Increased soluble vascular adhesion molecule-1 concentration is associated with impaired coronary flow reserve in

Byung Ju Shim1, Dong Hyeon Lee, Ho Joong Youn

  • 1Division of Cardiology, Department of Internal Medicine, College of Medicine, The Catholic University of Korea, Seoul, Korea.

Heart and Vessels
|November 1, 2013
PubMed

Insights

Early atherosclerosis markers like soluble vascular cell adhesion molecule-1 (sVCAM-1) are inversely associated with coronary flow reserve (CFR) in cardiac syndrome X patients. This suggests sVCAM-1 may indicate subclinical coronary atherosclerosis.

Area of Science:

  • Cardiology
  • Vascular Biology
  • Inflammation Research

Background:

  • Endothelial dysfunction and inflammation drive atherosclerosis.
  • Coronary flow reserve (CFR) assesses coronary microcirculation function.
  • Cardiac Syndrome X involves chest pain with normal coronary angiograms, often linked to microvascular dysfunction.

Purpose of the Study:

  • To investigate the association between early atherosclerotic inflammatory markers and CFR.
  • To evaluate soluble vascular cell adhesion molecule-1 (sVCAM-1) in relation to CFR in cardiac syndrome X.

Main Methods:

  • 135 cardiac syndrome X patients underwent transthoracic echocardiography (TTE) for CFR assessment.
  • Blood samples measured inflammatory biomarkers: sVCAM-1, IL-6, MCP-1, Lp-PLA2.
  • CFR was measured using TTE with adenosine or dipyridamole within two weeks of coronary angiography.

Main Results:

  • An inverse correlation was found between sVCAM-1 and CFR (r = -0.225, P = 0.014).
  • Patients with CFR < 2.0 had significantly higher sVCAM-1 levels (757 ± 323 ng/ml) compared to those with CFR ≥ 2.0 (628 ± 146 ng/ml, P = 0.007).
  • Multivariate analysis identified sVCAM-1 as an independent factor related to CFR < 2.0 (OR 1.003, P = 0.023).

Conclusions:

  • sVCAM-1 levels are inversely associated with CFR in cardiac syndrome X patients.
  • Elevated sVCAM-1 may reflect subclinical coronary atherosclerosis and microvascular dysfunction.
  • Further research is needed to confirm sVCAM-1's role as an inflammatory modulator in early atherosclerosis.

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