Combination of blood oxygen level–dependent functional magnetic resonance imaging and visual evoked potential recordings for abnormal visual cortex in two types of amblyopia

Purpose To elucidate the different neuromechanisms of subjects with strabismic and anisometropic amblyopia compared with normal vision subjects using blood oxygen level–dependent functional magnetic resonance imaging (BOLD-fMRI) and pattern-reversal visual evoked potential (PR-VEP). Methods Fifty-three subjects, age range seven to 12 years, diagnosed with strabismic amblyopia (17 cases), anisometropic amblyopia (20 cases), and normal vision (16 cases), were examined using the BOLD-fMRI and PR-VEP of UTAS-E3000 techniques. Cortical activation by binocular viewing of reversal checkerboard patterns was examined in terms of the calcarine region of interest (ROI)-based and spatial frequency–dependent analysis. The correlation of cortical activation in fMRI and the P100 amplitude in VEP were analyzed using the SPSS 12.0 software package. Results In the BOLD-fMRI procedure, reduced areas and decreased activation levels were found in Brodmann area (BA) 17 and other extrastriate areas in subjects with amblyopia compared with the normal vision group. In general, the reduced areas mainly resided in the striate visual cortex in subjects with anisometropic amblyopia. In subjects with strabismic amblyopia, a more significant cortical impairment was found in bilateral BA 18 and BA 19 than that in subjects with anisometropic amblyopia. The activation by high-spatial-frequency stimuli was reduced in bilateral BA 18 and 19 as well as BA 17 in subjects with anisometropic amblyopia, whereas the activation was mainly reduced in BA 18 and BA 19 in subjects with strabismic amblyopia. These findings were further confirmed by the ROI-based analysis of BA 17. During spatial frequency–dependent VEP detection, subjects with anisometropic amblyopia had reduced sensitivity for high spatial frequency compared to subjects with strabismic amblyopia. The cortical activation in fMRI with the calcarine ROI-based analysis of BA 17 was significantly correlated with the P100 amplitude in VEP recording. Conclusions This study suggested that different types of amblyopia had different cortical responses and combinations of spatial frequency–dependent BOLD-fMRI with PR-VEP could differentiate among various kinds of amblyopia according to the different cortical responses. This study can supply new methods for amblyopia neurology study.

[1]  Stephen J Anderson,et al.  Neuroimaging in Human Amblyopia , 2006, Strabismus.

[2]  R. Hess,et al.  Detection, discrimination and integration of second-order orientation information in strabismic and anisometropic amblyopia , 2005, Vision Research.

[3]  Karl J. Friston,et al.  Posterior probability maps and SPMs , 2003, NeuroImage.

[4]  J Anthony Movshon,et al.  The pattern of visual deficits in amblyopia. , 2003, Journal of vision.

[5]  G. Curio,et al.  Dipole source localization and fMRI of simultaneously recorded data applied to somatosensory categorization , 2003, NeuroImage.

[6]  F. Kruggel,et al.  Hemodynamic and Electroencephalographic Responses to Illusory Figures: Recording of the Evoked Potentials during Functional MRI , 2001, NeuroImage.

[7]  Ravi S. Menon,et al.  Brief visual stimulation allows mapping of ocular dominance in visual cortex using fMRI , 2001, Human brain mapping.

[8]  R. Harrad,et al.  Screening for amblyopia in preschool children: Results of a population-based, randomised controlled trial , 2001, Ophthalmic epidemiology.

[9]  Louis Lemieux,et al.  Comparison of Spike-Triggered Functional MRI BOLD Activation and EEG Dipole Model Localization , 2001, NeuroImage.

[10]  D. Levi,et al.  Is second-order spatial loss in amblyopia explained by the loss of first-order spatial input? , 2001, Vision Research.

[11]  Afraim Salek-Haddadi,et al.  Event-Related fMRI with Simultaneous and Continuous EEG: Description of the Method and Initial Case Report , 2001, NeuroImage.

[12]  M Bach,et al.  Coupling of neural activity and BOLD fMRI response: New insights by combination of fMRI and VEP experiments in transition from single events to continuous stimulation , 2001, Magnetic resonance in medicine.

