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Prognostic factors in patients with hepatitis C virus infection and systemic vasculitis
Objective Hepatitis C virus (HCV)–related systemic vasculitis can cause significant morbidity and mortality. Most studies of the prognosis of patients with HCV‐related systemic vasculitis are based on heterogeneous studies performed before the era of antiviral therapy. The aim of this study was to a...
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Published in: | Arthritis & rheumatology (Hoboken, N.J.) N.J.), 2011-06, Vol.63 (6), p.1748-1757 |
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creator | Terrier, Benjamin Semoun, Oren Saadoun, David Sène, Damien Resche‐Rigon, Matthieu Cacoub, Patrice |
description | Objective
Hepatitis C virus (HCV)–related systemic vasculitis can cause significant morbidity and mortality. Most studies of the prognosis of patients with HCV‐related systemic vasculitis are based on heterogeneous studies performed before the era of antiviral therapy. The aim of this study was to analyze the clinical, biologic, and therapeutic factors associated with prognosis in a homogeneous series of patients with HCV‐related systemic vasculitis who were followed up during the era of antiviral therapy.
Methods
One hundred fifty‐one consecutive HCV RNA–positive patients with vasculitis were prospectively followed up between 1993 and 2009 and were analyzed for clinical, biologic, and therapeutic factors associated with survival.
Results
After a median followup period of 54 months, 32 patients (21%) had died, mainly of infection and end‐stage liver disease. The 1‐year, 3‐year, 5‐year, and 10‐year survival rates were 96%, 86%, 75%, and 63%, respectively. Baseline factors associated with a poor prognosis were the presence of severe liver fibrosis (hazard ratio [HR] 5.31), central nervous system involvement (HR 2.74), kidney involvement (HR 1.91), and heart involvement (HR 4.2). The Five‐Factors Score (FFS), a vasculitis scoring system, was significantly associated with outcome. In multivariate analysis, severe fibrosis (HR 10.8) and the FFS (HR 2.49) were significantly associated with a poor prognosis. Treatment with the combination of PEGylated interferon plus ribavirin was associated with a good prognosis (HR 0.34), whereas treatment with immunosuppressive agents was associated with a poor outcome, after adjustment for the severity of vasculitis (HR 4.05). Among patients without severe fibrosis, the FFS was a good predictor of outcome, while among those with severe fibrosis, the severity of vasculitis had no prognostic value.
Conclusion
At the time of the diagnosis of HCV‐related systemic vasculitis, severe liver fibrosis and the severity of vasculitis were the main prognostic factors. Use of antiviral agents was associated with a good prognosis, whereas treatment with immunosuppressant agents had a negative impact. |
doi_str_mv | 10.1002/art.30319 |
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Hepatitis C virus (HCV)–related systemic vasculitis can cause significant morbidity and mortality. Most studies of the prognosis of patients with HCV‐related systemic vasculitis are based on heterogeneous studies performed before the era of antiviral therapy. The aim of this study was to analyze the clinical, biologic, and therapeutic factors associated with prognosis in a homogeneous series of patients with HCV‐related systemic vasculitis who were followed up during the era of antiviral therapy.
Methods
One hundred fifty‐one consecutive HCV RNA–positive patients with vasculitis were prospectively followed up between 1993 and 2009 and were analyzed for clinical, biologic, and therapeutic factors associated with survival.
Results
After a median followup period of 54 months, 32 patients (21%) had died, mainly of infection and end‐stage liver disease. The 1‐year, 3‐year, 5‐year, and 10‐year survival rates were 96%, 86%, 75%, and 63%, respectively. Baseline factors associated with a poor prognosis were the presence of severe liver fibrosis (hazard ratio [HR] 5.31), central nervous system involvement (HR 2.74), kidney involvement (HR 1.91), and heart involvement (HR 4.2). The Five‐Factors Score (FFS), a vasculitis scoring system, was significantly associated with outcome. In multivariate analysis, severe fibrosis (HR 10.8) and the FFS (HR 2.49) were significantly associated with a poor prognosis. Treatment with the combination of PEGylated interferon plus ribavirin was associated with a good prognosis (HR 0.34), whereas treatment with immunosuppressive agents was associated with a poor outcome, after adjustment for the severity of vasculitis (HR 4.05). Among patients without severe fibrosis, the FFS was a good predictor of outcome, while among those with severe fibrosis, the severity of vasculitis had no prognostic value.
