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BOLD fMRI and DTI in strabismic amblyopes following occlusion therapy

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Abstract

Evaluation of brain cluster activation using the functional magnetic resonance imaging (fMRI) and diffusion tensor imaging (DTI) was sought in strabismic amblyopes. In this hospital-based case–control cross-sectional study, fMRI and DTI were conducted in strabismic amblyopes before initiation of any therapy and after visual recovery following the administration of occlusion therapy. FMRI was performed in 10 strabismic amblyopic subjects (baseline group) and in 5 left strabismic amblyopic children post-occlusion therapy after two-line visual improvement. Ten age-matched healthy children with right ocular dominance formed control group. Structural and functional MRI was carried out on 1.5T MR scanner. The visual task consisted of 8 Hz flickering checkerboard with red dot and occasional green dot. Blood-oxygen-level-dependent (BOLD) fMRI was analyzed using statistical parametric mapping and DTI on NordicIce (NordicNeuroLab) softwares. Reduced occipital activation was elicited when viewing with the amblyopic eye in amblyopes. An ‘ipsilateral to viewing eye’ pattern of calcarine BOLD activation was observed in controls and left amblyopes. Activation of cortical areas associated with visual processing differed in relation to the viewing eye. Following visual recovery on occlusion therapy, enhanced activity in bilateral hemispheres in striate as well as extrastriate regions when viewing with either eye was seen. Improvement in visual acuity following occlusion therapy correlates with hemodynamic activity in amblyopes.

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Abbreviations

fMRI:

Functional magnetic resonance imaging

DTI:

Diffusion tensor imaging

BOLD:

Blood oxygen level dependent

SPM8:

Statistical parametric mapping

LGN:

Lateral geniculate nucleus

FA:

Fractional anisotropy

EPI:

Echo planar imaging

CBRG:

Flickering checkerboard with red dot and occasional green dot

ANOVA:

Analysis of variance

BA:

Brodmann areas

RE:

Right eye

LE:

Left eye

ROI:

Region of interest

References

  1. Flom MC, Neumaier RW (1966) Prevalence of amblyopia. Public Health Rep 81:329–341

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  2. Friedman DS, Repka MX, Katz J, Giordano L, Ibironke J, Hawse P, Tielsch JM (2009) Prevalence of amblyopia and strabismus in white and African American children aged 6 through 71 months the Baltimore Pediatric Eye Disease Study. Ophthalmology 116:2128-34.e1-2

  3. Pai AS, Rose KA, Leone JF, Sharbini S, Burlutsky G, Varma R, Wong TY, Mitchell P (2012) Amblyopia prevalence and risk factors in Australian preschool children. Ophthalmology 119:138–144

    Article  PubMed  Google Scholar 

  4. Algaze A, Roberts CJ, Leguire LE et al (2002) Functional magnetic resonance imaging as a tool for investigating amblyopia in the human visual cortex. J AAPOS 6:300–308

    Article  PubMed  Google Scholar 

  5. Barnes GR, Hess RF, Dumoulin SO et al (2001) The cortical deficit in humans with strabismic amblyopia. J Physiol 533:281–297

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  6. Imamura K, Richter H, Fischer H et al (1997) Reduced activity in the extrastriate visual cortex of individuals with strabismic amblyopia. Neurosci Lett 225:173–176

    Article  CAS  PubMed  Google Scholar 

  7. Li C, Cheng L, Yu Q et al (2012) Relationship of visual cortex function and visual acuity in anisometropic amblyopic children. Int J Med Sci 9:115–120

    Article  PubMed  Google Scholar 

  8. Hess RF, Thompson B, Gole G, Mullen KT (2009) Deficient responses from the lateral geniculate nucleus in humans with amblyopia. Eur J Neurosci 29:1064–1070

    Article  PubMed  PubMed Central  Google Scholar 

  9. Hess RF, Thompson B, Gole G, Mullen KT (2010) The amblyopic deficit and its relationship to geniculo-cortical processing streams. J Neurophysiol 104:475–483

    Article  PubMed  Google Scholar 

  10. Choi MY, Lee K, Hwang J et al (2001) Comparison between anisometropic and strabismic amblyopia using functional magnetic resonance imaging. Br J Ophthalmol 85:1052–1056

