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Diagnosis and personalized management of hepatitis B including significance of genotypes

机译:乙型肝炎的诊断和个性化治疗,包括基因型的意义

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Purpose of Review: Chronic hepatitis B virus (HBV) infection is a leading cause of cirrhosis and hepatocellular carcinoma globally. This article reviews recent therapeutic developments and highlights the significance of HBV genotypes. Recent Findings: Seven drugs (two interferons and five oral antiviral drugs) are currently available for the treatment of chronic hepatitis B. Peginterferon has the advantage of finite treatment duration and higher off-treatment durability, but causes more side effects. On-treatment monitoring with hepatitis B surface antigen and HBV DNA levels can predict response and serve as a stopping rule. Oral antiviral therapy carries fewer side effects, but long-term treatment is often required. Regular HBV DNA monitoring is essential for detecting drug resistance and suboptimal responders. HBV is divided into eight genotypes based on a difference in genetic sequence of 8% or more. Genotype C is associated with prolonged immune clearance and a higher risk of progression to cirrhosis and hepatocellular carcinoma. Patients with genotype D HBV infection have low response rate of 7-25% to peginterferon. Summary: The availability of effective antiviral therapy and virological assays has transformed HBV treatment in the past two decades. The differences in response rate and side-effect profile call for individualized treatment selection.
机译:审查目的:慢性乙型肝炎病毒(HBV)感染是全球肝硬化和肝细胞癌的主要原因。本文回顾了近期的治疗进展,并强调了HBV基因型的重要性。最新发现:目前有七种药物(两种干扰素和五种口服抗病毒药物)可用于治疗慢性乙型肝炎。聚乙二醇干扰素具有治疗持续时间有限,治疗持久性更高的优势,但会带来更多的副作用。用乙型肝炎表面抗原和HBV DNA水平进行治疗中的监测可以预测反应,并作为终止规则。口服抗病毒治疗副作用较小,但通常需要长期治疗。定期监测HBV DNA对于检测耐药性和次优反应者至关重要。根据8%或更高的遗传序列差异,HBV分为八种基因型。 C基因型与延长的免疫清除率和发展为肝硬化和肝细胞癌的较高风险有关。 D基因型HBV感染的患者对聚乙二醇干扰素的应答率较低,为7-25%。简介:在过去的二十年中,有效的抗病毒治疗和病毒学检测方法已经改变了HBV的治疗方法。反应率和副作用的差异要求个体化治疗选择。

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