Conclusion
At the time of the diagnosis of HCV‐related systemic vasculitis, severe liver fibrosis and the severity of vasculitis were the main prognostic factors. Use of antiviral agents was associated with a good prognosis, whereas treatment with immunosuppressant agents had a negative impact.</description><identifier>ISSN: 0004-3591</identifier><identifier>ISSN: 2326-5191</identifier><identifier>ISSN: 1529-0131</identifier><identifier>EISSN: 1529-0131</identifier><identifier>EISSN: 2326-5205</identifier><identifier>DOI: 10.1002/art.30319</identifier><identifier>PMID: 21400476</identifier><identifier>CODEN: ARHEAW</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Adult ; Aged ; Aged, 80 and over ; Antiviral agents ; Antiviral Agents - therapeutic use ; Biological and medical sciences ; Central nervous system ; Cohort Studies ; Diseases of the osteoarticular system ; Drug Therapy, Combination ; Female ; Fibrosis ; Heart ; Hepatitis ; Hepatitis C virus ; Hepatitis C, Chronic - complications ; Human viral diseases ; Humans ; Immunosuppressive agents ; Immunosuppressive Agents - adverse effects ; Immunosuppressive Agents - therapeutic use ; Infection ; Infectious diseases ; Interferon ; Interferon-alpha - therapeutic use ; Kidney ; Liver Cirrhosis - drug therapy ; Liver Cirrhosis - virology ; Liver diseases ; Male ; Medical prognosis ; Medical sciences ; Middle Aged ; Morbidity ; Mortality ; Multivariate analysis ; Polyethylene Glycols - therapeutic use ; Prognosis ; Prospective Studies ; Recombinant Proteins ; Ribavirin ; Ribavirin - therapeutic use ; Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis ; Severity of Illness Index ; Survival ; Systemic vasculitis ; Systemic Vasculitis - drug therapy ; Systemic Vasculitis - mortality ; Systemic Vasculitis - virology ; Treatment Outcome ; Vasculitis ; Viral diseases ; Viral hepatitis</subject><ispartof>Arthritis & rheumatology (Hoboken, N.J.), 2011-06, Vol.63 (6), p.1748-1757</ispartof><rights>Copyright © 2011 by the American College of Rheumatology</rights><rights>2015 INIST-CNRS</rights><rights>Copyright © 2011 by the American College of Rheumatology.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4159-d14afd28c4dde24abf62e549449f8d8f41f0e9b8f72fe8b8846d81b33a5b56c73</citedby><cites>FETCH-LOGICAL-c4159-d14afd28c4dde24abf62e549449f8d8f41f0e9b8f72fe8b8846d81b33a5b56c73</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=24336104$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/21400476$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Terrier, Benjamin</creatorcontrib><creatorcontrib>Semoun, Oren</creatorcontrib><creatorcontrib>Saadoun, David</creatorcontrib><creatorcontrib>Sène, Damien</creatorcontrib><creatorcontrib>Resche‐Rigon, Matthieu</creatorcontrib><creatorcontrib>Cacoub, Patrice</creatorcontrib><title>Prognostic factors in patients with hepatitis C virus infection and systemic vasculitis</title><title>Arthritis & rheumatology (Hoboken, N.J.)</title><addtitle>Arthritis Rheum</addtitle><description>Objective
Hepatitis C virus (HCV)–related systemic vasculitis can cause significant morbidity and mortality. Most studies of the prognosis of patients with HCV‐related systemic vasculitis are based on heterogeneous studies performed before the era of antiviral therapy. The aim of this study was to analyze the clinical, biologic, and therapeutic factors associated with prognosis in a homogeneous series of patients with HCV‐related systemic vasculitis who were followed up during the era of antiviral therapy.
