Hepatitis C virus infection in renal transplant patients: a comparative study with immunocompetent patients

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Data
2005-12-01
Autores
Perez, R. M.
Ferreira, ASP
Souza e Silva, Ivonete Sandra de [UNIFESP]
Medina-Pestana, J. O.
Lanzoni, V. P.
Silva, AEB
Ferraz, MLG
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The behavior of hepatitis C in states of immunodeficiency is poorly understood and it is still unclear whether the characteristics of hepatitis C virus (HCV) infection in renal transplant patients differ from those observed in immunocompetent subjects. the aim of this study was to compare the biochemical and histologic characteristics of chronic HCV infection between renal transplant and immunocompetent patients. Forty-one HCV-RNA-positive renal transplant patients and 41 immunocompetent controls matched for gender, age at infection and time of infection were included in the study. the groups were compared regarding laboratory and histologic variables. Renal transplant patients showed lower alanine aminotransferase (ALT) levels (p = 0.005) and higher levels of gamma-glutamyltransferase (p = 0.003), alkaline phosphatase (p < 0.001), and direct bilirubin (p < 0.001) when compared with controls. Histologic analysis revealed less intense portal (p < 0.001) and periportal (p = 0.046) inflammatory infiltrate in renal transplant patients but a larger proportion of cases with confluent necrosis (p = 0.043). No difference in the presence of septal fibrosis, hepatic steatosis, bile duct injury and siderosis was observed. However, there was a difference in the presence of lymphoid aggregates, which were less frequent in the renal transplant group (p < 0.001). in conclusion, the characteristics of hepatitis C in renal transplant patients differ from that observed in immunocompetent patients. in renal transplant patients, HCV infection is biochemically characterized by lower ALT levels and higher frequency of cholestasis. Regarding histology, despite lower frequency of lymphoid aggregates and less intense portal/periportal inflammatory infiltrate, a greater lobular damage was observed. the impact of these differences on the progression of fibrosis remains to be established.
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Clinical Transplantation. Oxford: Blackwell Publishing, v. 19, n. 6, p. 763-768, 2005.