Prins Doety, Jansonius Nomdo M, Cornelissen Frans W
Laboratory of Experimental Ophthalmology, Department of Ophthalmology, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
Invest Ophthalmol Vis Sci. 2017 Feb 1;58(2):1304-1313. doi: 10.1167/iovs.16-20404.
Chronic ocular pathology, such as glaucoma and macular degeneration, is associated with neuroanatomic changes in the visual pathways. It is a challenge to determine the mechanism responsible for these changes. This could be functional deprivation or transsynaptic degeneration. Acquired monocular blindness provides a unique opportunity to establish which mechanism underlies neuroanatomic changes in ocular pathology in general, since the loss of input is well defined, and it causes selective functional deprivation due to the loss of stereopsis. Here, we assessed whether acquired monocular blindness is associated with neuroanatomic changes, and if so, where these changes are located.
High-resolution T1-weighted magnetic resonance images were obtained in 15 monocularly blind patients and 18 healthy controls. We used voxel- and surface-based morphometry to compare gray and white matter volume, cortical thickness, mean curvature, and surface area between these groups.
The gray matter volume in the bilateral superior lateral occipital cortices was decreased in the monocular blind patients, in the absence of volumetric differences in their early visual cortex.
The volumetric decrease in the superior lateral occipital cortices is consistent with specific functional deprivation, as the superior lateral occipital cortices play an important role in depth perception. Moreover, in the absence of differences in the early visual cortex, the decrease is inconsistent with transsynaptic degeneration propagating from the degenerated retinal axons.
慢性眼部病变,如青光眼和黄斑变性,与视觉通路的神经解剖学变化相关。确定导致这些变化的机制具有挑战性。这可能是功能性剥夺或跨突触变性。后天性单眼失明提供了一个独特的机会来确定一般眼部病变中神经解剖学变化的潜在机制,因为输入的丧失是明确的,并且由于立体视觉的丧失导致选择性功能性剥夺。在此,我们评估后天性单眼失明是否与神经解剖学变化相关,如果是,这些变化位于何处。
对15名单眼失明患者和18名健康对照者进行高分辨率T1加权磁共振成像。我们使用基于体素和表面的形态测量法来比较两组之间的灰质和白质体积、皮质厚度、平均曲率和表面积。
单眼失明患者双侧枕叶上外侧皮质的灰质体积减少,而其早期视觉皮质的体积没有差异。
枕叶上外侧皮质的体积减少与特定的功能性剥夺一致,因为枕叶上外侧皮质在深度感知中起重要作用。此外,由于早期视觉皮质没有差异,这种减少与从退化的视网膜轴突传播的跨突触变性不一致。