Future Treatment Options and Regimens for Nonalcoholic Fatty Liver Disease.
暂无分享,去创建一个
[1] M. Wolf,et al. Hepatic and renal improvements with FXR agonist vonafexor in individuals with suspected fibrotic NASH. , 2022, Journal of hepatology.
[2] A. Sanyal,et al. Digital pathology with artificial intelligence analyses provides greater insights into treatment-induced fibrosis regression in NASH. , 2022, Journal of hepatology.
[3] A. Sanyal,et al. Breakthroughs in therapies for NASH and remaining challenges. , 2022, Journal of hepatology.
[4] Shimona Starling. A new GLP1, GIP and glucagon receptor triagonist , 2022, Nature Reviews Endocrinology.
[5] B. Neuschwander‐Tetri,et al. Complexity of ballooned hepatocyte feature recognition: Defining a training atlas for artificial intelligence-based imaging in NAFLD. , 2022, Journal of hepatology.
[6] R. Loomba,et al. Fenofibrate Mitigates Hypertriglyceridemia in Nonalcoholic Steatohepatitis Patients Treated With Cilofexor/Firsocostat. , 2022, Clinical gastroenterology and hepatology : the official clinical practice journal of the American Gastroenterological Association.
[7] M. Ziol,et al. Common genetic variation in alcohol-related hepatocellular carcinoma: a case-control genome-wide association study. , 2021, The Lancet. Oncology.
[8] Hongliang Li,et al. Targeting ACC for NASH resolution. , 2021, Trends in molecular medicine.
[9] A. Sanyal,et al. Expert Panel Review to Compare FDA and EMA Guidance on Drug Development and Endpoints in Nonalcoholic Steatohepatitis. , 2021, Gastroenterology.
[10] B. Neuschwander‐Tetri,et al. EDP-305 in patients with NASH: A phase II double-blind placebo-controlled dose-ranging study. , 2021, Journal of hepatology.
[11] N. Lanthier,et al. A Randomized, Controlled Trial of the Pan-PPAR Agonist Lanifibranor in NASH. , 2021, The New England journal of medicine.
[12] B. Neuschwander‐Tetri,et al. Prospective Study of Outcomes in Adults with Nonalcoholic Fatty Liver Disease. , 2021, The New England journal of medicine.
[13] V. Wong,et al. Cirrhosis regression is associated with improved clinical outcomes in patients with nonalcoholic steatohepatitis , 2021, Hepatology.
[14] M. Karsdal,et al. BMS‐986263 in patients with advanced hepatic fibrosis: 36‐week results from a randomized, placebo‐controlled phase 2 trial , 2021, Hepatology.
[15] L. Kupčinskas,et al. Aramchol in patients with nonalcoholic steatohepatitis: a randomized, double-blind, placebo-controlled phase 2b trial , 2021, Nature Medicine.
[16] G. Marchesini,et al. Non-alcoholic fatty liver disease: A patient guideline , 2021, JHEP reports : innovation in hepatology.
[17] Y. Eguchi,et al. Randomised clinical trial: Pemafibrate, a novel selective peroxisome proliferator‐activated receptor α modulator (SPPARMα), versus placebo in patients with non‐alcoholic fatty liver disease , 2021, Alimentary pharmacology & therapeutics.
[18] B. Neuschwander‐Tetri,et al. TVB-2640 (FASN inhibitor) for the treatment of nonalcoholic steatohepatitis: FASCINATE-1, a randomized, placebo-controlled Ph2a trial. , 2021, Gastroenterology.
[19] P. Galle,et al. Impact of thyroid disorders on the incidence of non‐alcoholic fatty liver disease in Germany , 2021, United European gastroenterology journal.
[20] Ben L. Da,et al. Semaglutide or Placebo for Nonalcoholic Steatohepatitis. , 2021, The New England journal of medicine.
[21] T. Rolph,et al. Efruxifermin in non-alcoholic steatohepatitis: a randomized, double-blind, placebo-controlled, phase 2a trial , 2021, Nature Medicine.
[22] J. Rosenstock,et al. Tirzepatide versus Semaglutide Once Weekly in Patients with Type 2 Diabetes. , 2021, The New England journal of medicine.
[23] E. Schiff,et al. Saroglitazar, a PPAR‐α/γ Agonist, for Treatment of NAFLD: A Randomized Controlled Double‐Blind Phase 2 Trial , 2021, Hepatology.
[24] D. Drucker,et al. GIPR Signaling in Immune Cells Maintains Metabolically Beneficial Type 2 Immune Responses in the White Fat From Obese Mice , 2021, Frontiers in Immunology.
