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Clinics ; 70(12): 790-796, Dec. 2015. tab, graf
Article Dans Anglais | LILACS | ID: lil-769706

Résumé

OBJECTIVE: To determine peroxisome proliferator activated receptor α and γ mRNA expression in liver tissue of hepatitis C virus-infected patients with and without human immunodeficiency virus and its possible contribution to an acceleration of liver disease progression. METHODS: We measured peroxisome proliferator-activated receptor α and γ mRNA expression by real-time polymerase chain reaction in liver tissues from 40 subjects infected only with hepatitis C virus, 36 subjects co-infected with hepatitis C virus and human immunodeficiency virus and 11 normal adults. RESULTS: Hepatic mRNA expression of both peroxisome proliferator-activated receptors was significantly lower in hepatitis C virus-infected subjects with and without human immunodeficiency virus co-infection compared to the controls. Non-black race was also identified as a predictor of lower peroxisome receptor α and γ mRNA expression. Compared to subjects infected only with hepatitis C virus, liver peroxisome receptor γ mRNA expression was significantly lower in hepatitis C virus/human immunodeficiency virus-co-infected subjects (0.0092 in hepatitis C virus/human immunodeficiency virus-co-infection vs. 0.0120 in hepatitis C virus-only; p=0.004). Hepatic peroxisome receptor α mRNA expression in the hepatitis C virus-infected patients was lower in the presence of human immunodeficiency virus co-infection in non-black subjects (0.0769 vs. 0.1061; p=0.02), whereas the levels did not vary based on human immunodeficiency virus status among black subjects. CONCLUSION: mRNA expression of both peroxisome proliferator-activated receptors is impaired in hepatitis C virus-infected liver and further reduced by human immunodeficiency virus co-infection, although the suppressive effects of the viruses are substantially mitigated in black patients.


Sujets)
Adulte , Sujet âgé , Femelle , Humains , Mâle , Adulte d'âge moyen , Co-infection/anatomopathologie , Infections à VIH/anatomopathologie , Hépatite C chronique/anatomopathologie , Récepteur PPAR alpha/analyse , Récepteur PPAR gamma/analyse , ARN messager/analyse , Analyse de variance , Biopsie , Études transversales , Co-infection/complications , Co-infection/ethnologie , Infections à VIH/complications , Infections à VIH/ethnologie , Hépatite C chronique/complications , Hépatite C chronique/ethnologie , Modèles linéaires , Cirrhose du foie/étiologie , Cirrhose du foie/anatomopathologie , Foie/anatomopathologie , Récepteur PPAR alpha/génétique , Récepteur PPAR gamma/génétique , Réaction de polymérisation en chaine en temps réel , Valeurs de référence , Indice de gravité de la maladie
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