Affiliation: | 1. Cardiovascular Center, Taichung Veterans General Hospital, Taichung, Taiwan;2. School of Medicine, National Yang Ming University, Taipei, Taiwan;3. Department of Medicine, China Medical University, Taichung, Taiwan;4. School of Medicine, National Yang Ming University, Taipei, Taiwan;5. Division of Endocrinology and Metabolism, Department of Medicine, Taichung Veterans General Hospital, Taichung, Taiwan;6. Institute of Biomedical Sciences, National Chung Hsing University, Taichung, Taiwan;7. School of Medicine, National Defense Medical Center, Taipei, Taiwan;8. Department of Medical Research, Taichung Veterans General Hospital, Taichung, Taiwan;9. Tung-Hai University, Taichung, Taiwan;10. Division of Endocrinology and Metabolism, Department of Medicine, Taichung Veterans General Hospital, Taichung, Taiwan |
Abstract: | Context: Inflammation is one of the mechanisms underlying cardiac syndrome X (CSX). Objectives: Few studies have compared the expression of inflammatory or adhesion molecules between coronary artery disease (CAD) versus CSX. Materials and methods: Ninety-two CSX and 145 CAD subjects without known diabetes mellitus underwent coronary angiogram for angina. Results: Vascular cell adhesion molecule (VCAM)-1 (median, 507 versus 431?ng/ml, p?=?0.001) was significantly higher in the CAD group. In the binary regression, VCAM-1 was a significant differential factor for CAD versus CSX. Discussion and conclusion: Adhesion molecules might be implicated in the differential expression of macro versus microvascular coronary disease. Trial registration number: NCT01198730 at https://clinicaltrials.gov |