Recent Projects

(home)


MR methods


Visual localizers at 3T

While working in David Heeger's lab, I wanted to investigate the temporal dynamics of high- and low-resolution gradient echo (GE) BOLD at 3T.  GE BOLD is the standard fMRI method, and it is well known that large draining veins can dominate regions of the image.  Large vein-dominated voxels in analysis can degrade both spatial and temporal characteristics of the data.  The hope was that using small voxels would let us identify and remove vein-dominated voxels from the data, and that we would show a measurable decrease in the delay and dispersion of the hemodynamic response in high-resolution data.  We found little difference in the temporal dynamics of the low- and high-resolution data, but we did find that using small voxels greatly increased our ability to accurately localize the cortical response to visual stimuli.  We measured the accuracy of two different kinds of localizer scans: differential and single-condition.  The particular pattern of results we measured indicates that directional blood flow in large draining veins can shift the observed BOLD response (not surprising), and that this results in a mismatch between the ROIs defined by differential and single-condition localizers.  What was surprising was that the ROIs defined by differential localizers were not a subset of the ROIs defined by the less spatially restrictive single-condition localizer, particularly with low resolution imaging.  The conclusion I draw from this data is that, while differential localizers are better at localizing cortical responses, spatial accuracy does not necessarily lead to functional accuracy, and many analyses may be better off useing a less spatially accurate ROI.  This work has been submitted for consideration as an abstract at VSS '06, and is in the process of being submitted for publication.


High resolution imaging in medial temporal lobe (MTL)

distorted anatomies and EPI images demonstrate decreased distortion and drop-out with zoomed EPICollaborating with Lila Davachi and Souheil Inati, I studied the accuracy of signal localization in MTL.  This is a region famous for distortion and signal loss, both due to spurious magnetic field gradients induced by the air/tissue interface of the auditory canal, as well as other places in the inferior regions of the brain where materials with different magnetic suscetibility abut.  Using established methods for quantifying distortion, we found that the short read-out time allowed by zoomed EPI (using outer-volume suppression) provided images with moderately high resolution, acceptable signal-to-noise ratio, and little distortion.  Signal drop-out in anterior parahippocampal gyrus was the most significant problem, and one which varied significantly from subject to subject.  We are in the process of preparing this data for publication.

Point spread function for BOLD fMRI (spatial accuracy)

Since scanner technologies allow routine acquisition of high resolution functional images (in-plane resolution ~1 mm), the intrinisic spatial resolution of the hemodynamic response is becoming a critical question. One way of quantifying the spatial blurring in a system is to measure the modulation transfer function (MTF): the magnitude of response as a function of spatial frequency. To measure the MTF in V1 (primary visual cortex), we present visual stimuli of increasing spatial frequency, then measure the amplitude of BOLD response. The inverse Fourier transform of this MTF yields an estimate of the point spread function (PSF) for BOLD fMRI.

Taking advantage of the ultra-high field scanners at the CMRR, I completed a set of experiments measuring the MTF/PSF for both gradient echo and spin echo BOLD fMRI at 7 Tesla, as well as gradient echo BOLD at 3 Tesla. Early analyses (presented as a poster at the 12th Scientific Meeting of the International Society for Magnetic Resonance in Medicine) told an interesting story:

While these results are consistent with other reports on the spatial accuracy of BOLD, I believe that the conclusions cited above are based on a confound in the data, originating in A) experiment design and B) the fact that the point spread function is not uniform across the cortical surface.  Therefore, these results were not submitted for publication.

Z-shimming

Air-tissue interfaces above the auditory canals and frontal sinuses create susceptibility-induced artifacts in EPI sequences that lead to either data loss or poor registration between functional and anatomical images. Real-time correction for susceptibility-induced artifacts is possbile but time consuming. However, parallel imaging technologies - particularly advantageous at high field - buy the necessary time to use z-shimming to improve image quality and recover data in frontal lobe and inferior temporal cortex. I am in the process of finishing up a short demonstration of the strengths and limitations of z-shimming at 7 Telsa.

Presented as a poster at the 11th Scientific Meeting of the ISMRM, July 2003.


Vision science

Contrast response to broadband images
Contrast response for natural images is stronger and saturates more rapidly.
Perhaps the most basic property of early vision (V1) is the contrast response - the rate at which neural firing rates increase with increasing image contrast - and contrast response functions for individual sine wave gratings (narrow spatial frequency content) are well known.  However extrapolating from isolated patches of sine wave gratings to complicated patterns with broadband spatial frequency content is not simple.  We combined fMRI and computational modeling to measure and understand the contrast response to natural images, with typical 1/f amplitude specta, and to natural images with whitened (flat) spatial frequency spectra.  The general result is not surprising - the contrast response saturates at a rate not much different from the contrast response to sine wave gratings.  However, the subtle differences measured between the contrast response functions for natural and whitened images were intriguing.  We successfully modeled this with a class of models which could account for both the contrast sensitivity function at low contrast and contrast constancy at high contrast. pdf

BOLD response to images formed from random placement of Gabor patches

This project was motivated by the following question:  is specification of RMS contrast and spatial frequency content sufficient to predict the V1 BOLD response?  A simple thought experiment, illustrated by the images shown below (which all have the same RMS contrast and spatial frequency content), gives the answer - no! The problem is in the posing of the question:  global
contrast and global BOLD response are the wrong questions to be asking in V1.  At VSS 2004 I presented preliminary work testing our ability to predict and quantify local BOLD responses to local image features (abstract published in JOV); this is a line of research I plan to continue.

low density 1 cpd Gabor patches     high density 1 cpd Gabors     scrambled image (1 cpd noise)



Vision beyond V1

Example of generic quadruped.
One intriguing question is how the visual system efficiently reconstructs three-dimensional object and scene perception from two-dimensional retinal information. The stick figure paper is a brief investigation into the adaptation of classification image techniques for the study of three dimensional form perception.  In this paper, we emphasize the importance of using a three-dimensional generative model to create the stimulus space that is used to probe visual processes, even though the images are displayed in two dimensions.