Natural History of Myocardial α_vβ₃ Integrin Expression After Acute Myocardial Infarction: Correlation with Changes in Myocardial Blood Flow.

Abstract

Angiogenesis is an essential part of the cardiac repair process after myocardial infarction, but its spatiotemporal dynamics remain to be fully deciphered.⁶⁸Ga-NODAGA-Arg-Gly-Asp (RGD) is a PET tracer targeting α_vβ₃ integrin expression, which is a marker of angiogenesis. <b>Methods:</b> In this prospective single-center trial, we aimed to monitor angiogenesis through myocardial integrin α_vβ₃ expression in 20 patients with ST-segment elevation myocardial infarction (STEMI). In addition, the correlations between the expression levels of myocardial α_vβ₃ integrin and the subsequent changes in ⁸²Rb PET/CT parameters, including rest and stress myocardial blood flow (MBF), myocardial flow reserve (MFR), and wall motion abnormalities, were assessed. The patients underwent ⁶⁸Ga-NODAGA-RGD PET/CT and rest and stress ⁸²Rb-PET/CT at 1 wk, 1 mo, and 3 mo after STEMI. To assess ⁶⁸Ga-NODAGA-RGD uptake, the summed rest ⁸²Rb and ⁶⁸Ga-NODAGA-RGD images were coregistered, and segmental SUVs were calculated (RGD SUV). <b>Results:</b> At 1 wk after STEMI, 19 participants (95%) presented increased ⁶⁸Ga-NODAGA-RGD uptake in the infarcted myocardium. Seventeen participants completed the full imaging series. The values of the RGD SUV in the infarcted myocardium were stable 1 mo after STEMI (1 wk vs. 1 mo, 1.47 g/mL [interquartile range (IQR), 1.37-1.64 g/mL] vs. 1.47 g/mL [IQR, 1.30-1.66 g/mL]; <i>P</i> = 0.9), followed by a significant partial decrease at 3 mo (1.32 g/mL [IQR, 1.12-1.71 g/mL]; <i>P</i> = 0.011 vs. 1 wk and 0.018 vs. 1 mo). In segment-based analysis, positive correlations were found between RGD SUV at 1 wk and the subsequent changes in stress MBF (Spearman ρ: <i>r</i> = 0.17, <i>P</i> = 0.0033) and MFR (Spearman ρ: <i>r</i> = 0.31, <i>P</i> < 0.0001) at 1 mo. A negative correlation was found between RGD SUV at 1 wk and the subsequent changes in wall motion abnormalities at 3 mo (Spearman ρ: <i>r</i> = <i>-</i>0.12, <i>P</i> = 0.035). <b>Conclusion:</b> The present study found that α_vβ₃ integrin expression is significantly increased in the infarcted myocardium 1 wk after STEMI. This expression remains stable after 1 mo and partially decreases after 3 mo. Initial α_vβ₃ integrin expression at 1 wk is significantly weakly correlated with subsequent improvements in stress MBF, MFR, and wall motion analysis.