Evidence map›Paper›PMID 38262275›Full record

ArticleAtherosclerosis2024

Comprehensive biomechanical and anatomical atherosclerotic plaque metrics predict major adverse cardiovascular events: A new tool for clinical decision making.

Sophie Z Gu, Mona E Ahmed, Yuan Huang, Diaa Hakim, Charles Maynard, Nicholas V Cefalo, Ahmet U Coskun, Charis Costopoulos, Akiko Maehara, Gregg W Stone and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Atherosclerosis, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
7.4field-weighted citation impact, top 2% 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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Review
  3. Considerations on the Development of Therapeutics in Vascular Calcification.Journal of cardiovascular development and disease · 2025
    Review
  4. Review
  5. Review
  6. Article
  7. In vivo atherosclerotic plaque characterization using 7T quantitative T2*mapping distinguishes symptomatic middle cerebral artery plaques.Journal of cardiovascular magnetic resonance : official journal of the Society for Cardiovascular Magnetic Resonance
    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 at 7 institutions in 3 countries.

Sophie Z GuSection of Cardiorespiratory Medicine, Department of Medicine, University of Cambridge, Cambridge, UK.
Mona E AhmedCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA; Department of Molecular Medicine and Surgery, Karolinska Institutet Karolinska University Hospital Solna, 171 76, Stockholm, Sweden.
Yuan HuangCentre for Mathematical and Statistical Analysis of Multimodal Imaging, University of Cambridge, Cambridge, UK; Department of Radiology, University of Cambridge, Cambridge, UK.
Diaa HakimCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Charles MaynardDepartment of Health Services, University of Washington, Seattle, WA, USA.
Nicholas V CefaloCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA.
Ahmet U CoskunMechanical and Industrial Engineering, Northeastern University, Boston, MA, USA.
Charis CostopoulosDepartment of Cardiology, Royal Papworth Hospital, Cambridge, UK.
Akiko MaeharaCardiovascular Research Foundation, New York City, New York, USA.
Gregg W StoneThe Zena and Michael A. Wiener Cardiovascular Institute, Icahn School of Medicine at Mount Sinai, New York, USA.
Peter H StoneCardiovascular Division, Brigham and Women's Hospital, Harvard Medical School, Boston, MA, USA. Electronic address: pstone@bwh.harvard.edu.
Martin R BennettSection of Cardiorespiratory Medicine, Department of Medicine, University of Cambridge, Cambridge, UK. Electronic address: mrb24@medschl.cam.ac.uk.
Brigham and Women's Hospital · USUniversity of Cambridge · GBCardiovascular Institute of the South · USCardiovascular Research Foundation · USNortheastern University · USPapworth Hospital · GBUniversity of Washington · US

Funding

Unique value of real-time shear stress to enhance coronary disease managementR01HL140498 · NHLBI · MASSACHUSETTS GENERAL HOSPITAL · PI STONE, PETER HOWARD, TEARNEY, GUILLERMO J · 2018 to 2022
$3.9M
Integrating Coronary Atherosclerosis with Physiologic Features for Optimized Risk StratificationR01HL146144 · NHLBI · BRIGHAM AND WOMEN'S HOSPITAL · PI MIN, JAMES K, STONE, PETER HOWARD · 2021 to 2024
$2.5M
British Heart Foundation CH/2000003/12800British Heart Foundation FS/19/66/34658British Heart Foundation PG/16/24/32090British Heart Foundation PG/18/14/33562British Heart Foundation RG/20/2/34763British Heart Foundation TA/F/20/210001NHLBI NIH HHS R01 HL140498NHLBI NIH HHS R01 HL146144
6 · The paper itself

Abstract

BACKGROUND AND

aimsAnatomical imaging alone of coronary atherosclerotic plaques is insufficient to identify risk of future adverse events and guide management of non-culprit lesions. Low endothelial shear stress (ESS) and high plaque structural stress (PSS) are associated with events, but individually their predictive value is insufficient for risk prediction. We determined whether combining multiple complementary, biomechanical and anatomical plaque characteristics improves outcome prediction sufficiently to inform clinical decision-making.

methodsWe examined baseline ESS, ESS gradient (ESSG), PSS, and PSS heterogeneity index (HI), and plaque burden in 22 lesions that developed subsequent events and 64 control lesions that remained quiescent from the PROSPECT study.

results86 fibroatheromas were analysed from 67 patients. Lesions with events showed higher PSS HI (0.32 vs. 0.24, p<0.001), lower local ESS (0.56Pa vs. 0.91Pa, p = 0.007), and higher ESSG (3.82 Pa/mm vs. 1.96 Pa/mm, p = 0.007), while high PSS HI (hazard ratio [HR] 3.9, p = 0.006), high ESSG (HR 3.4, p = 0.007) and plaque burden>70 % (HR 2.6, p = 0.02) were independent outcome predictors in multivariate analysis. Combining low ESS, high ESSG, and high PSS HI gave both high positive predictive value (80 %), which increased further combined with plaque burden>70 %, and negative predictive value (81.6 %). Low ESS, high ESSG, and high PSS HI co-localised spatially within 1 mm in lesions with events, and importantly, this cluster was distant from the minimum lumen area site.

conclusionsCombining complementary biomechanical and anatomical metrics significantly improves risk-stratification of individual coronary lesions. If confirmed from larger prospective studies, our results may inform targeted revascularisation vs. conservative management strategies.

Indexed as

Coronary Artery DiseasePlaque, AtheroscleroticClinical Decision-MakingCoronary AngiographyCoronary VesselsHumansPredictive Value of TestsProspective StudiesRisk FactorsUltrasonography, InterventionalAcute coronary syndromeAtherosclerotic plaquesIntravascular ultrasoundPatient outcomesRisk stratification

Identifiers

PMID38262275
PMCPMC10939719
OpenAlexW4390754442

What OpenQuestion holds

Textmetadata
LicenceTDM
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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.