Methods
One hundred fifty‐one consecutive HCV RNA–positive patients with vasculitis were prospectively followed up between 1993 and 2009 and were analyzed for clinical, biologic, and therapeutic factors associated with survival.
Results
After a median followup period of 54 months, 32 patients (21%) had died, mainly of infection and end‐stage liver disease. The 1‐year, 3‐year, 5‐year, and 10‐year survival rates were 96%, 86%, 75%, and 63%, respectively. Baseline factors associated with a poor prognosis were the presence of severe liver fibrosis (hazard ratio [HR] 5.31), central nervous system involvement (HR 2.74), kidney involvement (HR 1.91), and heart involvement (HR 4.2). The Five‐Factors Score (FFS), a vasculitis scoring system, was significantly associated with outcome. In multivariate analysis, severe fibrosis (HR 10.8) and the FFS (HR 2.49) were significantly associated with a poor prognosis. Treatment with the combination of PEGylated interferon plus ribavirin was associated with a good prognosis (HR 0.34), whereas treatment with immunosuppressive agents was associated with a poor outcome, after adjustment for the severity of vasculitis (HR 4.05). Among patients without severe fibrosis, the FFS was a good predictor of outcome, while among those with severe fibrosis, the severity of vasculitis had no prognostic value.
Conclusion
At the time of the diagnosis of HCV‐related systemic vasculitis, severe liver fibrosis and the severity of vasculitis were the main prognostic factors. Use of antiviral agents was associated with a good prognosis, whereas treatment with immunosuppressant agents had a negative impact.</description><subject>Adult</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Antiviral agents</subject><subject>Antiviral Agents - therapeutic use</subject><subject>Biological and medical sciences</subject><subject>Central nervous system</subject><subject>Cohort Studies</subject><subject>Diseases of the osteoarticular system</subject><subject>Drug Therapy, Combination</subject><subject>Female</subject><subject>Fibrosis</subject><subject>Heart</subject><subject>Hepatitis</subject><subject>Hepatitis C virus</subject><subject>Hepatitis C, Chronic - complications</subject><subject>Human viral diseases</subject><subject>Humans</subject><subject>Immunosuppressive agents</subject><subject>Immunosuppressive Agents - adverse effects</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Infection</subject><subject>Infectious diseases</subject><subject>Interferon</subject><subject>Interferon-alpha - therapeutic use</subject><subject>Kidney</subject><subject>Liver Cirrhosis - drug therapy</subject><subject>Liver Cirrhosis - virology</subject><subject>Liver diseases</subject><subject>Male</subject><subject>Medical prognosis</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Morbidity</subject><subject>Mortality</subject><subject>Multivariate analysis</subject><subject>Polyethylene Glycols - therapeutic use</subject><subject>Prognosis</subject><subject>Prospective Studies</subject><subject>Recombinant Proteins</subject><subject>Ribavirin</subject><subject>Ribavirin - therapeutic use</subject><subject>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</subject><subject>Severity of Illness Index</subject><subject>Survival</subject><subject>Systemic vasculitis</subject><subject>Systemic Vasculitis - drug therapy</subject><subject>Systemic Vasculitis - mortality</subject><subject>Systemic Vasculitis - virology</subject><subject>Treatment Outcome</subject><subject>Vasculitis</subject><subject>Viral diseases</subject><subject>Viral hepatitis</subject><issn>0004-3591</issn><issn>2326-5191</issn><issn>1529-0131</issn><issn>1529-0131</issn><issn>2326-5205</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2011</creationdate><recordtype>article</recordtype><recordid>eNp90VtLwzAYBuAgis7DhX9AAiLqRWeObXI5hicQFJl4WdI00UjXziRV9u_N3FQQ9Cp85OHN4QVgH6MhRoicKR-HFFEs18AAcyIzhCleBwOEEMsol3gLbIfwkkZCOd0EWwSztFXkA_B457untgvRaWiVjp0P0LVwpqIzbQzw3cVn-GwWc3QBjuGb8_2CWKOj61qo2hqGeYhmmhLeVNB9s5C7YMOqJpi91boDHi7OJ-Or7Ob28no8usk0w1xmNWbK1kRoVteGMFXZnBjOJGPSilpYhi0yshK2INaISgiW1wJXlCpe8VwXdAccL3NnvnvtTYjl1AVtmka1putDKXJZSIEET_LkX4kRQYLmmMlED3_Rl673bXpHiTkukJCU50mdLpX2XQje2HLm3VT5eYoqF72UqZfys5dkD1aJfTU19bf8KiKBoxVIX6ga61WrXfhxjKarIZbc2dK9u8bM_z6xHN1Plkd_AKjso90</recordid><startdate>201106</startdate><enddate>201106</enddate><creator>Terrier, Benjamin</creator><creator>Semoun, Oren</creator><creator>Saadoun, David</creator><creator>Sène, Damien</creator><creator>Resche‐Rigon, Matthieu</creator><creator>Cacoub, Patrice</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley</general><general>Wiley Subscription Services, Inc</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>7QL</scope><scope>7QP</scope><scope>7T5</scope><scope>7TM</scope><scope>7U7</scope><scope>C1K</scope><scope>H94</scope><scope>K9.