We investigated whether SPET studies of neuroactivation might benefit
from a similar approach used in PET; that is, increase the number of s
cans per task and accept poorer individual scan quality. Different stu
dy paradigms were simulated by varying the scanning parameters: (1) ad
ministered radiation activity per scan, (2) number of scans per task a
nd (3) scan acquisition time. The maximum total dose received by each
simulated subject remained the same. Areas of activation of varying si
gnal strength were added to the scans using a customized graphics pack
age. To establish the statistical benefits of a replication paradigm v
ersus a non-replication paradigm, the datasets were analysed using SPM
95 statistics software. This simulation was able to show that, when an
SPM investigation is used for data analysis, study replication is mor
e important than the individual image quality typically available from
a high-performance SPET system.