# Targeting Triglycerides in Cardiovascular Disease Prevention: Evidence, Mechanisms, and Emerging Therapies

**Authors:** Usman Alam, Sheetal V. Mathai, Annalisa Filtz, Toshiki Kuno, Juan J. Badimon, Allan D. Sniderman, Salim S. Virani, Peter P. Toth, Michael D. Shapiro, Carl J. Lavie, Deepak L. Bhatt, Leandro Slipczuk

PMC · DOI: 10.1007/s11886-025-02337-1 · 2026-01-03

## TL;DR

This review explores how targeting triglycerides and related lipoproteins may help reduce cardiovascular disease risk, especially in high-risk patients.

## Contribution

The paper highlights emerging therapies and evidence for targeting triglyceride-rich lipoproteins to reduce residual cardiovascular risk.

## Key findings

- Mendelian randomization and clinical data support a causal link between remnant lipoproteins and atherosclerotic CVD.
- ApoC-III and ANGPTL3 inhibitors show robust lipid-lowering effects, unlike selective PPAR modulators.
- Targeting apolipoprotein B in triglyceride-rich lipoproteins may benefit high-risk patients, though more outcome data are needed.

## Abstract

The goal of this review is to evaluate the evolving role of triglycerides (TGs) and TG-rich lipoproteins (TRLs) in cardiovascular disease (CVD) risk and prevention. We examine the mechanistic rationale, genetic and epidemiological evidence, and therapeutic potential of targeting TGs in residual risk reduction, particularly in high-risk populations.

Emerging data from Mendelian randomization studies and large clinical cohorts support a causal link between elevated remnant lipoproteins and atherosclerotic CVD, in which apolipoprotein B may be the principal driver. Although traditional triglyceride-lowering agents have produced mixed results on cardiovascular outcomes, emerging therapies—such as ApoC-III and ANGPTL3 inhibitors—show robust lipid-lowering effects, while selective PPAR modulators have thus far not demonstrated cardiovascular benefit. However, outcome data remain limited.

Residual CVD risk persists despite aggressive LDL-C reduction, especially in patients with diabetes, metabolic syndrome, or chronic kidney disease. Selective TG-lowering strategies targeting TRLs—especially those that decrease apolipoprotein B—may provide clinical benefit in high-risk phenotypes. Ongoing trials will clarify whether these promising agents confer meaningful cardiovascular protection and warrant integration into future guidelines.

## Linked entities

- **Genes:** APOC3 (apolipoprotein C3) [NCBI Gene 345], ANGPTL3 (angiopoietin like 3) [NCBI Gene 27329]
- **Diseases:** cardiovascular disease (MONDO:0004995), diabetes (MONDO:0005015), metabolic syndrome (MONDO:0000816), chronic kidney disease (MONDO:0005300)

## Full-text entities

- **Genes:** PPARA (peroxisome proliferator activated receptor alpha) [NCBI Gene 5465] {aka NR1C1, PPAR, PPAR-alpha, PPARalpha, hPPAR}, ANGPTL3 (angiopoietin like 3) [NCBI Gene 27329] {aka ANG-5, ANGPT5, ANL3, FHBL2}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, APOC3 (apolipoprotein C3) [NCBI Gene 345] {aka APOCIII, Apo-C3, ApoC-3}
- **Diseases:** CVD (MESH:D002318), chronic kidney disease (MESH:D051436), metabolic syndrome (MESH:D024821), atherosclerotic CVD (MESH:D050197), diabetes (MESH:D003920)
- **Chemicals:** lipid (MESH:D008055), TG (MESH:D014280), LDL-C (-)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12764623/full.md

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Source: https://tomesphere.com/paper/PMC12764623