PMID- 12791819 OWN - NLM STAT- MEDLINE DCOM- 20030724 LR - 20191210 IS - 0161-5505 (Print) IS - 0161-5505 (Linking) VI - 44 IP - 6 DP - 2003 Jun TI - Calf flow reserve with H(2)(15)O PET as a quantifiable index of lower extremity flow. PG - 915-9 AB - Objective measures of recruitable blood flow are of importance in angiogenesis trials. We validated a new PET-derived flow reserve (FR) measurement in healthy subjects and subjects with peripheral artery disease (PAD). METHODS: Five healthy volunteers and 5 subjects with PAD underwent cannulation of the femoral artery and vein. Basal and maximal flow (100 micro g/kg/min of adenosine infused intraarterially) in the lower extremity was determined using thermodilution (TD) techniques. Subjects then underwent plethysmography (PL) followed by PET measurements of blood flow at the calf level. For the PET studies, a transmission scan followed by injection of 1.85 GBq (50 mCi) H(2)(15)O and dynamic scanning for 5 min were acquired in five 1-min frames. Regions of interest were drawn on successive PET image slices, and radioactivity was quantified from the first-minute scan after injection. FR for each of the 3 modalities was expressed as the ratio of adenosine to basal flow. RESULTS: PET-derived FR correlated strongly with TD (r = 0.82; P = 0.004) but not with PL (r = 0.17; P = 0.85). The mean average difference in FR between healthy volunteers and PAD subjects was 13.0 with PET and 4.5 with TD. The intra- and intersubject variability for PET expressed as the coefficient of variation was 10.5% and 29.0% for healthy subjects and 7.0% and 52.9% in PAD, respectively. CONCLUSION: As expected, FR was significantly lower in PAD subjects compared with healthy subjects as assessed with TD and PET but not with PL. PET-derived FR appears to be reproducible and generates sharper and higher indices of recruitable flow in healthy subjects and PAD. These findings have implications for the use of PET-derived FR as a sensitive index of recruitable flow in angiogenesis trials. FAU - Schmidt, Michael A AU - Schmidt MA AD - Section of Vascular Medicine, Division of Cardiology, University of Michigan, Ann Arbor, Michigan, USA. FAU - Chakrabarti, Anjan AU - Chakrabarti A FAU - Shamim-Uzzaman, Qurratul AU - Shamim-Uzzaman Q FAU - Kaciroti, Niko AU - Kaciroti N FAU - Koeppe, Robert A AU - Koeppe RA FAU - Rajagopalan, Sanjay AU - Rajagopalan S LA - eng PT - Clinical Trial PT - Controlled Clinical Trial PT - Journal Article PT - Validation Study PL - United States TA - J Nucl Med JT - Journal of nuclear medicine : official publication, Society of Nuclear Medicine JID - 0217410 RN - 0 (Oxygen Radioisotopes) RN - 0 (Radiopharmaceuticals) RN - 7YNJ3PO35Z (Hydrogen) RN - K72T3FS567 (Adenosine) SB - IM MH - Adenosine MH - Adult MH - Arteries/diagnostic imaging/physiopathology MH - Blood Flow Velocity MH - Female MH - Femoral Artery/physiopathology MH - Humans MH - *Hydrogen/pharmacokinetics MH - Lower Extremity/blood supply/diagnostic imaging MH - Male MH - Middle Aged MH - Muscle, Skeletal/*blood supply/*diagnostic imaging MH - Neovascularization, Physiologic MH - *Oxygen Radioisotopes/pharmacokinetics MH - Peripheral Vascular Diseases/*diagnostic imaging/physiopathology MH - Plethysmography MH - Radiopharmaceuticals/pharmacokinetics MH - Regional Blood Flow MH - Thermodilution MH - Thigh/blood supply/diagnostic imaging MH - Tomography, Emission-Computed/methods EDAT- 2003/06/07 05:00 MHDA- 2003/07/25 05:00 CRDT- 2003/06/07 05:00 PHST- 2003/06/07 05:00 [pubmed] PHST- 2003/07/25 05:00 [medline] PHST- 2003/06/07 05:00 [entrez] PST - ppublish SO - J Nucl Med. 2003 Jun;44(6):915-9.