Drugs for Non-alcoholic Steatohepatitis (NASH): Quest for the Holy Grail

被引:46
作者
Sharma, Mithun [1 ]
Premkumar, Madhumita [2 ]
Kulkarni, Anand, V [1 ]
Kumar, Pramod [1 ]
Reddy, D. Nageshwar [3 ]
Rao, Nagaraja Padaki [1 ]
机构
[1] Asian Inst Gastroenterol, Dept Hepatol, Hyderabad, India
[2] PGIMER, Dept Hepatol, Chandigarh, India
[3] Asian Inst Gastroenterol, Dept Gastroenterol, Hyderabad, India
关键词
Fatty liver; NAFLD; NASH; Obeticholic acid; Saroglitazar; FATTY LIVER-DISEASE; VITAMIN-E; URSODEOXYCHOLIC ACID; INSULIN SENSITIVITY; INTERIM ANALYSIS; OBETICHOLIC ACID; LIPID-METABOLISM; SKELETAL-MUSCLE; SCORING SYSTEM; PLACEBO;
D O I
10.14218/JCTH.2020.00055
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Nonalcoholic fatty liver disease (NAFLD) is a global epidemic that is likely to become the most common cause of chronic liver disease in the next decade, worldwide. Though numerous drugs have been evaluated in clinical trials, most of them have returned inconclusive results and shown poorly-tolerated adverse effects. None of the drugs have been approved by the Food and Drug Administration for treating biopsy-proven non-alcoholic steatohepatitis (NASH). Vitamin E and pioglitazone have been extensively used in treatment of biopsy-proven nondiabetic NASH patients. Although some amelioration of inflammation has been seen, these drugs did not improve the fibrosis component of NASH. Therefore, dietary modification and weight reduction have remained the cornerstone of treatment of NASH; moreover, they have shown to improve histological activity as well as fibrosis. The search for an ideal drug or 'Holy Grail' within this landscape of possible agents continues, as weight reduction is achieved only in less than 10% of patients. In this current review, we summarize the drugs for NASH which are under investigation, and we provide a critical analysis of their up-to-date results and outcomes.
引用
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页码:40 / 50
页数:11
相关论文
共 125 条
[1]  
Abner Erin L, 2011, Curr Aging Sci, V4, P158
[2]  
[Anonymous], 2019, HEPATOLOGY, V70, p1477A, DOI 10.1002/hep.31033
[3]  
[Anonymous], 2019, HEPATOLOGY, V70, P188, DOI [10.1002/hep.30941, DOI 10.1002/HEP.30941]
[4]   Cenicriviroc for the treatment of liver fibrosis in adults with nonalcoholic steatohepatitis: AURORA Phase 3 study design [J].
Anstee, Quentin M. ;
Neuschwander-Tetri, Brent A. ;
Wong, Vincent Wai-Sun ;
Abdelmalek, Manal F. ;
Younossi, Zobair M. ;
Yuan, Jiacheng ;
Pecoraro, Maria Lucia ;
Seyedkazemi, Star ;
Fischer, Laurent ;
Bedossa, Pierre ;
Goodman, Zachary ;
Alkhouri, Naim ;
Tacke, Frank ;
Sanyal, Arun .
CONTEMPORARY CLINICAL TRIALS, 2020, 89
[5]   Progression of NAFLD to diabetes mellitus, cardiovascular disease or cirrhosis [J].
Anstee, Quentin M. ;
Targher, Giovanni ;
Day, Christopher P. .
NATURE REVIEWS GASTROENTEROLOGY & HEPATOLOGY, 2013, 10 (06) :330-344
[6]   Effects of n-3 fish oil on metabolic and histological parameters in NASH: A double-blind, randomized, placebo-controlled trial [J].
Argo, Curtis K. ;
Patrie, James T. ;
Lackner, Carolin ;
Henry, Thomas D. ;
de lange, Eduard E. ;
Weltman, Arthur L. ;
Shah, Neeral L. ;
Al-Osaimi, Abdullah M. ;
Pramoonjago, Patcharin ;
Jayakumar, Saumya ;
Binder, Lukas P. ;
Simmons-Egolf, Winsor D. ;
Burks, Sandra G. ;
Bao, Yongde ;
Taylor, Ann Gill ;
Rodriguez, Jessica ;
Caldwell, Stephen H. .
JOURNAL OF HEPATOLOGY, 2015, 62 (01) :190-197
[7]   Glucagon-like peptide 1 decreases lipotoxicity in non-alcoholic steatohepatitis [J].
Armstrong, Matthew J. ;
Hull, Diana ;
Guo, Kathy ;
Barton, Darren ;
Hazlehurst, Jonathan M. ;
Gathercole, Laura L. ;
Nasiri, Maryam ;
Yu, Jinglei ;
Gough, Stephen C. ;
Newsome, Philip N. ;
Tomlinson, Jeremy W. .
JOURNAL OF HEPATOLOGY, 2016, 64 (02) :399-408
[8]   Liraglutide safety and efficacy in patients with non-alcoholic steatohepatitis (LEAN): a multicentre, double-blind, randomised, placebo-controlled phase 2 study [J].
Armstrong, Matthew James ;
Gaunt, Piers ;
Aithal, Guruprasad P. ;
Barton, Darren ;
Hull, Diana ;
Parker, Richard ;
Hazlehurst, Jonathan M. ;
Guo, Kathy ;
Abouda, George ;
Aldersley, Mark A. ;
Stocken, Deborah ;
Gough, Stephen C. ;
Tomlinson, Jeremy W. ;
Brown, Rachel M. ;
Huebscher, Stefan G. ;
Newsome, Philip N. .
LANCET, 2016, 387 (10019) :679-690
[9]   Activation of the AMPK/Sirt1 pathway by a leucine-metformin combination increases insulin sensitivity in skeletal muscle, and stimulates glucose and lipid metabolism and increases life span in Caenorhabditis elegans [J].
Banerjee, Jheelam ;
Bruckbauer, Antje ;
Zemel, Michael B. .
METABOLISM-CLINICAL AND EXPERIMENTAL, 2016, 65 (11) :1679-1691
[10]   The pan-caspase inhibitor Emricasan (IDN-6556) decreases liver injury and fibrosis in a murine model of non-alcoholic steatohepatitis [J].
Barreyro, Fernando J. ;
Holod, Silvia ;
Finocchietto, Paola V. ;
Camino, Alejandra M. ;
Aquino, Jorge B. ;
Avagnina, Alejandra ;
Carreras, Maria C. ;
Poderoso, Juan J. ;
Gores, Gregory J. .
LIVER INTERNATIONAL, 2015, 35 (03) :953-966