Evidence map›Paper›PMID 41483441›Full record

ReviewCurrent cardiology reports2026

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 and 2 more

Abstract readReview
In one paragraph

Review in Current cardiology reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

12 authors.

Usman AlamDivision of Cardiology, Montefiore Health System/Albert Einstein College of Medicine, Bronx, NY, USA.
Sheetal V MathaiDivision of Cardiology, Montefiore Health System/Albert Einstein College of Medicine, Bronx, NY, USA.
Annalisa FiltzDivision of Cardiology, Montefiore Health System/Albert Einstein College of Medicine, Bronx, NY, USA.
Toshiki KunoDivision of Cardiology, Beth Israel Deaconess Medical Center, Harvard Medical School, Boston, MA, USA.
Juan J BadimonAtherothrombosis Research Unit, Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Allan D SnidermanDepartment of Medicine, Mike and Valeria Rosenbloom Centre for Cardiovascular Prevention, McGill University Health Centre-Royal Victoria Hospital, 1001 Boulevard Décarie, Montreal, QC, Canada.
Salim S ViraniSection of Cardiology, Department of Medicine, Aga Khan University, Karachi, Pakistan.
Peter P TothSterling Rock Falls Clinic and CGH Medical Center, Sterling, IL, USA.
Michael D ShapiroSection of Cardiovascular Medicine, Wake Forest University School of Medicine, Winston-Salem, NC, USA.
Carl J LavieOchsner Clinical School, John Ochsner Heart and Vascular Institute, The University of Queensland School of Medicine, New Orleans, LA, USA.
Deepak L BhattMount Sinai Fuster Heart Hospital, Icahn School of Medicine at Mount Sinai, New York, NY, USA.
Leandro SlipczukDivision of Cardiology, Montefiore Health System/Albert Einstein College of Medicine, Bronx, NY, USA. lslipczukb@montefiore.org.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purpose of reviewThe 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. RECENT

findingsEmerging 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.

Indexed as

Cardiovascular DiseasesHypolipidemic AgentsTriglyceridesHumansLipoproteinsHypolipidemic AgentsLipoproteinsTriglyceridesANGPTL3ApoC-IIILipid-lowering therapyRemnant lipoproteinsTriglycerides

Identifiers

PMID41483441
PMCPMC12764623

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.