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  11. Anderson SJ, Holliday IE, Harding GF (1999) Assessment of cortical dysfunction in human strabismic amblyopia using magnetoencephalography (MEG). Vision Res 39:1723–1738

    Article  CAS  PubMed  Google Scholar 

  12. Conner IP, Odom JV, Schwartz TL, Mendola JD (2007) Retinotopic maps and foveal suppression in the visual cortex of amblyopic adults. J Physiol 583(Pt 1):159–173

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  13. Simons K, Gotzler KC, Vitale S (1997) Penalization versus parttime occlusion and binocular outcome in treatment of strabismicamblyopia. Ophthalmology 104:2156–2160

    Article  CAS  PubMed  Google Scholar 

  14. Harrad R (2000) The efficacy of occlusion for strabismic amblyopia. Can an optimal duration be identified? Br J Ophthalmol 84:561

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  15. Rogers GL (2003) Functional magnetic resonance imaging (fMRI) and effects of l-dopa on visual function in normal and amblyopic subjects. Trans Am Ophthalmol Soc 101:401–415

    PubMed  PubMed Central  Google Scholar 

  16. Beaulieu C (2002) The basis of anisotropic water diffusion in the nervous system: a technical review. NMR Biomed 15:435–455

    Article  PubMed  Google Scholar 

  17. Andersson JL, Hutton C, Ashburner J et al (2001) Modeling geometric deformations in EPI time series. Neuroimage. 13:903–919

    Article  CAS  PubMed  Google Scholar 

  18. Eickhoff SB, Laird AR, Grefkes C, Wang LE, Zilles K, Fox PT (2009) Coordinate-based activation likelihood estimation meta-analysis of neuroimaging data: a random-effects approach based on empirical estimates of spatial uncertainty. Hum Brain Mapp 30:2907–2926

    Article  PubMed  PubMed Central  Google Scholar 

  19. Talairach J (1988) Tournoux P in “co-planar stereotaxic atlas of the human brain”. Thieme Medical Publishers, New York

    Google Scholar 

  20. de Marco G, Menuel C, Guillevin R et al (2008) Clinical interest of fMRI and functional exploration methods of brain activity and interactivity: physical and neurophysiological considerations. J Neuroradiol 35:131–143

    Article  PubMed  Google Scholar 

  21. Fox PT, Raichle ME (1984) Stimulus rate dependence of regional cerebral blood flow in human striate cortex, demonstrated by positron emission tomography. J Neurophysiol 51:1109–1120

    CAS  PubMed  Google Scholar 

  22. Mentis MJ, Alexander GE, Grady CL et al (1997) Frequency variation of a pattern-flash visual stimulus during PET differentially activates brain from striate through frontal cortex. Neuroimage 5:116–128

    Article  CAS  PubMed  Google Scholar 

  23. Tankus A, Fried I (2012) Visuomotor coordination and motor representation by human temporal lobe neurons. J Cogn Neurosci 24:600–610

    Article  PubMed  Google Scholar 

  24. Kravitz DJ, Saleem KS, Baker CI, Mishkin M (2011) A new neural framework for visuospatial processing. Nat Rev Neurosci 12:217–230

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  25. Liu H, Stufflebeam SM, Sepulcre J et al (2009) Evidence from intrinsic activity that asymmetry of the human brain is controlled by multiple factors. Proc Natl Acad Sci USA 106:20499–20503

    Article  CAS  PubMed  PubMed Central  Google Scholar 

  26. Le Grand R, Mondloch CJ, Maurer D, Brent HP (2003) Expert face processing requires visual input to the right hemisphere during infancy. Nat Neurosci 6:1108–1112

    Article  PubMed  Google Scholar 

  27. Hamsher KD (1978) Stereopsis and unilateral brain disease. Invest Ophthalmol Vis Sci 17:336–343

    CAS  PubMed  Google Scholar 

  28. De Renzi E (1986) Prosopagnosia in two patients with CT scan evidence of damage confined to the right hemisphere. Neuropsychologia 24:385–389

