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      Altered anterior visual system development following early monocular enucleation

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          Abstract

          Purpose

          Retinoblastoma is a rare eye cancer that generally occurs before 5 years of age and often results in enucleation (surgical removal) of the cancerous eye. In the present study, we sought to determine the consequences of early monocular enucleation on the morphological development of the anterior visual pathway including the optic chiasm and lateral geniculate nucleus.

          Methods

          A group of adults who had one eye enucleated early in life due to retinoblastoma was compared to binocularly intact controls. Although structural changes have previously been reported in late enucleation, we also collected data from one late enucleated participant to compare to our early enucleated participants. Measurements of the optic nerves, optic chiasm, optic tracts and lateral geniculate nuclei were evaluated from T 1 weighted and proton density weighted images collected from each participant.

          Results

          The early monocular enucleation group exhibited overall degeneration of the anterior visual system compared to controls. Surprisingly, however, optic tract diameter and geniculate volume decreases were less severe contralateral to the remaining eye. Consistent with previous research, the late enucleated participant showed no asymmetry and significantly larger volume decreases in both geniculate nuclei compared to controls.

          Conclusions

          The novel finding of an asymmetry in morphology of the anterior visual system following long-term survival from early monocular enucleation indicates altered postnatal visual development. Possible mechanisms behind this altered development include recruitment of deafferented cells by crossing nasal fibres and/or geniculate cell retention via feedback from primary visual cortex. These data highlight the importance of balanced binocular input during postnatal maturation for typical anterior visual system morphology.

          Highlights

          • Morphology of the anterior visual system in early monocular enucleation was assessed.

          • Optic tract diameter, and optic chiasm and lateral geniculate volumes were decreased.

          • A contralateral bias was observed for optic tract diameter and geniculate volume.

          • One late enucleate exhibited severe geniculate volume decreases but no asymmetry.

          • Altered visual development occurs to compensate for early enucleation.

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          Most cited references63

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          Investigation of the single case in neuropsychology: confidence limits on the abnormality of test scores and test score differences.

          Neuropsychologists often need to estimate the abnormality of an individual patient's test score, or test score discrepancies, when the normative or control sample against which the patient is compared is modest in size. Crawford and Howell [The Clinical Neuropsychologist 12 (1998) 482] and Crawford et al. [Journal of Clinical and Experimental Neuropsychology 20 (1998) 898] presented methods for obtaining point estimates of the abnormality of test scores and test score discrepancies in this situation. In the present study, we extend this work by developing methods of setting confidence limits on the estimates of abnormality. Although these limits can be used with data from normative or control samples of any size, they will be most useful when the sample sizes are modest. We also develop a method for obtaining point estimates and confidence limits on the abnormality of a discrepancy between a patient's mean score on k-tests and a test entering into that mean. Computer programs that implement the formulae for the confidence limits (and point estimates) are described and made available.
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            EFFECTS OF VISUAL DEPRIVATION ON MORPHOLOGY AND PHYSIOLOGY OF CELLS IN THE CATS LATERAL GENICULATE BODY.

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              Age-related total gray matter and white matter changes in normal adult brain. Part I: volumetric MR imaging analysis.

              A technique of segmenting total gray matter (GM) and total white matter (WM) in human brain is now available. We investigated the effects of age and sex on total fractional GM (%GM) and total fractional WM (%WM) volumes by using volumetric MR imaging in healthy adults. Fifty-four healthy volunteers (22 men, 32 women) aged 20-86 years underwent dual-echo fast spin-echo MR imaging. Total GM, total WM, and intracranial space volumes were segmented by using MR image-based computerized semiautomated software. Volumes were normalized as a percentage of intracranial volume (%GM and %WM) to adjust for variations in head size. Age and sex effects were then assessed. Both %GM and %WM in the intracranial space were significantly less in older subjects (> or =50 years) than in younger subjects (<50 years) (P <.0001 and P =.02, respectively). Consistently, %GM decreased linearly with age, beginning in the youngest subjects. %WM decreased in a quadratic fashion, with a greater rate beginning only in adult midlife. Although larger GM volumes were observed in men before adjustments for cranium size, no significant differences in %GM or %WM were observed between the sexes. GM volume loss appears to be a constant, linear function of age throughout adult life, whereas WM volume loss seems to be delayed until middle adult life. Both appear to be independent of sex. Quantitative analysis of %GM and %WM volumes can improve our understanding of brain atrophy due to normal aging; this knowledge may be valuable in distinguishing atrophy of disease patterns from characteristics of the normal aging process.
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                Author and article information

                Journal
                Neuroimage Clin
                Neuroimage Clin
                NeuroImage : Clinical
                Elsevier
                2213-1582
                1 November 2013
                1 November 2013
                2014
                : 4
                : 72-81
                Affiliations
                [a ]Department of Psychology, York University, Toronto, Canada
                [b ]Centre for Vision Research, York University, Toronto, Canada
                [c ]Department of Biology, York University, Toronto, Canada
                [d ]Department of Ophthalmology and Visual Sciences, The Hospital for Sick Children, Toronto, Canada
                [e ]Department of Ophthalmology, University of Toronto, Toronto, Canada
                [f ]Princess Margaret Cancer Centre, University Health Network, Toronto, Canada
                Author notes
                [* ]Corresponding author at: Department of Psychology and Centre for Vision Research, York University, 4700 Keele St., Toronto, ON M3J 1P3, Canada. Tel.: + 1 416 736 2100x20452; fax: + 1 416 736 5814. steeves@ 123456yorku.ca
                Article
                S2213-1582(13)00144-7
                10.1016/j.nicl.2013.10.014
                3853349
                24319655
                e9edb994-b788-47de-ace2-61886342ebdc
                © 2013 The Authors

                This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution and reproduction in any medium, provided the original author and source are credited.

                History
                : 24 August 2013
                : 11 October 2013
                : 19 October 2013
                Categories
                Article

                anterior visual system development,retinoblastoma,lateral geniculate nucleus,optic chiasm,monocular enucleation

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