A Ankeeta1, s Senthil Kumaran1, and Rohit Saxena2
1NMR and MRI facility, All India Institute of Medical Sciences, New Delhi, India, 2RP centre, Opthalmology, All India Institute of Medical Sciences, New Delhi, India
Synopsis
Anatomical and functional MRI data for Braille and
phonological noun pair assessment test was acquired in 40
early blind (EB), forty late blind (LB) subjects
and thirty sighted controls (SC) in two age groups 6-12 years and 13-19 years
(all right-handed). Visual impairment induces structural and functional modification in the
visual cortex. Late blind subjects exhibited differences in the V1 13-19 years
age range, but not in the 6-12 years age group. Duration
of blindness and education influence the extent of plasticity of the V1
and language network.
Introduction
Visual deprivation
during different developmental periods leads to different structural and
functional alterations in the brain. However, the effects of visual deprivation
on the spontaneous functional organization of the brain remain largely unknown.
In this study, we used voxel-based functional connectivity density (FCD)
analyses to investigate the effects of visual deprivation during different
developmental periods on the spontaneous functional organization of the brain1,2.
Onset of blindness and age of blindness may play a significant role in cortical thickness of
occipital cortex.Objective
To observe the
structural alteration and functional connectivity based on the age differences
for haptic language task versus phonological task and if any changes persist,
then correlation with duration of braille reading to recognise the aspect of
alteration for the plasticity in visual area.Methodology
Forty early blind (EB) and Forty late
blind (LB) subjects and thirty sighted controls (SC) in two age groups 6-12
years and 13-19 years (all right-handed) were recruited from the clinics of our
institute (Table 1). Standard diagnostic and exclusion criteria were followed.
Anatomical and functional data for Braille and phonological noun pair
assessment test was acquired in a 3T MR scanner (Achieva 3.0T TX, Philips,
Netherlands), with the following imaging parameters: slices per slab: 160,
distance factor 50%, orientation: sagittal; slice thickness: 1mm; T1:1100ms; TR: 1900ms; TE: 3.37ms; averages:
1; FOV: 256mm, FOV phase: 93.8%; Base
resolution: 256; Phase resolution 100; Phase encoding direction: A>>P;
Band width: 130 Hz; echo spacing: 8.6ms. Data processing were carried out using
SPM12 with the help of CAT12 and CONN toolbox3,4. The clusters were
converted from MNI template to the Talairach and Tornoux coordinates, for
estimation of anatomical areas5. Two-sample
t-test and multiple comparison (post-hoc analysis) (p<0.001, cluster
threshold 10) were used for inter-group comparisons.Result
During phonological language task
in early blind, bilateral superior frontal gyrus, left hemispheric middle
frontal gyrus, para hippocampal gyrus, precuneus, superior temporal gyrus,
thalamus and right cerebral cingulate gyrus, medial frontal gyrus exhibited
BOLD activation. In late blind, bilateral activation in fusiform gyrus, para
hippocampal gyrus, cuneus, post-central gyrus along-with right hemispheric
thalamus, superior temporal gyrus, primary and auditory association cortex,
dorsal posterior cingulate cortex, somatosensory association cortex, brainstem,
lingual gyrus, superior frontal gyrus, and precentral gyrus, and left hemispheric
inferior parietal lobule, insula, precuneus, cerebellum, primary somatosensory
cortex, associative visual cortex (v3,v4,v5), premotor cortex and supplementary
motor area, medial frontal gyrus were associated during the phonological task (Figure 1). During Braille reading task, in late blind bold activation was observed in right
cuneus, inferior frontal gyrus, middle frontal gyrus, para hippocampal gyrus,
precentral gyrus, superior frontal gyrus, superior temporal gyrus and left hemispheric
fusiform gyrus, inferior parietal lobule, lingual gyrus, medial frontal gyrus,
middle temporal gyrus, para hippocampal gyrus. Early blind subjects exhibited bilateral activation in superior
temporal gyrus, precuneus in the two age groups. Right hemispheric lentiform
nucleus, brainstem and left inferior parietal lobule, para hippocampal gyrus
and left hemispheric medial frontal gyrus, para hippocampal gyrus, middle
occipital gyrus, precuneus, thalamus, cerebellum, middle frontal gyrus were
also active in both the groups.Discussion
Bilateral activation of middle temporal gyrus and superior
temporal gyrus (with left hemispheric dominance) was observed irrespective of
age difference in all the groups (p < 0.05, FWE corrected). Visual cortical
area response was higher in 13-19 years than 6-12 years of early blind and late
blind groups, for the Braille reading and phonological tasks (Figure 2). The Pearson correlation analyses for the visual activation with age is positive for the
non-visual language perception in both late and early blind groups (Figure 3).
During
the Braille reading task, the children group exhibited inferior frontal area (IFG) and Wernicke’s area, whereas adolescent group revealed in prefrontal,
Wernicke’s area and Broca’s area. During the phonological language task,
children group of early and late blind invoked the inferior frontal and Broca’s
areas along with hippocampus and middle temporal gyrus. The same task revealed activation
in IFG, prefrontal areas Wernicke’s and Broca’s area in adolescent groups.
Hence early and late blind children have reduced language selectivity in
prefrontal cortex relative to sighted group and
adolescent group language pathway is intact and in correlation with the
left visual cortex than children group.1,2
Voxel
based anatomical analysis and functional connectivity revealed decreased
connectivity (both short and long range) in primary visual area and
somatosenso ry area in 6-12 years, than 13 -19 years (Figure 4) of both early and late
blind groups6. For the phonological language area, a
decreased connectivity was observed between visual area, somatosensory area and
primary auditory cortex. These results reflect cross-modal plasticity due to
adaptive compensatory mechanism in brain of visually deprived subjects. On
comparing the EB with the LB, we can deduce that the age of onset of blindness
and the total duration of blindness play a role in cortical thickness7.Conclusion
VBM and functional connectivity revealed cross modal
plasticity in visual and language areas, which are dependent on duration of
blindness and duration of education.Acknowledgements
Authors acknowledge the grant by Cognitive Science Research Initiative CSRI - DST; Government of India. Also we acknowledge participants from National Association of Blind for the participation and cooperation throughout the study.
References
- Zhou Z, Xu J, Shi L, et al. (2019) Alterations of the brain
microstructure and corresponding functional connectivity in early‐blind
adolescents. Neural Plast 2019: 2747460.
- Liu Y et al (2007) Whole brain functional connectivity in the
early blind. Brain; 130:2085-96.
- Ashburner J., (2010) VBM tutorial, UCL (http://www.fil.ion.ucl.ac.uk/ ~john/misc/
VBMclass10.pdf)
- Whitfield-Gabrieli, S; Nieto-Castanon, A (2012). "Conn: a
functional connectivity toolbox for correlated and anticorrelated brain
networks". Brain Connect. 2: 125–41.
- Talairach J, and Tornoux P 1988 Stuttgart: thieme
- Atilgan H Collignon O, Hasson U, (2017) Structural
neuroplasticity of the superior temporal plane in early and late blindness, Brain
and Language;170:71-81.
- Hou, F., Liu, X., Zhou, Z., Zhou, J. & Li, H. (2017). Reduction
of Interhemispheric Functional Brain Connectivity in Early Blindness: A
Resting-State fMRI Study, BioMed Research International 2017, 1–8.