Evidence map›Paper›PMID 39287909›Full record

ArticleAnnals of biomedical engineering2025

Relative Residence Time Can Account for Half of the Anatomical Variation in Fatty Streak Prevalence Within the Right Coronary Artery.

Pratik Kandangwa, Kevin Cheng, Miten Patel, Spencer J Sherwin, Ranil de Silva, Peter D Weinberg

Abstract read
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Article in Annals of biomedical engineering, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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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

3 citing papers in PubMed.

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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.

Pratik KandangwaDepartment of Bioengineering, Imperial College London, London, SW7 2AZ, UK.
Kevin ChengNational Heart and Lung Institute, Imperial College London, London, SW3 6LY, UK.
Miten PatelNational Heart and Lung Institute, Imperial College London, London, SW3 6LY, UK.
Spencer J SherwinDepartment of Aeronautics, Imperial College London, London, SW7 2AZ, UK.
Ranil de SilvaNational Heart and Lung Institute, Imperial College London, London, SW3 6LY, UK.
Peter D WeinbergDepartment of Bioengineering, Imperial College London, London, SW7 2AZ, UK. p.weinberg@imperial.ac.uk.ORCID http://orcid.org/0000-0001-6114-5498

Funding

British Heart Foundation SP/17/1/32702Engineering and Physical Sciences Research Council Studentship from CDT in Fluid Dynamics Across Scales
6 · The paper itself

Abstract

purposeThe patchy anatomical distribution of atherosclerosis has been attributed to variation in haemodynamic wall shear stress (WSS). The consensus is that low WSS and a high Oscillatory Shear Index (OSI) trigger the disease. We found that atherosclerosis at aortic branch sites correlates threefold better with transverse WSS (transWSS), a metric which quantifies multidirectional near-wall flow. Coronary artery disease has greater clinical significance than aortic disease but computation of WSS metrics is complicated by the substantial vessel motion occurring during each cardiac cycle. Here we present the first comparison of the distribution of atherosclerosis with WSS metrics computed for moving coronary arteries.

methodsMaps of WSS metrics were computed using dynamic geometries reconstructed from angiograms of ten non-stenosed human right coronary arteries (RCAs). They were compared with maps of fatty streak prevalence derived from a previous study of 1852 RCAs.

resultsTime average WSS (TAWSS), OSI, transWSS and the cross-flow index (CFI), a non-dimensional form of the transWSS, gave non-significant or significant but low spatial correlations with lesion prevalence. The highest correlation coefficient (0.71) was for the relative residence time (RRT), a metric that decreases with TAWSS and increases with OSI. The coefficient was not changed if RRT was calculated using CFI, which captures multidirectional WSS only, rather than OSI, which encompasses both multidirectional and oscillatory WSS.

conclusionContrary to our earlier findings in the aorta, low WSS in combination with highly multidirectional flow correlates best with lesion location in the RCA, explaining approximately half of its anatomical variation.

Indexed as

Coronary Artery DiseaseCoronary VesselsModels, CardiovascularFemaleHumansMaleStress, MechanicalComputational fluid dynamicsCoronary artery diseaseEndothelial cell activation potentialHemodynamicsPathobiological determinants of atherosclerosis in youth

Identifiers

PMID39287909
PMCPMC11782302

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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.