TABLE 1

Summary of Metabolic Radiotracers Used for PET/CT Imaging of Atherosclerosis

TracerMetabolic targetsAdvantages and key findingsLimitationsStudy
18F-FDGGlucose transport and phosphorylationTracer is readily available and the most extensively validated in preclinical and clinical studies; uptake correlates with overall inflammatory burden of plaques, for example, macrophage content; early detection of response to statins is possibleTracer targets nearly ubiquitous metabolic process, with limited specificity for individual cell type or phenotype(1215)
18F-FMISOCellular hypoxiaUptake is higher in symptomatic carotid plaques; positive correlation exists between 18F-FMISO and 18F-FDG uptakeDiffusion barrier limits uptake; cell specificity is lacking(27)
18F-HX4Cellular hypoxiaPositive correlation exists between 18F-HX4 and 18F-FDG uptakeDiffusion barrier limits uptake; cell specificity is lacking(26)
64Cu-ATSMCellular hypoxiaUptake correlates with plaque hypoxia and macrophage content; hypoxic cell uptake is higher than for 18F-FMISO, and washout from normoxic tissues is fasterDiffusion barrier limits uptake; cell specificity is lacking(28)
11C-acetateTCA, FAO, FAS, OxPhosFocal uptake occurs in calcified plaques and arterial segments without calcificationsHalf-life is short, limiting availability(30)
11C-cholineFAS, biosynthesisUptake is mostly in arterial segments with thickening and increased lipid content; cardiac uptake is lower than that of 18F-FDGHalf-life is short, limiting availability(37)
18F-FMCFAS, biosynthesisUptake is mostly in arterial segments with thickening and increased lipid contentTracer may be substrate for distinct set of transporters from those used to transport choline(36)
18F-FECFAS, biosynthesisUptake correlates with cardiovascular risk factors; no association exists between uptake and prior cerebrovascular or cardiovascular eventsTracer may be substrate for distinct set of transporters from those used to transport choline(38)
  • ATSM = diacetyl-bis(N4-methylthiosemicarbazone); FAO = fatty acid oxidation; FAS = fatty acid synthesis; FMC = fluoromethylcholine; FEC = fluoroethylcholine.