4.7 Article

Virologic, Clinical, and Immune Response Outcomes of Patients With Hepatitis C Virus-Associated Cryoglobulinemia Treated With Direct-Acting Antivirals

期刊

CLINICAL GASTROENTEROLOGY AND HEPATOLOGY
卷 15, 期 4, 页码 575-+

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ELSEVIER SCIENCE INC
DOI: 10.1016/j.cgh.2016.09.158

关键词

Cryoglobulinemic Vasculitis; Hepatitis C; DAA; Antiviral Therapy

资金

  1. Instituto de Salud Carlos III [PI15/00151]
  2. Ministerio de Economia y Competitividad [SAF 14/57708-R]
  3. Fondo Europeo de Desarrollo Regional, Union Europea, Una Manera de Hacer Europa, Plan Estrategico de la Hepatitis C (Ministerio de Sanidad)
  4. Secretaria d'Universitats i Recerca del Departament d'Economia i Coneixement [2014_SGR_605]
  5. Spanish Health Ministry (Plan Estrategico Nacional Contra la Hepatitis C)
  6. Fondo Europeo de Desarrollo Regional, Union Europea, and Una Manera de Hacer Europa (Instituto de Salud Carlos III)
  7. Fondo Europeo de Desarrollo Regional, Union Europea, and Una Manera de Hacer Europa (Fondo Europeo de desarrollo regional) [PIE 13/00033]

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BACKGROUND & AIMS: Cryoglobulins (circulating immune complexes of polyclonal IgG, monoclonal IgM, and rheumatoid factor) are detected in the circulation of 40% to 60% of patients with chronic hepatitis C virus infection, and cryoglobulinemic vasculitis (CV) is observed in approximately 10% of patients. We aimed to assess the clinical and immune effects of direct-acting antiviral treatment. METHODS: We performed a prospective study of 64 patients with HCV infection with circulating cryoglobulins receiving direct-acting antiviral therapy at a single center in Barcelona, Spain, from January 2014 through April 2016. Patients were classified as having CV (n = 35) or asymptomatic circulating cryoglobulins (ACC, n = 29). Clinical response was considered complete if a patient's Birmingham Vasculitis Activity Score (version 3) was 0, or if all affected organs improved 12 weeks after the end of therapy. A complete immunologic response (CIR) was defined as no detection of circulating cryoglobulins and normalized levels of complement and/or rheumatoid factor. RESULTS: Clinical manifestations of CV included purpura (65%), weakness (70%), arthralgia (31%), myalgia (20%), peripheral neuropathy (50%), and renal involvement (20%). At baseline, patients with CV had significantly higher levels of rheumatoid factor and lower levels of C4 complement than patients with ACC, whereas cryocrits were similar between groups (3.2% vs 2.6%). Overall, 60 patients (94%) had a sustained viral response 12 weeks after therapy. Among patients with CV, the median Birmingham Vasculitis Activity Score (version 3) decreased from 9 (range, 2-31) to 3 (range, 0-12) (P <.001). Twenty-five patients with CV (71%) achieved a complete clinical response. Immune-suppressive therapy was reduced for 4 of 13 patients and withdrawn for 6 of 13. Overall, 48% of patients achieved a CIR. A low baseline cryocrit level (< 2.7%) was the only factor associated with CIR (odds ratio, 9.8; 95% confidence interval, 2.2-44; P =.03). CONCLUSIONS: Viral eradication was associated with clinical improvement in most patients with CV. Markers of immune activation, including circulating cryoglobulins, persisted in 52% of patients with CV or ACC, despite a sustained viral response 12 weeks after therapy. A longer follow-up period after viral eradication might be necessary to ensure a normal immune response.

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