# Genetic determinants of lipid metabolism in cardioprotection: From mechanisms to clinical practice

**Authors:** Mia Manojlovic, Diana Mahmoud, Magdalena Pantic, Melaku Taye Amogne

PMC · DOI: 10.17305/bb.2025.13176 · 2025-12-04

## TL;DR

This paper reviews how genetic factors influence lipid metabolism and offer insights for preventing and treating cardiovascular diseases.

## Contribution

The paper highlights novel genetic variants linked to cardioprotection and their therapeutic implications in lipid metabolism.

## Key findings

- Genetic variations that maintain lifelong low LDL levels significantly reduce ASCVD risk.
- Genetic studies inform new therapies and improve prediction of drug responses and side effects.
- Understanding protective genetic mechanisms can guide therapeutic strategies for cardiovascular risk.

## Abstract

Atherosclerotic cardiovascular diseases (ASCVD) continue to be the leading causes of morbidity and mortality globally. Disorders of lipoprotein metabolism contribute significantly to the development of atherosclerosis, which begins with the subendothelial retention of plasma-derived apolipoprotein B-containing lipoproteins, particularly low-density lipoprotein (LDL) and its remnants. Elevated LDL cholesterol levels and triglycerides, coupled with low high-density lipoprotein (HDL) cholesterol levels, are critical risk factors for ASCVD. Landmark epidemiological studies have identified dyslipidemia as a key modifiable risk factor for these diseases, elucidating the essential role of lipid abnormalities in atherogenesis and highlighting significant opportunities for cardiovascular disease prevention and risk stratification. Genetic epidemiology studies have shown that lifelong low levels of LDL due to genetic variations markedly reduce the risk of ASCVD. Recent advancements in lipid-lowering pharmacology are increasingly informed by genetic studies that reveal naturally occurring mutations offering lifelong cardioprotection. Furthermore, these genetic studies have facilitated the development of novel therapeutics and enhanced the prediction of potential side effects, variability in individual drug responses, and improved risk stratification. This narrative review article aims to summarize key genetic variants that influence lipid metabolism and examine their therapeutic potential in cardiovascular therapy. Given the central role of atherosclerosis in determining cardiovascular risk, it is vital to consider lipid metabolism in the context of genetic factors that affect individual susceptibility to hyperlipidemia. Defining cardioprotective genetic determinants is equally important, as it may provide a foundation for therapeutic strategies by emphasizing protective mechanisms.

## Linked entities

- **Diseases:** hyperlipidemia (MONDO:0021187)

## Full-text entities

- **Genes:** APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}
- **Diseases:** hyperlipidemia (MESH:D006949), Atherosclerotic cardiovascular diseases (MESH:D050197), lipoprotein (MESH:C563618), dyslipidemia (MESH:D050171), cardiovascular disease (MESH:D002318), lipid abnormalities (MESH:D011017)
- **Chemicals:** lipid (MESH:D008055), cholesterol (MESH:D002784), triglycerides (MESH:D014280)

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC12873742/full.md

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Source: https://tomesphere.com/paper/PMC12873742