PMID- 33864798 OWN - NLM STAT- MEDLINE DCOM- 20210624 LR - 20210624 IS - 1532-8600 (Electronic) IS - 0026-0495 (Linking) VI - 119 DP - 2021 Jun TI - Non-alcoholic fatty liver disease, insulin resistance, metabolic syndrome and their association with vascular risk. PG - 154770 LID - S0026-0495(21)00070-6 [pii] LID - 10.1016/j.metabol.2021.154770 [doi] AB - The prevalence of non-alcoholic fatty liver disease (NAFLD), one of the most common liver diseases, is rising. About 25% of adults worldwide are probably affected by NAFLD. Insulin resistance (IR) and fat accumulation in the liver are strongly related. The association between NAFLD, metabolic syndrome (MetS) and IR is established, but an independent impact of NAFLD on vascular risk and progression of cardiovascular (CV) disease (CVD) still needs to be confirmed. This narrative review considers the evidence regarding the link between NAFLD, IR and CVD risk. There is strong evidence for a "concomitantly rising incidence" of NAFLD, IR, MetS and CVD but there is no definitive evidence regarding whether NAFLD is, or is not, an independent and significant risk factor the development of CVD. There are also considerations that type 2 diabetes mellitus (T2DM) may be a common link between NAFLD/non-alcoholic steatohepatitis (NASH) and CVD. NAFLD may be associated with widespread abnormal peri-organ or intra-organ fat (APIFat) deposition (e.g. epicardial adipose tissue) which may further contribute to CV risk. It is clear that NAFLD patients have a greater CV risk (independent or not) which needs to be addressed in clinical practice. CI - Copyright (c) 2021 Elsevier Inc. All rights reserved. FAU - Muzurovic, Emir AU - Muzurovic E AD - Department of Internal Medicine, Endocrinology Section, Clinical Centre of Montenegro, Ljubljanska bb, 81000 Podgorica, Montenegro; Faculty of Medicine, University of Montenegro, Krusevac bb, 81000 Podgorica, Montenegro. Electronic address: dremir@t-com.me. FAU - Mikhailidis, Dimitri P AU - Mikhailidis DP AD - Department of Clinical Biochemistry, Royal Free Hospital Campus, University College London Medical School, University College London (UCL), Pond Street, London NW3 2QG, UK; Mohammed Bin Rashid University of Medicine and Health Sciences, Dubai, United Arab Emirates. FAU - Mantzoros, Christos AU - Mantzoros C AD - Department of Medicine, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA 02215, USA; Section of Endocrinology, Boston VA Healthcare System, Harvard Medical School, Boston, MA 02115, USA. LA - eng PT - Journal Article PT - Review DEP - 20210414 PL - United States TA - Metabolism JT - Metabolism: clinical and experimental JID - 0375267 SB - IM MH - Adult MH - Cardiometabolic Risk Factors MH - Cardiovascular Diseases/epidemiology/*etiology MH - Diabetes Mellitus, Type 2/complications/epidemiology/metabolism MH - Humans MH - Insulin Resistance/*physiology MH - Metabolic Syndrome/complications/*epidemiology MH - Non-alcoholic Fatty Liver Disease/*complications/epidemiology MH - Prevalence MH - Risk Factors OTO - NOTNLM OT - Diabetes mellitus OT - Insulin resistance OT - Metabolic syndrome OT - Non-alcoholic fatty liver disease OT - Treatment OT - Vascular risk COIS- Declaration of competing interest EM has given talks or attended conferences sponsored by Novo Nordisk, SANOFI, AstraZeneca, SERVIER and Merck. DPM has given talks, acted as a consultant or attended conferences sponsored by Amgen, Novo Nordisk and Libytec. The article is based on a lecture given by DPM as part of the 18th Annual World Congress Insulin Resistance Diabetes & Cardiovascular Disease meeting, Los Angeles, USA, December 3-5, 2020. DPM received a fee from the organizers of the meeting; there was no specific pharmaceutical industry funding or any involvement in the content of the lecture or present review. CM reports grants, personal fees and other from Coherus Inc., grants, personal fees and other from Novo Nordisk, personal fees and non-financial support from Ansh, personal fees and non-financial support from Aegerion, personal fees and non-financial support from PES, personal fees and non-financial support from California Walnut Commission, personal fees from Genfit, personal fees from Intercept, personal fees from Regeneron, personal fees from CardioMetabolic Health Conference - The Metabolic Institute of America, personal fees from Amgen, outside the submitted work. EDAT- 2021/04/18 06:00 MHDA- 2021/06/25 06:00 CRDT- 2021/04/17 20:07 PHST- 2021/02/05 00:00 [received] PHST- 2021/03/25 00:00 [revised] PHST- 2021/03/27 00:00 [accepted] PHST- 2021/04/18 06:00 [pubmed] PHST- 2021/06/25 06:00 [medline] PHST- 2021/04/17 20:07 [entrez] AID - S0026-0495(21)00070-6 [pii] AID - 10.1016/j.metabol.2021.154770 [doi] PST - ppublish SO - Metabolism. 2021 Jun;119:154770. doi: 10.1016/j.metabol.2021.154770. Epub 2021 Apr 14.