    Article  PubMed  Google Scholar 

  29. Van Kleeck MH (1989) Hemispheric differences in global versus local processing of hierarchical visual stimuli by normal subjects: new data and a meta-analysis of previous studies. Neuropsychologia 27:1165–1178

    Article  PubMed  Google Scholar 

  30. Sadato N, Okada T, Kubota K, Yonekura Y (2004) Tactile discrimination activates the visual cortex of the recently blind naive to Braille: a functional magnetic resonance imaging study in humans. Neurosci Lett 359:49–52

    Article  CAS  PubMed  Google Scholar 

  31. Everts R, Lidzba K, Wilke M, Kiefer C, Mordasini M, Schroth G, Perrig W, Steinlin M (2009) Strengthening of laterality of verbal and visuospatial functions during childhood and adolescence. Hum Brain Mapp 30:473–483

    Article  PubMed  Google Scholar 

  32. Crosson B, Moore AB, McGregor KM, Chang YL, Benjamin M, Gopinath K, Sherod ME, Wierenga CE, Peck KK, Briggs RW, Rothi LJ, White KD (2009) Regional changes in word-production laterality after a naming treatment designed to produce a rightward shift in frontal activity. Brain Lang 111:73–85

    Article  PubMed  PubMed Central  Google Scholar 

  33. Pizzagalli D, Pascual-Marqui RD, Nitschke JB, Oakes TR, Larson CL, Abercrombie HC, Schaefer SM, Koger JV, Benca RM, Davidson RJ (2001) Anterior cingulate activity as a predictor of degree of treatment response in major depression: evidence from brain electrical tomography analysis. Am J Psychiatry 158:405–415

    Article  CAS  PubMed  Google Scholar 

  34. Levy LM, Henkin RI, Lin CS, Hutter A, Schellinger D (1998) Increased brain activation in response to odors in patients with hyposmia after theophylline treatment demonstrated by fMRI. J Comput Assist Tomogr 22:760–770

    Article  CAS  PubMed  Google Scholar 

  35. Fridriksson J, Morrow-Odom L, Moser D, Fridriksson A, Baylis G (2006) Neural recruitment associated with anomia treatment in aphasia. Neuroimage 32:1403–1412

    Article  PubMed  Google Scholar 

  36. Sundgren PC (2009) Diffusion Tensor Imaging and Tractography: have They Come of Age? J Neuroophthalmol 29:93–95

    Article  PubMed  Google Scholar 

  37. Song HY, Qi S, Tang HH et al (2010) MR DTI and DTT study on the development of optic radiation in patients with anisometropia amblyopia. Sichuan Da Xue Xue Bao Yi Xue Ban 41:648–651

    PubMed  Google Scholar 

  38. Xiao JX, Xie S, Ye JT et al (2007) Detection of abnormal visual cortex in children with amblyopia by voxel-based morphometry. Am J Ophthalmol 143:489–493

    Article  PubMed  Google Scholar 

  39. Barton JJ (2011) Disorders of higher visual processing. Handb Clin Neurol 102:223–261

    Article  PubMed  Google Scholar 

  40. Myers EH, Hampson M, Vohr B et al (2010) Functional connectivity to a right hemisphere language center in prematurely born adolescents. Neuroimage 51:1445–1452

    Article  PubMed  PubMed Central  Google Scholar 

  41. Skranes J, Lohaugen GC, Martinussen M, Indredavik MS, Dale AM, Haraldseth O, Vangberg TR, Brubakk AM (2009) White matter abnormalities and executive function in children with very low birth weight. NeuroReport 20:263–266

    Article  PubMed  Google Scholar 

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Correspondence to Senthil S. Kumaran.

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The study was approved by the institutional ethics committee and adheres to the tenets of declaration of Helsinki (1964) and its later amendments.

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This article does not contain any studies with animals performed by any of the authors.

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Informed consent was obtained from all individual participants/their parents included in this study.

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Gupta, S., Kumaran, S.S., Saxena, R. et al. BOLD fMRI and DTI in strabismic amblyopes following occlusion therapy. Int Ophthalmol 36, 557–568 (2016). https://doi.org/10.1007/s10792-015-0159-2

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  • DOI: https://doi.org/10.1007/s10792-015-0159-2

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