Evidence map›Paper›PMID 39304297›Full record

ArticleOpen heart2024

Interleukin 6 plasma levels are associated with progression of coronary plaques.

Jordan M Kraaijenhof, Nick S Nurmohamed, Evangelos Tzolos, Mo Meah, Jolien Geers, Yannick Kaiser, Jeffrey Kroon, G Kees Hovingh, Erik S G Stroes, Marc R Dweck

Abstract read
In one paragraph

Article in Open heart, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
–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

8 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
  4. Review
  5. A Review on the Role of Oral Bacteria in Stroke.International journal of molecular sciences · 2025
    Review
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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

10 authors.

Jordan M KraaijenhofDepartment of Vascular Medicine, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0001-7566-6403
Nick S NurmohamedDepartment of Vascular Medicine, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, The Netherlands.ORCID 0000-0001-9045-6009
Evangelos TzolosBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-0038-043X
Mo MeahBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-0806-9972
Jolien GeersBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-1109-5191
Yannick KaiserDepartment of Vascular Medicine, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, The Netherlands.
Jeffrey KroonDepartment of Experimental Vascular Medicine, Amsterdam University Medical Centers, University of Amsterdam, Amsterdam, The Netherlands.
G Kees HovinghDepartment of Vascular Medicine, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, The Netherlands.
Erik S G StroesDepartment of Vascular Medicine, Amsterdam University Medical Centres, University of Amsterdam, Amsterdam, The Netherlands.
Marc R DweckBritish Heart Foundation Centre for Cardiovascular Science, University of Edinburgh, Edinburgh, UK marc.dweck@ed.ac.uk.ORCID 0009-0005-1991-0017

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammation plays a pivotal role in atherogenesis and is a causal risk factor for atherosclerotic cardiovascular disease. Non-invasive coronary CT angiography (CCTA) enables evaluation of coronary plaque phenotype. This study investigates the relationship between a comprehensive panel of inflammatory markers and short-term plaque progression on serial CCTA imaging, hypothesising that inflammation is associated with increased plaque volume.

methodsA total of 161 patients aged ≥40 years with stable multivessel coronary artery disease were included, who underwent CCTA at baseline and 12 months follow-up. Baseline plasma levels of interleukin 6 (IL-6), high-sensitivity C-reactive protein and other inflammatory markers were measured. Plaque volumes were assessed using semiautomated software, calculating total, noncalcified, calcified and low-attenuation noncalcified plaque volumes. Linear regression models, adjusted for ASSIGN score, segment involvement score and body mass index, evaluated associations between inflammatory markers and plaque volume changes.

resultsThe mean±SD age was 65.4±8.4 years, with 129 (80.6%) male participants. Baseline total plaque volume was 1394 (1036, 1993) mm³. After 12 months, total plaque volume changed by 78 (-114, 244) mm³. IL-6 levels were associated with a 4.9% increase in total plaque volume (95% CI: 0.9 to 8.9, p=0.018) and a 4.8% increase in noncalcified plaque volume (95% CI: 0.7 to 8.9, p=0.022). No significant associations were observed for other inflammatory markers.

conclusionsPlasma IL-6 levels are significantly associated with increased total and noncalcified short-term plaque progression in patients with stable coronary artery disease. This supports the potential of IL-6 as a target for reducing plaque progression and cardiovascular risk.

Indexed as

BiomarkersComputed Tomography AngiographyCoronary AngiographyCoronary Artery DiseaseDisease ProgressionInterleukin-6Plaque, AtheroscleroticAgedCoronary VesselsFemaleFollow-Up StudiesHumansMaleMiddle AgedProspective StudiesRisk FactorsBiomarkersIL6 protein, humanInterleukin-6Computed Tomography AngiographyCoronary Artery DiseaseInflammation

Identifiers

PMID39304297
PMCPMC11418485

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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.