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Halting the natural history of hepatitis B viral infection: a paradigm shift.

机译:停止乙型肝炎病毒感染的自然史:范式转变。

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The 2007 American Association for the Study of Liver Diseases (AASLD) practice guidelines for managing chronic hepatitis B virus (HBV) infection recommend pharmacologic therapy for patients with alanine aminotransferase (ALT) activity higher than 2 times the upper limit of normal and serum HBV DNA concentration higher than 20,000 IU/mL. Findings reported over the past several years, however, indicate that HBV infection associated with ALT activity and serum HBV DNA concentrations below these treatment thresholds can progress to serious liver disease, such as cirrhosis or hepatocellular carcinoma. These findings suggest that these treatment thresholds may be too conservative. Moreover, emerging data suggest that, in some patient populations, the appropriate goal of therapy may be sustained suppression of HBV DNA with maintenance antiviral therapy. A satellite symposium conducted during the 57th Annual Meeting of the AASLD in Boston, Massachusetts, presented new findings relative to the course of HBV infection.
机译:2007年美国肝病研究协会(AASLD)管理慢性乙型肝炎病毒(HBV)感染的实践指南建议对丙氨酸转氨酶(ALT)活性高于正​​常和血清HBV DNA上限2倍的患者进行药物治疗浓度高于20,000 IU / mL。然而,过去几年的发现表明,与ALT活性和血清HBV DNA浓度低于这些治疗阈值相关的HBV感染可能会发展为严重的肝病,例如肝硬化或肝细胞癌。这些发现表明这些治疗阈值可能太保守了。此外,新出现的数据表明,在某些患者人群中,合适的治疗目标可能是维持抗病毒治疗持续抑制HBV DNA。在马萨诸塞州波士顿举行的AASLD第57届年会期间举行的卫星座谈会上,提出了有关HBV感染过程的新发现。

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