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

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.
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.…
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Taxonomy
TopicsLipid metabolism and disorders · Diabetes, Cardiovascular Risks, and Lipoproteins · Lipoproteins and Cardiovascular Health
