MOLECULAR AND BIOCHEMICAL STUDIES ON HEPATITIS C PATIENTS RELAPSED AFTER SOFOSBUVIR TREATMENT

Mostafa H. Diab, A. Mansour, M. E. Badry, A. Farrag
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Abstract

Hepatitis C viral infection is one of the most common diseases in Egypt in the 20 th century that leaded to liver diseases such as liver cirrhosis or hepatocellular carcinoma (HCC). sofosbuvir is one of the most successful direct-acting antiviral (DAA) that play an important role in treatment of HCV. Fifty thousand patients with HCV were admitted in Mabaret El-Asafra hospital, Alexandria, Egypt, during a duration period extended from Oct 2015 to Oct 2017. All patients treated with sofosbuvir and ribavirin for 6 months as first line therapy according Egyptian health authorities. At end treatment period with first line of therapy during the follow-up checking detected HCV by quantitative PCR in seventy patients. Liver enzymes for seventy patients were estimated after relapse. Seventy patients were treated with combined therapy sofosbuvir and simeprevir as second line therapy. Liver enzymes and PCR were estimated after treated with second line therapy. All our cohort treatment experienced was between 1 and 2 therapy including monitoring for their liver functions after 1 treatment, during relapse period and after receiving the 2 therapy. Patients that were treated with combination of sofosbuvir and ribavirin at the first therapy achieved SVR after 24 weeks, a decrease in liver functions (ALT & AST) 94% achieving normal values, while 6% had mid elevation in ALT; 84% had normal values of AST and 16% had abnormal results with a negative PCR results. After following up (4 w to 48w) 36 % had normal ALT, 64% had abnormal results; 11.2 % had normal AST, 89% were abnormal. Patients were relapsed in 48weeks, and their viral load ranged from 7.0 X 10 to 9.90 X 10IU/m. After receiving the 2 therapy, patients achieved SVR in a period ranged from 4 weeks to 12 weeks with no apparent changes in ALT, AST values, while the viral load was negative in all patients. Combination therapy (sofosbuvir and simeprevir ) for 12 weeks in patients with genotype 4 infection is an effective regimen with an overall SVR rate of 100%. Keyword: Hepatitis c Virus; sofosbuvir; simeprevir; ribavirin and HCV relapsed patients.
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索非布韦治疗后丙型肝炎复发患者的分子生化研究
丙型肝炎病毒感染是20世纪埃及最常见的疾病之一,可导致肝硬化或肝细胞癌(HCC)等肝脏疾病。索非布韦是最成功的直接作用抗病毒药物(DAA)之一,在HCV治疗中发挥重要作用。2015年10月至2017年10月期间,埃及亚历山大市Mabaret El-Asafra医院收治了5万名HCV患者。根据埃及卫生当局的说法,所有患者接受索非布韦和利巴韦林6个月的一线治疗。在第一线治疗结束后的随访检查中,70例患者通过定量PCR检测出HCV。70例患者复发后肝酶测定。70例患者采用索非布韦和西莫普韦联合治疗作为二线治疗。二线治疗后肝酶和PCR检测。我们所有的队列治疗经历都在1到2种治疗之间,包括在1种治疗后、复发期间和接受2种治疗后监测肝功能。在第一次治疗时接受索非布韦和利巴韦林联合治疗的患者在24周后达到SVR,肝功能(ALT和AST)下降94%达到正常值,而ALT中等升高6%;84%的人AST值正常,16%的人PCR结果异常,阴性。随访(4 ~ 48w), 36% ALT正常,64% ALT异常;11.2% AST正常,89% AST异常。患者在48周内复发,病毒载量范围为7.0 × 10 ~ 9.90 × 10IU/m。在接受2种治疗后,患者在4周至12周期间达到SVR, ALT、AST值无明显变化,所有患者的病毒载量均为阴性。基因4型感染患者联合治疗(索非布韦和西莫普韦)12周是一种有效的方案,总SVR率为100%。关键词:丙型肝炎病毒;sofosbuvir;simeprevir;利巴韦林和HCV复发患者。
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