TY - JOUR
T1 - Strategies to Diagnose Nonalcoholic Steatohepatitis
T2 - A Novel Approach to Take Advantage of Pharmacokinetic Alterations
AU - Marie, Soléne
AU - Tripp, David K.K.
AU - Cherrington, Nathan J.
N1 - Funding Information:
This work was supported by National Institutes of Health National Institute of Environmental Health Sciences [Grants ES028668 and ES006694]. 1S.M. and D.K.K.T. contributed equally to this work. dx.doi.org/10.1124/dmd.121.000413.
Publisher Copyright:
Copyright © 2022 by The American Society for Pharmacology and Experimental Therapeutics
PY - 2022/4/1
Y1 - 2022/4/1
N2 - 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.
AB - 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.
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U2 - 10.1124/dmd.121.000413
DO - 10.1124/dmd.121.000413
M3 - Review article
C2 - 34531312
AN - SCOPUS:85128488829
SN - 0090-9556
VL - 50
SP - 492
EP - 499
JO - Drug Metabolism and Disposition
JF - Drug Metabolism and Disposition
IS - 4
ER -