Evidence map›Paper›PMID 37823265›Full record

ReviewArteriosclerosis, thrombosis, and vascular biology2023

Engineering Organ-on-a-Chip Systems for Vascular Diseases.

Amid Shakeri, Ying Wang, Yimu Zhao, Shira Landau, Kevin Perera, Jonguk Lee, Milica Radisic

Abstract readReview
In one paragraph

Review in Arteriosclerosis, thrombosis, and vascular biology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 37 papers.

0numbers the graph read from it
0cells of the map it votes in
37citing 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

37 citing papers in PubMed.

  1. Review
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  5. Article
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  9. Article
  10. CD8Nature reviews. Cardiology · 2026
    Review
  11. Guidelines for evaluating endothelial function in vascular tissue.American journal of physiology. Heart and circulatory physiology · 2026
    Review
  12. Translational Geroscience Strategies for Delaying Multimorbidity.ACS pharmacology & translational science · 2026
    Review
  13. Review
  14. Review
  15. Review
  16. Review
  17. Considerations in the Use of Mouse Models of Vascular and Valvular Calcification.Arteriosclerosis, thrombosis, and vascular biology · 2026
    Review
  18. Review
  19. Review
  20. Review
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

7 authors.

Amid ShakeriInstitute of Biomedical Engineering (A.S., Y.W., Y.Z., S.L., J.L., M.R.), University of Toronto, Ontario, Canada.ORCID 0000-0002-4534-382X
Ying WangInstitute of Biomedical Engineering (A.S., Y.W., Y.Z., S.L., J.L., M.R.), University of Toronto, Ontario, Canada.
Yimu ZhaoInstitute of Biomedical Engineering (A.S., Y.W., Y.Z., S.L., J.L., M.R.), University of Toronto, Ontario, Canada.
Shira LandauInstitute of Biomedical Engineering (A.S., Y.W., Y.Z., S.L., J.L., M.R.), University of Toronto, Ontario, Canada.
Kevin PereraDepartment of Mechanical and Industrial Engineering (K.P.), University of Toronto, Ontario, Canada.
Jonguk LeeInstitute of Biomedical Engineering (A.S., Y.W., Y.Z., S.L., J.L., M.R.), University of Toronto, Ontario, Canada.
Milica RadisicInstitute of Biomedical Engineering (A.S., Y.W., Y.Z., S.L., J.L., M.R.), University of Toronto, Ontario, Canada.ORCID 0000-0003-1249-4135

Funding

Engineering Vascularized Cardiac MuscleR01HL076485 · NHLBI · COLUMBIA UNIV NEW YORK MORNINGSIDE · PI Gordana Vunjak-Novakovic · 2005 to 2026
$9.2M
NHLBI NIH HHS R01 HL076485
6 · The paper itself

Abstract

Vascular diseases, such as atherosclerosis and thrombosis, are major causes of morbidity and mortality worldwide. Traditional in vitro models for studying vascular diseases have limitations, as they do not fully recapitulate the complexity of the in vivo microenvironment. Organ-on-a-chip systems have emerged as a promising approach for modeling vascular diseases by incorporating multiple cell types, mechanical and biochemical cues, and fluid flow in a microscale platform. This review provides an overview of recent advancements in engineering organ-on-a-chip systems for modeling vascular diseases, including the use of microfluidic channels, ECM (extracellular matrix) scaffolds, and patient-specific cells. We also discuss the limitations and future perspectives of organ-on-a-chip for modeling vascular diseases.

Indexed as

Microphysiological SystemsVascular DiseasesExtracellular MatrixHumansLab-On-A-Chip DevicesMicrofluidicsendothelial cellshemodynamicsmicrofluidicsmicrophysiological systemsvascular diseases

Identifiers

PMID37823265
PMCPMC10842627

What OpenQuestion holds

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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.