Evidence map›Paper›PMID 39012624›Full record

ArticleQJM : monthly journal of the Association of Physicians2024

Plasma NOTCH3 and the risk of cardiovascular recurrence in patients with ischemic stroke.

R C S Seet, A M L Quek, O Teng, S Krishnan, G J L Ng, M Y Ng, A Mahadevan, F W J Chioh, K P Yeo, H Y Lim and 7 more

Abstract read
In one paragraph

Article in QJM : monthly journal of the Association of Physicians, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Observational
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

17 authors.

R C S SeetDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID 0000-0001-8946-3578
A M L QuekDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.ORCID 0000-0002-0569-0472
O TengDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
S KrishnanLee Kong Chian School of Medicine, Nanyang Technological University Singapore, Singapore, Singapore.
G J L NgDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
M Y NgDepartment of Medicine, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
A MahadevanLee Kong Chian School of Medicine, Nanyang Technological University Singapore, Singapore, Singapore.
F W J ChiohLee Kong Chian School of Medicine, Nanyang Technological University Singapore, Singapore, Singapore.
K P YeoImmunology Translational Research Programme, Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
H Y LimImmunology Translational Research Programme, Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
J KimDepartment of Physiology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
C L F SwaInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
N M Q PekInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
T V ArumugamCentre for Cardiovascular Biology and Disease Research, La Trobe University, Melbourne, Australia.
V AngeliImmunology Translational Research Programme, Department of Microbiology and Immunology, Yong Loo Lin School of Medicine, National University of Singapore, Singapore, Singapore.
J GunaratneInstitute of Molecular and Cell Biology, Agency for Science, Technology and Research, Singapore, Singapore.
C CheungLee Kong Chian School of Medicine, Nanyang Technological University Singapore, Singapore, Singapore.

Funding

Campus for Research Excellence and Technological EnterpriseHuman Frontier Science Program RGY0069/2019Lee Kong Chian School of MedicineMinistry of Education RG88/21MOE MOET15-T2-1-019National Medical Research Council NMRC/CSA-SI/0005/2021National Medical Research Council NMRC/OFIRG/0036/2017National Research FoundationTemasek Foundation-Singapore Millennium FoundationVascular Research Initiative
6 · The paper itself

Abstract

backgroundIschemic stroke patients are more prone to developing another cardiovascular event.

aimThis study aims to examine potential biological predispositions to cardiovascular recurrence in patients with ischemic stroke.

designHuman and preclinical studies.

methodsQuantitative proteomic analysis, animal stroke, atherosclerosis models and circulating endothelial cells (CECs) were employed to examine candidate biomarkers derived from an ischemic stroke cohort in Singapore.

resultsProteomic analysis of pooled microvesicles of 'Event' (n = 24) and without 'Event' (n = 24) samples identified NOTCH3 as a candidate marker; plasma NOTCH3 were shown to be elevated in 'Event' patients compared to those without 'Events' and age-matched controls. In a validation cohort comprising 431 prospectively recruited ischemic stroke patients (mean age 59.1 years; median follow-up 3.5 years), men with plasma NOTCH3 (>1600 pg/ml) harbored increased risk of cardiovascular recurrence (adjusted hazards ratio 2.29, 95% CI 1.10-4.77); no significant association was observed in women. Chronic renal failure, peripheral artery disease and NT-pro-brain natriuretic peptide were significant predictors of plasma NOTCH3 in men without ischemic stroke (adjusted r2 = 0.43). Following middle cerebral artery occlusion, NOTCH3 expression in mouse sera increased and peaked at 24 h, persisting thereafter for at least 72 h. In Apoe-/- atherosclerotic mice, NOTCH3 stained the endothelium of defective arterial lining and atherosclerotic plaques. Analysis of CECs isolated from stroke patients revealed increased gene expression of NOTCH3, further supporting endothelial damage underpinning NOTCH3-mediated atherosclerosis.

conclusionFindings from this study suggests that NOTCH3 could be important in cardiovascular recurrence following an ischemic stroke.

Indexed as

Cardiovascular DiseasesIschemic StrokeReceptor, Notch3StrokeAgedAnimalsBiomarkersFemaleHumansMaleMiceMiddle AgedProspective StudiesProteomicsRecurrenceRisk FactorsBiomarkersNOTCH3 protein, humanNotch3 protein, mouseReceptor, Notch3

Identifiers

PMID39012624
PMCPMC11760494

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.