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Naglaa S Elabd,1 Safaa I Tayel,2 Moamena S Elhamouly,1 Shaimaa A Hassanein,3 Samar M Kamaleldeen,4 Fatma E Ahmed,5 Mahmoud Rizk,6 Abdelnaser A Gadallah,7 Soma E Ajlan,8 Ahmed S Sief9 1Tropical Medicine Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt; 2Medical Biochemistry and Molecular Biology Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt; 3Diagnostic Radiology Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt; 4Clinical Pathology Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt; 5Clinical Pharmacology Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt; 6Internal Medicine Department, Faculty of Medicine, Banha University, Banha, Egypt; 7Internal Medicine Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt; 8Microbiology and Immunology Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt; 9Hepatology and Gastroenterology Department, Shebin Elkom Teaching Hospital, Menoufia, EgyptCorrespondence: Safaa I TayelMedical Biochemistry and Molecular Biology Department, Faculty of Medicine, Menoufia University, Shebin El-Kom, Menoufia, 32511, EgyptTel +20 1003383097Email drsafaa_tayel@yahoo.comBackground: Treatment response to antiviral drugs is a challenging issue in patients with chronic hepatitis C virus (HCV) infection. Although microRNA-122 represents the majority of the microRNA content in hepatic tissues, few studies have evaluated its role in the treatment response, so we aimed to study its role in chronic HCV patients and in predicting the treatment response to direct-acting antivirals (DAAs).Methods: The study included 125 chronic HCV patients (89 naïve and 36 with a prior failed peginterferon/ribavirin response) and 50 apparently healthy subjects. Complete blood count, liver function, α-fetoprotein, lipid profiles, serum creatinine, abdominal ultrasound, and FibroScan® were assessed. Viral markers, HCV antibodies, and hepatitis B surface antigen were measured by enzyme-linked fluorescent immunoassay, with quantitative estimation of HCV RNA and microRNA-122 levels by real-time PCR.Results: The microRNA-122 level in HCV patients (those with a sustained virologic response 12 weeks after finishing therapy [SVR12] and non-responders) was significantly increased compared with controls and expressed more in non-responders versus SVR12 (p=0.042). ROC curve analysis of microRNA-122 for differentiating HCV patients from healthy controls revealed that a cut-off point of > 1.45 had a sensitivity of 67.20%, specificity of 94.0%, AUC=0.861, and p< 0.001; and for predicting response to treatment a cut-off point ≤ 5.66 could significantly (p=0.022) predict the occurrence of SVR, with a sensitivity of 60.34%, specificity of 66.67%, and AUC=0.729. Logistic regression analysis showed significant values for microRNA-122 in multivariate and univariate analysis for the prediction of response to DAAs.Conclusion: The results demonstrated the possible function of microRNA-122 as an indicative tool for distinguishing chronic HCV patients from controls and in the assessment of the therapeutic reaction to DAAs.Keywords: CHC, FibroScan, microRNA-122, DAAs |
