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Published on: June 23, 2014
Hepatitis C virus-associated polyarteritis nodosa
D Saadoun1, B Terrier, O Semoun
1Assistance Publique Hôpitaux de Paris, Groupe Hospitalier Pitié-Salpêtrière, Paris, France.
Insights
Hepatitis C virus (HCV)-associated polyarteritis nodosa (PAN) presents more severely than other HCV vasculitis but achieves higher remission rates. This study analyzed 31 HCV-PAN patients, finding distinct clinical features and outcomes.
Area of Science:
- Rheumatology
- Infectious Diseases
- Internal Medicine
Background:
- Hepatitis C virus (HCV) infection is linked to various systemic vasculitides.
- Polyarteritis nodosa (PAN) is a rare but serious vasculitis that can be associated with HCV.
- Understanding the specific characteristics of HCV-associated PAN is crucial for effective management.
Purpose of the Study:
- To characterize the clinical presentation and outcomes of patients with polyarteritis nodosa (PAN) specifically related to hepatitis C virus (HCV).
- To compare the features of HCV-PAN with other HCV-related vasculitides, such as mixed cryoglobulinemia vasculitis.
- To identify factors associated with treatment response in HCV- vasculitis.
Main Methods:
- A retrospective analysis of 31 patients with chronic HCV infection diagnosed with PAN between 1990 and 2009.
- Patients met established criteria for PAN (ACR and Chapel Hill).
- Comparison of clinical and laboratory data between HCV-PAN and HCV-mixed cryoglobulinemia vasculitis cohorts.
Main Results:
- HCV-PAN constituted 19.3% of the HCV vasculitis cohort.
- HCV-PAN patients exhibited more severe symptoms including fever, weight loss, severe hypertension, gastrointestinal issues, neuropathy, and microaneurysms.
- Complete clinical remission was achieved in 79.3% of HCV-PAN patients, significantly higher than in HCV-MC patients (57.5%).
- Skin involvement and PAN-type vasculitis were independently associated with complete clinical response.
Conclusions:
- HCV-PAN represents a significant subset of HCV-related vasculitis with distinct clinical characteristics.
- Despite a more severe presentation, HCV-PAN demonstrates a higher rate of complete clinical remission.
- Early identification and management of factors like skin involvement are key for successful treatment outcomes.
Objective:
To analyze the main characteristics and outcome of polyarteritis nodosa (PAN)-type vasculitis associated with hepatitis C virus (HCV).
Methods:
We reported the characteristics and outcome of 31 patients chronically infected with HCV who satisfied the American College of Rheumatology and Chapel Hill criteria for PAN, seen between 1990 and 2009 in a university center.
Results:
Among a cohort of 161 patients with HCV-related vasculitis, 31 (19.3%) were diagnosed as having PAN. The median age was 64.5 years (interquartile range 49.5-70.5 years), with 54.8% women. Compared with HCV-associated mixed cryoglobulinemia (HCV-MC) vasculitis, HCV-PAN displayed a more severe and acute clinical presentation with more frequent fever and weight loss (P < 0.0001), severe hypertension (P = 0.0006), gastrointestinal tract involvement (P < 0.0001), severe acute sensory-motor multifocal mononeuropathy (P < 0.0001), kidney and liver microaneurysms (P = 0.002), and increased C-reactive protein level (P < 0.0001). Complete clinical remission of vasculitis was achieved in 79.3% of HCV-PAN patients compared to 57.5% of HCV-MC patients (P = 0.05). In multivariate analysis, skin involvement (odds ratio [OR] 2.81, 95% confidence interval [95% CI] 1.27-6.33) and PAN-type vasculitis (OR 3.01, 95% CI 1.16-8.96) were independently associated with a complete clinical response of HCV vasculitis. A glomerular filtration rate <70 ml/minute (OR 0.54, 95% CI 0.24-1.21) was negatively associated with a complete clinical response of HCV vasculitis. The 5-year survival rate was 86% in the entire cohort, regardless of the vasculitis type.
Conclusion:
HCV-PAN accounts for 19.3% of our cohort of HCV vasculitis. HCV-PAN displays a more severe and acute clinical presentation and a higher rate of clinical remission.
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