Atrophy of the lateral geniculate nucleus in human glaucoma detected by magnetic resonance imaging
Aim:To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal subjects.Methods:Following institutional St Michael’s Hospital Research Ethics Board approval, a prospective and masked neuroimaging study was conduc...
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Published in | British journal of ophthalmology Vol. 93; no. 1; pp. 56 - 60 |
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Main Authors | , , , , , |
Format | Journal Article |
Language | English |
Published |
BMA House, Tavistock Square, London, WC1H 9JR
BMJ Publishing Group Ltd
01.01.2009
BMJ Publishing Group BMJ Publishing Group LTD |
Subjects | |
Online Access | Get full text |
ISSN | 0007-1161 1468-2079 1468-2079 |
DOI | 10.1136/bjo.2008.138172 |
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Abstract | Aim:To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal subjects.Methods:Following institutional St Michael’s Hospital Research Ethics Board approval, a prospective and masked neuroimaging study was conducted on glaucoma patients with visual-field defects affecting both eyes (n = 10) and age-matched controls (n = 8). Following informed consent, all subjects underwent 1.5-Tesla MRI. Coronal proton density magnetic resonance images of both LGNs were obtained, and LGN height measurements were measured by consensus by three neuroradiologists masked to the diagnosis. Glaucoma and control groups were compared using the t test.Results:Both LGNs were identified and visualised by 1.5-Tesla MRI for every subject. Compared with controls, the mean LGN heights in glaucoma were decreased in right (4.09 (0.89) mm vs 4.74 (0.54) mm, p>0.05) and left LGNs (3.98 (0.57) mm vs 4.83 (0.95) mm; p = 0.033). The combined right and left LGN height in glaucoma was significantly decreased compared with controls (8.07 (1.06) mm vs 9.56 (0.86) mm; p = 0.005).Conclusion:In vivo MRI evidence of LGN degeneration in human glaucoma is consistent with ex vivo primate and human neuropathological studies. LGN atrophy may be a relevant biomarker of visual system injury and/or progression in some glaucoma patients. |
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AbstractList | Aim:To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal subjects.Methods:Following institutional St Michael’s Hospital Research Ethics Board approval, a prospective and masked neuroimaging study was conducted on glaucoma patients with visual-field defects affecting both eyes (n = 10) and age-matched controls (n = 8). Following informed consent, all subjects underwent 1.5-Tesla MRI. Coronal proton density magnetic resonance images of both LGNs were obtained, and LGN height measurements were measured by consensus by three neuroradiologists masked to the diagnosis. Glaucoma and control groups were compared using the t test.Results:Both LGNs were identified and visualised by 1.5-Tesla MRI for every subject. Compared with controls, the mean LGN heights in glaucoma were decreased in right (4.09 (0.89) mm vs 4.74 (0.54) mm, p>0.05) and left LGNs (3.98 (0.57) mm vs 4.83 (0.95) mm; p = 0.033). The combined right and left LGN height in glaucoma was significantly decreased compared with controls (8.07 (1.06) mm vs 9.56 (0.86) mm; p = 0.005).Conclusion:In vivo MRI evidence of LGN degeneration in human glaucoma is consistent with ex vivo primate and human neuropathological studies. LGN atrophy may be a relevant biomarker of visual system injury and/or progression in some glaucoma patients. To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal subjects.AIMTo determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal subjects.Following institutional St Michael's Hospital Research Ethics Board approval, a prospective and masked neuroimaging study was conducted on glaucoma patients with visual-field defects affecting both eyes (n = 10) and age-matched controls (n = 8). Following informed consent, all subjects underwent 1.5-Tesla MRI. Coronal proton density magnetic resonance images of both LGNs were obtained, and LGN height measurements were measured by consensus by three neuroradiologists masked to the diagnosis. Glaucoma and control groups were compared using the t test.METHODSFollowing institutional St Michael's Hospital Research Ethics Board approval, a prospective