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Abstract Hepatitis C is the most pressing public health challenge in Egypt where hepatitis C Virus (HCV) prevalence is the highest in the world. The success of antiviral treatment in patients with chronic HCV (CHC) depends on factors related to the virus and host. The earlier work with telomerase showed that expression of the human telomerase reverse transcriptase mRNA (hTERT) was increased in hepatocyte cultures after overexpression of HCV core protein as compared to normal human liver and uninfected cells. The aim of the present study is to evaluate hTERT as an early prognostic factor for non-fibrotic CHC patients schedule for 24 weeks treatment with pegylated interferon and ribavirin (Peg-IFN/RBV) and the correlation between hTERT follow-up with patients host factors. The study was conducted on 50 chronic non-fibrotic HCV newly diagnosed and recruited from Ain Shams University hospitals. All patients (37 males/13 females) were aged 30 years or older; they were seropositive for HCV antibodies, with detectable HCV RNA; seronegative for other viruses; and free of any other liver or metabolic disease at enrollment. They have received antiviral combination therapy with Peg-IFN/RBV scheduled for 24 weeks. All patients’ data were collected after admission (baseline) and followed up after 4 and 24 weeks of treatment for Prothrombin time (PT), complete blood count (CBC), liver function tests, total cholesterol, alpha fetoprotein (AFP) and real time PCR for HCV and hTERT. The response rate at 24 weeks was 35/50 patients (70%). We found that the factors that contribute to virological response in detected hTERT patients were leukocytes count (LR 34.1, p < 0.001), hTERT (LR=13; p<0.004), and HCV (LR=9; p<0.01). This study concluded that hTERT is a good early predictor factor of virological response for non-fibrotic CHC patients treated with combined therapy of Peg-IFN/ RBV taking into consideration the patient’s leukocyte count and hTERT at baseline. We recommend that patients with leukocyte count lower than 2.7 x 10^3 /μL with undetected baseline hTERT are not good candidates for treatment with combination therapy of Peg-IFN/RBV and may better shift to another line of treatment. |