@article{a4a679b7c3ea4c45b70d5e570e9bb9e5,
title = "Clinical assessment for high-risk patients with non-alcoholic fatty liver disease in primary care and diabetology practices",
abstract = "Background: Primary care practitioners (PCPs) and diabetologists are at the frontline of potentially encountering patients with NASH. Identification of those at high risk for adverse outcomes is important. Aim: To provide practical guidance to providers on how to identify these patients and link them to specialty care. Methods: US members of the Global Council on NASH evaluated the evidence about NASH and non-invasive tests and developed a simple algorithm to identify high-risk NASH patients for diabetologists and primary care providers. These tools can assist frontline providers in decision-making and referral to gastroenterology/hepatology practices for additional assessments. Results: The presence of NASH-related advanced fibrosis is an independent predictor of adverse outcomes. These patients with NASH are considered high risk and referral to specialists is warranted. Given that staging of fibrosis requires a liver biopsy, non-invasive tests for fibrosis would be preferred. Consensus recommendation from the group is to risk-stratify patients based on metabolic risk factors using the FIB-4 as the initial non-invasive test due to its simplicity and ease of use. A FIB-4 score ≥1.3 can be used for further assessment and linkage to specialty care where additional technology to assess liver stiffness or serum fibrosis test will be available. Conclusion: Due to the growing burden of NAFLD and NASH, PCPs and diabetologists are faced with increased patient encounters in their clinical practices necessitating referral decisions. To assist in identifying high-risk NASH patients requiring specialty care, we provide a simple and easy to use algorithm.",
author = "Younossi, {Zobair M.} and Corey, {Kathleen E.} and Naim Alkhouri and Mazen Noureddin and Ira Jacobson and Brian Lam and Stephen Clement and Rita Basu and Stuart Gordon and Natarajan Ravendhra and Puneet Puri and Mary Rinella and Peter Scudera and Singal, {Ashwani K.} and Linda Henry",
note = "Funding Information: Funding for this work was received from Intercept Pharmaceuticals. Declaration of personal interests: ZMY has received research funds or served as consultant to Gilead Sciences, Intercept, NovoNordisk, BMS, Allergan, Terns, Viking, Abbvie, Siemens, Merck, Novartis and Quest Diagnostics, MN has received served as a consultant to Gilead, Intercept, Pfizer, Novartis, Allergan, Blade, EchoSens North America, OWL, Terns, Simenes, Zydus and Abbott, has received research support from Allergan, BMS, Gilead, Galmed, Galectin, Genfit, Conatus, Enanta, Novartis, Shire and Zydus and is a minor shareholder or has stocks in Anaetos and Viking. KC serves on the advisory boards for BMS, Novo Nordisk, Gilead. Grants from Boehringer Ingelheim and Novartis. NA has served on advisory boards for Allergan, Gilead, Intercept, Pfizer and Zydus; he has served as a speaker for AbbVie, Alexion, Gilead, Intercept and Simply Speaking; and has received research support from Akero, Albireo, Allergan, Axcella, BI, BMS, Celgene, Gilead, Galmed, Galectin, Genfit, Enanta, Enyo, Hanmi, Inventiva, Madrigal, Merck, Novartis, Novo Nordisk, Pfizer, Poxel and Zydus. MR has received consulting funds from Gilead Sciences, NGM Biopharmaceuticals, Enanta, Immuron, Fractyl, Prociento, Gelesis, Merck, Metacrine, Viking Therapeutics, Allergan, Cymabay, Boehringer Ingelheim, Genentech, Sagimet Bio, Terns, Siemens and Novartis, Bristol-Myers Squibb, Intercept Pharmaceuticals and has received independent research grant funding from Novartis and support in kind from Owl. NR has received research grants from Gilead, BMS, Allergan, Novartis, Enanta, Shire and Cellgene. IJ and SG have received research funds or honoria from Intercept Pharmaceuticals. All other authors have no disclosures at this time. Funding Information: : ZMY has received research funds or served as consultant to Gilead Sciences, Intercept, NovoNordisk, BMS, Allergan, Terns, Viking, Abbvie, Siemens, Merck, Novartis and Quest Diagnostics, MN has received served as a consultant to Gilead, Intercept, Pfizer, Novartis, Allergan, Blade, EchoSens North America, OWL, Terns, Simenes, Zydus and Abbott, has received research support from Allergan, BMS, Gilead, Galmed, Galectin, Genfit, Conatus, Enanta, Novartis, Shire and Zydus and is a minor shareholder or has stocks in Anaetos and Viking. KC serves on the advisory boards for BMS, Novo Nordisk, Gilead. Grants from Boehringer Ingelheim and Novartis. NA has served on advisory boards for Allergan, Gilead, Intercept, Pfizer and Zydus; he has served as a speaker for AbbVie, Alexion, Gilead, Intercept and Simply Speaking; and has received research support from Akero, Albireo, Allergan, Axcella, BI, BMS, Celgene, Gilead, Galmed, Galectin, Genfit, Enanta, Enyo, Hanmi, Inventiva, Madrigal, Merck, Novartis, Novo Nordisk, Pfizer, Poxel and Zydus. MR has received consulting funds from Gilead Sciences, NGM Biopharmaceuticals, Enanta, Immuron, Fractyl, Prociento, Gelesis, Merck, Metacrine, Viking Therapeutics, Allergan, Cymabay, Boehringer Ingelheim, Genentech, Sagimet Bio, Terns, Siemens and Novartis, Bristol‐Myers Squibb, Intercept Pharmaceuticals and has received independent research grant funding from Novartis and support in kind from Owl. NR has received research grants from Gilead, BMS, Allergan, Novartis, Enanta, Shire and Cellgene. IJ and SG have received research funds or honoria from Intercept Pharmaceuticals. All other authors have no disclosures at this time. Declaration of personal interests Funding Information: Funding for this work was received from Intercept Pharmaceuticals. Publisher Copyright: {\textcopyright} 2020 John Wiley & Sons Ltd",
year = "2020",
month = aug,
day = "1",
doi = "10.1111/apt.15830",
language = "English (US)",
volume = "52",
pages = "513--526",
journal = "Alimentary Pharmacology and Therapeutics",
issn = "0269-2813",
publisher = "Wiley",
number = "3",
}