Therapeutic pipeline in nonalcoholic steatohepatitis

被引:210
作者
Vuppalanchi, Raj [1 ]
Noureddin, Mazen [2 ]
Alkhouri, Naim [3 ]
Sanyal, Arun J. [4 ]
机构
[1] Indiana Univ Sch Med, Div Gastroenterol & Hepatol, Indianapolis, IN 46202 USA
[2] Cedar Sinai Med Ctr, Div Gastroenterol & Hepatol, Los Angeles, CA USA
[3] Arizona Liver Hlth, Tucson, AZ USA
[4] Virginia Commonwealth Univ, Dept Internal Med, Div Gastroenterol Hepatol & Nutr, Richmond, VA 23284 USA
关键词
D O I
10.1038/s41575-020-00408-y
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
The therapeutic pipeline for nonalcoholic steatohepatitis (NASH) is expanding as insights into disease pathophysiology are gained. This Review summarizes progress in the development of NASH therapies, current and ongoing clinical trials, and potential challenges with emerging therapies. Our understanding of nonalcoholic fatty liver disease pathophysiology continues to advance rapidly. Accordingly, the field has moved from describing the clinical phenotype through the presence of nonalcoholic steatohepatitis (NASH) and degree of fibrosis to deep phenotyping with a description of associated comorbidities, genetic polymorphisms and environmental influences that could be associated with disease progression. These insights have fuelled a robust therapeutic pipeline across a variety of new targets to resolve steatohepatitis or reverse fibrosis, or both. Additionally, some of these therapies have beneficial effects that extend beyond the liver, such as effects on glycaemic control, lipid profile and weight loss. In addition, emerging therapies for NASH cirrhosis would have to demonstrate either reversal of fibrosis with associated reduction in portal hypertension or at least delay the progression with eventual decrease in liver-related outcomes. For non-cirrhotic NASH, it is the expectation that reversal of fibrosis by one stage or resolution of NASH with no worsening in fibrosis will need to be accompanied by overall survival benefits. In this Review, we summarize NASH therapies that have progressed to phase II and beyond. We also discuss some of the potential clinical challenges with the use of these new therapies when approved.
引用
收藏
页码:373 / 392
页数:20
相关论文
共 205 条
  • [1] Efficacy and safety of once-weekly semaglutide versus once-daily sitagliptin as an add-on to metformin, thiazolidinediones, or both, in patients with type 2 diabetes (SUSTAIN 2): a 56-week, double-blind, phase 3a, randomised trial
    Ahren, Bo
    Masmiquel, Luis
    Kumar, Harish
    Sargin, Mehmet
    Karsbol, Julie Derving
    Jacobsen, Sanja Hald
    Chow, Francis
    [J]. LANCET DIABETES & ENDOCRINOLOGY, 2017, 5 (05) : 341 - 354
  • [2] Clinical Utility of an Increase in Magnetic Resonance Elastography in Predicting Fibrosis Progression in Nonalcoholic Fatty Liver Disease
    Ajmera, Veeral H.
    Liu, Amy
    Singh, Seema
    Yachoa, Georg
    Ramey, Matthew
    Bhargava, Meera
    Zamani, Ava
    Lopez, Scarlett
    Mangla, Neeraj
    Bettencourt, Ricki
    Rizo, Emily
    Valasek, Mark
    Behling, Cynthia
    Richards, Lisa
    Sirlin, Claude
    Loomba, Rohit
    [J]. HEPATOLOGY, 2020, 71 (03) : 849 - 860
  • [3] Obeticholic acid may increase the risk of gallstone formation in susceptible patients
    Al-Dury, Samer
    Wahlstrom, Annika
    Panzitt, Katrin
    Thorell, Anders
    Stahlman, Marcus
    Trauner, Michael
    Fickert, Peter
    Backhed, Fredrik
    Fandriks, Lars
    Wagner, Martin
    Marschall, Hanns-Ulrich
    [J]. JOURNAL OF HEPATOLOGY, 2019, 71 (05) : 986 - 991
  • [4] The TGR5 receptor mediates bile acid-induced itch and analgesia
    Alemi, Farzad
    Kwon, Edwin
    Poole, Daniel P.
    Lieu, TinaMarie
    Lyo, Victoria
    Cattaruzza, Fiore
    Cevikbas, Ferda
    Steinhoff, Martin
    Nassini, Romina
    Materazzi, Serena
    Guerrero-Alba, Raquel
    Valdez-Morales, Eduardo
    Cottrell, Graeme S.
    Schoonjans, Kristina
    Geppetti, Pierangelo
    Vanner, Stephen J.
    Bunnett, Nigel W.
    Corvera, Carlos U.
    [J]. JOURNAL OF CLINICAL INVESTIGATION, 2013, 123 (04) : 1513 - 1530
  • [5] Recent advances in the development of farnesoid X receptor agonists
    Ali, Ahmad H.
    Carey, Elizabeth J.
    Lindor, Keith D.
    [J]. ANNALS OF TRANSLATIONAL MEDICINE, 2015, 3 (01)
  • [6] Alkhouri, 2020, LIV M
  • [7] Diagnosis and Management of Statin Intolerance
    Alonso, Rodrigo
    Cuevas, Ada
    Cafferata, Alberto
    [J]. JOURNAL OF ATHEROSCLEROSIS AND THROMBOSIS, 2019, 26 (03) : 207 - 215
  • [8] Amin N, 2019, HEPATOLOGY, V70, p21A
  • [9] Bile Acids Activate YAP to Promote Liver Carcinogenesis
    Anakk, Sayeepriyadarshini
    Bhosale, Manoj
    Schmidt, Valentina A.
    Johnson, Randy L.
    Finegold, Milton J.
    Moore, David D.
    [J]. CELL REPORTS, 2013, 5 (04): : 1060 - 1069
  • [10] Liver Fibrosis, but No Other Histologic Features, Is Associated With Long-term Outcomes of Patients With Nonalcoholic Fatty Liver Disease
    Angulo, Paul
    Kleiner, David E.
    Dam-Larsen, Sanne
    Adams, Leon A.
    Bjornsson, Einar S.
    Charatcharoenwitthaya, Phunchai
    Mills, Peter R.
    Keach, Jill C.
    Lafferty, Heather D.
    Stahler, Alisha
    Haflidadottir, Svanhildur
    Bendtsen, Flemming
    [J]. GASTROENTEROLOGY, 2015, 149 (02) : 389 - +