Objective: To evaluate the development of optic radiations (ORs) in patients with anisometropia amblyopia using magnetic resonance diffusion tensor imaging (DTI) and diffusion tensor tractography (DTT), and to explore possible mechanism of pathogenesis of amblyopia.
Methods: Brain scan was performed with 3.0 Tesla scanner on 8 patients with anisometropia amblyopia and 15 control subjects with normal sights. The fractional anisotropy (FA) values, the apparent diffusion coefficient (ADC) values, the numbers of neural fiber bundle of ORs, and the voxel numbers of ORs were compared between the patients with anisometropia amblyopia and those with normal sights and between the ipsilateral ORs and the contralateral ORs in the patients with amblyopia.
Results: No differences in the FA values, the ADC values, the numbers of neural fiber bundle of ORs and the voxel numbers of ORs were found between the ipsilateral ORs and the contralateral ORs in the patients with amblyopia (P > 0.05). Significant decreases in the FA values and the voxel numbers of ORs were found in the patients with amblyopia compared with the controls (P < 0.05). No differences in the voxel numbers of both ORs in the anterior parts were found between the patients with amblyopia and the controls (P > 0.05). However, the patients with amblyopia had more voxel numbers of ORs in the posterior parts than the controls (P < 0.05). The differences in the ADC values and the numbers of neural fiber bundle of ORs between the patients with amblyopia and the controls were not significant (P > 0.05).
Conclusion: The compactability, integrity and directivity of ORs decrease in patients with anisometropia amblyopia. The projection of OR fibers is abnormal. The ORs are underdeveloped, especially in the posterior parts, although no abnormal morphologic changes occur. The DTI and DTT can detect the underdevelopment of optic radiations in patients with anisometropia amblyopia indirectly.