Coronary Computed Tomography Angiography Analysis of Calcium Content to Identify Non-culprit Vulnerable Plaques in Patients With Acute Coronary Syndrome.

coronary calcification coronary computed tomographic angiography (CCTA) non-ST elevation myocardial infarction (NSTEMI) optical coherence tomography (OCT) vulnerable plaque

Journal

Frontiers in cardiovascular medicine
ISSN: 2297-055X
Titre abrégé: Front Cardiovasc Med
Pays: Switzerland
ID NLM: 101653388

Informations de publication

Date de publication:
2022
Historique:
received: 15 02 2022
accepted: 22 03 2022
entrez: 2 5 2022
pubmed: 3 5 2022
medline: 3 5 2022
Statut: epublish

Résumé

Aside from the culprit plaque, the presence of vulnerable plaques in patients with acute coronary syndrome (ACS) may be associated with future cardiac events. A link between calcification and plaque rupture has been previously described. To assess whether analysis of the calcium component of coronary plaques using CT angiography, coronary computed tomographic angiography (CCTA) can help to detect additional vulnerable plaques in patients with non-ST elevation myocardial infarction (NSTEMI). Cross sectional study of consecutive patients referred for NSTEMI from 30 July to 30 August 2018 with CCTA performed before coronary angiography with systematic optical coherence tomography (OCT) analysis of all coronary arteries within 24 h of clinical onset of NSTEMI. Three types of plaques were defined: culprit plaques defined by angiography (vulnerable culprit plaques-VCP) - plaques with a fibrous cap thickness < 65 microns or thrombus in OCT (vulnerable non-culprit plaque-VNCP) - plaques with a fibrous cap thickness ≥ 65 microns in OCT (stable plaque-SP). A total of 134 calcified plaques were identified in 29 patients (73% male, 59 ± 14 years) with 29(22%) VCP, 28(21%) VNCP and 77(57%) SP. Using CCTA analysis of the calcium component, factors associated with vulnerable plaques were longer calcification length, larger calcification volume, lower calcium mass, higher Agatston score plaque-specific (ASp), presence of spotty calcifications and an intimal position in the wall. In multivariate analysis, ASp, calcification length and spotty calcifications were independently associated to vulnerable plaques. There was no difference between VCP and VNCP. CCTA analysis of calcium component of the plaque could help to identify additional vulnerable plaques in NSTEMI patients.

Sections du résumé

Background UNASSIGNED
Aside from the culprit plaque, the presence of vulnerable plaques in patients with acute coronary syndrome (ACS) may be associated with future cardiac events. A link between calcification and plaque rupture has been previously described.
Aim UNASSIGNED
To assess whether analysis of the calcium component of coronary plaques using CT angiography, coronary computed tomographic angiography (CCTA) can help to detect additional vulnerable plaques in patients with non-ST elevation myocardial infarction (NSTEMI).
Materials And Methods UNASSIGNED
Cross sectional study of consecutive patients referred for NSTEMI from 30 July to 30 August 2018 with CCTA performed before coronary angiography with systematic optical coherence tomography (OCT) analysis of all coronary arteries within 24 h of clinical onset of NSTEMI. Three types of plaques were defined: culprit plaques defined by angiography (vulnerable culprit plaques-VCP) - plaques with a fibrous cap thickness < 65 microns or thrombus in OCT (vulnerable non-culprit plaque-VNCP) - plaques with a fibrous cap thickness ≥ 65 microns in OCT (stable plaque-SP).
Results UNASSIGNED
A total of 134 calcified plaques were identified in 29 patients (73% male, 59 ± 14 years) with 29(22%) VCP, 28(21%) VNCP and 77(57%) SP. Using CCTA analysis of the calcium component, factors associated with vulnerable plaques were longer calcification length, larger calcification volume, lower calcium mass, higher Agatston score plaque-specific (ASp), presence of spotty calcifications and an intimal position in the wall. In multivariate analysis, ASp, calcification length and spotty calcifications were independently associated to vulnerable plaques. There was no difference between VCP and VNCP.
Conclusions UNASSIGNED
CCTA analysis of calcium component of the plaque could help to identify additional vulnerable plaques in NSTEMI patients.

Identifiants

pubmed: 35498013
doi: 10.3389/fcvm.2022.876730
pmc: PMC9051337
doi:

Types de publication

Journal Article

Langues

eng

Pagination

876730

Informations de copyright

Copyright © 2022 Pezel, Sideris, Dillinger, Logeart, Manzo-Silberman, Cohen-Solal, Beauvais, Devasenapathy, Laissy and Henry.

