TY - JOUR
T1 - Current and future therapeutic regimens for nonalcoholic fatty liver disease and nonalcoholic steatohepatitis
AU - Younossi, Zobair M.
AU - Loomba, Rohit
AU - Rinella, Mary E.
AU - Bugianesi, Elisabetta
AU - Marchesini, Giulio
AU - Neuschwander-Tetri, Brent A.
AU - Serfaty, Lawrence
AU - Negro, Francesco
AU - Caldwell, Stephen H.
AU - Ratziu, Vlad
AU - Corey, Kathleen E.
AU - Friedman, Scott L.
AU - Abdelmalek, Manal F.
AU - Harrison, Stephen A.
AU - Sanyal, Arun J.
AU - Lavine, Joel E.
AU - Mathurin, Philippe
AU - Charlton, Michael R.
AU - Chalasani, Naga P.
AU - Anstee, Quentin M.
AU - Kowdley, Kris V.
AU - George, Jacob
AU - Goodman, Zachary D.
AU - Lindor, Keith
N1 - Funding Information:
Copyright VC 2017 by the American Association for the Study of Liver Diseases. View this article online at wileyonlinelibrary.com. DOI 10.1002/hep.29724 Potential conflicts of interest: Zobair M. Younossi consults for Bristol-Myers Squibb, Intercept, Gilead, Allergan, NovoNordisk, Novartis, and GlaxoSmithKline. He advises Vertex and Janssen. Mary E. Rinella consults for Intercept, Gilead, Immuron, NGM, Nusirt, Enanta, and Novartis. Elisabetta Bugianesi consults for Gilead and Genfit. Giulio Marchesini advises for and has received grants from Gilead and Eli Lilly. He has received grants from Novo Nordisk, Genfit, and Janssen. Brent A. Neuschwander-Tetri consults and advises for Nimbus, Bristol-Myers Squibb, Boehringer Ingelheim, Janssen, Enanta, Novartis, Galmed, Zafgen, Receptos, Pfizer, Allergan, MedImmue/AstraZeneca, ConSynance, Tobira, Karos, Afimmune, NuSirt, Arrowhead, Reset, Intercept, Gilead, Abide, and Cymabay. Francesco Negro consults for and has received grants from Gilead and AbbVie. He consults for Merck. Stephen H. Caldwell consults for Shionogi and Gencia. He has received grants from Gilead, Genfit, Galmed, NGM, Immuron, Conatus, Vital Therapy, Target, and TaiwanJ. Vlad Ratziu consults for and has received grants from Intercept. He consults for Galmed, Genfit, Boehringer-Ingelhim, Pfizer, and Allergan. He has received grants from Gilead. Scott L. Friedman consults for, has research contracts with, and owns stock in Scholar Rock. He consults for and has research contracts with Bristol-Myers Squibb, Enanta, and Zafgen. He consults and owns stock in Exalenz, Blade, DeuteRx, Galectin, Genfit, Glympse, Jecure, Lifemax, and Northern Biologics. He consults for Abide, Affimune, Allegan, Angion, Arubutus, Arrowheard, Avaliv, Axcella, Boehringer Ingelheim, Can-Fite, ChemomAb, Contravir, CymaBay, Five Prime, Fortress, Gemphire, Glycotest, Inception, Lexicon, Metacrine, Metagenix, Morphic Rock, Nitto, Novartis, Ocera, Perspectum, Pfizer, Revive, RiverVest, Roche/Genentech, Sandhill, Second Genome, Surrozen, Takeda, Teva, Third Rock, Tokai, Viking, Vivace, VL-45, X-Tuit, and Zydus. He has research contracts with AbbVie and 3V Bio. He owns stock in Akarna, BirdRock, Conatus, Intercept, Nimbus, and Tobira. Manal F. Abdelmalek advises for and has received grants from NGM, Bristol-Myers Squibb, TaiwanJ, and Allergan. She has received grants from Gilead, Galmed, Conatus, Intercept, Immuron, Excelenz, Madrigal, Shire, Galactin, Genfit, Boehringher Ingelheim, Metabolon, and Prometheus. Stephen A. Harrison consults for and owns stock in Cirius and Madrigal. He consults for Cymetrix, Novartis, Perspectum, Intercept, Novo Nordisk, Capulus, CiVi, NGM, CLDF, Genfit, Echosens, High Index, and Prometheus. He advises for Gilead. He is on the speakers’ bureau for Alexion. Arun J. Sanyal consults for and has received grants from Gilead, Malinckrodt, and Salix. He consults for and is employed by Sanyal Bio. He consults for Pfizer, Nimbus, Nitto Denko, Hemoshear, and Lilly. He has received grants from Conatus, Novartis, Galectin, Bristol-Myers Squibb, Merck, and Sequana. He has received royalties from Elsevier and Uptodate. He owns stock in Akarna, GenFit, and NewCo. Philippe Mathurin consults for and is on the speakers’ bureau for Gilead. He consults for Sanofi and Verlyx. Michael R. Charlton consults for and has received grants from Gilead, Intercept, NGM, Genfit, and Novartis. He has received grants from Conatus. Naga P. Chalasani consults for Lilly, AbbVie, Tobira (Allergan), Shire, Madrigal, Axovant, Afimmune, Nusirt, and Imuran. He has received grants from Gilead, Galectin, Intercept, and Cumberland. Quentin M. Anstee consults for, is on the speakers’ bureau for, and has received grants from Allergan/Tobira and Genfit. He consults and is on the speakers’ bureau for Abbott. He consults for and has received grants from Eli Lilly, Intercept, Novartis, and Pfizer. He consults for Acuitas, E3Bio, Galmed, Gilead, Grunthal, Imperial Innoations, Inventiva, Janssen, Kenes, MedImmune, NewGene, and Raptor. He is on the speakers’ bureau for Clinical Care Options. He has received grants from AbbVie, Antaros, AstraZeneca, Boehringer Ingelheim, Ellegaard Gottigen, Exalenz, GlaxoSmithKline, Vertex, iXscient, Nordic Bioscience, Novo Nordisk, One Way Liver Genomics, Perspectum, Sanofi-Aventis, SomaLogic, and Takeda. Kris V. Kowdley consults for, advises for, is on the speakers’ bureau for, and has received grants from Gilead and Intercept. He advises for and has received grants from Allergan. He consults for Verlyx. He advises for Conatus. He has received grants from Galectin and Immuron. Zachary D. Goodman consults for and has received grants from Allergan. He consults for Pfizer. He received grants from Gilead, Galectin, Conatus, Exalenz, Intercept, Sanofi, Novartis, and Bristol-Myers Squibb.
