Rapid Progression to Decompensated Cirrhosis, Liver Transplant, and Death in HIV-infected Men After Primary Hepatitis C Virus Infection

Background. We and others have shown that primary hepatitis C (HCV) infection in men infected with human immunodeficiency virus (HIV) causes early-onset liver fibrosis; however, little is known about the long-term natural history of the liver disease in these HIV-infected men. Methods. We followed a...

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Veröffentlicht in:Clinical infectious diseases 2013-04, Vol.56 (7), p.1038-1043
Hauptverfasser: Fierer, Daniel S., Dieterich, Douglas T., Fiel, M. Isabel, Branch, Andrea D., Marks, Kristen M., Fusco, Dahlene N., Hsu, Ricky, Smith, Davey M., Fierer, Joshua
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container_end_page 1043
container_issue 7
container_start_page 1038
container_title Clinical infectious diseases
container_volume 56
creator Fierer, Daniel S.
Dieterich, Douglas T.
Fiel, M. Isabel
Branch, Andrea D.
Marks, Kristen M.
Fusco, Dahlene N.
Hsu, Ricky
Smith, Davey M.
Fierer, Joshua
description Background. We and others have shown that primary hepatitis C (HCV) infection in men infected with human immunodeficiency virus (HIV) causes early-onset liver fibrosis; however, little is known about the long-term natural history of the liver disease in these HIV-infected men. Methods. We followed a cohort of HIV-infected men with primary HCV infection in New York City. Results. Four men who were not cured after their primary HCV infection developed decompensated cirrhosis within 17 months to 6 years after primary HCV infection. Three died within 8 years of primary HCV infection, and 1 survived after liver transplant done 2 years after primary HCV infection. Three of the 4 men had AIDS at the time of primary HCV infection, and the most rapid progression occurred in the 2 men with the lowest CD4 counts at the time of HCV infection. Liver histopathology was most consistent with HCV-induced damage even though some had exposures to other potential hepatotoxins. Conclusions. Primary HCV infection resulted in decompensated cirrhosis and death within 2–8 years in 4 HIV-infected men. The rapid onset of fibrosis due to primary HCV infection in HIV-infected men cannot therefore be considered benign. The rate of continued progression to liver failure may be proportional to the degree of underlying immunocompromise caused by HIV infection. More research is needed to better define the mechanisms behind accelerated liver damage.
doi_str_mv 10.1093/cid/cis1206
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Isabel ; Branch, Andrea D. ; Marks, Kristen M. ; Fusco, Dahlene N. ; Hsu, Ricky ; Smith, Davey M. ; Fierer, Joshua</creator><creatorcontrib>Fierer, Daniel S. ; Dieterich, Douglas T. ; Fiel, M. Isabel ; Branch, Andrea D. ; Marks, Kristen M. ; Fusco, Dahlene N. ; Hsu, Ricky ; Smith, Davey M. ; Fierer, Joshua</creatorcontrib><description>Background. We and others have shown that primary hepatitis C (HCV) infection in men infected with human immunodeficiency virus (HIV) causes early-onset liver fibrosis; however, little is known about the long-term natural history of the liver disease in these HIV-infected men. Methods. We followed a cohort of HIV-infected men with primary HCV infection in New York City. Results. Four men who were not cured after their primary HCV infection developed decompensated cirrhosis within 17 months to 6 years after primary HCV infection. Three died within 8 years of primary HCV infection, and 1 survived after liver transplant done 2 years after primary HCV infection. Three of the 4 men had AIDS at the time of primary HCV infection, and the most rapid progression occurred in the 2 men with the lowest CD4 counts at the time of HCV infection. Liver histopathology was most consistent with HCV-induced damage even though some had exposures to other potential hepatotoxins. Conclusions. Primary HCV infection resulted in decompensated cirrhosis and death within 2–8 years in 4 HIV-infected men. The rapid onset of fibrosis due to primary HCV infection in HIV-infected men cannot therefore be considered benign. The rate of continued progression to liver failure may be proportional to the degree of underlying immunocompromise caused by HIV infection. More research is needed to better define the mechanisms behind accelerated liver damage.