[25] A. Sanyal,et al. Potent suppression of hydrophobic bile acids by aldafermin, an FGF19 analogue, across metabolic and cholestatic liver diseases , 2021, JHEP reports : innovation in hepatology.
[26] M. Bashir,et al. A structurally optimized FXR agonist, MET409, reduced liver fat content over 12 weeks in patients with non-alcoholic steatohepatitis. , 2021, Journal of hepatology.
[27] Christopher D. Brown,et al. A genome-wide association study for nonalcoholic fatty liver disease identifies novel genetic loci and trait-relevant candidate genes in the Million Veteran Program. , 2021, medRxiv.
[28] B. Andersen,et al. FGF19 and FGF21 for the Treatment of NASH—Two Sides of the Same Coin? Differential and Overlapping Effects of FGF19 and FGF21 From Mice to Human , 2020, Frontiers in Endocrinology.
[29] F. Anania,et al. Nonalcoholic Steatohepatitis: Current Thinking From the Division of Hepatology and Nutrition at the Food and Drug Administration , 2020, Hepatology.
[30] K. Cusi,et al. A Placebo-Controlled Trial of Subcutaneous Semaglutide in Nonalcoholic Steatohepatitis. , 2020, The New England journal of medicine.
[31] V. Wong,et al. Combination Therapies Including Cilofexor and Firsocostat for Bridging Fibrosis and Cirrhosis Attributable to NASH , 2020, Hepatology.
[32] J. Ludvigsson,et al. Mortality in Biopsy-Confirmed Nonalcoholic Fatty Liver Disease , 2020, Gut.
[33] J. Trotter,et al. Efficacy and Safety of Aldafermin, an Engineered FGF19 Analog, in a Randomized, Double-Blind, Placebo-Controlled Trial of Patients With Nonalcoholic Steatohepatitis. , 2020, Gastroenterology.
[34] G. Koch,et al. Suboptimal reliability of liver biopsy evaluation has implications for randomized clinical trials. , 2020, Journal of hepatology.
[35] V. Ratziu,et al. Why do so many NASH trials fail? , 2020, Gastroenterology.
[36] F. Tacke,et al. Differential effects of selective- and pan-PPAR agonists on experimental steatohepatitis and hepatic macrophages. , 2020, Journal of hepatology.
[37] A. Hollenberg,et al. Thyroid Hormone Signaling and the Liver , 2020, Hepatology.
[38] K. Duffin,et al. Effects of Novel Dual GIP and GLP-1 Receptor Agonist Tirzepatide on Biomarkers of Nonalcoholic Steatohepatitis in Patients With Type 2 Diabetes , 2020, Diabetes Care.
[39] K. Clément,et al. Genome-wide association study of non-alcoholic fatty liver and steatohepatitis in a histologically-characterised cohort. , 2020, Journal of hepatology.
[40] L. Groop,et al. Hydroxysteroid 17-β dehydrogenase 13 variant increases phospholipids and protects against fibrosis in nonalcoholic fatty liver disease. , 2020, JCI insight.
[41] V. Wong,et al. Selonsertib for Patients with Bridging Fibrosis or Compensated Cirrhosis Due to NASH: Results from Randomized Ph III STELLAR Trials. , 2020, Journal of hepatology.
[42] V. Wong,et al. Cilofexor, a Nonsteroidal FXR Agonist, in Patients With Noncirrhotic NASH: A Phase 2 Randomized Controlled Trial , 2020, Hepatology.
[43] N. Bhala,et al. Association Between Fibrosis Stage and Outcomes of Patients with Non-Alcoholic Fatty Liver Disease: a Systematic Review and Meta-Analysis. , 2020, Gastroenterology.
[44] D. Erion,et al. Acetyl-CoA carboxylase 1 and 2 inhibition ameliorates steatosis and hepatic fibrosis in a MC4R knockout murine model of nonalcoholic steatohepatitis , 2020, PloS one.
[45] V. Wong,et al. Cenicriviroc Treatment for Adults With Nonalcoholic Steatohepatitis and Fibrosis: Final Analysis of the Phase 2b CENTAUR Study , 2020, Hepatology.
[46] Manfred von der Ohe,et al. Obeticholic acid for the treatment of non-alcoholic steatohepatitis: interim analysis from a multicentre, randomised, placebo-controlled phase 3 trial , 2019, The Lancet.
[47] Marcos C. Pedrosa,et al. A randomized, double-blind, multicenter, phase 2b study to evaluate the safety and efficacy of a combination of tropifexor and cenicriviroc in patients with nonalcoholic steatohepatitis and liver fibrosis: Study design of the TANDEM trial. , 2019, Contemporary clinical trials.
