Caitlin O'Connell1, Leon Ho2,3, Matthew Murphy2, Yolandi van der Merwe1,2, Ian Conner1,2, Gadi Wollstein1,2, Joel Schuman1,2, Rakie Cham1, and Kevin Chan1,2
1Department of Bioengineering, University of Pittsburgh, Pittsburgh, PA, United States, 2UPMC Eye Center, Eye and Ear Institute, Ophthalmology and Visual Science Research Center, Department of Ophthalmology, University of Pittsburgh, Pittsburgh, PA, United States, 3Department of Electrical and Electronic Engineering, The University of Hong Kong, Pokfulam, Hong Kong
Synopsis
Human
visual performance has been observed to exhibit superiority in the lower visual
field and horizontal meridian compared to the upper visual field and vertical
meridian, respectively, in response to many classes of stimuli, but the
underlying neural mechanisms remain unclear. This study determines if processing of visual
information is dependent on the location of stimuli in the visual field using
functional MRI. The
results show stronger brain responses and larger activation volumes upon flickering
visual stimulation to the lower hemifield compared to upper hemifield, while
only the activation size differed between visual presentations to the
horizontal and vertical meridians.Purpose
Human
visual performance has been shown to be better in the lower visual field than
upper visual field [1-3], and in the horizontal meridian than vertical
meridian in many classes of stimuli [4, 5]. However, the neural mechanisms of such lower
visual field and horizontal meridian advantages in human visual processing
remain incompletely understood [6-9]. Understanding
the neural correlates of visual field responses may also be clinically
important. This study aims to determine if processing of visual information in
the brain is dependent on the location of stimuli in the visual field. We quantitatively
examined brain activity in response to visual presentations to (1) the upper
and lower hemifields and (2) the vertical and horizontal meridians using
functional MRI (fMRI).
Methods
Fourteen
healthy young participants (8 males and 6 females) aged 27.4±3.5 years old (age range=22-32
years old) were recruited and informed consent was obtained prior to participation. All fMRI data were collected on a 3 Tesla
Siemens Allegra scanner.
Blood-oxygenation-level-dependent (BOLD) images were collected using a
single-shot echo planar imaging pulse sequence with the following parameters:
TR=2 s, TE=26 ms, field of view=24x24 cm2, 96x96 imaging matrix,
2.5x2.5mm2 in-plane resolution and 28 contiguous 2.5 mm thick axial
slices.
Brain activity was assessed with 2 fMRI scans
with both eyes open and focusing on a fixation point to establish the center of
the visual field. Each scan was 5 minutes long consisting of 12 trials of
alternating 12 seconds of rest and 12 seconds of visual stimulation. Each
participant underwent two fMRI scans, where two visual stimulus patterns were
compared during each scan by alternating the stimulus pattern between odd and
even trials:
1. Upper (Fig. 1a) versus
lower hemifield (Fig 1b)
2. Vertical (Fig. 1c) versus
horizontal meridian (Fig 1d)
The stimuli were checkerboard patterns flashing
at 8 Hz and were presented using the e-prime software (Psychology Software
Tools, Inc., Sharpsburg, PA, USA).
Mean BOLD
% change was calculated in the activated brain regions for each participant using
a z-score threshold of 2.3 after slice-timing correction and image realignment in
the FSL software [11]. Paired Student’s t-tests were performed comparing the mean BOLD %
change or brain activation volume of all participants between upper and lower
hemifields, or between vertical and horizontal meridians with significance set
at p<0.05.
Results
Figure 1
shows the visual presentation patterns and representative brain activation in
response to visual stimulation to the upper (Fig. 1a) and lower hemifields (Fig.
1b) and horizontal (Fig. 1c) and vertical meridians (Fig. 1d). Upper and lower
hemifield presentations predominantly activated the ventral and dorsal regions
of the occipital cortex, respectively, whereas vertical and horizontal meridian
presentations activated different retinotopic regions of the occipital cortex. Both
BOLD % change (Fig. 2a) and activation volume (Fig. 2b) were significantly greater
for lower hemifield stimulation than upper hemifield stimulation. No apparent difference
in BOLD % change was observed between vertical and horizontal meridian visual
presentations (p=0.11) (Fig. 2a).
However, visual presentation to horizontal meridian appeared to activate
larger brain areas than visual presentation to vertical meridian (Fig. 2b).
Discussion & Conclusion
The
present results agree with recent psychophysical and neurophysiological studies
which showed asymmetries between upper and lower field visual information
processing [1-3, 6-9]. Specifically, lower hemifield visual
stimulation produced stronger brain responses and larger activated brain areas than
upper hemifield, suggesting that the human brain may be more sensitive to the
lower visual field than the upper visual field. The vertical and horizontal
meridians are known to retinotopically map to the V1-V2 and V2-V3 borders,
respectively, and may possess horizontal-vertical anisotropy in the human brain
[5,6]. Although visual stimulation to the horizontal meridian activated larger
brain areas than the vertical meridian, the lack of difference between strengths
of brain responses to vertical and horizontal meridian visual stimulation
suggests that the asymmetry in visual brain processing between upper and lower
visual fields is more pronounced than that between vertical and horizontal
meridians using current testing visual presentation paradigms. The current
results may provide insight into functional deficits seen in individuals with visual
field loss.
Acknowledgements
This
work was supported by the National Institutes of Health Contracts P30-EY008098,
T32-EY017271, and UL1-TR000005 (Bethesda, Maryland); BrightFocus Foundation
G2013077 (Clarksburg, Maryland); Alcon Research Institute Young Investigator
Grant (Fort Worth, Texas); Eye and Ear Foundation (Pittsburgh, Pennsylvania);
and Research to Prevent Blindness (New York, New York).References
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