</description><identifier>ISSN: 1058-4838</identifier><identifier>EISSN: 1537-6591</identifier><identifier>DOI: 10.1093/cid/cis1206</identifier><identifier>PMID: 23264364</identifier><identifier>CODEN: CIDIEL</identifier><language>eng</language><publisher>Oxford: Oxford University Press</publisher><subject>Adult ; AIDS ; Biological and medical sciences ; Biopsies ; CD4 Lymphocyte Count ; Cirrhosis ; Cohort Studies ; Fatal Outcome ; Fibrosis ; Gastroenterology. Liver. Pancreas. Abdomen ; Hepacivirus ; Hepatitis ; Hepatitis C ; Hepatitis C - complications ; Hepatitis C - therapy ; Histocytochemistry ; HIV ; HIV Infections - complications ; HIV Infections - immunology ; HIV/AIDS ; Human immunodeficiency virus ; Human viral diseases ; Humans ; Infections ; Infectious diseases ; Liver ; Liver - pathology ; Liver cirrhosis ; Liver Cirrhosis - complications ; Liver Cirrhosis - diagnosis ; Liver diseases ; Liver failure ; Liver Failure - complications ; Liver Failure - diagnosis ; Liver Transplantation ; Liver. Biliary tract. Portal circulation. Exocrine pancreas ; Male ; Medical sciences ; Mens health ; Middle Aged ; New York City ; Other diseases. Semiology ; Survival analysis ; Time Factors ; Transplants &amp; implants ; Viral diseases ; Viral diseases of the lymphoid tissue and the blood. Aids ; Viral hepatitis</subject><ispartof>Clinical infectious diseases, 2013-04, Vol.56 (7), p.1038-1043</ispartof><rights>Copyright © 2013 Oxford University Press on behalf of the Infectious Diseases Society of America</rights><rights>2014 INIST-CNRS</rights><rights>Copyright Oxford University Press, UK Apr 1, 2013</rights><rights>The Author 2012. Published by Oxford University Press on behalf of the Infectious Diseases Society of America. All rights reserved. For Permissions, please e-mail: . 2012</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c527t-2912a43c1897e859c957d0431e35cd5e99ddc6dbdb3de533e59926f4070319a23</citedby><cites>FETCH-LOGICAL-c527t-2912a43c1897e859c957d0431e35cd5e99ddc6dbdb3de533e59926f4070319a23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.jstor.org/stable/pdf/23481987$$EPDF$$P50$$Gjstor$$H</linktopdf><linktohtml>$$Uhttps://www.jstor.org/stable/23481987$$EHTML$$P50$$Gjstor$$H</linktohtml><link.rule.ids>230,314,776,780,799,881,27903,27904,57995,58228</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=27140485$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/23264364$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fierer, Daniel S.</creatorcontrib><creatorcontrib>Dieterich, Douglas T.</creatorcontrib><creatorcontrib>Fiel, M. Isabel</creatorcontrib><creatorcontrib>Branch, Andrea D.</creatorcontrib><creatorcontrib>Marks, Kristen M.</creatorcontrib><creatorcontrib>Fusco, Dahlene N.</creatorcontrib><creatorcontrib>Hsu, Ricky</creatorcontrib><creatorcontrib>Smith, Davey M.</creatorcontrib><creatorcontrib>Fierer, Joshua</creatorcontrib><title>Rapid Progression to Decompensated Cirrhosis, Liver Transplant, and Death in HIV-infected Men After Primary Hepatitis C Virus Infection</title><title>Clinical infectious diseases</title><addtitle>Clin Infect Dis</addtitle><description>Background. We and others have shown that primary hepatitis C (HCV) infection in men infected with human immunodeficiency virus (HIV) causes early-onset liver fibrosis; however, little is known about the long-term natural history of the liver disease in these HIV-infected men. Methods. We followed a cohort of HIV-infected men with primary HCV infection in New York City. Results. Four men who were not cured after their primary HCV infection developed decompensated cirrhosis within 17 months to 6 years after primary HCV infection. Three died within 8 years of primary HCV infection, and 1 survived after liver transplant done 2 years after primary HCV infection. Three of the 4 men had AIDS at the time of primary HCV infection, and the most rapid progression occurred in the 2 men with the lowest CD4 counts at the time of HCV infection. Liver histopathology was most consistent with HCV-induced damage even though some had exposures to other potential hepatotoxins. Conclusions. Primary HCV infection resulted in decompensated cirrhosis and death within 2–8 years in 4 HIV-infected men. The rapid onset of fibrosis due to primary HCV infection in HIV-infected men cannot therefore be considered benign. The rate of continued progression to liver failure may be proportional to the degree of underlying immunocompromise caused by HIV infection. More research is needed to better define the mechanisms behind accelerated liver damage.