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诊断非酒精性脂肪性肝炎的策略:利用药代动力学改变的新方法。

Strategies to Diagnose Nonalcoholic Steatohepatitis: A Novel Approach to Take Advantage of Pharmacokinetic Alterations.

机构信息

Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, Arizona.

Department of Pharmacology and Toxicology, College of Pharmacy, University of Arizona, Tucson, Arizona

出版信息

Drug Metab Dispos. 2022 Apr;50(4):492-499. doi: 10.1124/dmd.121.000413. Epub 2021 Sep 16.

Abstract

Nonalcoholic steatohepatitis (NASH) is the progressive form of nonalcoholic fatty liver disease (NAFLD) and is diagnosed by a liver biopsy. Because of the invasiveness of a biopsy, the majority of patients with NASH are undiagnosed. Additionally, the prevalence of NAFLD and NASH creates the need for a simple screening method to differentiate patients with NAFLD versus NASH. Noninvasive strategies for diagnosing NAFLD versus NASH have been developed, typically relying on imaging techniques and endogenous biomarker panels. However, each technique has limitations, and none can accurately predict the associated functional impairment of drug metabolism and disposition. The function of several drug-metabolizing enzymes and drug transporters has been described in NASH that impacts drug pharmacokinetics. The aim of this review is to give an overview of the existing noninvasive strategies to diagnose NASH and to propose a novel strategy based on altered pharmacokinetics using an exogenous biomarker whose disposition and elimination pathways are directly impacted by disease progression. Altered disposition of safe and relatively inert exogenous compounds may provide the sensitivity and specificity needed to differentiate patients with NAFLD and NASH to facilitate a direct indication of hepatic impairment on drug metabolism and prevent subsequent adverse drug reactions. SIGNIFICANCE STATEMENT: This review provides an overview of the main noninvasive techniques (imaging and panels of biomarkers) used to diagnose NAFLD and NASH along with a biopsy. Pharmacokinetic changes have been identified in NASH, and this review proposes a new approach to predict NASH and the related risk of adverse drug reactions based on the assessment of drug elimination disruption using exogenous biomarkers.

摘要

非酒精性脂肪性肝炎(NASH)是一种非酒精性脂肪性肝病(NAFLD)的进展形式,通过肝活检诊断。由于活检具有侵袭性,大多数 NASH 患者都未被诊断。此外,NAFLD 和 NASH 的流行程度需要一种简单的筛选方法来区分 NAFLD 与 NASH 患者。已经开发出用于诊断 NAFLD 与 NASH 的非侵入性策略,通常依赖于成像技术和内源性生物标志物组。然而,每种技术都有其局限性,并且没有一种技术可以准确预测与药物代谢和处置相关的功能损害。在 NASH 中已经描述了几种药物代谢酶和药物转运体的功能,这些功能会影响药物药代动力学。本综述的目的是概述现有的用于诊断 NASH 的非侵入性策略,并提出一种基于使用外源性生物标志物的改变药代动力学的新策略,该生物标志物的处置和消除途径直接受疾病进展的影响。改变安全且相对惰性的外源性化合物的处置可能提供区分 NAFLD 和 NASH 患者所需的灵敏度和特异性,以促进对药物代谢的肝损伤的直接指示,并防止随后发生不良反应。意义陈述:本综述概述了用于诊断 NAFLD 和 NASH 的主要非侵入性技术(成像和生物标志物组),以及肝活检。在 NASH 中已经确定了药代动力学变化,本综述提出了一种新的方法,基于使用外源性生物标志物评估药物消除中断来预测 NASH 及相关不良反应风险。

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