</scope><scope>7U9</scope><scope>7X8</scope></search><sort><creationdate>201106</creationdate><title>Prognostic factors in patients with hepatitis C virus infection and systemic vasculitis</title><author>Terrier, Benjamin ; Semoun, Oren ; Saadoun, David ; Sène, Damien ; Resche‐Rigon, Matthieu ; Cacoub, Patrice</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4159-d14afd28c4dde24abf62e549449f8d8f41f0e9b8f72fe8b8846d81b33a5b56c73</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2011</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Antiviral agents</topic><topic>Antiviral Agents - therapeutic use</topic><topic>Biological and medical sciences</topic><topic>Central nervous system</topic><topic>Cohort Studies</topic><topic>Diseases of the osteoarticular system</topic><topic>Drug Therapy, Combination</topic><topic>Female</topic><topic>Fibrosis</topic><topic>Heart</topic><topic>Hepatitis</topic><topic>Hepatitis C virus</topic><topic>Hepatitis C, Chronic - complications</topic><topic>Human viral diseases</topic><topic>Humans</topic><topic>Immunosuppressive agents</topic><topic>Immunosuppressive Agents - adverse effects</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Infection</topic><topic>Infectious diseases</topic><topic>Interferon</topic><topic>Interferon-alpha - therapeutic use</topic><topic>Kidney</topic><topic>Liver Cirrhosis - drug therapy</topic><topic>Liver Cirrhosis - virology</topic><topic>Liver diseases</topic><topic>Male</topic><topic>Medical prognosis</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Morbidity</topic><topic>Mortality</topic><topic>Multivariate analysis</topic><topic>Polyethylene Glycols - therapeutic use</topic><topic>Prognosis</topic><topic>Prospective Studies</topic><topic>Recombinant Proteins</topic><topic>Ribavirin</topic><topic>Ribavirin - therapeutic use</topic><topic>Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis</topic><topic>Severity of Illness Index</topic><topic>Survival</topic><topic>Systemic vasculitis</topic><topic>Systemic Vasculitis - drug therapy</topic><topic>Systemic Vasculitis - mortality</topic><topic>Systemic Vasculitis - virology</topic><topic>Treatment Outcome</topic><topic>Vasculitis</topic><topic>Viral diseases</topic><topic>Viral hepatitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Terrier, Benjamin</creatorcontrib><creatorcontrib>Semoun, Oren</creatorcontrib><creatorcontrib>Saadoun, David</creatorcontrib><creatorcontrib>Sène, Damien</creatorcontrib><creatorcontrib>Resche‐Rigon, Matthieu</creatorcontrib><creatorcontrib>Cacoub, Patrice</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>Calcium & Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Nucleic Acids Abstracts</collection><collection>Toxicology Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Virology and AIDS Abstracts</collection><collection>MEDLINE - Academic</collection><jtitle>Arthritis & rheumatology (Hoboken, N.J.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Terrier, Benjamin</au><au>Semoun, Oren</au><au>Saadoun, David</au><au>Sène, Damien</au><au>Resche‐Rigon, Matthieu</au><au>Cacoub, Patrice</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prognostic factors in patients with hepatitis C virus infection and systemic vasculitis</atitle><jtitle>Arthritis & rheumatology (Hoboken, N.J.)</jtitle><addtitle>Arthritis Rheum</addtitle><date>2011-06</date><risdate>2011</risdate><volume>63</volume><issue>6</issue><spage>1748</spage><epage>1757</epage><pages>1748-1757</pages><issn>0004-3591</issn><issn>2326-5191</issn><issn>1529-0131</issn><eissn>1529-0131</eissn><eissn>2326-5205</eissn><coden>ARHEAW</coden><abstract>Objective
Hepatitis C virus (HCV)–related systemic vasculitis can cause significant morbidity and mortality. Most studies of the prognosis of patients with HCV‐related systemic vasculitis are based on heterogeneous studies performed before the era of antiviral therapy. The aim of this study was to analyze the clinical, biologic, and therapeutic factors associated with prognosis in a homogeneous series of patients with HCV‐related systemic vasculitis who were followed up during the era of antiviral therapy.
