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1.
Radiology ; 310(3): e231557, 2024 03.
Article in English | MEDLINE | ID: mdl-38441097

ABSTRACT

Background Coronary artery calcium (CAC) has prognostic value for major adverse cardiovascular events (MACE) in asymptomatic individuals, whereas its role in symptomatic patients is less clear. Purpose To assess the prognostic value of CAC scoring for MACE in participants with stable chest pain initially referred for invasive coronary angiography (ICA). Materials and Methods This prespecified subgroup analysis from the Diagnostic Imaging Strategies for Patients With Stable Chest Pain and Intermediate Risk of Coronary Artery Disease (DISCHARGE) trial, conducted between October 2015 and April 2019 across 26 centers in 16 countries, focused on adult patients with stable chest pain referred for ICA. Participants were randomly assigned to undergo either ICA or coronary CT. CAC scores from noncontrast CT scans were categorized into low, intermediate, and high groups based on scores of 0, 1-399, and 400 or higher, respectively. The end point of the study was the occurrence of MACE (myocardial infarction, stroke, and cardiovascular death) over a median 3.5-year follow-up, analyzed using Cox proportional hazard regression tests. Results The study involved 1749 participants (mean age, 60 years ± 10 [SD]; 992 female). The prevalence of obstructive coronary artery disease (CAD) at CT angiography rose from 4.1% (95% CI: 2.8, 5.8) in the CAC score 0 group to 76.1% (95% CI: 70.3, 81.2) in the CAC score 400 or higher group. Revascularization rates increased from 1.7% to 46.2% across the same groups (P < .001). The CAC score 0 group had a lower MACE risk (0.5%; HR, 0.08 [95% CI: 0.02, 0.30]; P < .001), as did the 1-399 CAC score group (1.9%; HR, 0.27 [95% CI: 0.13, 0.59]; P = .001), compared with the 400 or higher CAC score group (6.8%). No significant difference in MACE between sexes was observed (P = .68). Conclusion In participants with stable chest pain initially referred for ICA, a CAC score of 0 showed very low risk of MACE, and higher CAC scores showed increasing risk of obstructive CAD, revascularization, and MACE at follow-up. Clinical trial registration no. NCT02400229 © RSNA, 2024 Supplemental material is available for this article. See also the editorial by Hanneman and Gulsin in this issue.


Subject(s)
Coronary Artery Disease , Myocardial Infarction , Adult , Humans , Female , Middle Aged , Calcium , Coronary Artery Disease/diagnostic imaging , Chest Pain/diagnostic imaging
2.
Pharmacology ; 77(4): 188-94, 2006.
Article in English | MEDLINE | ID: mdl-16877874

ABSTRACT

The physiological effects of a novel MRI contrast agent, Gd(ABE-DTTA), were investigated in dogs, monitoring parameters in blood samples. Each animal (n = 8 in the short-term, n = 4 in the long-term group) underwent isoflurane anesthesia followed by the generation of myocardial infarction and received a contrast agent at the MRI effective dose. Blood samples were collected 24 and 48 h, and 7, 14, 28, 35, 49 and 56 days after contrast agent administration. No significant changes exceeding the normal range were detected in any of the investigated parameters except in alanine aminotransferase (ALT). ALT enzyme activity increased in the short-term group 24 and 48 h after agent administration as expected from the effect of isoflurane anesthesia. Between days 7 and 56 no elevation in ALT was observed. In dogs no substantial short- or long-term effect was observed on the investigated, physiological parameters after Gd(ABE-DTTA) administration at the MRI effective dose.


Subject(s)
Contrast Media/pharmacology , Magnetic Resonance Imaging/methods , Organometallic Compounds/pharmacology , Alanine Transaminase/blood , Amylases/blood , Amylases/metabolism , Anesthetics, Inhalation/administration & dosage , Animals , Blood Proteins/analysis , Blood Proteins/metabolism , Contrast Media/chemistry , Contrast Media/toxicity , Dogs , Drug Evaluation, Preclinical/methods , Electrolytes/blood , Erythrocyte Count , Isoflurane/administration & dosage , Kidney Function Tests/methods , Leukocyte Count , Liver Function Tests/methods , Male , Molecular Structure , Myocardial Ischemia/chemically induced , Myocardial Ischemia/diagnosis , Organometallic Compounds/blood , Organometallic Compounds/chemistry , Pentetic Acid/blood , Pentetic Acid/chemistry , Pentetic Acid/pharmacology , Time Factors
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