What the Future Holds for NASH: An Augmented Reality Look into Disease Stating and Targeted Therapies

Faculty

Zobair M. Younossi, MD, MPH, FACP, FACG, AGAF, FAASLD
President, Inova Medicine Services
Chairman, Clinical Research, Inova Health System
Professor and Chairman of Department of Medicine Inova Fairfax Medical Campus Falls Church, VA
Zobair M. Younossi, MD, MPH, FACP, FACG, AGAF, FAASLD
President, Inova Medicine Services

Dr. Younossi earned his medical degree from the University of Rochester School of Medicine and Dentistry (Alpha Omega Alpha 1989) in Rochester, NY, USA. He completed his residency in internal medicine with a fellowship in gastroenterology and hepatology at Scripps Clinic and Research Foundation in La Jolla, California, USA, while earning his Master of Public Health degree from San Diego State University School of Public Health, San Diego, California, USA. He served as Staff Hepatologist and Senior Researcher at the Cleveland Clinic Foundation, Cleveland, Ohio, USA, before establishing the Center for Liver Diseases at Inova Fairfax Hospital, which is now renowned for research related to non-alcoholic fatty liver disease (NAFLD) and outcomes research in liver disease. He has served as Vice President of Research for Inova Health System and currently serves as the President and Chairman of the Board of Trustees of the Chronic Liver Disease Foundation (2018-Present) and the Board of Inova Health System Foundation (2011-Present). Dr. Younossi was appointed by Governors T. Kaine and B. McDonnell of Virginia to the Board of Directors of Virginia Biotechnology Research Partnership Authority (2008-2014). He also served on the Virginia Tobacco & Health Research Repository (VTHRR), Board of Directors, America Heart Association, Mid-Atlantic Affiliate (2010-2012) and Board of the American College of Gastroenterology Institute for Clinical Research & Education (2013-Present). He has served on multiple committees for American Association for the Study of Liver Diseases, American College of Gastroenterology, American Gastrointestinal Association, and George Mason University as well as on numerous committees at Inova Fairfax Hospital and Inova Health System.

Dr. Younossi pioneered research in NAFLD and has been a leader in the field of patient-reported outcomes (PROs), economic assessment and other areas of outcomes research in liver disease. He leads a number of international efforts related to NAFLD and PROs in liver disease though global collaborations, including the Chair of Global NASH Council and the Global Liver and NASH Registries. In addition to research and administrative duties, Dr. Younossi has been actively involved in teaching students, residents, and fellows. He has also served as Chair, Director or faculty of a number of international scientific, and CME-related courses.

Dr. Younossi specializes in hepatology and gastroenterology and has authored over 510 articles, 3 books, 6 journal supplements, over 25 book chapters, and over 800 abstracts at the international scientific meetings. He is a highly sought-after speaker providing over 420 faculty lectures in national and international meetings. His academic productivity has led to an H-index of 82. Dr. Younossi also serves as the co-editor of Liver International, Associate Editor of Journal of Hepatology, and on the editorial board of a number of important medical journals. He has represented the American Association of Liver Disease and American Gastroenterological Association at different congressional meetings.

Rohit Loomba, MD, MHSc
Director, NAFLD Research Center
Professor of Medicine
Director of Hepatology and Vice Chief, Division of Gastroenterology
Adjunct Professor, Division of Epidemiology University of California at San Diego San Diego, CA
Rohit Loomba, MD, MHSc
Director, NAFLD Research Center

Dr. Rohit Loomba is a Professor of Medicine (with tenure), Director of Hepatology, at University of California at San Diego. He is an internationally recognized thought leader in translational research and innovative clinical trial design in nonalcoholic steatohepatitis (NASH), and non-invasive assessment of NAFLD using advanced imaging modalities.

Dr. Loomba is the founding director of the UCSD NAFLD Research Center where his team is conducting cutting edge research in all aspects of NAFLD including non-invasive biomarkers, genetics, epidemiology, clinical trial design, imaging endpoints, and integrated OMICs using microbiome, metabolome, and lipidome. This integrated approach has led to several innovative applications such as establishment of MRI-PDFF as a non-invasive biomarker of treatment response in early phase trials in NASH, which has now been adopted in more than 50 clinical trials conducted worldwide. He holds a patent on non-invasive biomarkers of NASH and fibrosis.

His research is funded by the National Institutes of Health including two R01s, three U01 (two NIDDK and one from NIAAA), core director of P30 (NIDDK) and project director P01 (NHLBI) grant mechanisms, Foundation of NIH, National Science Foundation, as well as several investigator-initiated research projects funded by the industry. He is the Principal Investigator, UCSD, for the NIDDK-sponsored NASH Clinical Research Network. He served as the elected Chair of the NAFLD, Special Interest Group of the American Association for the Study of Liver Diseases and is the elected member to the National Board of Directors of the American Liver Foundation.

