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Quantification of Skeletal Muscle Perfusion in Peripheral Artery Disease Using 18F-Sodium Fluoride Positron Emission Tomography Imaging.
Chou, Ting-Heng; Nabavinia, Mahboubeh; Tram, Nguyen K; Rimmerman, Eleanor T; Patel, Surina; Musini, Kumudha Narayana; Eisert, Susan Natalie; Wolfe, Tatiana; Wynveen, Molly K; Matsuzaki, Yuichi; Kitsuka, Takahiro; Iwaki, Ryuma; Janse, Sarah A; Bobbey, Adam J; Breuer, Christopher K; Goodchild, Laurie; Malbrue, Raphael; Shinoka, Toshiharu; Atway, Said A; Go, Michael R; Stacy, Mitchel R.
Affiliation
  • Chou TH; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Nabavinia M; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Tram NK; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Rimmerman ET; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Patel S; Biophysics Graduate Program Ohio State University Columbus OH.
  • Musini KN; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Eisert SN; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Wolfe T; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Wynveen MK; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Matsuzaki Y; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Kitsuka T; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Iwaki R; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Janse SA; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Bobbey AJ; Center for Biostatistics Ohio State University Columbus OH.
  • Breuer CK; Department of Radiology Nationwide Children's Hospital Columbus OH.
  • Goodchild L; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Malbrue R; Animal Resources Core Research Institute at Nationwide Children's Hospital Columbus OH.
  • Shinoka T; Animal Resources Core Research Institute at Nationwide Children's Hospital Columbus OH.
  • Atway SA; Center for Regenerative Medicine Research Institute at Nationwide Children's Hospital Columbus OH.
  • Go MR; Department of Orthopaedics Ohio State University College of Medicine Columbus OH.
  • Stacy MR; Division of Vascular Diseases & Surgery, Department of Surgery Ohio State University College of Medicine Columbus OH.
J Am Heart Assoc ; 13(4): e031823, 2024 Feb 20.
Article in En | MEDLINE | ID: mdl-38353265
ABSTRACT

BACKGROUND:

Perfusion deficits contribute to symptom severity, morbidity, and death in peripheral artery disease (PAD); however, no standard method for quantifying absolute measures of skeletal muscle perfusion exists. This study sought to preclinically test and clinically translate a positron emission tomography (PET) imaging approach using an atherosclerosis-targeted radionuclide, fluorine-18-sodium fluoride (18F-NaF), to quantify absolute perfusion in PAD. METHODS AND

RESULTS:

Eight Yorkshire pigs underwent unilateral femoral artery ligation and dynamic 18F-NaF PET/computed tomography imaging on the day of and 2 weeks after occlusion. Following 2-week imaging, calf muscles were harvested to quantify microvascular density. PET methodology was validated with microspheres in 4 additional pig studies and translated to patients with PAD (n=39) to quantify differences in calf perfusion across clinical symptoms/stages and perfusion responses in a case of revascularization. Associations between PET perfusion, ankle-brachial index, toe-brachial index, and toe pressure were assessed in relation to symptoms. 18F-NaF PET/computed tomography quantified significant deficits in calf perfusion in pigs following arterial occlusion and perfusion recovery 2 weeks after occlusion that coincided with increased muscle microvascular density. Additional studies confirmed that PET-derived perfusion measures agreed with microsphere-derived perfusion measures. Translation of imaging methods demonstrated significant decreases in calf perfusion with increasing severity of PAD and quantified perfusion responses to revascularization. Perfusion measures were also significantly associated with symptom severity, whereas traditional hemodynamic measures were not.

CONCLUSIONS:

18F-NaF PET imaging quantifies perfusion deficits that correspond to clinical stages of PAD and represents a novel perfusion imaging strategy that could be partnered with atherosclerosis-targeted 18F-NaF PET imaging using a single radioisotope injection. REGISTRATION URL https//www.clinicaltrials.gov; Unique identifier NCT03622359.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscle, Skeletal / Peripheral Arterial Disease Limits: Animals / Humans Language: En Journal: J Am Heart Assoc Year: 2024 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Muscle, Skeletal / Peripheral Arterial Disease Limits: Animals / Humans Language: En Journal: J Am Heart Assoc Year: 2024 Document type: Article