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Mechanisms Linking Metabolic-Associated Fatty Liver Disease (MAFLD) to Cardiovascular Disease

Research output: Contribution to journalReview articlepeer-review

63 Scopus citations

Abstract

Purpose of Review: Metabolic-associated fatty liver disease (MAFLD) is a condition of fat accumulation in the liver that occurs in the majority of patients in combination with metabolic dysfunction in the form of overweight or obesity. In this review, we highlight the cardiovascular complications in MAFLD patients as well as some potential mechanisms linking MAFLD to the development of cardiovascular disease and highlight potential therapeutic approaches to treating cardiovascular diseases in patients with MAFLD. Recent Findings: MAFLD is associated with an increased risk of cardiovascular diseases (CVD), including hypertension, atherosclerosis, cardiomyopathies, and chronic kidney disease. While clinical data have demonstrated the link between MAFLD and the increased risk of CVD development, the mechanisms responsible for this increased risk remain unknown. Summary: MAFLD can contribute to CVD through several mechanisms including its association with obesity and diabetes, increased levels of inflammation, and oxidative stress, as well as alterations in hepatic metabolites and hepatokines. Therapies to potentially treat MAFLD-induced include statins and lipid-lowering drugs, glucose-lowering agents, antihypertensive drugs, and antioxidant therapy.

Original languageEnglish
Pages (from-to)151-162
Number of pages12
JournalCurrent Hypertension Reports
Volume25
Issue number8
DOIs
StatePublished - Aug 2023

Bibliographical note

Publisher Copyright:
© 2023, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.

Funding

This work was supported by the National Institutes of Health R01DK126884 (D.E.S.), R01DK121797 (T.D.H.J.), the National Heart, Lung and Blood Institute P01HL05197-11 (D.E.S.), the National Institute of General Medical Sciences P20GM104357-02 (D.E.S.), and the American Heart Association Postdoctoral Award 1020493 (O.O.B.)

FundersFunder number
National Institutes of Health (NIH)
National Heart, Lung, and Blood Institute (NHLBI)P01HL05197-11
National Institute of General Medical Sciences DP2GM119177 Sophie Dumont National Institute of General Medical SciencesP20GM104357-02
National Institute of Diabetes and Digestive and Kidney DiseasesR01DK126884, R01DK121797
American the American Heart Association1020493

    UN SDGs

    This output contributes to the following UN Sustainable Development Goals (SDGs)

    1. SDG 3 - Good Health and Well-being
      SDG 3 Good Health and Well-being

    Keywords

    • Diastolic dysfunction
    • Heart failure
    • Hepatic steatosis
    • Hypertension
    • NAFLD
    • Systolic dysfunction
    • Vascular dysfunction

    ASJC Scopus subject areas

    • Internal Medicine

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