He serves on the Editorial Board of Gastroenterology, Journal of Hepatology, GUT and Nature Reviews in gastroenterology and hepatology. He recently completed a 5-year term as the Deputy Editor of HEPATOLOGY, the official journal of the AASLD. Currently, he serves as the co-Editor of Alimentary Pharmacology and Therapeutics, an international journal in the field of gastroenterology and hepatology.

Dr. Loomba has published more than 300 manuscripts and has an H-index of 92. He is among the top 1% of the globally highly cited scientists across all fields in 2019 and 2020 by Web of Science. He is an elected member of American Society of Clinical Investigation.

Mazen Noureddin, MD, MHSc
Director, Fatty Liver Program
Karsh Division of Gastroenterology and Hepatology
Comprehensive Transplant Center
Cedars-Sinai Medical Center Los Angeles, CA
Mazen Noureddin, MD, MHSc
Director, Fatty Liver Program

Dr. Mazen Noureddin is the founding Director of Cedars-Sinai’s Fatty Liver Program in Los Angeles, California. The research of Mazen Noureddin, MD, MHSc, focuses on the underlying mechanisms of non- alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis (NASH), new imaging modalities, non-invasive biomarkers, and exploring new treatments. He has conducted several original studies that have been featured in publications in Gastroenterology, Journal of Hepatology, Gut, Hepatology, The American Journal of Gastroenterology, and many others. The Fatty Liver Program at Cedars- Sinai is conducting a number of breakthrough studies and clinical trials targeting new therapies in patients NAFLD and NASH, including those with advanced fibrosis and cirrhosis.

Statement of Need

Given the rising prevalence of non-alcoholic fatty liver disease (NAFLD) and the societal and economic burden of its aggressive subtype, non-alcoholic steatohepatitis (NASH), it is important that hepatologists and gastroenterologists are equipped with the latest tools to diagnose NASH. While there are currently no approved therapies for the treatment of NASH, several targeted therapies are being investigated in clinical trials, with high probability of being approved in the near future. Hence, it is imperative that hepatologists and gastroenterologists have up to date knowledge regarding the latest clinical data on NASH therapies.

This CME Outfitters symposium will feature expert faculty integrating augmented reality (AR) to discuss pathways, therapeutic targets, and disease progression providing the learners with the best visual experience to enable them to integrate the latest tools for diagnosis and management of patients with NASH.

Learning Objectives

At the end of this CME/CE activity, participants should be able to:

  • Describe the role of immune, inflammatory, and metabolic pathways in the pathogenesis of NASH.
  • Select appropriate non-invasive and invasive modalities for the identification of advanced fibrosis in patients with NAFLD.
  • Evaluate the efficacy of emerging therapies for improving fibrosis in patients with NASH.

The following learning objectives pertain only to those requesting CNE or CPE credit:

  • Describe the role of immune, inflammatory, and metabolic pathways in the pathogenesis of NASH.
  • Determine appropriate non-invasive and invasive modalities for the identification of advanced fibrosis in patients with NAFLD.
  • Evaluate the efficacy of emerging therapies for improving fibrosis in patients with NASH.

Financial Support

Supported by an educational grant from Intercept Pharmaceuticals.

Target Audience

Hepatologists, gastroenterologists, endocrinologists, diabetologists, primary care physicians, physician assistants, nurse practitioners, nurses, and pharmacists.

Credit Information

Physicians (ACCME) 1.5

CME Outfitters, LLC, is accredited by the Accreditation Council for Continuing Medical Education (ACCME) to provide continuing medical education for physicians. CME Outfitters, LLC, designates this enduring activity for a maximum of 1.5 AMA PRA Category 1 Credit(s). Physicians should claim only the credit commensurate with the extent of their participation in the activity.

Pharmacists/Pharmacy Tech (ACPE) 1.5

This application-based activity is approved for 1.5 contact hours (0.15 CEUs) of continuing pharmacy credit.
Activity UAN: 0376-0000-19-038-H01-P

Note to Nurse Practitioners

Nurse Practitioners can apply for AMA PRA Category 1 Credit through the American Academy of Nurse Practitioners (AANP). AANP will accept AMA PRA Category 1 Credit  from organizations accredited by the Accreditation Council for Continuing Medical Education. Nurse practitioners can also apply for credit through their state boards.

Note to PAs

AAPA accepts certificates of participation for educational activities certified for AMA PRA Category 1 Credit  from organizations accredited by the Accreditation Council for Continuing Medical Education.

MIPS Improvement Activity

Completion of this accredited CME activity meets the expectations of an Accredited Safety or Quality Improvement Program (IA_PSPA_28) for the Merit-based Incentive Payment Program (MIPS). Clinicians should submit their improvement activities by attestation via the CMS Quality Payment Program website.