and masked neuroimaging study was conducted on glaucoma patients with visual-field defects affecting both eyes (n = 10) and age-matched controls (n = 8). Following informed consent, all subjects underwent 1.5-Tesla MRI. Coronal proton density magnetic resonance images of both LGNs were obtained, and LGN height measurements were measured by consensus by three neuroradiologists masked to the diagnosis. Glaucoma and control groups were compared using the t test.Both LGNs were identified and visualised by 1.5-Tesla MRI for every subject. Compared with controls, the mean LGN heights in glaucoma were decreased in right (4.09 (0.89) mm vs 4.74 (0.54) mm, p>0.05) and left LGNs (3.98 (0.57) mm vs 4.83 (0.95) mm; p = 0.033). The combined right and left LGN height in glaucoma was significantly decreased compared with controls (8.07 (1.06) mm vs 9.56 (0.86) mm; p = 0.005).RESULTSBoth LGNs were identified and visualised by 1.5-Tesla MRI for every subject. Compared with controls, the mean LGN heights in glaucoma were decreased in right (4.09 (0.89) mm vs 4.74 (0.54) mm, p>0.05) and left LGNs (3.98 (0.57) mm vs 4.83 (0.95) mm; p = 0.033). The combined right and left LGN height in glaucoma was significantly decreased compared with controls (8.07 (1.06) mm vs 9.56 (0.86) mm; p = 0.005).In vivo MRI evidence of LGN degeneration in human glaucoma is consistent with ex vivo primate and human neuropathological studies. LGN atrophy may be a relevant biomarker of visual system injury and/or progression in some glaucoma patients.CONCLUSIONIn vivo MRI evidence of LGN degeneration in human glaucoma is consistent with ex vivo primate and human neuropathological studies. LGN atrophy may be a relevant biomarker of visual system injury and/or progression in some glaucoma patients. To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal subjects. Following institutional St Michael's Hospital Research Ethics Board approval, a prospective and masked neuroimaging study was conducted on glaucoma patients with visual-field defects affecting both eyes (n = 10) and age-matched controls (n = 8). Following informed consent, all subjects underwent 1.5-Tesla MRI. Coronal proton density magnetic resonance images of both LGNs were obtained, and LGN height measurements were measured by consensus by three neuroradiologists masked to the diagnosis. Glaucoma and control groups were compared using the t test. Both LGNs were identified and visualised by 1.5-Tesla MRI for every subject. Compared with controls, the mean LGN heights in glaucoma were decreased in right (4.09 (0.89) mm vs 4.74 (0.54) mm, p>0.05) and left LGNs (3.98 (0.57) mm vs 4.83 (0.95) mm; p = 0.033). The combined right and left LGN height in glaucoma was significantly decreased compared with controls (8.07 (1.06) mm vs 9.56 (0.86) mm; p = 0.005). In vivo MRI evidence of LGN degeneration in human glaucoma is consistent with ex vivo primate and human neuropathological studies. LGN atrophy may be a relevant biomarker of visual system injury and/or progression in some glaucoma patients. Aim: To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal subjects. Methods: Following institutional St Michael's Hospital Research Ethics Board approval, a prospective and masked neuroimaging study was conducted on glaucoma patients with visual-field defects affecting both eyes (nâ[euro]S=â[euro]S10) and age-matched controls (nâ[euro]S=â[euro]S8). Following informed consent, all subjects underwent 1.5-Tesla MRI. Coronal proton density magnetic resonance images of both LGNs were obtained, and LGN height measurements were measured by consensus by three neuroradiologists masked to the diagnosis. Glaucoma and control groups were compared using the t test. Results: Both LGNs were identified and visualised by 1.5-Tesla MRI for every subject. Compared with controls, the mean LGN heights in glaucoma were decreased in right (4.09 (0.89) mm vs 4.74 (0.54) mm, p>0.05) and left LGNs (3.98 (0.57) mm vs 4.83 (0.95) mm; pâ[euro]S=â[euro]S0.033). The combined right and left LGN height in glaucoma was significantly decreased compared with controls (8.07 (1.06) mm vs 9.56 (0.86) mm; pâ[euro]S=â[euro]S0.005). Conclusion: In vivo MRI evidence of LGN degeneration in human glaucoma is consistent with ex vivo primate and human neuropathological studies. LGN atrophy may be a relevant biomarker of visual system injury and/or progression in some glaucoma patients. |
