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@ARTICLE{Albertini:281514,
author = {Albertini, Tobia and Dörner, Marc and Giannopoulos,
Andreas A and von Känel, Roland and Benz, Dominik C and
Mikail, Nidaa and de Wilde, Daniel and Voegel, Clarissa D
and Binz, Tina M and Kaufmann, Philipp A and Gebhard,
Catherine and Buechel, Ronny R and Pazhenkottil, Aju P},
title = {{A}ssociation between inflammatory biomarkers, chronic
stress, and pericoronary adipose tissue attenuation obtained
with coronary {CT}.},
journal = {European heart journal - cardiovascular imaging},
volume = {26},
number = {10},
issn = {2047-2404},
address = {Oxford},
publisher = {Oxford University Press},
reportid = {DZNE-2025-01133},
pages = {1664 - 1672},
year = {2025},
abstract = {Pericoronary adipose tissue (PCAT) attenuation is a novel
imaging biomarker of coronary inflammation associated with
an increased risk of coronary artery disease (CAD). However,
no studies have examined the relationship between chronic
stress and PCAT. This study aimed to evaluate the
intersection between chronic stress, inflammatory
biomarkers, coronary plaque features, and PCAT attenuation.A
total of 98 participants without known CAD were included.
PCAT attenuation, total plaque volume (TPV) quantification,
and vulnerable plaque features were assessed by coronary CT
angiography and chronic stress was measured by hair cortisol
concentration (HCC) and vital exhaustion questionnaire.
Regression models were used to analyse associations of PCAT
with the inflammatory biomarkers interleukin-6 (IL-6) and
tumour necrosis factor-α (TNF-α), TPV, vulnerable plaque
features, and coronary stenosis. Moderating analyses were
performed to test whether chronic stress modulated the
association between inflammatory biomarkers and PCAT
attenuation. PCAT attenuation was significantly associated
with IL-6 (mean difference 1.05, $95\%$ CI 0.21-1.89, P =
0.014), TNF-α (mean difference 0.60, $95\%$ CI 0.06-1.13, P
= 0.027), and a greater TPV (mean difference 3.51, $95\%$ CI
0.02-7.00, P = 0.048), but not vulnerable plaque features or
coronary stenosis. HCC (interaction term -0.12, $95\%$ CI
-0.22 to -0.02, P = 0.019) and vital exhaustion (interaction
term 0.13, $95\%$ CI 0.01-0.25, P = 0.024) moderated the
relationship between IL-6, but not TNF-α, and PCAT
attenuation.This study suggests that circulating
inflammatory biomarkers are associated with PCAT
attenuation, which was further correlated with TPV. Chronic
stress may moderate the relationship between inflammatory
cytokines and PCAT attenuation.},
keywords = {Humans / Male / Female / Middle Aged / Biomarkers: blood /
Computed Tomography Angiography: methods / Adipose Tissue:
diagnostic imaging / Coronary Artery Disease: diagnostic
imaging / Coronary Artery Disease: blood / Coronary
Angiography: methods / Stress, Psychological / Inflammation
/ Plaque, Atherosclerotic: diagnostic imaging / Aged /
Interleukin-6: blood / Chronic Disease / Tumor Necrosis
Factor-alpha: blood / Epicardial Adipose Tissue / chronic
stress (Other) / coronary artery disease (Other) / hair
cortisol (Other) / interleukin-6 (Other) / pericoronary
adipose tissue attenuation (Other) / vital exhaustion
(Other) / Biomarkers (NLM Chemicals) / Interleukin-6 (NLM
Chemicals) / Tumor Necrosis Factor-alpha (NLM Chemicals)},
cin = {AG Schreiber},
ddc = {610},
cid = {I:(DE-2719)1310010},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40886153},
doi = {10.1093/ehjci/jeaf217},
url = {https://pub.dzne.de/record/281514},
}