chronic hepatitis C infection. To determine the impact of hepatitis G virus co‐infection on morbidity and mortality following liver transplantation, we measured HGV RNA by polymerase chain reaction in pre and posttransplantation sera from a cohort of patients transplanted for chronic hepatitis C and a control group of patients transplanted for nonviral causes who were negative for hepatitis C virus (HCV) RNA in serum. The overall prevalence rate of HGV RNA in transplanted patients with chronic hepatitis C was 20.7%. HGV infection was present before transplantation in 13% while it appeared to have been acquired at the time of transplantation in 7.4%. Mean serum alanine aminotransferase activity, hepatic histological activity, and patient and graft survival were similar between HGV‐positive and HGV‐negative patients. The prevalence rate of HGV RNA in transplanted controls was 64% (P < .01) with a significantly higher rate of acquisition of HGV infection following transplantation (53%, P < .001) when compared with patients with chronic hepatitis C. Mean serum alanine aminotransferase activity was significantly lower in the control patients with HGV infection alone following transplantation than in patients co‐infected with hepatitis C (37 ± 9 vs. 70 ± 33 U/L, P < .01). Thus, HGV is frequently found in transplantation patients co‐infected with hepatitis C although it appears to have minimal clinical impact. In patients transplanted for nonviral causes of end‐stage liver disease, a high rate of hepatitis G acquisition at the time of transplantation may occur but does not appear to predispose to chronic hepatitis.</description><subject>Adult</subject><subject>Biological and medical sciences</subject><subject>Chronic Disease</subject><subject>Female</subject><subject>Flaviviridae - isolation & purification</subject><subject>Hepatitis C - mortality</subject><subject>Hepatitis C - virology</subject><subject>Hepatitis, Viral, Human - mortality</subject><subject>Hepatitis, Viral, Human - virology</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Liver Diseases - mortality</subject><subject>Liver Diseases - surgery</subject><subject>Liver Diseases - virology</subject><subject>Liver Transplantation - adverse effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>RNA, Viral - blood</subject><subject>Survival Analysis</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><issn>0270-9139</issn><issn>1527-3350</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1997</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kMFu1DAURS0EKtPCsstKXqDuUp4dJ7GXaNR2kCrBAtbRs_OiMco4wc606q6fwDf2SzCdUbpj5cU9Os_3MnYu4EoAyM9bmq4qAbKCqqzfsJWoZFOUZQVv2QpkA4URpXnPTlP6BQBGSX3CToxQQlVixZ42NOHsZ5_4Lb_3cZ-4G5-f_vjQk5v9GLgPfPD3FPkcMaRpwDDjSxDJ-clTmBN_8POWu20cg3d8uxjXHEPHwxiyGIcFOOg6nwgTfWDvehwSfTy-Z-znzfWP9aa4-3b7df3lrnAKVF2gampLZAEaKXJb3fSdBezIStS9AJRGKq10aY3orKn6yhLYGlFY6aBR5Rm7PHinOP7eU5rbnU-OhtyHxn1qG22M1FpnsDiALo4pRerbKfodxsdWQPtv8TYXbJfFM39xFO_tjrqFPk6c80_HHJPDoc8rOp8WTNY1SCUz1hywBz_Q4_9vtpvr768f-As9YpyV</recordid><startdate>199705</startdate><enddate>199705</enddate><creator>Fried, M W</creator><creator>Khudyakov, Y E</creator><creator>Smallwood, G A</creator><creator>Cong, M</creator><creator>Nichols, B</creator><creator>Diaz, E</creator><creator>Siefert, P</creator><creator>Gutekunst, K</creator><creator>Gordon, R D</creator><creator>Boyer, T D</creator><creator>Fields, H 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>199705</creationdate><title>Hepatitis G virus co‐infection in liver transplantation recipients with chronic hepatitis C and nonviral chronic liver disease</title><author>Fried, M W ; Khudyakov, Y E ; Smallwood, G A ; Cong, M ; Nichols, B ; Diaz, E ; Siefert, P ; Gutekunst, K ; Gordon, R D ; Boyer, T D ; Fields, H A</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4046-a476beeb0072110287fdb0adeb2a8f10a29248483b91db95f5be0b6aa1b2c0743</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1997</creationdate><topic>Adult</topic><topic>Biological and medical sciences</topic><topic>Chronic Disease</topic><topic>Female</topic><topic>Flaviviridae - isolation & purification</topic><topic>Hepatitis C - mortality</topic><topic>Hepatitis C - virology</topic><topic>Hepatitis, Viral, Human - mortality</topic><topic>Hepatitis, Viral, Human - virology</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Liver Diseases - mortality</topic><topic>Liver Diseases - surgery</topic><topic>Liver Diseases - virology</topic><topic>Liver Transplantation - adverse effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>RNA, Viral - blood</topic><topic>Survival Analysis</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Fried, M W</creatorcontrib><creatorcontrib>Khudyakov, Y E</creatorcontrib><creatorcontrib>Smallwood, G A</creatorcontrib><creatorcontrib>Cong, M</creatorcontrib><creatorcontrib>Nichols, B</creatorcontrib><creatorcontrib>Diaz, E</creatorcontrib><creatorcontrib>Siefert, P</creatorcontrib><creatorcontrib>Gutekunst, K</creatorcontrib><creatorcontrib>Gordon, R D</creatorcontrib><creatorcontrib>Boyer, T D</creatorcontrib><creatorcontrib>Fields, H 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>Fried, M W</au><au>Khudyakov, Y E</au><au>Smallwood, G A</au><au>Cong, M</au><au>Nichols, B</au><au>Diaz, E</au><au>Siefert, P</au><au>Gutekunst, K</au><au>Gordon, R D</au><au>Boyer, T D</au><au>Fields, H A</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Hepatitis G virus co‐infection in liver transplantation recipients with chronic hepatitis C and nonviral chronic liver disease</atitle><jtitle>Hepatology (Baltimore, Md.)</jtitle><addtitle>Hepatology</addtitle><date>1997-05</date><risdate>1997</risdate><volume>25</volume><issue>5</issue><spage>1271</spage><epage>1275</epage><pages>1271-1275</pages><issn>0270-9139</issn><eissn>1527-3350</eissn><coden>HPTLD9</coden><abstract>Hepatitis G virus (HGV) is a newly described RNA virus that is parenterally transmitted and has been found frequently in patients with chronic hepatitis C infection. To determine the impact of hepatitis G virus co‐infection on morbidity and mortality following liver transplantation, we measured HGV RNA by polymerase chain reaction in pre and posttransplantation sera from a cohort of patients transplanted for chronic hepatitis C and a control group of patients transplanted for nonviral causes who were negative for hepatitis C virus (HCV) RNA in serum. The overall prevalence rate of HGV RNA in transplanted patients with chronic hepatitis C was 20.7%. HGV infection was present before transplantation in 13% while it appeared to have been acquired at the time of transplantation in 7.4%. Mean serum alanine aminotransferase activity, hepatic histological activity, and patient and graft survival were similar between HGV‐positive and HGV‐negative patients. The prevalence rate of HGV RNA in transplanted controls was 64% (P < .01) with a significantly higher rate of acquisition of HGV infection following transplantation (53%, P < .001) when compared with patients with chronic hepatitis C. Mean serum alanine aminotransferase activity was significantly lower in the control patients with HGV infection alone following transplantation than in patients co‐infected with hepatitis C (37 ± 9 vs. 70 ± 33 U/L, P < .01). Thus, HGV is frequently found in transplantation patients co‐infected with hepatitis C although it appears to have minimal clinical impact. In patients transplanted for nonviral causes of end‐stage liver disease, a high rate of hepatitis G acquisition at the time of transplantation may occur but does not appear to predispose to chronic hepatitis.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>9141451</pmid><doi>10.1002/hep.510250536</doi><tpages>5</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Adult Biological and medical sciences Chronic Disease Female Flaviviridae - isolation & purification Hepatitis C - mortality Hepatitis C - virology Hepatitis, Viral, Human - mortality Hepatitis, Viral, Human - virology Human viral diseases Humans Infectious diseases Liver Diseases - mortality Liver Diseases - surgery Liver Diseases - virology Liver Transplantation - adverse effects Male Medical sciences Middle Aged RNA, Viral - blood Survival Analysis Viral diseases Viral hepatitis |
title | Hepatitis G virus co‐infection in liver transplantation recipients with chronic hepatitis C and nonviral chronic liver disease |
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