Evidence map›Paper›PMID 35722127›Full record

ArticleFrontiers in cardiovascular medicine2022

Morphological and Physiological Characteristics of Ruptured Plaques in Native Arteries and Neoatherosclerotic Segments: An OCT-Based and Computational Fluid Dynamics Study.

Chongying Jin, Ryo Torii, Anantharaman Ramasamy, Vincenzo Tufaro, Callum D Little, Klio Konstantinou, Yi Ying Tan, Nathan A L Yap, Jackie Cooper, Tom Crake and 9 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in cardiovascular medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
1.1field-weighted citation impact, top 24% of its field
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

2 citing papers in PubMed, 5 citations in OpenAlex.

  1. Review
  2. 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

19 authors at 9 institutions in 5 countries.

Chongying JinDepartment of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom.
Ryo ToriiDepartment of Mechanical Engineering, University College London, London, United Kingdom.
Anantharaman RamasamyDepartment of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom.
Vincenzo TufaroDepartment of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom.
Callum D LittleRoyal Free Hospital, University College London, London, United Kingdom.
Klio KonstantinouEssex Cardiothoracic Centre, Anglia Ruskin School of Medicine, Essex, United Kingdom.
Yi Ying TanDepartment of Mechanical Engineering, University College London, London, United Kingdom.
Nathan A L YapBarts and The London School of Medicine and Dentistry, London, United Kingdom.
Jackie CooperCentre for Cardiovascular Medicine and Devices, William Harvey Research Institute, Queen Mary University of London, London, United Kingdom.
Tom CrakeDepartment of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom.
Constantinos O'MahonyDepartment of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom.
Roby RakhitRoyal Free Hospital, University College London, London, United Kingdom.
Mohaned EgredFreeman Hospital, Newcastle University, Newcastle upon Tyne, United Kingdom.
Javed AhmedFreeman Hospital, Newcastle University, Newcastle upon Tyne, United Kingdom.
Grigoris KaramasisEssex Cardiothoracic Centre, Anglia Ruskin School of Medicine, Essex, United Kingdom.
Lorenz RäberDepartment of Cardiology, University of Bern, Bern, Switzerland.
Andreas BaumbachDepartment of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom.
Anthony MathurDepartment of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom.
Christos V BourantasDepartment of Cardiology, Barts Heart Centre, Barts Health NHS Trust, London, United Kingdom.
Barts Health NHS Trust · GBEssex Cardiothoracic Centre · GBThe Royal Free Hospital · GBUniversity College London · GBWilliam Harvey Research Institute · GBFreeman Hospital · GBNewcastle University · GBUniversity of Bern · CHYale University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Intravascular imaging has been used to assess the morphology of lesions causing an acute coronary syndrome (ACS) in native vessels (NV) and identify differences between plaques that ruptured (PR) and caused an event and those that ruptured without clinical manifestations. However, there is no data about the morphological and physiological characteristics of neoatherosclerotic plaques that ruptured (PR-NA) which constitute a common cause of stent failure. Methods: We retrospectively analyzed data from patients admitted with an acute myocardial infarction that had optical coherence tomography (OCT) imaging of the culprit vessel before balloon pre-dilation. OCT pullbacks showing PR were segmented at every 0.4 mm. The extent of the formed cavity, lipid and calcific tissue, thrombus, and macrophages were measured, and the fibrous cap thickness (FCT) and the incidence of micro-channels and cholesterol crystals were reported. These data were used to reconstruct a representative model of the native and neoatherosclerotic lesion geometry that was processed with computational fluid dynamics (CFD) techniques to estimate the distribution of the endothelial shear stress and plaque structural stress. Result: Eighty patients were included in the present analysis: 56 had PR in NV (PR-NV group) and 24 in NA segments (PR-NA group). The PR-NV group had a larger minimum lumen area (2.93 ± 2.03 vs. 2.00 ± 1.26 mm Conclusion: We reported significant morphological and physiological differences between culprit ruptured plaques in native and stented segments. Further research is needed to better understand the causes of these differences and the mechanisms regulating neoatherosclerotic lesion destabilization.

Indexed as

computational fluid dynamics (CFD)endothelial shear stressneoatherosclerosisoptical coherence tomographyplaque ruptureplaque structural stress

Identifiers

PMID35722127
PMCPMC9204481
OpenAlexW4281779110

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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.