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Iron overload in patients with chronic hepatitis C virus infection: clinical and histological study
Ivonete S S Silva1, Renata M Perez, Pedro V Oliveira
1Department of Gastroenterology, Federal University of Sao Paulo, Rua Botucatu 740, 2nd floor, CEP 04023-900 São Paulo-SP, Brazil. nett@uol.com.br
Insights
Iron overload is uncommon in chronic hepatitis C virus (HCV) infection and doesn't appear to significantly impact liver damage. Histochemical liver iron is a reliable marker for estimating hepatic iron concentration (HIC) when overload is present.
Area of Science:
- Hepatology
- Iron Metabolism
- Viral Hepatitis
Background:
- Iron plays a role in the natural history of hepatitis C.
- Elevated serum markers of iron stores are common in chronic hepatitis C virus (HCV) carriers.
- The impact of hepatic iron overload in HCV is not well understood.
Purpose of the Study:
- Determine the prevalence of iron overload in chronic HCV carriers.
- Investigate the relationship between hepatic iron concentration (HIC) and clinical, biochemical, and histological factors.
Main Methods:
- Analyzed 96 patients with anti-HCV and HCV-RNA.
- Measured hepatic iron concentration (HIC) using atomic absorption spectrophotometry.
- Correlated HIC with various clinical, biochemical, and histological parameters using statistical analysis.
Main Results:
- Iron overload (HIC >30 mmol/g dry weight) was found in 5% of patients.
- Higher HIC was associated with male gender, elevated serum ferritin, and stainable iron.
- Stainable iron was the only independent predictor of HIC.
Conclusions:
- Iron overload is uncommon in chronic HCV patients.
- Hepatic iron content does not appear to be related to liver damage.
- Histochemical liver iron is a useful marker for estimating HIC in cases of iron overload.
Background:
Recently it has been found that iron is an important element in the natural history of hepatitis C. Serum markers of iron stores are frequently increased in chronic hepatitis C virus (HCV)-infected carriers but the real impact of the hepatic iron overload is poorly understood. The purpose of the present paper was to determine the prevalence of iron overload and to study the relationship between hepatic iron concentration (HIC) and clinical, biochemical and histological characteristics in chronic HCV-infected carriers.
Methods:
Patients presenting with anti-HCV and HCV-RNA were included. Hepatic iron concentration was determined in liver tissue by atomic absorption spectrophotometry. The association between HIC and age, gender, risk factor of transmission, duration of infection, aspartate aminotransferase (AST) and alanine aminotransferase (ALT) levels, iron and serum ferritin, transferrin saturation, HCV-RNA level, grading of inflammatory activity, staging of fibrosis, hepatic steatosis, and stainable iron was analyzed. Statistical analysis included the Mann-Whitney test and a multiple linear regression model.
Results:
Ninety-six patients (58% male) with a mean age of 44 +/- 10 years were studied. Serum iron, ferritin and transferrin saturation were elevated in 28%, 27% and 12.5% of patients, respectively. Stainable iron was detected in few patients (15.6%). Higher grades of stainable iron (2 and 3) were observed in only 7%. The HIC (>30 mmol/g dry weight) was elevated in five patients (5%). Neither grading nor staging were related to HIC. Higher HIC were observed in male patients (P < 0.001), in patients with elevated serum ferritin (P = 0.001) and in patients with stainable iron (grades 2 and 3; P = 0.001). Multiple linear regression analysis showed that only stainable iron was independently correlated with HIC (P = 0.003).
Conclusions:
Iron overload in chronically HCV-infected patients was uncommon and hepatic iron content seemed not to be related to the liver damage process. In the eventuality of iron overload, histochemical liver iron is a useful marker to estimate HIC.
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