Methods
One hundred fifty‐one consecutive HCV RNA–positive patients with vasculitis were prospectively followed up between 1993 and 2009 and were analyzed for clinical, biologic, and therapeutic factors associated with survival.
Results
After a median followup period of 54 months, 32 patients (21%) had died, mainly of infection and end‐stage liver disease. The 1‐year, 3‐year, 5‐year, and 10‐year survival rates were 96%, 86%, 75%, and 63%, respectively. Baseline factors associated with a poor prognosis were the presence of severe liver fibrosis (hazard ratio [HR] 5.31), central nervous system involvement (HR 2.74), kidney involvement (HR 1.91), and heart involvement (HR 4.2). The Five‐Factors Score (FFS), a vasculitis scoring system, was significantly associated with outcome. In multivariate analysis, severe fibrosis (HR 10.8) and the FFS (HR 2.49) were significantly associated with a poor prognosis. Treatment with the combination of PEGylated interferon plus ribavirin was associated with a good prognosis (HR 0.34), whereas treatment with immunosuppressive agents was associated with a poor outcome, after adjustment for the severity of vasculitis (HR 4.05). Among patients without severe fibrosis, the FFS was a good predictor of outcome, while among those with severe fibrosis, the severity of vasculitis had no prognostic value.
Conclusion
At the time of the diagnosis of HCV‐related systemic vasculitis, severe liver fibrosis and the severity of vasculitis were the main prognostic factors. Use of antiviral agents was associated with a good prognosis, whereas treatment with immunosuppressant agents had a negative impact.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>21400476</pmid><doi>10.1002/art.30319</doi><tpages>10</tpages></addata></record> |
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subjects | Adult Aged Aged, 80 and over Antiviral agents Antiviral Agents - therapeutic use Biological and medical sciences Central nervous system Cohort Studies Diseases of the osteoarticular system Drug Therapy, Combination Female Fibrosis Heart Hepatitis Hepatitis C virus Hepatitis C, Chronic - complications Human viral diseases Humans Immunosuppressive agents Immunosuppressive Agents - adverse effects Immunosuppressive Agents - therapeutic use Infection Infectious diseases Interferon Interferon-alpha - therapeutic use Kidney Liver Cirrhosis - drug therapy Liver Cirrhosis - virology Liver diseases Male Medical prognosis Medical sciences Middle Aged Morbidity Mortality Multivariate analysis Polyethylene Glycols - therapeutic use Prognosis Prospective Studies Recombinant Proteins Ribavirin Ribavirin - therapeutic use Sarcoidosis. Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. Vasculitis Severity of Illness Index Survival Systemic vasculitis Systemic Vasculitis - drug therapy Systemic Vasculitis - mortality Systemic Vasculitis - virology Treatment Outcome Vasculitis Viral diseases Viral hepatitis |
title | Prognostic factors in patients with hepatitis C virus infection and systemic vasculitis |
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