Author | Polemidiotis, M Yücel, Y H Gupta, N Greenberg, G Gray, B de Tilly, L Noël |
AuthorAffiliation | 3 Glaucoma and Nerve Protection Unit, St Michael’s Hospital, University of Toronto, Toronto, Canada 1 Ophthalmology & Vision Sciences, Faculty of Medicine, University of Toronto, Toronto, Canada 4 Keenan Research Center at the Li Ka Shing Knowledge Institute of St Michael’s Hospital, University of Toronto, Toronto, Canada 5 Division of Neuroradiology, Department of Diagnostic Imaging, St Michael’s Hospital, University of Toronto, Toronto, Canada 2 Laboratory Medicine & Pathobiology, Faculty of Medicine, University of Toronto, Toronto, Canada 6 Ophthalmic Pathology Laboratory, University of Toronto, Toronto, Canada |
AuthorAffiliation_xml | – name: 5 Division of Neuroradiology, Department of Diagnostic Imaging, St Michael’s Hospital, University of Toronto, Toronto, Canada – name: 2 Laboratory Medicine & Pathobiology, Faculty of Medicine, University of Toronto, Toronto, Canada – name: 6 Ophthalmic Pathology Laboratory, University of Toronto, Toronto, Canada – name: 1 Ophthalmology & Vision Sciences, Faculty of Medicine, University of Toronto, Toronto, Canada – name: 3 Glaucoma and Nerve Protection Unit, St Michael’s Hospital, University of Toronto, Toronto, Canada – name: 4 Keenan Research Center at the Li Ka Shing Knowledge Institute of St Michael’s Hospital, University of Toronto, Toronto, Canada |
Author_xml | – sequence: 1 givenname: N surname: Gupta fullname: Gupta, N email: guptan@smh.toronto.on.ca organization: Keenan Research Center at the Li Ka Shing Knowledge Institute of St Michael’s Hospital, University of Toronto, Toronto, Canada – sequence: 2 givenname: G surname: Greenberg fullname: Greenberg, G email: guptan@smh.toronto.on.ca organization: Division of Neuroradiology, Department of Diagnostic Imaging, St Michael’s Hospital, University of Toronto, Toronto, Canada – sequence: 3 givenname: L Noël surname: de Tilly fullname: de Tilly, L Noël email: guptan@smh.toronto.on.ca organization: Division of Neuroradiology, Department of Diagnostic Imaging, St Michael’s Hospital, University of Toronto, Toronto, Canada – sequence: 4 givenname: B surname: Gray fullname: Gray, B email: guptan@smh.toronto.on.ca organization: Division of Neuroradiology, Department of Diagnostic Imaging, St Michael’s Hospital, University of Toronto, Toronto, Canada – sequence: 5 givenname: M surname: Polemidiotis fullname: Polemidiotis, M email: guptan@smh.toronto.on.ca organization: Division of Neuroradiology, Department of Diagnostic Imaging, St Michael’s Hospital, University of Toronto, Toronto, Canada – sequence: 6 givenname: Y H surname: Yücel fullname: Yücel, Y H email: guptan@smh.toronto.on.ca organization: Ophthalmic Pathology Laboratory, University of Toronto, Toronto, Canada |
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Keywords | Atrophy Glaucoma Human Protozoa Eye disease Glaucoma (eye) Medical imagery Ciliata Ophthalmology Nuclear magnetic resonance imaging |
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PublicationTitle | British journal of ophthalmology |
PublicationTitleAlternate | Br J Ophthalmol |
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Snippet | Aim:To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal... Aim: To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal... To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal subjects.... To determine in vivo whether the lateral geniculate nucleus (LGN) undergoes atrophy in patients with glaucoma and vision loss compared with normal... |
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SubjectTerms | Age Aged Atrophy - pathology Biological and medical sciences Case-Control Studies Disease Disease Progression Female Geniculate Bodies - pathology Glaucoma Glaucoma - pathology Glaucoma and intraocular pressure Humans Magnetic Resonance Imaging Male Medical imaging Medical sciences Middle Aged Miscellaneous Nerve Degeneration - pathology NMR Nuclear magnetic resonance Ophthalmology Original Pathology Patients Primates Prospective Studies Studies |
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Title | Atrophy of the lateral geniculate nucleus in human glaucoma detected by magnetic resonance imaging |
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