Interplay Between Zero CAC, Quantitative Plaque Analysis, and Adverse Events in a Diverse Patient Cohort.


Journal

Circulation. Cardiovascular imaging
ISSN: 1942-0080
Titre abrégé: Circ Cardiovasc Imaging
Pays: United States
ID NLM: 101479935

Informations de publication

Date de publication:
08 2023
Historique:
pmc-release: 10 08 2024
medline: 17 8 2023
pubmed: 15 8 2023
entrez: 15 8 2023
Statut: ppublish

Résumé

Coronary artery calcium scoring (CAC) has garnered attention in the diagnostic approach to chest pain patients. However, little is known about the interplay between zero CAC, sex, race, ethnicity, and quantitative coronary plaque analysis. We conducted a retrospective analysis from our computed tomography registry of patients with stable angina without prior myocardial infarction or revascularization undergoing coronary computed tomography angiography at Montefiore Healthcare System. Follow-up end points collected included invasive angiography, type-1 myocardial infarction, coronary revascularization, cardiovascular and all-cause death. A total of 2249 patients were included (66% female). The median follow-up was 5.5 years. The median age of those without CAC was 52 years (interquartile range, 44-59) and 60 years (interquartile range, 53-68) in those with CAC. Most patients were Hispanic (58%), and the rest were non-Hispanic Black (28%), non-Hispanic White (10%), and non-Hispanic Asian (5%). The majority had CAC=0 (55%). The negative predictive value of CAC=0 was 92.8%, 99.9%, and 99.9% for any plaque, obstructive coronary artery stenosis, and the composite outcome of all-cause death, myocardial infarction, or coronary revascularization, respectively. Among patients without CAC (n=1237), 89 patients (7%) had evidence of plaque on their coronary computed tomography angiography with a median low-attenuation noncalcified plaque burden of 4% (2-7). There were no significant differences in the negative predictive value for CAC=0 by sex, race, or ethnicity. Patients with ≥2 risk factors had higher odds of having plaque with zero CAC. In summary, no sex, race, or ethnicity differences were demonstrated in the negative predictive value of a zero CAC; however, patients with ≥2 risk factors had a higher prevalence of plaque. A small percentage (7%) of symptomatic patients undergoing coronary computed tomography angiography with zero CAC had noncalcified coronary plaque, with the implication that caution is needed for downscaling of preventive treatment in patients with zero CAC, chest pain, and multiple risk factors.

Sections du résumé

BACKGROUND
Coronary artery calcium scoring (CAC) has garnered attention in the diagnostic approach to chest pain patients. However, little is known about the interplay between zero CAC, sex, race, ethnicity, and quantitative coronary plaque analysis.
METHODS
We conducted a retrospective analysis from our computed tomography registry of patients with stable angina without prior myocardial infarction or revascularization undergoing coronary computed tomography angiography at Montefiore Healthcare System. Follow-up end points collected included invasive angiography, type-1 myocardial infarction, coronary revascularization, cardiovascular and all-cause death.
RESULTS
A total of 2249 patients were included (66% female). The median follow-up was 5.5 years. The median age of those without CAC was 52 years (interquartile range, 44-59) and 60 years (interquartile range, 53-68) in those with CAC. Most patients were Hispanic (58%), and the rest were non-Hispanic Black (28%), non-Hispanic White (10%), and non-Hispanic Asian (5%). The majority had CAC=0 (55%). The negative predictive value of CAC=0 was 92.8%, 99.9%, and 99.9% for any plaque, obstructive coronary artery stenosis, and the composite outcome of all-cause death, myocardial infarction, or coronary revascularization, respectively. Among patients without CAC (n=1237), 89 patients (7%) had evidence of plaque on their coronary computed tomography angiography with a median low-attenuation noncalcified plaque burden of 4% (2-7). There were no significant differences in the negative predictive value for CAC=0 by sex, race, or ethnicity. Patients with ≥2 risk factors had higher odds of having plaque with zero CAC.
CONCLUSIONS
In summary, no sex, race, or ethnicity differences were demonstrated in the negative predictive value of a zero CAC; however, patients with ≥2 risk factors had a higher prevalence of plaque. A small percentage (7%) of symptomatic patients undergoing coronary computed tomography angiography with zero CAC had noncalcified coronary plaque, with the implication that caution is needed for downscaling of preventive treatment in patients with zero CAC, chest pain, and multiple risk factors.

Identifiants

pubmed: 37582155
doi: 10.1161/CIRCIMAGING.123.015236
pmc: PMC10430772
mid: NIHMS1919177
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

e015236

Subventions

Organisme : NHLBI NIH HHS
ID : P50 HL120163
Pays : United States
Organisme : NHLBI NIH HHS
ID : K02 HL004199
Pays : United States
Organisme : CLC NIH HHS
ID : 75N90019D00011
Pays : United States
Organisme : NHLBI NIH HHS
ID : 75N92021D00011
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL148787
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL151266
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL146204
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL144707
Pays : United States

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Auteurs

Michael Fattouh (M)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Toshiki Kuno (T)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Pamela Pina (P)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

John P Skendelas (JP)

Cardiothoracic and Vascular Surgery Department, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (J.P.S.).

Daniel Lorenzatti (D)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Javier Arce (J)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Jonathan Daich (J)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Gustavo Duarte (G)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Carol Fernandez-Hazim (C)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Miguel Rodriguez-Guerra (M)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Patrick Neshiwat (P)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Aldo L Schenone (AL)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Lili Zhang (L)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Carlos J Rodriguez (CJ)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Armin Arbab-Zadeh (A)

Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD (A.A.-Z., M.J.B.).

Piotr J Slomka (PJ)

Department of Imaging, Cedars-Sinai Medical Center, Los Angeles, CA (P.J.S., D.S.B., D.D.).

Salim S Virani (SS)

Section of Cardiology, Department of Medicine, The Aga Khan Universit, Karachi, Pakistan (S.S.V.).
Section of Cardiology, Texas Heart Institute & Baylor College of Medicine, Houston (S.S.V.).

Michael J Blaha (MJ)

Division of Cardiology, Johns Hopkins University School of Medicine, Baltimore, MD (A.A.-Z., M.J.B.).

Daniel S Berman (DS)

Department of Imaging, Cedars-Sinai Medical Center, Los Angeles, CA (P.J.S., D.S.B., D.D.).

Damini Dey (D)

Department of Imaging, Cedars-Sinai Medical Center, Los Angeles, CA (P.J.S., D.S.B., D.D.).

Mario J Garcia (MJ)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

Leandro Slipczuk (L)

Division of Cardiology, Montefiore Medical Center/Albert Einstein College of Medicine, Bronx, NY (M.F., T.K., P.P., D.L., J.A., J.D., G.D., C.F.-H., M.R.-G., P.N., A.L.S., L.Z., C.J.R., M.J.G., L.S.).

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