Giorgio Antonio, Zhang Jian, Costantino Francesco, De Stefano Nicola, Frezzotti Paolo
Department of Medicine, Surgery and Neuroscience, University of Siena, Italy.
Hum Brain Mapp. 2018 Jan;39(1):532-541. doi: 10.1002/hbm.23862. Epub 2017 Oct 24.
Brain changes within and beyond the visual system have been demonstrated in primary open angle glaucoma (POAG), the most common type of glaucoma. These changes have been often interpreted as a neurodegenerative process due, at least partially, to the raised intraocular pressure (IOP). In this context, normal tension glaucoma (NTG), a form of POAG with IOP <21 mm Hg despite the typical glaucomatous findings, represents the most suitable model of glaucoma to test the validity of this hypothesis. We acquired multimodal brain MRI in NTG patients (n = 17) and compared them with demographically matched groups of POAG patients with raised IOP (n = 17) and normal controls (NC, n = 29). Voxelwise statistics was performed with nonparametric permutation testing. Both NTG and POAG patients showed, compared to NC, significantly more gray matter atrophy in both the visual system and in nonvisual brain regions and altered diffusion tensor imaging-derived anatomical connectivity (AC; lower fractional anisotropy and/or higher diffusivities). Compared with NTG, POAG had both more atrophic visual cortex and higher axial diffusivity in nonvisual regions. Functional connectivity (FC) with respect to NC was altered in NTG at short-range level [visual network (VN), ventral attention network] and in POAG at long-range level (between secondary VN and limbic network). FC of POAG was higher than NTG in both VN and executive network. This study provides further evidence that diffuse structural and functional abnormalities across glaucoma brain may be, at least partially, independent of raised IOP and the consequent retinal degeneration. This further defines glaucoma as a condition with neurodegeneration spreading. Hum Brain Mapp 39:532-541, 2018. © 2017 Wiley Periodicals, Inc.
在原发性开角型青光眼(POAG,最常见的青光眼类型)中,已证实视觉系统内外均存在脑部变化。这些变化常被解释为一种神经退行性过程,至少部分原因是眼内压(IOP)升高。在此背景下,正常眼压性青光眼(NTG),即一种尽管有典型青光眼表现但眼压<21 mmHg的POAG形式,是检验该假设有效性的最合适的青光眼模型。我们对NTG患者(n = 17)进行了多模态脑MRI检查,并将其与年龄、性别匹配的眼压升高的POAG患者组(n = 17)和正常对照组(NC,n = 29)进行比较。采用非参数置换检验进行体素统计。与NC相比,NTG和POAG患者在视觉系统和非视觉脑区均显示出明显更多的灰质萎缩,以及扩散张量成像衍生的解剖连接性(AC;较低的分数各向异性和/或较高的扩散率)改变。与NTG相比,POAG的视觉皮层萎缩更严重,非视觉区域的轴向扩散率更高。与NC相比,NTG在短程水平[视觉网络(VN)、腹侧注意网络]的功能连接性(FC)发生改变,POAG在长程水平(次级VN和边缘网络之间)的FC发生改变。POAG在VN和执行网络中的FC均高于NTG。本研究提供了进一步的证据,表明青光眼患者脑部广泛的结构和功能异常可能至少部分独立于眼压升高及随之而来的视网膜变性。这进一步将青光眼定义为一种神经退行性病变扩散的疾病。《人类大脑图谱》39:532 - 541,2018年。© 2017威利期刊公司。