Evidence map›Paper›PMID 42403465›Full record

ArticleAmerican journal of preventive cardiology2026

The effect of colchicine on pericoronary adipose tissue attenuation by serial coronary CT angiography: A substudy of the Ekstrom trial.

J R Colasurdo, R Mora, D Verghese, M Bhandari, K Irannejad, N Punnanithinont, B Iskander, V Garikapati, A Kinninger, S Roy and 2 more

Abstract read
In one paragraph

Article in American journal of preventive cardiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

J R ColasurdoDepartment of Medicine, Harbor-UCLA Medical Center, Torrance, CA, USA.
R MoraThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
D VergheseThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
M BhandariThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
K IrannejadThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
N PunnanithinontThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
B IskanderThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
V GarikapatiThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
A KinningerThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
S RoyThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
M BudoffThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.
S LakshmananThe Lundquist Institute for Biomedical Innovation at Harbor-UCLA Medical Center, Torrance, CA, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Inflammation plays a pivotal role in initiation and progression of coronary artery disease (CAD). Pericoronary adipose tissue (PCAT) attenuation on coronary CT angiography (CCTA) is a novel non-invasive biomarker of coronary inflammation. Low dose colchicine has been shown to safely lower cardiovascular events among patients with stable CAD. We sought to investigate whether colchicine is associated with changes in PCAT by serial CCTA in patients enrolled in the Effect of Colchicine on Progression of Known Coronary Atherosclerosis in Patients with STable CoROnary Artery Disease CoMpared to Placebo (EKSTROM) trial. Methods: This is a post-hoc analysis of the EKSTROM trial, a prospective, placebo-controlled serial CCTA trial that randomized patients with stable CAD to receive either colchicine (0.5 mg/day) or placebo, and followed for 12 months. PCAT attenuation was quantified using partially-automated Medis QAngioCT software. Multivariable linear regression models were adjusted for traditional cardiovascular risk factors and baseline PCAT attenuation to examine the change in mean PCAT attenuation between the treatment groups. Results: The analysis included 71 participants (12% female, mean age 64.6 ± 7.3, mean hsCRP 0.8 mg/L). Mean PCAT attenuation in the colchicine group was -73.6 HU ±8.0 at baseline which increased to -73.1 HU ±8.2 at 12-month follow-up. Mean PCAT attenuation in the placebo group was -75.3 HU ±7.4 at baseline, which increased to 74.5 HU ±6.8 at follow-up, with a between group change of 0.3 HU ±8.0 ( Conclusion: Colchicine was not associated with a significant change in PCAT over 12 months in participants in the EKSTROM trial with stable CAD. Larger studies with long-term follow up are needed to evaluate the mechanistic benefits of colchicine on the complex interactions of coronary atherosclerosis, inflammation, and adverse CV risk.

Indexed as

atherosclerosisColchicineCoronary CT angiographyInflammationPeri coronary adipose tissue

Identifiers

PMID42403465
PMCPMC13329530

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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.