[Prevalence and clinical significance of antiphospholipid antibodies in chronic hepatitis C]
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Published on: February 3, 2012
M Romero Gómez1, D López Lacomba, E García-Díaz
1Servicio de Digestivo, Hospital Universitario de Valme, Sevilla. mromerog@meditex.es
Insights
Antiphospholipid antibodies (APA), specifically anticardiolipin IgG (ACA-IgG), are prevalent in chronic hepatitis C patients and correlate with advanced liver disease and fibrosis progression. These findings suggest ACA-IgG may contribute to liver damage in chronic hepatitis C.
Area of Science:
- Hepatology
- Immunology
- Virology
Context:
- Chronic hepatitis C is a significant global health concern.
- Antiphospholipid antibodies (APA) are associated with autoimmune conditions.
- The role of APA in viral hepatitis is not fully understood.
Purpose:
- To determine the prevalence of antiphospholipid antibodies (APA) in patients with chronic hepatitis C.
- To investigate the association between APA and the progression of liver disease in chronic hepatitis C.
Summary:
- A study of 128 chronic hepatitis C patients and 93 controls found 25% of patients had positive APA.
- Anticardiolipin IgG (ACA-IgG) was significantly higher in patients (22%) than controls (3.2%) and correlated with advanced fibrosis (F4 staging), portal hypertension, and cirrhosis complications.
- Lupus anticoagulant (LA) was absent, and ACA-IgM levels were similar between groups. Anti-beta 2 glycoprotein I antibodies were detected in 43.5% of ACA-positive patients.
Impact:
- ACA-IgG positivity is linked to more severe liver disease in chronic hepatitis C.
- These findings highlight a potential role for ACA-IgG in driving fibrosis and liver disease progression.
- Further research may explore therapeutic strategies targeting ACA-IgG in chronic hepatitis C.
Background:
To know the prevalence of antiphospholipid antibodies in chronic hepatitis C and their relationship with disease progression.
Methods:
One hundred and twenty-eight patients with chronic hepatitis C and 93 healthy controls were enrolled up. We determined platelets, ALT, gamma GT, RNAHCV in serum and liver and non-organ specific antibodies, grade and stage in liver biopsy, risk factors, duration of disease and alcohol intake were also included. Portal hypertension and liver function parameters were studied. Antiphospholipid antibodies (APA): lupus anticoagulant (LA) and anticardiolipin antibodies (ACA) (IgG and IgM) were measured by EIA. Anti-beta 2 glycoprotein I antibodies were also detected by EIA in ACA positive patients.
Results:
Thirty one out of 128 (25%; 95% CI: 17.8%-33.4%) showed positive antiphospholipid antibodies. Positive ACA-IgG was higher in patients than controls (22% vs 3.2%; p < 0.05), whereas, ACA-IgM was similar (5% vs 3.2%; p = NS), and LA was absent in both groups. ALT levels, viraemia, viral load in liver, platelets, or ANA titre were similar in patients with and without positive ACA-IgG. Risk factors, duration of disease or alcohol intake were not related yet. Patients with staging F1 showed positive ACA-IgG 4 of 44 (9%; 95% CI: 2.5%-21.7%), in staging F2 7 of 39 (18%; 95% CI: 7.5%-33.5%) and in staging F4 17 of 45 (38%; 95% CI: 23.8%-53.5%; p < 0.005). ACA-IgG was significantly related to portal hypertension, Child-Pugh stage and presence of cirrhosis complications. Anti-beta 2 glycoprotein I antibodies were detected in ten (43.5%; CI 95%: 23.2%-65.5%) out of 23 ACA positive patients.
Conclusions:
ACA-IgG seems to be associated with chronic hepatitis C, and could play a potential role in fibrosis progression and liver disease in these patients.
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