Cell proliferation detected using [18F]FLT PET/CT as an early marker of abdominal aortic aneurysm

BACKGROUND: Abdominal aortic aneurysm (AAA) is a focal aortic dilatation progressing towards rupture. Non-invasive AAA-associated cell proliferation biomarkers are not yet established. We investigated the feasibility of the cell proliferation radiotracer, fluorine-18-fluorothymidine ([18F]FLT) with...

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Veröffentlicht in:JOURNAL OF NUCLEAR CARDIOLOGY 2021-10, Vol.28 (5), p.1961-1971
Hauptverfasser: Gandhi, Richa, Cawthorne, Christopher, Craggs, Lucinda J.L, Wright, John D, Domarkas, Juozas, He, Ping, Koch-Paszkowski, Joanna, Shires, Michael, Scarsbrook, Andrew F, Archibald, Stephen J, Tsoumpas, Charalampos, Bailey, Marc A
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Sprache:eng
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Zusammenfassung:BACKGROUND: Abdominal aortic aneurysm (AAA) is a focal aortic dilatation progressing towards rupture. Non-invasive AAA-associated cell proliferation biomarkers are not yet established. We investigated the feasibility of the cell proliferation radiotracer, fluorine-18-fluorothymidine ([18F]FLT) with positron emission tomography/computed tomography (PET/CT) in a progressive pre-clinical AAA model (angiotensin II, AngII infusion). METHODS AND RESULTS: Fourteen-week-old apolipoprotein E-knockout (ApoE-/-) mice received saline or AngII via osmotic mini-pumps for 14 (n = 7 and 5, respectively) or 28 (n = 3 and 4, respectively) days and underwent 90-minute dynamic [18F]FLT PET/CT. Organs were harvested from independent cohorts for gamma counting, ultrasound scanning, and western blotting. [18F]FLT uptake was significantly greater in 14- (n = 5) and 28-day (n = 3) AAA than in saline control aortae (n = 5) (P 
ISSN:1071-3581