Disclosure Declaration

It is the policy of CME Outfitters, LLC, to ensure independence, balance, objectivity, and scientific rigor and integrity in all of their CE activities. Faculty must disclose to the participants any relationships with commercial companies whose products or devices may be mentioned in faculty presentations, or with the commercial supporter of this CE activity. CME Outfitters, LLC, has evaluated, identified, and attempted to resolve any potential conflicts of interest through a rigorous content validation procedure, use of evidence-based data/research, and a multidisciplinary peer review process. The following information is for participant information only. It is not assumed that these relationships will have a negative impact on the presentations.


Dr. Younossi reports he receives research support from Bristol-Myers Squibb Company; Gilead Sciences, Inc.; and Intercept Pharmaceuticals, Inc. He is a consultant for Gilead Sciences, Inc.; Intercept Pharmaceuticals, Inc.; Novo Nordisk; Siemens; Terns Pharmaceuticals, Inc.; and Viking Therapeutics.


Dr. Loomba reports his institution receives grants from Allergan, Boehringer-Ingelheim, Bristol-Myers Squibb Company; Cirius Therapeutics; Eli Lilly and Company; Galectin Therapeutics Inc.; Galmed Pharmaceuticals Ltd.; GE Healthcare Life Sciences; Genfit; Gilead Sciences, Inc.; Intercept Pharmaceuticals, Inc.; GRAIL, Inc.; Janssen Pharmaceuticals, Inc.; Madrigal Pharmaceuticals, Inc.; Merck & Co., Inc.; NGM Biopharmaceuticals; NuSirt Biopharma; Pfizer Inc.; pH Pharma Co., Ltd.; Prometheus Laboratories Inc.; and Siemens. He is a consultant or advisory board member for Alnylam Pharmaceuticals, Inc./ Regeneron Pharmaceuticals Inc. ; Arrowhead Pharmaceuticals, Inc.; AstraZeneca; Bird Rock Bio; Boehringer Ingelheim; Bristol-Myer Squibb Company; Celgene Corporation; Cirius Therapeutics; CohBar, Inc.; Conatus Pharmaceuticals Inc.; Eli Lilly and Company; Galmed Pharmaceuticals Ltd.; Gemphire Therapeutics Inc.; Gilead Sciences, Inc.; Glympse Bio; GNI Group Ltd.; GRI Bio; Inipharm, Inc.; Intercept Pharmaceuticals, Inc.; Ionis Pharmaceuticals, Inc.; Janssen Pharmaceuticals, Inc.; Merck & Co., Inc.; Metacrine, Inc.; NGM Biopharmaceuticals; Novartis Pharmaceuticals Corporation; Novo Nordisk; Pfizer Inc.; Prometheus Laboratories Inc.; Promethera Biosciences; sanofi-aventis U.S. LLC; Siemens; and Viking Therapeutics, Inc. He the Co-founder of Liponexus, Inc.


Dr. Noureddin reports that he receives research support from Allergan; Bristol-Myers Squibb Company; Conatus Pharmaceuticals Inc.; Enanta Pharmaceuticals, Inc.; Galectin Therapeutics Inc.; Galmed Pharmaceuticals; GENFIT; Gilead Sciences, Inc.; Novartis; Shire and Zydus Pharmaceuticals, Inc. He is on the advisory board or speakers bureau for Abbott; Allergan; Blade Therapeutics; EchosensTM North America; Gilead Sciences, Inc.; Intercept Pharmaceuticals, Inc.; Novartis; OWL; Pfizer Inc.; Roche Diagnostics, North America; and Siemens. He is a stock shareholder (directly purchased) of Ananetos and Viking Therapeutics, Inc.


Disclosures were obtained from the CME Outfitters, LLC staff: No disclosures to report.

  • Tony Graham, MD (peer reviewer)
  • Mae Ochoa, RPh (peer reviewer)
  • Evan Luberger (planning committee)
  • Kavitha Ramachandran, PhD (planning committee)
  • Jan Perez (planning committee)
  • Sharon Tordoff (planning committee)

Faculty of this CE activity may include discussions of products or devices that are not currently labeled for use by the FDA. The faculty has been informed of their responsibility to disclose to the audience if they will be discussing off-label or investigational uses (any uses not approved by the FDA) of products or devices.

Obtaining Credit

Post-tests, credit request forms, and activity evaluations must be completed online (requires free account activation), and participants can print their certificate or statement of credit immediately (75% pass rate required). This website supports all browsers except Internet Explorer for Mac. For complete technical requirements and privacy policy, visit our Privacy & Confidentiality page.

 


NOTE: Pharmacist CE Universal Activity Number, Enduring: 0376-0000-19-038-H01-P.

Questions about this activity?

Call us at 877.CME.PROS (877.263.7767).

MMV-095-122319-60

What the Future Holds for NASH: An Augmented Reality Look into Disease Stating and Targeted Therapies
Event Date: 12/23/2019