[48] B. Neuschwander‐Tetri,et al. Resmetirom (MGL-3196) for the treatment of non-alcoholic steatohepatitis: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial , 2019, The Lancet.
[49] O. Cummings,et al. Association of Histologic Disease Activity With Progression of Nonalcoholic Fatty Liver Disease , 2019, JAMA network open.
[50] B. Singh,et al. Non-alcoholic fatty liver disease and hypercholesterolemia: Roles of thyroid hormones, metabolites, and agonists. , 2019, Thyroid : official journal of the American Thyroid Association.
[51] D. Koeberl,et al. A liver-specific thyromimetic, VK2809, decreases hepatosteatosis in glycogen storage disease type Ia (GSD Ia). , 2019, Thyroid : official journal of the American Thyroid Association.
[52] P. Bedossa,et al. Regenerate: Design of a pivotal, randomised, phase 3 study evaluating the safety and efficacy of obeticholic acid in patients with fibrosis due to nonalcoholic steatohepatitis. , 2019, Contemporary clinical trials.
[53] U. Kaul,et al. New dual peroxisome proliferator activated receptor agonist—Saroglitazar in diabetic dyslipidemia and non-alcoholic fatty liver disease: integrated analysis of the real world evidence , 2019, Cardiovascular Diabetology.
[54] K. Cusi,et al. Role of Vitamin E for Nonalcoholic Steatohepatitis in Patients With Type 2 Diabetes: A Randomized Controlled Trial , 2019, Diabetes Care.
[55] E. Speliotes,et al. 17‐Beta Hydroxysteroid Dehydrogenase 13 Is a Hepatic Retinol Dehydrogenase Associated With Histological Features of Nonalcoholic Fatty Liver Disease , 2019, Hepatology.
[56] L. Vonghia,et al. Pharmacological Treatment for Non-alcoholic Fatty Liver Disease , 2019, Advances in Therapy.
[57] Richard G. Lee,et al. Pnpla3 silencing with antisense oligonucleotides ameliorates nonalcoholic steatohepatitis and fibrosis in Pnpla3 I148M knock-in mice , 2019, Molecular metabolism.
[58] D. Drucker,et al. GIP regulates inflammation and body weight by restraining myeloid-cell-derived S100A8/A9 , 2018, Nature Metabolism.
[59] V. Wong,et al. Repeating measurements by transient elastography in non‐alcoholic fatty liver disease patients with high liver stiffness , 2018, Journal of gastroenterology and hepatology.
[60] B. Neuschwander‐Tetri,et al. Improvements in Histologic Features and Diagnosis Associated With Improvement in Fibrosis in Nonalcoholic Steatohepatitis: Results From the Nonalcoholic Steatohepatitis Clinical Research Network Treatment Trials , 2018, Hepatology.
[61] D. Rockey,et al. Simtuzumab Is Ineffective for Patients With Bridging Fibrosis or Compensated Cirrhosis Caused by Nonalcoholic Steatohepatitis. , 2018, Gastroenterology.
[62] Dongmei Wang,et al. Deciphering the Roles of PPARγ in Adipocytes via Dynamic Change of Transcription Complex , 2018, Front. Endocrinol..
[63] D. Drucker. Mechanisms of Action and Therapeutic Application of Glucagon-like Peptide-1. , 2018, Cell metabolism.
[64] J. Trotter,et al. NGM282 for treatment of non-alcoholic steatohepatitis: a multicentre, randomised, double-blind, placebo-controlled, phase 2 trial , 2018, The Lancet.
[65] J. Binet,et al. Design, Synthesis, and Evaluation of a Novel Series of Indole Sulfonamide Peroxisome Proliferator Activated Receptor (PPAR) α/γ/δ Triple Activators: Discovery of Lanifibranor, a New Antifibrotic Clinical Candidate. , 2018, Journal of medicinal chemistry.
[66] V. Ratziu. A critical review of endpoints for non-cirrhotic NASH therapeutic trials. , 2018, Journal of hepatology.
[67] V. Wong,et al. A randomized, placebo‐controlled trial of cenicriviroc for treatment of nonalcoholic steatohepatitis with fibrosis , 2018, Hepatology.
[68] G. Shulman,et al. Nonalcoholic Fatty Liver Disease as a Nexus of Metabolic and Hepatic Diseases. , 2018, Cell metabolism.
[69] W. Wahli,et al. Dual PPARα/γ agonist saroglitazar improves liver histopathology and biochemistry in experimental NASH models , 2017, Liver international : official journal of the International Association for the Study of the Liver.
