Background: The association of age with coronary plaque dynamics is not well characterized by coronary computed tomography angiography (CCTA). Methods: From a multinational registry of patients who underwent serial CCTA, 1153 subjects (61 ± 5 years old, 61.1% male) were analyzed. Annualized volume changes of total, fibrous, fibrofatty, necrotic core, and dense calcification plaque components of the whole heart were compared by age quartile groups. Clinical events, a composite of all-cause death, acute coronary syndrome, and any revascularization after 30 days of the initial CCTA, were also analyzed. Random forest analysis was used to define the relative importance of age on plaque progression. Results: With a 3.3-years’ median interval between the two CCTA, the median annual volume changes of total plaque in each age quartile group was 7.8, 10.5, 10.8, and 12.1 mm3/year and for dense calcification, 2.5, 4.6, 5.4, and 7.1 mm3/year, both of which demonstrated a tendency to increase by age (p-for-trend = 0.001 and < 0.001, respectively). However, this tendency was not observed in any other plaque components. The annual volume changes of total plaque and dense calcification were also significantly different in the propensity score-matched lowest age quartile group versus the other age groups as was the composite clinical event (log-rank p = 0.003). In random forest analysis, age had comparable importance in the total plaque volume progression as other traditional factors. Conclusions: The rate of whole-heart plaque progression and dense calcification increases depending on age. Age is a significant factor in plaque growth, the importance of which is comparable to other traditional risk factors. Clinical trial registration: URL: http://www.clinicaltrials.gov. Unique identifiers: NCT02803411.

Impact of age on coronary artery plaque progression and clinical outcome: A PARADIGM substudy / M. Kim, S.-. Lee, S. Kwak, S. Yang, Y.-. Kim, D. Andreini, M.H. Al-Mallah, M.J. Budoff, F. Cademartiri, K. Chinnaiyan, J.H. Choi, E. Conte, H. Marques, P. de Araujo Goncalves, I. Gottlieb, M. Hadamitzky, J.A. Leipsic, E. Maffei, G. Pontone, G.L. Raff, S. Shin, B.K. Lee, E.J. Chun, J.M. Sung, S.-. Lee, D.S. Berman, F.Y. Lin, R. Virmani, H. Samady, P.H. Stone, J. Narula, J.J. Bax, L.J. Shaw, J.K. Min, H.-. Chang. - In: JOURNAL OF CARDIOVASCULAR COMPUTED TOMOGRAPHY. - ISSN 1934-5925. - 15:3(2021 Jun), pp. 232-239. [10.1016/j.jcct.2020.09.009]

Impact of age on coronary artery plaque progression and clinical outcome: A PARADIGM substudy

D. Andreini;E. Conte;G. Pontone;
2021

Abstract

Background: The association of age with coronary plaque dynamics is not well characterized by coronary computed tomography angiography (CCTA). Methods: From a multinational registry of patients who underwent serial CCTA, 1153 subjects (61 ± 5 years old, 61.1% male) were analyzed. Annualized volume changes of total, fibrous, fibrofatty, necrotic core, and dense calcification plaque components of the whole heart were compared by age quartile groups. Clinical events, a composite of all-cause death, acute coronary syndrome, and any revascularization after 30 days of the initial CCTA, were also analyzed. Random forest analysis was used to define the relative importance of age on plaque progression. Results: With a 3.3-years’ median interval between the two CCTA, the median annual volume changes of total plaque in each age quartile group was 7.8, 10.5, 10.8, and 12.1 mm3/year and for dense calcification, 2.5, 4.6, 5.4, and 7.1 mm3/year, both of which demonstrated a tendency to increase by age (p-for-trend = 0.001 and < 0.001, respectively). However, this tendency was not observed in any other plaque components. The annual volume changes of total plaque and dense calcification were also significantly different in the propensity score-matched lowest age quartile group versus the other age groups as was the composite clinical event (log-rank p = 0.003). In random forest analysis, age had comparable importance in the total plaque volume progression as other traditional factors. Conclusions: The rate of whole-heart plaque progression and dense calcification increases depending on age. Age is a significant factor in plaque growth, the importance of which is comparable to other traditional risk factors. Clinical trial registration: URL: http://www.clinicaltrials.gov. Unique identifiers: NCT02803411.
English
Aging; atherosclerotic plaque; Computed tomography; Coronary artery disease; Disease progression; Adult; Age Factors; Aged; Coronary Artery Disease; Disease Progression; Female; Heart Disease Risk Factors; Humans; Male; Middle Aged; Predictive Value of Tests; Prognosis; Prospective Studies; Registries; Risk Assessment; Vascular Calcification; Computed Tomography Angiography; Plaque, Atherosclerotic
Settore MED/11 - Malattie dell'Apparato Cardiovascolare
Articolo
Esperti anonimi
Pubblicazione scientifica
Goal 3: Good health and well-being
giu-2021
1-ott-2020
Elsevier
15
3
232
239
8
Pubblicato
Periodico con rilevanza internazionale
scopus
pubmed
crossref
wos
datacite
Aderisco
info:eu-repo/semantics/article
Impact of age on coronary artery plaque progression and clinical outcome: A PARADIGM substudy / M. Kim, S.-. Lee, S. Kwak, S. Yang, Y.-. Kim, D. Andreini, M.H. Al-Mallah, M.J. Budoff, F. Cademartiri, K. Chinnaiyan, J.H. Choi, E. Conte, H. Marques, P. de Araujo Goncalves, I. Gottlieb, M. Hadamitzky, J.A. Leipsic, E. Maffei, G. Pontone, G.L. Raff, S. Shin, B.K. Lee, E.J. Chun, J.M. Sung, S.-. Lee, D.S. Berman, F.Y. Lin, R. Virmani, H. Samady, P.H. Stone, J. Narula, J.J. Bax, L.J. Shaw, J.K. Min, H.-. Chang. - In: JOURNAL OF CARDIOVASCULAR COMPUTED TOMOGRAPHY. - ISSN 1934-5925. - 15:3(2021 Jun), pp. 232-239. [10.1016/j.jcct.2020.09.009]
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M. Kim, S.-. Lee, S. Kwak, S. Yang, Y.-. Kim, D. Andreini, M.H. Al-Mallah, M.J. Budoff, F. Cademartiri, K. Chinnaiyan, J.H. Choi, E. Conte, H. Marques, P. de Araujo Goncalves, I. Gottlieb, M. Hadamitzky, J.A. Leipsic, E. Maffei, G. Pontone, G.L. Raff, S. Shin, B.K. Lee, E.J. Chun, J.M. Sung, S.-. Lee, D.S. Berman, F.Y. Lin, R. Virmani, H. Samady, P.H. Stone, J. Narula, J.J. Bax, L.J. Shaw, J.K. Min, H.-. Chang
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/2434/909075
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