Evidence map›Paper›PMID 41673471›Full record

ReviewNature reviews. Cardiology2026

Heart-on-a-chip and vasculature-on-a-chip platforms as models of cardiovascular disease.

Ramak Khosravi, Milica Radisic

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Cardiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. Review
  2. Review
  3. Review
  4. Decoding Vascular Senescence: Cellular Insights and Therapeutic Strategies.International journal of biological sciences · 2026
    Review
  5. 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

2 authors.

Ramak KhosraviToronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada.
Milica RadisicToronto General Hospital Research Institute, University Health Network, Toronto, Ontario, Canada. m.radisic@utoronto.ca.ORCID http://orcid.org/0000-0003-1249-4135

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Organ-on-a-chip platforms have revolutionized the modelling of cardiovascular pathophysiology, enabling researchers to elucidate underlying mechanisms and drug responses for a variety of inherited and acquired diseases. This emerging technology can overcome the limitations of traditional in vitro culture systems and animal models such as poor biological relevance and species-specific differences. Heart-on-a-chip and vasculature-on-a-chip models consist of 3D structures incorporating relevant cell populations (often derived from pluripotent stem cell sources) with precisely controlled electromechanical conditions and biochemical stimuli to form functional biomimetic microenvironments. These tunable platforms hold great promise in establishing patient-specific disease models and accelerating drug discovery and development, an important step in the direction of personalized cardiovascular medicine. In this Review, we highlight organ-on-a-chip models that have successfully mimicked cardiovascular disease phenotypes and contributed to the development of novel therapeutics, and summarize the technical and biological barriers to the widespread utilization of this technology.

Indexed as

Cardiovascular DiseasesLab-On-A-Chip DevicesModels, CardiovascularAnimalsHumansMicrophysiological Systems

Identifiers

What OpenQuestion holds

Textmetadata
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.