Distribution Volume Ratios without Blood Sampling from Graphical Analysis of PET Data

Journal of Cerebral Blood Flow and Metabolism - Tập 16 Số 5 - Trang 834-840 - 1996
Jean Logan1, Joanna S. Fowler1, Nora D. Volkow2,3, Gene‐Jack Wang3, Yu‐Shin Ding1, David Alexoff1
1Chemistry, Brookhaven National Laboratory, Upton
2Department of Psychiatry, SUNY-Stony Brook, Stony Brook, New York, U.S.A.
3Medical Departments, Brookhaven National Laboratory, Upton

Tóm tắt

The distribution volume ratio (DVR), which is a linear function of receptor availability, is widely used as a model parameter in imaging studies. The DVR corresponds to the ratio of the DV of a receptor-containing region to a nonreceptor region and generally requires the measurement of an arterial input function. Here we propose a graphical method for determining the DVR that does not require blood sampling. This method uses data from a nonreceptor region with an average tissue-to-plasma efflux constant k2 to approximate the plasma integral. Data from positron emission tomography studies with [15C]raclopride (n = 20) and [11C] d-threo-methylphenidate ([11C]dMP) (n = 8) in which plasma data were taken and used to compare results from two graphical methods, one that uses plasma data and one that does not. k2 was 0.163 and 0.051 min−1 for [11C]raclopride and [11C]dMP, respectively. Results from both methods were very similar, and the average percentage difference between the methods was −0.11% for [11C]raclopride and 0.46% for [11C]dMP for DVR of basal ganglia (BG) to cerebellum (CB). Good agreement between the two methods was also achieved for DVR images created by both methods. This technique provides an alternative method of analysis not requiring blood sampling that gives equivalent results for the two ligands studied. It requires initial studies with blood sampling to determine the average kinetic constant and to test applicability. In some cases, it may be possible to neglect the b̅2 term if the BG/CB ratio becomes reasonably constant for a sufficiently long period of time over the course of the experiment.

Từ khóa


Tài liệu tham khảo

10.1016/0969-8051(95)00042-V

10.1038/jcbfm.1993.6

10.1002/syn.890130407

10.1002/jlcr.2580341012

10.1073/pnas.82.11.3863

10.1038/jcbfm.1991.131

Ichise M, 1995, J Nud Med, 36, 1

10.1038/jcbfm.1991.130

10.1097/00004647-199601000-00005

10.1038/jcbfm.1990.127

10.1038/jcbfm.1994.132

10.1038/jcbfm.1985.87

10.1152/jappl.1976.40.3.458

10.1111/j.1471-4159.1977.tb10649.x

10.1002/syn.890160402

Volkow ND, 1995, J Nucl Med, 36, 2162

10.1126/science.6334363