Pulse Brain · Growing Health Evidence Index
Tier 4 — Narrative / commentaryPeer-reviewed

Metabolic dysfunction-associated steatotic liver disease and atherosclerosis

Yulino Castillo-Núñez, Paloma Almeda‐Valdés, Guillermo González-Gálvez, María del Rosario Arechavaleta-Granell

Current Diabetes Reports · 2024

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Summary

This 2024 narrative review in Current Diabetes Reports synthesises evidence on mechanistic links between metabolic dysfunction-associated steatotic liver disease (MASLD) and atherosclerosis. The authors propose that shared metabolic pathways—likely involving dyslipidaemia, insulin resistance, and systemic inflammation—underpin the epidemiological association between hepatic steatosis and cardiovascular disease risk in individuals with metabolic dysregulation. The review integrates current understanding of how liver metabolic dysfunction may contribute to atherosclerosis development.

Regional applicability

As a mechanistic review of metabolic disease pathways, the findings are broadly applicable to United Kingdom clinical and public health contexts, where metabolic dysfunction-associated liver disease and atherosclerosis represent significant health burdens. Transferability depends on whether the proposed pathways operate similarly across populations with varying genetic backgrounds and dietary patterns.

Key measures

Mechanistic pathways linking liver metabolic dysfunction to atherosclerosis; dyslipidaemia; insulin resistance; systemic inflammation markers; cardiovascular disease risk

Outcomes reported

The review synthesises evidence on mechanistic links between metabolic dysfunction-associated steatotic liver disease (MASLD) and atherosclerosis risk. It examines shared metabolic pathways including dyslipidaemia, insulin resistance, and systemic inflammation that may connect hepatic steatosis to cardiovascular disease development.

Theme
Nutrition & health
Subject
Dietary patterns & chronic disease
Study type
Narrative Review
Study design
Narrative review
Source type
Peer-reviewed study
Status
Published
System type
Human clinical
DOI
10.1007/s11892-024-01542-6
Catalogue ID
SNmp6e6v86-os1xmt

Topic tags

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