ON THE USE OF TEMPORAL CORRELATION-COEFFICIENTS FOR MAGNETIC-RESONANCE MAPPING OF FUNCTIONAL BRAIN ACTIVATION - INDIVIDUALIZED THRESHOLDS AND SPATIAL RESPONSE DELINEATION
A. Kleinschmidt et al., ON THE USE OF TEMPORAL CORRELATION-COEFFICIENTS FOR MAGNETIC-RESONANCE MAPPING OF FUNCTIONAL BRAIN ACTIVATION - INDIVIDUALIZED THRESHOLDS AND SPATIAL RESPONSE DELINEATION, International journal of imaging systems and technology, 6(2-3), 1995, pp. 238
Functional activation of the human visual and motor system was studied
by magnetic resonance imaging (MRI) at 2.0 T using dynamic series of
oxygenation-sensitive gradient-echo images at high spatial resolution.
Activation maps were computed by correlating signal intensity time co
urses with a reference waveform on a pixel-by-pixel basis. Although th
is strategy readily demonstrates stimulus-related functional cooperati
vity of activated regions in thresholded maps of correlation coefficie
nts, intertrial variability in the underlying distributions of correla
tion coefficients precludes the use of correlation coefficients as dir
ect thresholds for defining activation. Because stimulus-related effec
ts emerge as positive deviations from an otherwise symmetric distribut
ion of correlation coefficients, invariance against intertrial differe
nces as well as adequate visualization of activated areas may be achie
ved by the following procedure. First, a symmetrized noise distributio
n is reconstructed from the actual activation map that allows rescalin
g of correlation coefficients into percentile ranks with respect to th
e integral of the noise distribution. Second, a high percentile rank (
or correspondingly low error probability) can be used as threshold to
define primary sites of activation with high specificity. And third, t
he spatial extent of activation may be delineated by adding directly n
eighboring pixels with lower values provided their correlation coeffic
ients are high enough to contribute to the positive deviation from the
noise distribution. The outlined approach yields robust activation ma
ps but still awaits a more thorough statistical treatment of activatio
n in MRI correlational mapping. (C) 1995 John Wiley & Sons, Inc.