Non-invasive diagnosis of liver fibrosis in the transplant setting

Gonzalo Crespo, Zoe Mariño
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引用次数: 1

Abstract

Recurrent hepatitis C after liver transplantation is a rapidly evolving condition in which fibrosis deposition is accelerated, with 30% of patients developing graft cirrhosis within the first 5 years after transplantation. Antiviral therapy after transplantation achieves sustained virological response (SVR) in approximately 30% of patients, and a milder fibrosis stage at treatment seems to increase the probabilities of response to treatment. Importantly, SVR to antiviral therapy in this setting has been shown to modify the natural history of the disease, given the excellent prognosis of patients who are able to clear the virus. In this regard, an early recognition of these patients can help to start antiviral therapy in less advanced stages of the recurrence, with higher probabilities of achieving SVR. Non-invasive methods, and especially Fibroscan™, have been shown to significantly correlate with fibrosis stage and, more importantly, to permit early identification of those patients at higher risk of presenting worse outcomes. In addition, they can also confidently distinguish those patients who will present a good outcome and in which a significant number of protocol liver biopsies may be avoided.

移植后肝纤维化的无创诊断
肝移植后复发性丙型肝炎是一种快速发展的疾病,其中纤维化沉积加速,30%的患者在移植后的前5年内发生移植物肝硬化。移植后抗病毒治疗在大约30%的患者中实现了持续的病毒学反应(SVR),治疗时较轻的纤维化阶段似乎增加了对治疗反应的可能性。重要的是,鉴于能够清除病毒的患者预后良好,在这种情况下抗病毒治疗的SVR已被证明可以改变疾病的自然史。在这方面,早期识别这些患者可以帮助在复发的较不晚期阶段开始抗病毒治疗,实现SVR的可能性更高。非侵入性方法,特别是Fibroscan™,已被证明与纤维化分期显著相关,更重要的是,可以早期识别那些预后较差的高风险患者。此外,他们还可以自信地区分哪些患者将呈现良好的结果,并且可以避免大量的方案肝活检。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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