[70] Z. Goodman,et al. The ASK1 inhibitor selonsertib in patients with nonalcoholic steatohepatitis: A randomized, phase 2 trial , 2017, Hepatology.
[71] Shelly C. Lu,et al. Role of aramchol in steatohepatitis and fibrosis in mice , 2017, Hepatology communications.
[72] Jonathan C. Cohen,et al. The PNPLA3 variant associated with fatty liver disease (I148M) accumulates on lipid droplets by evading ubiquitylation , 2017, Hepatology.
[73] C. Mcwherter,et al. The selective peroxisome proliferator–activated receptor‐delta agonist seladelpar reverses nonalcoholic steatohepatitis pathology by abrogating lipotoxicity in diabetic obese mice , 2017, Hepatology communications.
[74] I. Leclercq,et al. The new‐generation pan‐peroxisome proliferator‐activated receptor agonist IVA337 protects the liver from metabolic disorders and fibrosis , 2017, Hepatology communications.
[75] B. Staels,et al. Bile acid control of metabolism and inflammation in obesity, type 2 diabetes, dyslipidemia and NAFLD. , 2017 .
[76] V. Wong,et al. Increased risk of mortality by fibrosis stage in nonalcoholic fatty liver disease: Systematic review and meta‐analysis , 2017, Hepatology.
[77] M. Beekman,et al. Fibroblast growth factor 21 reflects liver fat accumulation and dysregulation of signalling pathways in the liver of C57BL/6J mice , 2016, Scientific Reports.
[78] J. Hardies,et al. Long-Term Pioglitazone Treatment for Patients With Nonalcoholic Steatohepatitis and Prediabetes or Type 2 Diabetes Mellitus , 2016, Annals of Internal Medicine.
[79] Philippe Lehert,et al. Elafibranor, an Agonist of the Peroxisome Proliferator-Activated Receptor-α and -δ, Induces Resolution of Nonalcoholic Steatohepatitis Without Fibrosis Worsening. , 2016, Gastroenterology.
[80] Rachel M. Brown,et al. Liraglutide safety and efficacy in patients with non-alcoholic steatohepatitis (LEAN): a multicentre, double-blind, randomised, placebo-controlled phase 2 study , 2016, The Lancet.
[81] B. Staels,et al. Pathophysiology and Mechanisms of Nonalcoholic Fatty Liver Disease. , 2016, Annual review of physiology.
[82] Mary Brophy,et al. Million Veteran Program: A mega-biobank to study genetic influences on health and disease. , 2016, Journal of clinical epidemiology.
[83] F. Lv,et al. FGF19 promotes epithelial-mesenchymal transition in hepatocellular carcinoma cells by modulating the GSK3β/β- catenin signaling cascade via FGFR4 activation , 2015, Oncotarget.
[84] P. Bedossa,et al. A Post-Hoc Analysis ofthe Golden505 Trial Demonstrates Histological and Cardiometabolic Efficacy of Elafibranor-120 Mg in Patients with Moderate or Severe Nash That Are Eligible for Pharmacotherapy , 2016 .
[85] P. Bedossa,et al. Improvement in NASH histological activity highly correlates with fibrosis regression , 2016 .
[86] S. Friedman,et al. Challenges and opportunities in drug and biomarker development for nonalcoholic steatohepatitis: Findings and recommendations from an American Association for the Study of Liver Diseases–U.S. Food and Drug Administration Joint Workshop , 2015, Hepatology.
[87] B. Neuschwander‐Tetri,et al. Farnesoid X nuclear receptor ligand obeticholic acid for non-cirrhotic, non-alcoholic steatohepatitis (FLINT): a multicentre, randomised, placebo-controlled trial , 2015, The Lancet.
[88] M. Lazar,et al. Thiazolidinediones and the promise of insulin sensitization in type 2 diabetes. , 2014, Cell metabolism.
[89] A. Suzuki,et al. Repair-Related Activation of Hedgehog Signaling in Stromal Cells Promotes Intrahepatic Hypothyroidism , 2014, Endocrinology.
[90] J. Dufour,et al. Carriage of the PNPLA3 rs738409 C >G polymorphism confers an increased risk of non-alcoholic fatty liver disease associated hepatocellular carcinoma. , 2014, Journal of hepatology.
[91] S. So,et al. Discovery of 2-[3,5-dichloro-4-(5-isopropyl-6-oxo-1,6-dihydropyridazin-3-yloxy)phenyl]-3,5-dioxo-2,3,4,5-tetrahydro[1,2,4]triazine-6-carbonitrile (MGL-3196), a Highly Selective Thyroid Hormone Receptor β agonist in clinical trials for the treatment of dyslipidemia. , 2014, Journal of medicinal chemistry.
