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Liver damage in hemodialysis patients with hepatitis C virus viremia: a prospective 10-year study
N Furusyo1, J Hayashi, Y Kanamoto-Tanaka
1Department of General Medicine, Kyushu University Hospital, Fukuoka, Japan.
Insights
Hepatitis C virus (HCV) infection significantly impacts hemodialysis patients, causing extensive liver damage. Combined ultrasonography and fibrogenesis markers effectively detect liver damage in HCV-viremic hemodialysis patients.
Area of Science:
- Hepatology
- Virology
- Nephrology
Background:
- Hepatitis C virus (HCV) infection is a significant concern for patients undergoing hemodialysis.
- The extent and detection of liver damage in this population require further investigation.
Purpose of the Study:
- To evaluate the liver damage in hemodialysis patients with chronic HCV infection.
- To assess the utility of combined diagnostic methods for detecting liver damage.
Main Methods:
- A cohort of 233 hemodialysis patients was divided into HCV RNA positive (Group X, n=80) and negative (Group Y, n=153) groups.
- Serial alanine aminotransferase (ALT) levels were monitored from 1989-1998.
- Serum hyaluronic acid (HA), type-IV collagen (IV-C), platelet counts, and liver ultrasonography were performed in 1998.
Main Results:
- Group X showed a higher prevalence of continuously abnormal ALT levels and a higher incidence of hepatocellular carcinoma (3 cases).
- Significantly elevated serum HA and IV-C levels were observed in Group X compared to Group Y (P < 0.05).
- Ultrasonographic findings correlated with HA levels and platelet counts, revealing more abnormalities in Group X (P < 0.05).
Conclusions:
- HCV infection leads to significant liver damage in hemodialysis patients.
- Combined ultrasonography and serum fibrogenesis markers are valuable tools for detecting liver damage in HCV-viremic hemodialysis patients.
Abstract:
Hepatitis C virus (HCV) infection is a major problem associated with hemodialysis. The extent of liver damage in hemodialysis patients with chronic HCV infection has not been thoroughly documented. The aim of this study was to evaluate liver damage of hemodialysis patients infected with HCV. A total of 233 hemodialysis patients were categorized into two groups at entry: group X, 80 positive for serum HCV RNA, and group Y, 153 negative for serum HCV RNA. All were tested for serum alanine aminotransferase (ALT) serially from 1989 to 1998, and serum hyaluronic acid (HA), serum type-IV collagen (IV-C), platelet counts, and ultrasonographic examination of the liver was done in 1998. In group X, 61.3% had continuously abnormal ALT levels for over six months followed by normal ALT levels. Of the group X patients, 11.3% had abnormal ALT levels in 1998, and in three, hepatocellular carcinoma occurred. Mean HA and IV-C levels in group X (648.8 and 188.7 ng/ml, respectively) were significantly higher than in group Y (213.1 and 165.5 ng/ml, respectively) (P < 0.05). Ultrasonographic findings significantly correlated with serum HA level and platelet counts and showed significantly more abnormalities in group X than in group Y (P < 0.05). From these findings, a combined examination with ultrasonography and serum fibrogenesis markers is useful for detection of liver damage in hemodialysis patients with HCV viremia.
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