</description><subject>Adult</subject><subject>AIDS</subject><subject>Biological and medical sciences</subject><subject>Biopsies</subject><subject>CD4 Lymphocyte Count</subject><subject>Cirrhosis</subject><subject>Cohort Studies</subject><subject>Fatal Outcome</subject><subject>Fibrosis</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Hepacivirus</subject><subject>Hepatitis</subject><subject>Hepatitis C</subject><subject>Hepatitis C - complications</subject><subject>Hepatitis C - therapy</subject><subject>Histocytochemistry</subject><subject>HIV</subject><subject>HIV Infections - complications</subject><subject>HIV Infections - immunology</subject><subject>HIV/AIDS</subject><subject>Human immunodeficiency virus</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Infections</subject><subject>Infectious diseases</subject><subject>Liver</subject><subject>Liver - pathology</subject><subject>Liver cirrhosis</subject><subject>Liver Cirrhosis - complications</subject><subject>Liver Cirrhosis - diagnosis</subject><subject>Liver diseases</subject><subject>Liver failure</subject><subject>Liver Failure - complications</subject><subject>Liver Failure - diagnosis</subject><subject>Liver Transplantation</subject><subject>Liver. Biliary tract. Portal circulation. Exocrine pancreas</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Mens health</subject><subject>Middle Aged</subject><subject>New York City</subject><subject>Other diseases. Semiology</subject><subject>Survival analysis</subject><subject>Time Factors</subject><subject>Transplants &amp; implants</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. 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Isabel</au><au>Branch, Andrea D.</au><au>Marks, Kristen M.</au><au>Fusco, Dahlene N.</au><au>Hsu, Ricky</au><au>Smith, Davey M.</au><au>Fierer, Joshua</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Rapid Progression to Decompensated Cirrhosis, Liver Transplant, and Death in HIV-infected Men After Primary Hepatitis C Virus Infection</atitle><jtitle>Clinical infectious diseases</jtitle><addtitle>Clin Infect Dis</addtitle><date>2013-04-01</date><risdate>2013</risdate><volume>56</volume><issue>7</issue><spage>1038</spage><epage>1043</epage><pages>1038-1043</pages><issn>1058-4838</issn><eissn>1537-6591</eissn><coden>CIDIEL</coden><abstract>Background. We and others have shown that primary hepatitis C (HCV) infection in men infected with human immunodeficiency virus (HIV) causes early-onset liver fibrosis; however, little is known about the long-term natural history of the liver disease in these HIV-infected men. Methods. We followed a cohort of HIV-infected men with primary HCV infection in New York City. Results. Four men who were not cured after their primary HCV infection developed decompensated cirrhosis within 17 months to 6 years after primary HCV infection. Three died within 8 years of primary HCV infection, and 1 survived after liver transplant done 2 years after primary HCV infection. Three of the 4 men had AIDS at the time of primary HCV infection, and the most rapid progression occurred in the 2 men with the lowest CD4 counts at the time of HCV infection. Liver histopathology was most consistent with HCV-induced damage even though some had exposures to other potential hepatotoxins. Conclusions. Primary HCV infection resulted in decompensated cirrhosis and death within 2–8 years in 4 HIV-infected men. The rapid onset of fibrosis due to primary HCV infection in HIV-infected men cannot therefore be considered benign. The rate of continued progression to liver failure may be proportional to the degree of underlying immunocompromise caused by HIV infection. More research is needed to better define the mechanisms behind accelerated liver damage.</abstract><cop>Oxford</cop><pub>Oxford University Press</pub><pmid>23264364</pmid><doi>10.1093/cid/cis1206</doi><tpages>6</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
AIDS
Biological and medical sciences
Biopsies
CD4 Lymphocyte Count
Cirrhosis
Cohort Studies
Fatal Outcome
Fibrosis
Gastroenterology. Liver. Pancreas. Abdomen
Hepacivirus
Hepatitis
Hepatitis C
Hepatitis C - complications
Hepatitis C - therapy
Histocytochemistry
HIV
HIV Infections - complications
HIV Infections - immunology
HIV/AIDS
Human immunodeficiency virus
Human viral diseases
Humans
Infections
Infectious diseases
Liver
Liver - pathology
Liver cirrhosis
Liver Cirrhosis - complications
Liver Cirrhosis - diagnosis
Liver diseases
Liver failure
Liver Failure - complications
Liver Failure - diagnosis
Liver Transplantation
Liver. Biliary tract. Portal circulation. Exocrine pancreas
Male
Medical sciences
Mens health
Middle Aged
New York City
Other diseases. Semiology
Survival analysis
Time Factors
Transplants & implants
Viral diseases
Viral diseases of the lymphoid tissue and the blood. Aids
Viral hepatitis
title Rapid Progression to Decompensated Cirrhosis, Liver Transplant, and Death in HIV-infected Men After Primary Hepatitis C Virus Infection
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