Evidence map›Paper›PMID 38696700›Full record

ReviewCardiovascular research2024

Targeting macrophages with multifunctional nanoparticles to detect and prevent atherosclerotic cardiovascular disease.

Victoria Nankivell, Achini K Vidanapathirana, Ayla Hoogendoorn, Joanne T M Tan, Johan Verjans, Peter J Psaltis, Mark R Hutchinson, Brant C Gibson, Yiqing Lu, Ewa Goldys and 2 more

Abstract readReview
In one paragraph

Review in Cardiovascular research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing 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

21 citing papers in PubMed.

  1. Review
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  10. Preclinical Evaluation of Stable Integrin αPharmaceuticals (Basel, Switzerland) · 2025
    Article
  11. Article
  12. Review
  13. Review
  14. Review
  15. Article
  16. Nanotechnology-Based Therapeutics for Airway Inflammatory Diseases.Clinical reviews in allergy & immunology · 2025
    Review
  17. Review
  18. Review
  19. How Advanced Is Nanomedicine for Atherosclerosis?International journal of nanomedicine · 2025
    Review
  20. An oral microbiome model for predicting atherosclerotic cardiovascular disease.Frontiers in cellular and infection microbiology · 2025
    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.

Victoria NankivellAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Achini K VidanapathiranaAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Ayla HoogendoornAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Joanne T M TanVascular Research Centre, Lifelong Health, South Australian Health and Medical Research Institute (SAHMRI), North Terrace, Adelaide, 5000, Australia.
Johan VerjansAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Peter J PsaltisAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Mark R HutchinsonAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Brant C GibsonAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Yiqing LuAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Ewa GoldysAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Gang ZhengAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).
Christina A BursillAustralian Research Council (ARC) Centre of Excellence for Nanoscale BioPhotonics (CNBP).ORCID 0000-0002-0682-8760

Funding

ARC Future Fellowship FT180100565Australian Research Council CE140100003Lin Huddleston Heart Foundation Fellowship
6 · The paper itself

Abstract

Despite the emergence of novel diagnostic, pharmacological, interventional, and prevention strategies, atherosclerotic cardiovascular disease remains a significant cause of morbidity and mortality. Nanoparticle (NP)-based platforms encompass diverse imaging, delivery, and pharmacological properties that provide novel opportunities for refining diagnostic and therapeutic interventions for atherosclerosis at the cellular and molecular levels. Macrophages play a critical role in atherosclerosis and therefore represent an important disease-related diagnostic and therapeutic target, especially given their inherent ability for passive and active NP uptake. In this review, we discuss an array of inorganic, carbon-based, and lipid-based NPs that provide magnetic, radiographic, and fluorescent imaging capabilities for a range of highly promising research and clinical applications in atherosclerosis. We discuss the design of NPs that target a range of macrophage-related functions such as lipoprotein oxidation, cholesterol efflux, vascular inflammation, and defective efferocytosis. We also provide examples of NP systems that were developed for other pathologies such as cancer and highlight their potential for repurposing in cardiovascular disease. Finally, we discuss the current state of play and the future of theranostic NPs. Whilst this is not without its challenges, the array of multifunctional capabilities that are possible in NP design ensures they will be part of the next frontier of exciting new therapies that simultaneously improve the accuracy of plaque diagnosis and more effectively reduce atherosclerosis with limited side effects.

Indexed as

AtherosclerosisMacrophagesMultifunctional NanoparticlesPlaque, AtheroscleroticAnimalsHumansNanoparticle Drug Delivery SystemPredictive Value of TestsTheranostic NanomedicineNanoparticle Drug Delivery SystemAtherosclerosisMacrophagesNanoparticles

Identifiers

PMID38696700
PMCPMC11218693

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Registered trials

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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.