Evidence map›Paper›PMID 26951555›Full record

ArticleJournal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology2017

PET/CT evaluation of

Tomasz Mazurek, Małgorzata Kobylecka, Magdalena Zielenkiewicz, Aleksandra Kurek, Janusz Kochman, Krzysztof J Filipiak, Krzysztof Mazurek, Zenon Huczek, Leszek Królicki, Grzegorz Opolski

Abstract read
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In one paragraph

Article in Journal of nuclear cardiology : official publication of the American Society of Nuclear Cardiology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 46 papers.

0numbers the graph read from it
0cells of the map it votes in
46citing 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

46 citing papers in PubMed.

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  18. The Presence of Residual Vascular and Adipose Tissue Inflammation onNuclear medicine and molecular imaging · 2023
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

10 authors.

Tomasz MazurekFirst Chair and Department of Cardiology, Medical University of Warsaw, Banacha 1a, 02-097, Warsaw, Poland. tmazurek@kardia.pl.
Małgorzata KobyleckaDepartment of Nuclear Medicine, Medical University of Warsaw, Warsaw, Poland.
Magdalena ZielenkiewiczInsitiute of Mathematics, University of Warsaw, Warsaw, Poland.
Aleksandra KurekThe International Institute of Molecular and Cell Biology, Polish Academy of Sciences, Warsaw, Poland.
Janusz KochmanFirst Chair and Department of Cardiology, Medical University of Warsaw, Banacha 1a, 02-097, Warsaw, Poland.
Krzysztof J FilipiakFirst Chair and Department of Cardiology, Medical University of Warsaw, Banacha 1a, 02-097, Warsaw, Poland.
Krzysztof MazurekJózef Piłsudski University of Physical Education in Warsaw, Warsaw, Poland.
Zenon HuczekFirst Chair and Department of Cardiology, Medical University of Warsaw, Banacha 1a, 02-097, Warsaw, Poland.
Leszek KrólickiDepartment of Nuclear Medicine, Medical University of Warsaw, Warsaw, Poland.
Grzegorz OpolskiFirst Chair and Department of Cardiology, Medical University of Warsaw, Banacha 1a, 02-097, Warsaw, Poland.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInflammatory infiltrations in EAT which releases inflammatory cytokines correspond anatomically to the atheromatous plaques in underlying coronary vessels. However, it is unknown whether inflammatory activity of pericoronary adipose tissue (PCAT) promotes coronary atherosclerosis. METHODS AND

results35 non-diabetic patients with confirmed CAD and 35 non-CAD controls matched for age and BMI underwent 18F-FDG-PET/CT. Maximal SUV normalized by LA blood activity was measured on the sections corresponding to the respective coronaries (RCA, LCX, LAD), as well, as in subcutaneous fat, visceral fat, and epicardial fat. Extent of CAD was determined by % stenosis in segments corresponding to 18F-FDG-PET/CT sections in coronarography using quantitative coronary analysis. PCAT SUV was significantly greater than SUV in other fat locations, as well as PCAT SUV in the controls. In CAD patients with BMI >25, PCAT SUV was positively related to % stenosis of a respective coronary artery (RCA: 0.43; P < .05; LCX 0.58; P < .05; LAD 0.65; P < .05). PCAT SUV was the only independent predictor of coronary stenosis of LAD and RCA.

conclusionsInflammatory activity of PCAT is greater than in other fat locations, in CAD is greater than in non-CAD controls, and is independently associated with coronary stenosis. In overweight patients, PCAT SUV correlates with the extent of CAD.

Indexed as

AgedBiomarkersCoronary Artery DiseaseFemaleFluorodeoxyglucose F18HumansIntra-Abdominal FatMaleMyocardial Perfusion ImagingPanniculitisPositron Emission Tomography Computed TomographyPrognosisReproducibility of ResultsRisk FactorsSensitivity and SpecificityBiomarkersFluorodeoxyglucose F18adipose tissueatherosclerosisFDG-PET/CTstable coronary artery disease

Identifiers

What OpenQuestion holds

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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.