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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
Main Authors: Terrier, Benjamin, Semoun, Oren, Saadoun, David, Sène, Damien, Resche‐Rigon, Matthieu, Cacoub, Patrice
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container_title Arthritis & rheumatology (Hoboken, N.J.)
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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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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 &amp; 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&amp;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 &amp; 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. 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Granulomatous diseases of unproved etiology. Connective tissue diseases. Elastic tissue diseases. 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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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