[13]  K. Chang,et al.  Binocularity and spatial frequency dependence of calcarine activation in two types of amblyopia , 2001, Neuroscience Research.

[14]  A. M. Dale,et al.  Spatiotemporal Brain Imaging of Visual-Evoked Activity Using Interleaved EEG and fMRI Recordings , 2001, NeuroImage.

[15]  G Lennerstrand,et al.  Visual screening of Swedish children: an ophthalmological evaluation. , 2001, Acta ophthalmologica Scandinavica.

[16]  R F Hess,et al.  The cortical deficit in humans with strabismic amblyopia , 2001, The Journal of physiology.

[17]  Richard B Buxton,et al.  Putting spatial attention on the map: timing and localization of stimulus selection processes in striate and extrastriate visual areas , 2001, Vision Research.

[18]  Ravi S. Menon,et al.  BOLD fMRI response of early visual areas to perceived contrast in human amblyopia. , 2000, Journal of neurophysiology.

[19]  J. Naor,et al.  Early screening for amblyogenic risk factors lowers the prevalence and severity of amblyopia. , 2000, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

[20]  A. Norcia,et al.  Changes in cortical activity during suppression in stereoblindness , 2000, Neuroreport.

[21]  R. Hess,et al.  The orientation discrimination deficit in strabismic amblyopia depends upon stimulus bandwidth , 1999, Vision Research.

[22]  S. Anderson,et al.  Assessment of cortical dysfunction in human strabismic amblyopia using magnetoencephalography (MEG) , 1999, Vision Research.

[23]  Hugh R. Wilson,et al.  A deficit in strabismic amblyopia for global shape detection , 1999, Vision Research.

[24]  G. Lennerstrand,et al.  Screening for visual and ocular disorders in children, evaluation of the system in Sweden , 1998, Acta paediatrica.

[25]  Egill Rostrup,et al.  Visual Activation in Infants and Young Children Studied by Functional Magnetic Resonance Imaging , 1998, Pediatric Research.

[26]  R. Hess,et al.  A reduced motion aftereffect in strabismic amblyopia , 1997, Vision Research.

[27]  H. Onoe,et al.  Reduced activity in the extrastriate visual cortex of individuals with strabismic amblyopia , 1997, Neuroscience Letters.

[28]  Anthony J. Movshon,et al.  Visual Response Properties of Striate Cortical Neurons Projecting to Area MT in Macaque Monkeys , 1996, The Journal of Neuroscience.

[29]  C. Blakemore,et al.  Physiology of suppression in strabismic amblyopia. , 1996, The British journal of ophthalmology.

[30]  L. Kabasakal,et al.  Brain SPECT evaluation of the visual cortex in amblyopia. , 1995, Journal of nuclear medicine : official publication, Society of Nuclear Medicine.

[31]  J W Belliveau,et al.  Borders of multiple visual areas in humans revealed by functional magnetic resonance imaging. , 1995, Science.

[32]  Jonathan D. Cohen,et al.  Functional topographic mapping of the cortical ribbon in human vision with conventional MRI scanners , 1993, Nature.

[33]  R. Sireteanu,et al.  Distortions in two-dimensional visual space perception in strabismic observers , 1993, Vision Research.

[34]  S. H. Day,et al.  The classification of amblyopia on the basis of visual and oculomotor performance. , 1992, Transactions of the American Ophthalmological Society.

[35]  G. McCarthy,et al.  Dynamic mapping of the human visual cortex by high-speed magnetic resonance imaging. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[36]  M. Crawford,et al.  The lateral geniculate nucleus in human strabismic amblyopia. , 1992, Investigative ophthalmology & visual science.

[37]  Ian E. Holliday,et al.  The spatial localization deficit in amblyopia , 1992, Vision Research.

[38]  Ravi S. Menon,et al.  Intrinsic signal changes accompanying sensory stimulation: functional brain mapping with magnetic resonance imaging. , 1992, Proceedings of the National Academy of Sciences of the United States of America.

