NAFLD/NASH: The Cardiometabolic Connection
The prevalence of non-alcoholic fatty liver disease (NAFLD), one of the most common liver diseases, is rising. NAFLD affects up to a quarter of adults worldwide. NAFLD often accompanies obesity, type 2 diabetes mellitus (T2DM), dyslipidemia, and the metabolic syndrome. Its prevalence has risen dramatically since 1980, when it was a perplexing and sporadic disease when first reported by Ludwig and colleagues. NAFLD commonly leads to liver fibrosis (Non-Alcoholic Hepatosteatosis, NASH) and thus is a main cause of cirrhosis, the need for liver transplantation, and can lead to hepatocellular carcinoma.
Insulin resistance and fat accumulation in the liver relate closely, and link to ectopic fat deposits (e.g., epicardial adipose tissue) which may aggravate cardiovascular risk. The heightened cardiovascular risk in people with NAFLD requires management in clinical practice. Yet uncertainly surrounds the diagnosis and treatment for NAFLD. Clinicians, payers, and public health officials who grapple with this condition need to identify those with NAFLD who have a greater chance of liver disease progression and development of cardiovascular disease to deploy management strategies most effectively.
A holistic approach to diagnose and stratify NAFLD/NASH with use of biomarkers for liver disease severity (e.g., liver fat scores, fibrosis scores, fibroscan) and cardiovascular risk stratification with the use of clinical risk scores and/or detection of subclinical atherosclerosis may help identify individuals with a greater risk of liver disease progression or cardiovascular disease. Awareness, a multidisciplinary approach, and clinical advances are urgently needed to confront this challenge.
This series of video presentation aims to aid the practitioner to identify and manage fatty liver disease and its serious accompanying health risks.
Increase knowledge about the pathological link between NAFLD/NASH and ASCVD.
Improve the awareness about the need of a joint diagnosis and management of these combined conditions.
Improve the awareness about the need of implementing a multi-specialistic approach to NAFLD/NASH and ASCVD.
Acknowledge that lifestyle changes are important for both conditions. ASCVD can also be managed by several pharmacological strategies, while we wait for novel drug approaches for NAFLD/NASH.
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Disclosure: Inversago Pharma
Disclosures: Consultant/Speaker: CymaBay Therapeutics, Genfit, HighTide Therapeutics Inc., Intercept Pharmaceuticals, Inc., Gilead Sciences, Inc., Pliant Therapeutics, Inc., Mirum Pharmaceuticals, Inc., Madrigal Pharmaceuticals, Inc., NGM Biopharmaceuticals, AbbVie Inc. Research: CymaBay Therapeutics, Genfit, HighTide Therapeutics Inc., Intercept Pharmaceuticals, Inc., Gilead Sciences, Inc., Pliant Therapeutics, Inc., Mirum Pharmaceuticals, Inc., Madrigal Pharmaceuticals, Inc., NGM Biopharmaceuticals, AbbVie Inc., Metacrine, Pfizer Inc., Viking Therapeutics, Hanmi Pharm.Co.,Ltd.
Disclosures: Grant/Research support: Novartis. Unpaid Consultant and/or unpaid steering or executive committee of: Clinical trials: Amgen, Esperion, Genentech, Kowa, Merck, Novartis, Pfizer, Sanofi-Aventis-Regeneron. Scientific Advisory Board: Amgen, Beren, Caristo, Cartesian, CSL, Behring, DalCor, Dewpoint, Kancera, Medimmune, Novartis, NovoNordisk, Olatec, PlaqueTec, Xbiotech. Board: Xbiotech. Dr. Libby declines all personal compensation from pharma or device companies. Dr. Libby has a financial interest in Xbiotech, a company developing therapeutic human antibodies. Dr. Libby’s interests were reviewed and are managed by Brigham and Women’s Hospital and Partners HealthCare in accordance with their conflict-of-interest policies.
Disclosures: Daiichi-Sankyo, Montefarmaco OTC
Disclosures: Abbott, Aché, Amryt, Astra Zeneca, Amgen, EMS, Esperion, GETZ Pharma, Kowa, Libbs, Merck, MSD, Novo Nordisk, Pfizer, PTC Therapeutics , Roche, Sanofi
Disclosures: None