Therapeutic pipeline in nonalcoholic steatohepatitis

被引:228
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 [J].
Ahren, Bo ;
Masmiquel, Luis ;
Kumar, Harish ;
Sargin, Mehmet ;
Karsbol, Julie Derving ;
Jacobsen, Sanja Hald ;
Chow, Francis .
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 [J].
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 .
HEPATOLOGY, 2020, 71 (03) :849-860
[3]   Obeticholic acid may increase the risk of gallstone formation in susceptible patients [J].
Al-Dury, Samer ;
Wahlstrom, Annika ;
Panzitt, Katrin ;
Thorell, Anders ;
Stahlman, Marcus ;
Trauner, Michael ;
Fickert, Peter ;
Backhed, Fredrik ;
Fandriks, Lars ;
Wagner, Martin ;
Marschall, Hanns-Ulrich .
JOURNAL OF HEPATOLOGY, 2019, 71 (05) :986-991
[4]   The TGR5 receptor mediates bile acid-induced itch and analgesia [J].
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. .
JOURNAL OF CLINICAL INVESTIGATION, 2013, 123 (04) :1513-1530
[5]   Recent advances in the development of farnesoid X receptor agonists [J].
Ali, Ahmad H. ;
Carey, Elizabeth J. ;
Lindor, Keith D. .
ANNALS OF TRANSLATIONAL MEDICINE, 2015, 3 (01)
[6]  
Alkhouri, 2020, LIV M
[7]   Diagnosis and Management of Statin Intolerance [J].
Alonso, Rodrigo ;
Cuevas, Ada ;
Cafferata, Alberto .
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 [J].
Anakk, Sayeepriyadarshini ;
Bhosale, Manoj ;
Schmidt, Valentina A. ;
Johnson, Randy L. ;
Finegold, Milton J. ;
Moore, David D. .
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 [J].
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 .
GASTROENTEROLOGY, 2015, 149 (02) :389-+