Progression of whole-heart Atherosclerosis by coronary CT and major adverse cardiovascular events
Authors
van Rosendael, Alexander R. ; Lin, Fay Y. ; van den Hoogen, Inge J. ; Ma, Xiaoyue ; Gianni, Umberto ; Alawamlh, Omar Al Hussein ; Al'Aref, Subhi J. ; Pena, Jessica M. ; Andreini, Daniele ; Budoff, Matthew J. ; Cademartiri, Filippo ; Chinnaiyan, Kavitha ; Choi, Jung Hyun ; Conte, Edoardo ; Marques, Hugo ; Goncalves, Pedro de Araujo ; Gottlieb, Ilan ; Hadamitzky, Martin ; Leipsic, Jonathon ; Maffei, Erica ; Pontone, Gianluca ; Raff, Gilbert L. ; Shin, Sanghoon ; Kim, Yong-Jin ; Lee, Byoung Kwon ; Chun, Eun Ju ; Sung, Ji Min ; Lee, Sang Eun ; HAN, Donghee ; Berman, Daniel S. ; Virmani, Renu ; Samady, Habib ; Stone, Peter ; Narula, Jagat ; Bax, Jeroen J. ; Shaw, Leslee J. ; Min, James K. ; Chang, Hyuk-Jae
Citation
Journal of Cardiovascular Computed Tomography, Vol.15(4) : 322-330, 2021-07
Background: The current study aimed to examine the independent prognostic value of whole-heart atherosclerosis progression by serial coronary computed tomography angiography (CCTA) for major adverse cardiovascular events (MACE). Methods: The multi-center PARADIGM study includes patients undergoing serial CCTA for symptomatic reasons, >2 years apart. Whole-heart atherosclerosis was characterized on a segmental level, with co-registration of baseline and follow-up CCTA, and summed to per-patient level. The independent prognostic significance of atherosclerosis progression for MACE (non-fatal myocardial infarction [MI], death, unplanned coronary revascularization) was examined. Patients experiencing interval MACE were not omitted. Results: The study population comprised 1166 patients (age 60.5 +/- 9.5 years, 54.7% male) who experienced 139 MACE events during 8.2 (IQR 6.2, 9.5) years of follow up (15 death, 5 non-fatal MI, 119 unplanned revascularizations). Whole-heart percent atheroma volume (PAV) increased from 2.32% at baseline to 4.04% at follow-up. Adjusted for baseline PAV, the annualized increase in PAV was independently associated with MACE: OR 1.23 (95% CI 1.08, 1.39) per 1 standard deviation increase, which was consistent in multiple subpopulations. When categorized by composition, only non-calcified plaque progression associated independently with MACE, while calcified plaque did not. Restricting to patients without events before follow-up CCTA, those with future MACE showed an annualized increase in PAV of 0.93% (IQR 0.34, 1.96) vs 0.32% (IQR 0.02, 0.90), P < 0.001. Conclusions: Whole-heart atherosclerosis progression examined by serial CCTA is independently associated with MACE, with a prognostic threshold of 1.0% increase in PAV per year.