Déclaration de conflit d'intérêts

The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

Références

Nat Rev Cardiol. 2014 Jul;11(7):379-89
pubmed: 24776706
Circulation. 2003 Oct 7;108(14):1664-72
pubmed: 14530185
Eur Heart J Cardiovasc Imaging. 2015 Apr;16(4):373-9
pubmed: 25246503
Eur Heart J. 2016 Jan 14;37(3):267-315
pubmed: 26320110
Eur Heart J. 2016 Jan 21;37(4):390-9
pubmed: 26324537
N Engl J Med. 2017 Sep 21;377(12):1119-1131
pubmed: 28845751
Am J Cardiol. 2014 Nov 15;114(10):1497-503
pubmed: 25248815
J Cardiovasc Comput Tomogr. 2016 Jul-Aug;10(4):269-81
pubmed: 27318587
Atherosclerosis. 2013 Jul;229(1):124-9
pubmed: 23578355
PLoS One. 2020 Jul 13;15(7):e0235228
pubmed: 32658909
Mol Cell Biomech. 2008 Mar;5(1):37-47
pubmed: 18524245
Eur Heart J. 2020 Oct 1;41(37):3579-3586
pubmed: 32676644
Diagnostics (Basel). 2019 Sep 23;9(4):
pubmed: 31547506
J Cardiovasc Comput Tomogr. 2021 Jul-Aug;15(4):290-303
pubmed: 33926854
JACC Cardiovasc Imaging. 2015 Feb;8(2):198-209
pubmed: 25677892
J Am Coll Cardiol. 2012 Mar 20;59(12):1058-72
pubmed: 22421299
Circ Cardiovasc Imaging. 2017 May;10(5):
pubmed: 28483945
Circulation. 2015 Oct 27;132(17):1667-78
pubmed: 26503749
PLoS One. 2015 Jun 24;10(6):e0131254
pubmed: 26106881
JAMA. 2014 Jan 15;311(3):271-8
pubmed: 24247483
J Am Coll Cardiol. 2009 Jun 30;54(1):49-57
pubmed: 19555840
JACC Cardiovasc Imaging. 2015 Apr;8(4):451-460
pubmed: 25797121
Arterioscler Thromb Vasc Biol. 2000 May;20(5):1262-75
pubmed: 10807742
Int J Cardiol. 2017 Feb 1;228:11-22
pubmed: 27863350
J Am Coll Cardiol. 1990 Mar 15;15(4):827-32
pubmed: 2407762
Eur Radiol. 2015 Oct;25(10):3073-83
pubmed: 25994190
J Am Coll Cardiol. 1997 Feb;29(2):268-74
pubmed: 9014977
Front Cardiovasc Med. 2021 Jan 15;7:619798
pubmed: 33521068
J Am Coll Cardiol. 2015 Jul 28;66(4):337-46
pubmed: 26205589
J Am Coll Cardiol. 2009 May 5;53(18):1642-50
pubmed: 19406338
Circulation. 2001 Oct 2;104(14):1682-7
pubmed: 11581149
Nat Rev Cardiol. 2014 Jul;11(7):390-402
pubmed: 24755916
JACC Cardiovasc Imaging. 2016 Nov;9(11):1280-1288
pubmed: 27568114
JACC Cardiovasc Imaging. 2018 Jan;11(1):127-142
pubmed: 29301708
Proc Natl Acad Sci U S A. 2006 Oct 3;103(40):14678-83
pubmed: 17003118
Angiology. 2020 Nov;71(10):916-919
pubmed: 32633543
JACC Cardiovasc Imaging. 2009 Feb;2(2):153-60
pubmed: 19356549
BMC Cardiovasc Disord. 2020 May 6;20(1):212
pubmed: 32375648
Proc Natl Acad Sci U S A. 2013 Jun 25;110(26):10741-6
pubmed: 23733926

Auteurs

Théo Pezel (T)

Department of Cardiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.
Department of Radiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.

Georgios Sideris (G)

Department of Cardiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.

Jean-Guillaume Dillinger (JG)

Department of Cardiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.

Damien Logeart (D)

Department of Cardiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.

Stéphane Manzo-Silberman (S)

Department of Cardiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.

Alain Cohen-Solal (A)

Department of Cardiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.

Florence Beauvais (F)

Department of Cardiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.

Niveditha Devasenapathy (N)

Public Health Foundation of India, Indian Institute of Public Health, New Delhi, India.

Jean-Pierre Laissy (JP)

Department of Radiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.

Patrick Henry (P)

Department of Cardiology, Lariboisiere Hospital, Assistance Publique - Hôpitaux de Paris (APHP), University of Paris, Paris, France.

Classifications MeSH