NAFLD, and cardiovascular and cardiac diseases: Factors influencing risk, prediction and treatment

医学 内科学 心脏病学 疾病 脂肪肝 人口 胰岛素抵抗 风险因素 肥胖 环境卫生
作者
Giovanni Targher,Kathleen E. Corey,Christopher D. Byrne
出处
期刊:Diabetes & Metabolism [Elsevier BV]
卷期号:47 (2): 101215-101215 被引量:168
标识
DOI:10.1016/j.diabet.2020.101215
摘要

Abstract Background and aim Non-alcoholic fatty liver disease (NAFLD), affecting up to around 30% of the world’s adult population, causes considerable liver-related and extrahepatic morbidity and mortality. Strong evidence indicates that NAFLD (especially its more severe forms) is associated with a greater risk of all-cause mortality, and the predominant cause of mortality in this patient population is cardiovascular disease (CVD). This narrative review aims to discuss the strong association between NAFLD and increased risk of cardiovascular, cardiac and arrhythmic complications. Also discussed are the putative mechanisms linking NAFLD to CVD and other cardiac/arrhythmic complications, with a brief summary of CVD risk prediction/stratification and management of the increased CVD risk observed in patients with NAFLD. Results NAFLD is associated with an increased risk of CVD events and other cardiac complications (left ventricular hypertrophy, valvular calcification, certain arrhythmias) independently of traditional CVD risk factors. The magnitude of risk of CVD and other cardiac/arrhythmic complications parallels the severity of NAFLD (especially liver fibrosis severity). There are most likely multiple underlying mechanisms through which NAFLD may increase risk of CVD and cardiac/arrhythmic complications. Indeed, NAFLD exacerbates hepatic and systemic insulin resistance, promotes atherogenic dyslipidaemia, induces hypertension, and triggers synthesis of proatherogenic, procoagulant and proinflammatory mediators that may contribute to the development of CVD and other cardiac/arrhythmic complications. Conclusion Careful assessment of CVD risk is mandatory in patients with NAFLD for primary prevention of CVD, together with pharmacological treatment for coexisting CVD risk factors.
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