4.7 Article

Detection of Antecedent Myocardial Ischemia With Multiselectin Molecular Imaging

期刊

JOURNAL OF THE AMERICAN COLLEGE OF CARDIOLOGY
卷 60, 期 17, 页码 1690-1697

出版社

ELSEVIER SCIENCE INC
DOI: 10.1016/j.jacc.2012.07.027

关键词

contrast echocardiography; microbubbles; molecular imaging; myocardial ischemia; selectin

资金

  1. National Institutes of Health [T32-HL-094294-01]
  2. Swiss National Science Foundation [SNF 32323B_123919/1]
  3. Lichtenstein Foundation
  4. [R01-HL078610]
  5. [R01-DK063508]
  6. [R01-HL111969]
  7. [RC1-HL-100659]

向作者/读者索取更多资源

Objectives Our aim was to develop an echocardiographic molecular imaging approach for detecting recent myocardial ischemia by using recombinant P-selectin glycoprotein ligand (PSGL)-1 as a targeting ligand, which is a feasible approach for human use. Background Ischemic memory imaging using human PSGL-1 as a targeting moiety may extend the time window for postischemic detection by targeting the early (P-selectin) and late (E-selectin) endothelial ischemic response. Methods Lipid microbubbles bearing recombinant human PSGL-1 (MBYSPSL) or P-selectin antibody (MBAb) were prepared. Targeted attachment was evaluated by using flow chamber and intravital microscopy. In vivo ultrasound molecular imaging was first performed in the hindlimb in wild-type and P-selectin-deficient (P-/-) mice 45 to 360 min after brief ischemia-reperfusion injury. Myocardial contrast echocardiography molecular imaging was performed 1.5, 3, 6, and 18 h after brief left anterior descending coronary artery ischemia-reperfusion. Results Microbubble attachment to P-selectin-immunoglobulin G fusion protein in flow chamber experiments (shear stress 0.5 to 8.0 dyne/cm(2)) and to activated venular endothelium on intravital microscopy were similar for MBAb and MBYSPSL. Intense enhancement was seen for MBAb and MBYSPSL in postischemic muscle and was more stable over time for MBYSPSL. On myocardial contrast echocardiography, both MBYSPSL and MBAb produced similar signal enhancement at 90 min and 3 h after ischemia, which spatially correlated with the postischemic risk area. Signal significantly decreased but was still present at 6 to 18 h. Conclusions Echocardiographic molecular imaging with a human multi-selectin-targeted contrast agent bearing recombinant human PSGL-1 can detect myocardial ischemia hours after resolution. This approach may potentially be used for rapid bedside evaluation of patients with recent chest pain. (J Am Coll Cardiol 2012;60:1690-7) (C) 2012 by the American College of Cardiology Foundation

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