Publisher Copyright:
© 2017 by the American Association for the Study of Liver Diseases.
PY - 2018/7
Y1 - 2018/7
N2 - Nonalcoholic fatty liver disease (NAFLD) and its progressive form non-alcoholic steatohepatitis (NASH), are rapidly becoming among the top causes of cirrhosis, hepatocellular carcinoma, and indications for liver transplantation. Other than lifestyle modification through diet and exercise, there are currently no other approved treatments for NASH/NAFLD. Although weight loss can be effective, it is difficult to achieve and sustain. In contrast, bariatric surgery can improve metabolic conditions associated with NAFLD, and has been shown to improve liver histology. To have approved regimens for the treatment of NASH/NAFLD, several issues must be addressed. First, all stakeholders must agree on the most appropriate clinical trial endpoints for NASH. Currently, resolution of NASH (without worsening fibrosis) or reduction of fibrosis stage (without worsening NASH) are the accepted endpoints by the regulatory authorities. It is important to recognize the prognostic implication of histologic features of NASH. In this context, although histologic NASH has been associated with advanced fibrosis, it is not an independent predictor of long-term mortality. In contrast, there are significant data to suggest that fibrosis stage is the only robust and independent predictor of liver-related mortality. In addition to the primary endpoints, several important secondary endpoints, including noninvasive biomarkers, long-term outcomes, and patient-reported outcomes must be considered. In 2018, a few phase 3 clinical trials for the treatment of NASH have been initiated. Additionally, a number of phase 2a and 2b clinical trials targeting different pathogenic pathways in NASH are in the pipeline of emerging therapies. Conclusion: Over the next 5 years, some of these regimens are expected to provide potential new treatment options for patients with NASH/NAFLD. (Hepatology 2018;68:361-371).
AB - Nonalcoholic fatty liver disease (NAFLD) and its progressive form non-alcoholic steatohepatitis (NASH), are rapidly becoming among the top causes of cirrhosis, hepatocellular carcinoma, and indications for liver transplantation. Other than lifestyle modification through diet and exercise, there are currently no other approved treatments for NASH/NAFLD. Although weight loss can be effective, it is difficult to achieve and sustain. In contrast, bariatric surgery can improve metabolic conditions associated with NAFLD, and has been shown to improve liver histology. To have approved regimens for the treatment of NASH/NAFLD, several issues must be addressed. First, all stakeholders must agree on the most appropriate clinical trial endpoints for NASH. Currently, resolution of NASH (without worsening fibrosis) or reduction of fibrosis stage (without worsening NASH) are the accepted endpoints by the regulatory authorities. It is important to recognize the prognostic implication of histologic features of NASH. In this context, although histologic NASH has been associated with advanced fibrosis, it is not an independent predictor of long-term mortality. In contrast, there are significant data to suggest that fibrosis stage is the only robust and independent predictor of liver-related mortality. In addition to the primary endpoints, several important secondary endpoints, including noninvasive biomarkers, long-term outcomes, and patient-reported outcomes must be considered. In 2018, a few phase 3 clinical trials for the treatment of NASH have been initiated. Additionally, a number of phase 2a and 2b clinical trials targeting different pathogenic pathways in NASH are in the pipeline of emerging therapies. Conclusion: Over the next 5 years, some of these regimens are expected to provide potential new treatment options for patients with NASH/NAFLD. (Hepatology 2018;68:361-371).
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U2 - 10.1002/hep.29724
DO - 10.1002/hep.29724
M3 - Review article
C2 - 29222911
AN - SCOPUS:85045839702
SN - 0270-9139
VL - 68
SP - 361
EP - 371
JO - Hepatology
JF - Hepatology
IS - 1
ER -