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 |
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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. |
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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 & 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&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 & implants</subject><subject>Viral diseases</subject><subject>Viral diseases of the lymphoid tissue and the blood. Aids</subject><subject>Viral hepatitis</subject><issn>1058-4838</issn><issn>1537-6591</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkU9vEzEQxS1ERUvhxBlkCXGiC_6z3rUvSFVKm0hBVKj0ajn2bOMosRfbqcQn6NfGJWkph5FH8m_ePM1D6A0lnyhR_LP1rlamjHTP0BEVvG86oejz2hMhm1ZyeYhe5rwihFJJxAt0yDjrWt61R-juhxm9w5cp3iTI2ceAS8RnYONmhJBNAYcnPqVlzD6f4Lm_hYSvkgl5XJtQTrAJruKmLLEPeDq7bnwYwN6PfYOAT4dS-cvkNyb9xlMYTfHFZzzB1z5tM579hevWV-hgMOsMr_fvMfp5_vVqMm3m3y9mk9N5YwXrS8MUZabllkrVgxTKKtE70nIKXFgnQCnnbOcWbsEdCM5BKMW6oSU94VQZxo_Rl53uuF1swFkIJZm1HncOdTRe__8T_FLfxFvNhZT1fFXg_V4gxV9byEWv4jaF6llTTgXjPVOqUh93lE0x5wTD4wZK9H1quqam96lV-t1TU4_sQ0wV-LAHTLZmPdT719l_XE9b0kpRubc7bpVLTE90WkmV7Pkfclarnw</recordid><startdate>20130401</startdate><enddate>20130401</enddate><creator>Fierer, Daniel S.</creator><creator>Dieterich, Douglas T.</creator><creator>Fiel, M. 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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><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>Bacteriology Abstracts (Microbiology B)</collection><collection>Health and Safety Science Abstracts (Full archive)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Toxicology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Clinical infectious diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fierer, Daniel S.</au><au>Dieterich, Douglas T.</au><au>Fiel, M. 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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