Evidence map›Paper›PMID 30786744›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2019

Nanoparticle Therapy for Vascular Diseases.

Alyssa M Flores, Jianqin Ye, Kai-Uwe Jarr, Niloufar Hosseini-Nassab, Bryan R Smith, Nicholas J Leeper

Abstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 77 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
77citing papers in PubMed, 1 pooled it
–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

77 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  7. Article
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  9. Article
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  15. Nano Delivery System for Atherosclerosis.Journal of functional biomaterials · 2024
    Review
  16. Nanotheranostics for gynecological cancers: a path forward for Africa.Medical oncology (Northwood, London, England) · 2024
    Review
  17. Efferocytosis in atherosclerosis.Nature reviews. Cardiology · 2024
    Review
  18. Article
  19. Article
  20. Review

17 more citing papers are in PubMed but not listed here.

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

6 authors.

Alyssa M FloresFrom the Division of Vascular Surgery, Department of Surgery (A.M.F., J.Y., K.-U.J., N.J.L.), Stanford University School of Medicine, CA.
Jianqin YeFrom the Division of Vascular Surgery, Department of Surgery (A.M.F., J.Y., K.-U.J., N.J.L.), Stanford University School of Medicine, CA.
Kai-Uwe JarrFrom the Division of Vascular Surgery, Department of Surgery (A.M.F., J.Y., K.-U.J., N.J.L.), Stanford University School of Medicine, CA.
Niloufar Hosseini-NassabDepartment of Radiology (N.H.-N.), Stanford University School of Medicine, CA.
Bryan R SmithDepartment of Biomedical Engineering, Institute for Quantitative Health Science and Engineering, Michigan State University, East Lansing (B.R.S.).
Nicholas J LeeperFrom the Division of Vascular Surgery, Department of Surgery (A.M.F., J.Y., K.-U.J., N.J.L.), Stanford University School of Medicine, CA.

Funding

Clonal expansion, resistance to efferocytosis and innate immunity in atherosclerosisR35HL144475 · NHLBI · STANFORD UNIVERSITY · PI LEEPER, NICHOLAS JAMES · 2019 to 2024
$5.1M
The paradoxical role of CDKN2B in blood vessel sprouting and maturationR01HL125224 · NHLBI · STANFORD UNIVERSITY · PI LEEPER, NICHOLAS JAMES · 2015 to 2018
$1.9M
The role of CDKN2B in efferocytosis and atherosclerosisR01HL123370 · NHLBI · STANFORD UNIVERSITY · PI LEEPER, NICHOLAS JAMES · 2015 to 2018
$1.6M
NHLBI NIH HHS R01 HL123370NHLBI NIH HHS R01 HL125224NHLBI NIH HHS R35 HL144475
6 · The paper itself

Abstract

Nanoparticles promise to advance strategies to treat vascular disease. Since being harnessed by the cancer field to deliver safer and more effective chemotherapeutics, nanoparticles have been translated into applications for cardiovascular disease. Systemic exposure and drug-drug interactions remain a concern for nearly all cardiovascular therapies, including statins, antithrombotic, and thrombolytic agents. Moreover, off-target effects and poor bioavailability have limited the development of completely new approaches to treat vascular disease. Through the rational design of nanoparticles, nano-based delivery systems enable more efficient delivery of a drug to its therapeutic target or even directly to the diseased site, overcoming biological barriers and enhancing a drug's therapeutic index. In addition, advances in molecular imaging have led to the development of theranostic nanoparticles that may simultaneously act as carriers of both therapeutic and imaging payloads. The following is a summary of nanoparticle therapy for atherosclerosis, thrombosis, and restenosis and an overview of recent major advances in the targeted treatment of vascular disease.

Indexed as

AnimalsCardiovascular AgentsChemotaxis, LeukocyteCholesterolDrug CarriersDrug Evaluation, PreclinicalForecastingHumansInflammationMacrophagesMiceNanoparticlesNeointimaNeovascularization, PathologicPlaque, AtheroscleroticRNA InterferenceCardiovascular AgentsCholesterolDrug CarriersRNA, Small Interferingatherosclerosisnanotechnologyrestenosisthrombosisvascular diseases

Identifiers

PMID30786744
PMCPMC6436996

What OpenQuestion holds

Textmetadata
LicenceTDM
Read underepoch 390

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.