Liang Kae-Woei, Sheu Wayne H-H, Lee Wen-Jane, Lee Wen-Lieng, Fu Chia-Po, Wang Jun-Sing
a Cardiovascular Center , Taichung Veterans General Hospital , Taichung , Taiwan.
b School of Medicine , National Yang Ming University , Taipei , Taiwan.
Biomarkers. 2017 Dec;22(8):798-804. doi: 10.1080/1354750X.2017.1351003. Epub 2017 Jul 18.
Inflammation is one of the mechanisms underlying cardiac syndrome X (CSX).
Few studies have compared the expression of inflammatory or adhesion molecules between coronary artery disease (CAD) versus CSX.
Ninety-two CSX and 145 CAD subjects without known diabetes mellitus underwent coronary angiogram for angina.
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.
Adhesion molecules might be implicated in the differential expression of macro versus microvascular coronary disease.
NCT01198730 at https://clinicaltrials.gov.
炎症是心脏X综合征(CSX)的潜在机制之一。
很少有研究比较冠心病(CAD)与CSX之间炎症或黏附分子的表达。
92例CSX患者和145例无糖尿病的CAD患者因心绞痛接受冠状动脉造影。
CAD组血管细胞黏附分子(VCAM)-1(中位数,507对431 ng/ml,p = 0.001)显著更高。在二元回归中,VCAM-1是CAD与CSX的显著差异因素。
黏附分子可能与冠状动脉大血管与微血管疾病的差异表达有关。