# A narrative review of impacts of apolipoproteins on atherosclerotic coronary plaques

**Authors:** Tatsuya Fukase, Tomotaka Dohi

PMC · DOI: 10.1038/s44325-026-00104-x · npj Cardiovascular Health · 2026-02-02

## TL;DR

This review explores how different apolipoproteins affect coronary plaques and their potential as therapeutic targets.

## Contribution

The paper provides a narrative review of the clinical relevance of apolipoproteins in coronary plaque imaging and therapy.

## Key findings

- Apolipoproteins influence coronary plaque characteristics detectable through imaging.
- Therapeutic agents targeting apolipoproteins are being explored for clinical use.
- ApoA-I, ApoB, and ApoC-III have distinct roles in lipid metabolism and plaque formation.

## Abstract

Apolipoproteins are structural components of lipoproteins involved in assembly, enzyme regulation, structural integrity, and receptor binding. Apoprotein(a) forms lipoprotein(a), apolipoprotein A-I drives reverse cholesterol transport, apolipoprotein B reflects atherogenic particle number, and apolipoprotein C-III regulates triglycerides. This review highlights the clinical significance of these apolipoproteins in coronary plaque characteristics detected by imaging modality. Additionally, we summarize the current clinical status of therapeutic agents targeting these apolipoproteins and its future potential.

## Full-text entities

- **Genes:** HDL3 (Huntington-like neurodegenerative disorder 2) [NCBI Gene 53369] {aka HLN2}, APOA1 (apolipoprotein A1) [NCBI Gene 335] {aka AMYLD3, HPALP2, apo(a)}, VCAM1 (vascular cell adhesion molecule 1) [NCBI Gene 7412] {aka CD106, INCAM-100}, LPA (lipoprotein(a)) [NCBI Gene 4018] {aka AK38, APOA, LP}, MPO (myeloperoxidase) [NCBI Gene 4353], LAP (Laryngeal adductor paralysis) [NCBI Gene 7939], PON1 (paraoxonase 1) [NCBI Gene 5444] {aka ESA, MVCD5, PON}, JPH3 (junctophilin 3) [NCBI Gene 57338] {aka CAGL237, HDL2, JP-3, JP3, TNRC22}, LIPC (lipase C, hepatic type) [NCBI Gene 3990] {aka HDLCQ12, HL, HTGL}, APOB (apolipoprotein B) [NCBI Gene 338] {aka FCHL2, FLDB, LDLCQ4, apoB-100, apoB-48}, PCSK9 (proprotein convertase subtilisin/kexin type 9) [NCBI Gene 255738] {aka FH3, FHCL3, HCHOLA3, LDLCQ1, NARC-1, NARC1}, TNF (tumor necrosis factor) [NCBI Gene 7124] {aka DIF, IMD127, TNF-alpha, TNFA, TNFSF2, TNLG1F}, APOC2 (apolipoprotein C2) [NCBI Gene 344] {aka APO-CII, APOC-II}, APOA2 (apolipoprotein A2) [NCBI Gene 336] {aka APOA2D, Apo-AII, ApoA-II, apoAII}, IL1B (interleukin 1 beta) [NCBI Gene 3553] {aka IL-1, IL1-BETA, IL1F2, IL1beta}, CETP (cholesteryl ester transfer protein) [NCBI Gene 1071] {aka BPIFF, HDLCQ10}, ABCA1 (ATP binding cassette subfamily A member 1) [NCBI Gene 19] {aka ABC-1, ABC1, CERP, HDLCQTL13, HDLDT1, HPALP1}, SCARB1 (scavenger receptor class B member 1) [NCBI Gene 949] {aka CD36L1, CLA-1, CLA1, HDLCQ6, HDLQTL6, SR-BI}, LDLR (low density lipoprotein receptor) [NCBI Gene 3949] {aka LDLCQ2}, LPL (lipoprotein lipase) [NCBI Gene 4023] {aka HDLCQ11, LIPD}, ANGPTL3 (angiopoietin like 3) [NCBI Gene 27329] {aka ANG-5, ANGPT5, ANL3, FHBL2}, APOC3 (apolipoprotein C3) [NCBI Gene 345] {aka APOCIII, Apo-C3, ApoC-3}, APOE (apolipoprotein E) [NCBI Gene 348] {aka AD2, APO-E, ApoE4, LDLCQ5, LPG}, LCAT (lecithin-cholesterol acyltransferase) [NCBI Gene 3931]
- **Diseases:** death (MESH:D003643), ASCVD (MESH:D050197), thrombosis (MESH:D013927), familial hypercholesterolemia (MESH:D006938), acute myocardial infarction (MESH:D009203), cardiovascular death (MESH:D002318), thrombocytopenia (MESH:D013921), atherosclerotic coronary (MESH:D003324), inflammatory cytokines (MESH:D000080424), type 2 diabetic (MESH:D003924), hypercholesterolemia (MESH:D006937), unstable angina (MESH:D000789), chylomicronemia (MESH:D008072), hypertriglyceridemia (MESH:D015228), -cap fibroatheroma (MESH:D058226), calcified (MESH:D018333), coronary (MESH:D003323), necrotic (MESH:D009336), dyslipidemia (MESH:D050171), acute coronary syndrome (MESH:D054058), coronary heart disease (MESH:D003327), neurodegenerative disorders (MESH:D019636), inflammation (MESH:D007249), metabolic syndrome (MESH:D024821), hyperglycemia (MESH:D006943), acute pancreatitis (MESH:D010195), diabetes mellitus (MESH:D003920), plaque calcification (MESH:D003773), calcification (MESH:D002114), stable angina (MESH:D060050), stroke (MESH:D020521), obesity (MESH:D009765), coronary stenosis (MESH:D023921), stenosis (MESH:D003251), genetic disorders (MESH:D030342)
- **Chemicals:** glycosaminoglycans (MESH:D006025), disulfide (MESH:D004220), CE cholesterol ester (-), Mipomersen (MESH:C524142), CE (MESH:D002788), fatty acids (MESH:D005227), niacin (MESH:D009525), lipid (MESH:D008055), fibrates (MESH:D058607), glucose (MESH:D005947), ezetimibe (MESH:D000069438), omega-3 carboxylic acids (MESH:C000708078), pelacarsen (MESH:C000657224), TC (MESH:D013667), fat (MESH:D005223), evolocumab (MESH:C577155), TG (MESH:D014280), Evinacumab (MESH:C000621590), free fatty acids (MESH:D005230), lovastatin (MESH:D008148), phospholipid (MESH:D010743), cholesterol (MESH:D002784), nitric oxide (MESH:D009569), Volanesorsen (MESH:C000593612), N-acetylgalactosamine (MESH:D000116), oligonucleotide (MESH:D009841)
- **Species:** Homo sapiens (human, species) [taxon 9606], Mus musculus (house mouse, species) [taxon 10090]

## Full text

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## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12912438/full.md

## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12912438/full.md

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Source: https://tomesphere.com/paper/PMC12912438