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American Heart Association

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Final ID: MP1374

Validation of a Novel Reactive Oxygen Species-Targeted SPECT Tracer 67Ga-Galuminox in Pig Model of Myocardial Ischemia-Reperfusion Injury

Abstract Body (Do not enter title and authors here): Background: Reactive oxygen species (ROS) plays a major role in the pathogenesis of myocardial ischemia-reperfusion injury (IRI). However, molecular imaging probes enabling the in vivo detection of ROS are limited.
Aim: To evaluate and validate the myocardial uptake of a novel 67Ga-labeled SPECT tracer, 67Ga-Galuminox, for the in vivo quantitative assessment of myocardial IRI in relation to myocardial perfusion.
Methods: Three anesthetized Yorkshire pigs were subjected to myocardial IRI by 90 min balloon occlusion in the left anterior descending artery and reperfusion. In vivo SPECT/CT images of the heart were acquired on the day of injury or 3 days post injury with hybrid 360° CZT SPECT 64-slice CT (Veriton-CT 400, Spectrum Dynamics) with 67Ga-Galuminox (93 keV) in evaluation of ROS and 99mTc-Tetrofosmin (140.5 keV) to define myocardial perfusion. Quantitative segmental image analysis was performed and compared with tissue gamma well counting for the corresponding epicardial (EP) and endocardial (EN) segments.
Results: Myocardial uptake of 67Ga-Galuminox was increased in the area at risk as defined by 99mTc-Tetrofosmin (Figure 1). 67Ga-Galuminox uptake assessed by in vivo SPECT correlated positively with the tissue well counting in corresponding EP (r=0.57, p<0.005) and EN (r=0.43, p=0.002) segments. Uptake of 67Ga-Galuminox was significantly higher in the infarcted segments compared to remote area by both in vivo SPECT and gamma well counting. Regional myocardial 99mTc-Tetrofosmin and 67Ga-Galuminox uptake were negatively correlated in EP (r=-0.78, p<0.001) and EN (r=-0.8, p<0.001).
Conclusions: Myocardial 67Ga-Galuminox SPECT/CT imaging provides excellent image quality, enabling accurate non-invasive quantification of EN and EP activation of ROS in our porcine model of myocardial IRI.
  • Jang, Sun-joo  ( Yale University , New Haven , Connecticut , United States )
  • Sinusas, Albert  ( Yale University , New Haven , Connecticut , United States )
  • Sivapackiam, Jothilingam  ( Washington University School of Medicine , St. Louis , Missouri , United States )
  • Thorn, Stephanie  ( Yale University , New Haven , Connecticut , United States )
  • Nazari, Matthew  ( Yale University , New Haven , Connecticut , United States )
  • Zohora, Fatema Tuj  ( Yale University , New Haven , Connecticut , United States )
  • Burns, Rachel  ( Yale University , New Haven , Connecticut , United States )
  • Cho, Sang-geon  ( Chonnam National University , Gwangju , Korea (the Republic of) )
  • Gropler, Robert  ( Washington University School of Medicine , St. Louis , Missouri , United States )
  • Sharma, Vijay  ( Washington University School of Medicine , St. Louis , Missouri , United States )
  • Author Disclosures:
    Sun-Joo Jang: DO NOT have relevant financial relationships | Albert Sinusas: DO have relevant financial relationships ; Research Funding (PI or named investigator):Siemens:Active (exists now) ; Consultant:MicroVide:Active (exists now) ; Research Funding (PI or named investigator):Revalia:Active (exists now) ; Research Funding (PI or named investigator):Jubilant:Active (exists now) | Jothilingam Sivapackiam: No Answer | Stephanie Thorn: DO NOT have relevant financial relationships | Matthew Nazari: DO NOT have relevant financial relationships | Fatema Tuj Zohora: DO NOT have relevant financial relationships | Rachel Burns: DO NOT have relevant financial relationships | Sang-Geon Cho: No Answer | Robert Gropler: DO NOT have relevant financial relationships | Vijay Sharma: No Answer
Meeting Info:

Scientific Sessions 2025

2025

New Orleans, Louisiana

Session Info:
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