[39]  Ian E. Holliday,et al.  The coding of spatial position by the human visual system: Effects of spatial scale and contrast , 1992, Vision Research.

[40]  B. Rosen,et al.  Functional mapping of the human visual cortex by magnetic resonance imaging. , 1991, Science.

[41]  R. Demers,et al.  Peripheral vibratory sense deficits in solvent-exposed painters. , 1991, Journal of occupational medicine. : official publication of the Industrial Medical Association.

[42]  R. Sireteanu,et al.  [Visual field defects in strabismic amblyopes]. , 1989, Klinische Monatsblatter fur Augenheilkunde.

[43]  J A Movshon,et al.  Effects of early unilateral blur on the macaque's visual system. I. Behavioral observations , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[44]  J. Movshon,et al.  Effects of early unilateral blur on the macaque's visual system. III. Physiological observations , 1987, The Journal of neuroscience : the official journal of the Society for Neuroscience.

[45]  J. Movshon,et al.  Effects of early unilateral blur on the macaque's visual system. II. Anatomical observations , 1987 .

[46]  S. Klein,et al.  Vernier acuity, crowding and cortical magnification , 1985, Vision Research.

[47]  G. K. Noorden,et al.  Amblyopia: a multidisciplinary approach. Proctor lecture. , 1985, Investigative ophthalmology & visual science.

[48]  L. Garey,et al.  Structural development of the lateral geniculate nucleus and visual cortex in monkey and man , 1983, Behavioural Brain Research.

[49]  T. Wiesel Postnatal development of the visual cortex and the influence of environment , 1982, Nature.

[50]  Dennis M. Levi,et al.  Hyperacuity and amblyopia , 1982, Nature.

[51]  D E Mitchell,et al.  Normality of spatial resolution of retinal ganglion cells in cats with strabismic amblyopia. , 1982, The Journal of physiology.

[52]  J. Sjöstrand CONTRAST SENSITIVITY IN CHILDREN WITH STRABISMIC AND ANISOMETROPIC AMBLYOPIA. A STUDY OF THE EFFECT OF TREATMENT , 1981, Acta ophthalmologica.

[53]  G. K. Noorden,et al.  The effects of short-term experimental strabismus on the visual system in Macaca mulatta. , 1979, Investigative ophthalmology & visual science.

[54]  F. Campbell,et al.  On the nature of the neural abnormality in human amblyopia; neural aberrations and neural sensitivity loss , 1978, Pflügers Archiv.

[55]  R. F. Hess,et al.  The threshold contrast sensitivity function in strabismic amblyopia: Evidence for a two type classification , 1977, Vision Research.

[56]  D. G. Green,et al.  Laser interferometry in corneal opacification. Preoperative visual potential estimation. , 1972, Archives of ophthalmology.

[57]  D. Hubel,et al.  Comparison of the effects of unilateral and bilateral eye closure on cortical unit responses in kittens. , 1965, Journal of neurophysiology.

[58]  S. Crewther,et al.  Neural site of strabismic amblyopia in cats: spatial frequency deficit in primary cortical neurons , 2004, Experimental Brain Research.

[59]  M. Moseley,et al.  Amblyopia : a multidisciplinary approach , 2002 .

[60]  R. Harrad,et al.  Screening for amblyopia in preschool children , 2001 .

[61]  Sireteanu,et al.  Live vs. video observation in forced-choice preferential looking: a comparison of methods. , 1998, Strabismus.

[62]  G. V. von Noorden,et al.  Amblyopia: a multidisciplinary approach. Proctor lecture. , 1985, Investigative ophthalmology & visual science.

[63]  K. Sanderson,et al.  Primary visual cortex in the brushtailed possum: receptive field properties and corticocortical connections. , 1984, Brain, behavior and evolution.

[64]  T. Wiesel The postnatal development of the visual cortex and the influence of environment. , 1982, Bioscience reports.

[65]  D M Levi,et al.  Spatio-temporal interactions in anisometropic and strabismic amblyopia. , 1977, Investigative ophthalmology & visual science.