[92] B. Motta,et al. Recombinant PNPLA3 protein shows triglyceride hydrolase activity and its I148M mutation results in loss of function. , 2014, Biochimica et biophysica acta.
[93] D. Hum,et al. Hepatoprotective effects of the dual peroxisome proliferator‐activated receptor alpha/delta agonist, GFT505, in rodent models of nonalcoholic fatty liver disease/nonalcoholic steatohepatitis , 2013, Hepatology.
[94] L. N. Valenti,et al. PNPLA3 I148M polymorphism and progressive liver disease. , 2013, World journal of gastroenterology.
[95] J. Everhart,et al. Diurnal Variation in Serum Alanine Aminotransferase Activity in the US Population , 2013, Journal of clinical gastroenterology.
[96] B. Staels,et al. Roles of PPARs in NAFLD: potential therapeutic targets. , 2012, Biochimica et biophysica acta.
[97] K. Cusi,et al. Role of obesity and lipotoxicity in the development of nonalcoholic steatohepatitis: pathophysiology and clinical implications. , 2012, Gastroenterology.
[98] M. Yeh,et al. Peroxisome proliferator‐activated receptor‐α agonist, Wy 14 643, improves metabolic indices, steatosis and ballooning in diabetic mice with non‐alcoholic steatohepatitis , 2012, Journal of gastroenterology and hepatology.
[99] M. Negri,et al. 17β-Hydroxysteroid dehydrogenases (17β-HSDs) as therapeutic targets: Protein structures, functions, and recent progress in inhibitor development , 2011, The Journal of Steroid Biochemistry and Molecular Biology.
[100] M. Tschöp,et al. The metabolic actions of glucagon revisited , 2010, Nature Reviews Endocrinology.
[101] J. Hardies,et al. Pioglitazone in the treatment of NASH: the role of adiponectin , 2010, Alimentary pharmacology & therapeutics.
[102] M. Martínez-Chantar,et al. Increased fibroblast growth factor 21 in obesity and nonalcoholic fatty liver disease. , 2010, Gastroenterology.
[103] B. S. Mohammed,et al. Effect of fenofibrate and niacin on intrahepatic triglyceride content, very low-density lipoprotein kinetics, and insulin action in obese subjects with nonalcoholic fatty liver disease. , 2010, The Journal of clinical endocrinology and metabolism.
[104] K. Cusi,et al. Fenofibrate reduces systemic inflammation markers independent of its effects on lipid and glucose metabolism in patients with the metabolic syndrome. , 2010, The Journal of clinical endocrinology and metabolism.
[105] L. J. Hardies,et al. Importance of changes in adipose tissue insulin resistance to histological response during thiazolidinedione treatment of patients with nonalcoholic steatohepatitis , 2009, Hepatology.
[106] K. Laugero,et al. Pharmacological actions of the peptide hormone amylin in the long-term regulation of food intake, food preference, and body weight. , 2007, American journal of physiology. Regulatory, integrative and comparative physiology.
[107] H. Iwasaka,et al. An antisense oligonucleotide to HSP47 inhibits paraquat-induced pulmonary fibrosis in rats. , 2007, Toxicology.
[108] B. Spiegelman,et al. International Union of Pharmacology. LXI. Peroxisome Proliferator-Activated Receptors , 2006, Pharmacological Reviews.
[109] J. Hardies,et al. A placebo-controlled trial of pioglitazone in subjects with nonalcoholic steatohepatitis. , 2006, The New England journal of medicine.
[110] Ronald J A Wanders,et al. Biochemistry of mammalian peroxisomes revisited. , 2006, Annual review of biochemistry.
[111] T. Tuschl,et al. Functional anatomy of siRNAs for mediating efficient RNAi in Drosophila melanogaster embryo lysate , 2001, The EMBO journal.
[112] M. Matsuda,et al. PPARgamma ligands increase expression and plasma concentrations of adiponectin, an adipose-derived protein. , 2001, Diabetes.
[113] J. Auwerx,et al. The Organization, Promoter Analysis, and Expression of the Human PPARγ Gene* , 1997, The Journal of Biological Chemistry.
[114] J. Sauk,et al. Hsp47 and the translation-translocation machinery cooperate in the production of alpha 1(I) chains of type I procollagen. , 1994, The Journal of biological chemistry.
[115] Christine Dreyer,et al. Control of the peroxisomal β-oxidation pathway by a novel family of nuclear hormone receptors , 1992, Cell.
[116] S. J. Hampson. Nursing interventions for the first three postpartum months. , 1989, Journal of obstetric, gynecologic, and neonatal nursing : JOGNN.