Natural History of Myocardial α<sub>v</sub>β<sub>3</sub> Integrin Expression After Acute Myocardial Infarction: Correlation with Changes in Myocardial Blood Flow.

Détails

Ressource 1Télécharger: Dietz_JNM_RGDcoeur.pdf (967.46 [Ko])
Etat: Public
Version: Final published version
Licence: CC BY 4.0
ID Serval
serval:BIB_6979E661C78F
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Institution
Titre
Natural History of Myocardial α<sub>v</sub>β<sub>3</sub> Integrin Expression After Acute Myocardial Infarction: Correlation with Changes in Myocardial Blood Flow.
Périodique
Journal of nuclear medicine
Auteur⸱e⸱s
Dietz M., Kamani C.H., Bousige C., Dunet V., Delage J., Rubimbura V., Nicod Lalonde M., Treglia G., Schaefer N., Nammas W., Saraste A., Knuuti J., Mewton N., Prior J.O.
ISSN
1535-5667 (Electronic)
ISSN-L
0161-5505
Statut éditorial
Publié
Date de publication
01/07/2024
Peer-reviewed
Oui
Volume
65
Numéro
7
Pages
1107-1112
Langue
anglais
Notes
Publication types: Journal Article ; Clinical Trial
Publication Status: epublish
Résumé
Angiogenesis is an essential part of the cardiac repair process after myocardial infarction, but its spatiotemporal dynamics remain to be fully deciphered. <sup>68</sup> Ga-NODAGA-Arg-Gly-Asp (RGD) is a PET tracer targeting α <sub>v</sub> β <sub>3</sub> integrin expression, which is a marker of angiogenesis. Methods: In this prospective single-center trial, we aimed to monitor angiogenesis through myocardial integrin α <sub>v</sub> β <sub>3</sub> expression in 20 patients with ST-segment elevation myocardial infarction (STEMI). In addition, the correlations between the expression levels of myocardial α <sub>v</sub> β <sub>3</sub> integrin and the subsequent changes in <sup>82</sup> Rb PET/CT parameters, including rest and stress myocardial blood flow (MBF), myocardial flow reserve (MFR), and wall motion abnormalities, were assessed. The patients underwent <sup>68</sup> Ga-NODAGA-RGD PET/CT and rest and stress <sup>82</sup> Rb-PET/CT at 1 wk, 1 mo, and 3 mo after STEMI. To assess <sup>68</sup> Ga-NODAGA-RGD uptake, the summed rest <sup>82</sup> Rb and <sup>68</sup> Ga-NODAGA-RGD images were coregistered, and segmental SUVs were calculated (RGD SUV). Results: At 1 wk after STEMI, 19 participants (95%) presented increased <sup>68</sup> Ga-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]; P = 0.9), followed by a significant partial decrease at 3 mo (1.32 g/mL [IQR, 1.12-1.71 g/mL]; P = 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: r = 0.17, P = 0.0033) and MFR (Spearman ρ: r = 0.31, P < 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: r = -0.12, P = 0.035). Conclusion: The present study found that α <sub>v</sub> β <sub>3</sub> 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 <sub>v</sub> β <sub>3</sub> integrin expression at 1 wk is significantly weakly correlated with subsequent improvements in stress MBF, MFR, and wall motion analysis.
Mots-clé
Humans, Integrin alphaVbeta3/metabolism, Male, Female, Middle Aged, Myocardial Infarction/diagnostic imaging, Myocardial Infarction/metabolism, Myocardial Infarction/physiopathology, Positron Emission Tomography Computed Tomography, Coronary Circulation, Myocardium/metabolism, Aged, Heterocyclic Compounds, 1-Ring, Prospective Studies, Oligopeptides/metabolism, Rubidium Radioisotopes, Acetates, PET, RGD, angiogenesis, integrin αvβ3, myocardial infarction
Pubmed
Web of science
Open Access
Oui
Création de la notice
13/05/2024 13:32
Dernière modification de la notice
26/07/2024 6:02
Données d'usage