Prabhakaran Gokulraj T, Al-Nosairy Khaldoon O, Tempelmann Claus, Wagner Markus, Thieme Hagen, Hoffmann Michael B
Department of Ophthalmology, Otto-von-Guericke University, Magdeburg, Germany.
Department of Neurology, Otto-von-Guericke University, Magdeburg, Germany.
Front Neurosci. 2021 Jul 26;15:653632. doi: 10.3389/fnins.2021.653632. eCollection 2021.
In advanced retinitis pigmentosa with retinal lesions, the lesion projection zone (LPZ) in the early visual cortex can be driven during visual tasks, while it remains unresponsive during passive viewing. We tested whether this finding translates to advanced glaucoma, a major cause of acquired blindness. During visual stimulation, 3T fMRI scans were acquired for participants with advanced glaucoma ( = 4; age range: 51-72) and compared to two reference groups, i.e., advanced retinitis pigmentosa ( = 3; age range: 46-78) and age-matched healthy controls with simulated defects ( = 7). The participants viewed grating patterns drifting in 8 directions (12 s) alternating with uniform gray (12 s), either during passive viewing (PV), i.e., central fixation, or during a one-back task (OBT), i.e., reports of succeeding identical motion directions. As another reference, a fixation-dot task condition was included. Only in glaucoma and retinitis pigmentosa but not in controls, fMRI-responses in the lesion projection zone (LPZ) of V1 shifted from negative for PV to positive for OBT ( = 0.024 and = 0.012, respectively). In glaucoma, these effects also reached significance in V3 ( = 0.006), while in V2 there was a non-significant trend ( = 0.069). The general absence of positive responses in the LPZ during PV underscores the lack of early visual cortex bottom-up plasticity for acquired visual field defects in humans. Trends in our exploratory analysis suggesting the task-dependent LPZ responses to be inversely related to visual field loss, indicate the benefit of patient stratification strategies in future studies with greater sample sizes. We conclude that top-down mechanisms associated with task-elicited demands rather than visual cortex remapping appear to shape LPZ responses not only in retinitis pigmentosa, but also in glaucoma. These insights are of critical importance for the development of schemes for treatment and rehabilitation in glaucoma and beyond.
在患有视网膜病变的晚期视网膜色素变性患者中,早期视觉皮层中的病变投射区(LPZ)在视觉任务期间可被激活,而在被动观看时则无反应。我们测试了这一发现是否适用于晚期青光眼,这是后天性失明的主要原因。在视觉刺激期间,对患有晚期青光眼的参与者(n = 4;年龄范围:51 - 72岁)进行了3T功能磁共振成像(fMRI)扫描,并与两个参照组进行比较,即晚期视网膜色素变性患者(n = 3;年龄范围:46 - 78岁)和年龄匹配的有模拟缺陷的健康对照者(n = 7)。参与者观看在8个方向上漂移的光栅图案(12秒),并与均匀灰色交替出现(12秒),分别在被动观看(PV),即中央注视时,或在一个回溯任务(OBT),即报告连续相同运动方向时进行。作为另一个参照,还包括了一个注视点任务条件。仅在青光眼和视网膜色素变性患者中,而非对照组中,V1区的病变投射区(LPZ)的fMRI反应从被动观看时的负反应转变为一个回溯任务时的正反应(分别为p = 0.024和p = 0.012)。在青光眼中,这些效应在V3区也达到显著水平(p = 0.006),而在V2区有一个不显著的趋势(p = 0.069)。被动观看期间LPZ普遍缺乏正反应,这突出了人类后天性视野缺损缺乏早期视觉皮层自下而上的可塑性。我们探索性分析中的趋势表明,任务依赖的LPZ反应与视野缺损呈负相关,这表明在未来更大样本量的研究中患者分层策略的益处。我们得出结论,与任务引发的需求相关的自上而下机制而非视觉皮层重新映射,似乎不仅在视网膜色素变性中,而且在青光眼中塑造了LPZ反应。这些见解对于青光眼及其他疾病的治疗和康复方案的制定至关重要。