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DTI of the Visual Pathway - White Matter Tracts and Cerebral Lesions
Published on: August 26, 2014
Imaging reveals optic tract degeneration in hemianopia
Holly Bridge1, Panitha Jindahra, John Barbur
1FMRIB Centre, John Radcliffe Hospital, Oxford, United Kingdom. holly.bridge@clneuro.ox.ac.uk
Transsynaptic degeneration in the optic tract begins within 18 months of visual cortex or lateral geniculate nucleus damage in hemianopia. White matter integrity is compromised even before visible volume loss.
Area of Science:
- Neuroscience
- Ophthalmology
- Radiology
Background:
- Hemianopia, a visual field defect, can result from damage to the primary visual cortex (V1), lateral geniculate nucleus (LGN), or optic tract.
- Transsynaptic degeneration is a process where neuronal damage in one area leads to degeneration in connected areas.
Purpose of the Study:
- To investigate transsynaptic degeneration in the human optic tract in hemianopia.
- To determine how degeneration varies with the duration and location of the visual pathway insult.
Main Methods:
- Structural MRI scans were performed on seven hemianopic patients with damage to V1, LGN, or optic tract.
- Optic tract volume and cross-sectional area were computed using T1-weighted image intensity values.
- A laterality index was calculated to compare optic tract size between hemispheres at different intensity thresholds.
Main Results:
- Hemianopic patients with longstanding V1 or LGN damage showed significant optic tract degeneration (laterality index > 0.5) at high intensity values.
- Recent optic tract damage resulted in even higher laterality indices due to direct degeneration.
- Correlation between cross-section and volume indices was significant 18 months post-V1 lesion, unlike in controls.
Conclusions:
- Transsynaptic degeneration in the optic tract commences by 18 months after V1 lesion, compromising white matter integrity.
- Visible volume decrease in the optic tract requires longer durations of hemianopia.
- This MRI-based method offers a noninvasive approach to monitor optic tract degeneration timelines.
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