Department of Radiology, 42nd Hospital of PLA , Leshan, Sichuan, China.
Curr Eye Res. 2012 Sep;37(9):794-802. doi: 10.3109/02713683.2012.683506. Epub 2012 May 25.
To study changes in the morphometric characteristics of the whole brain visual-related cortex in various stages of primary open angle glaucoma (POAG) in vivo.
Thirty POAG patients (nine early stage cases and 21 advanced-late stage cases) and 30 gender-, education-, and age-matched healthy controls were enrolled in the study. Image data were obtained with a T1 weighted three-dimensional magnetization prepared rapid acquisition gradient echo sequence (T1WI 3D MP RAGE). Voxel-based morphometry (VBM) analysis was used to assess regional differences in gray matter (GM) densities on T1WI 3D MP RAGE scans of patients versus controls.
Compared with controls, brain regions with GM density changes were not found in the early stage of POAG patients but were found in the advanced-late stage of POAG patients. These changes with GM density reduction were mainly located in the bilateral primary visual cortex (BA17 and BA18), bilateral paracentral lobule (BA5), right precentral gyrus (BA6), right middle frontal gyrus (BA9), right inferior temporal gyrus (BA20), right angular gyrus (BA39), left praecuneus (BA7), left middle temporal gyrus (BA21), and superior temporal gyrus (BA22). Conversely, patients showed increased GM density in BA39 near the most damaged regions. In addition, in the advanced-late stage of POAG, some reduced GM density areas were related to binocular mean defect (MD) and disease duration (ranging from r = -0.761 to r = -0.458).
Our results suggest that there are different types of pathogenesis at different stages of POAG. Atrophy and degeneration of the visual-related cortex existed in the dorsal and ventral visual pathways in the advanced-late stage of POAG but were not found in the early stage of POAG using VBM. Such GM density changes are likely associated with the pathogenesis of POAG.
研究活体原发性开角型青光眼(POAG)各阶段全脑视觉相关皮质形态计量学特征的变化。
本研究纳入了 30 名 POAG 患者(早期 9 例,晚期 21 例)和 30 名性别、教育程度和年龄匹配的健康对照者。采用 T1 加权三维磁化准备快速获取梯度回波序列(T1WI 3D MP RAGE)获得图像数据。对患者和对照组 T1WI 3D MP RAGE 扫描的灰质(GM)密度进行基于体素的形态计量学(VBM)分析,以评估 GM 密度的区域性差异。
与对照组相比,早期 POAG 患者脑区未见 GM 密度变化,但晚期 POAG 患者脑区可见 GM 密度降低。这些 GM 密度降低的变化主要位于双侧初级视皮质(BA17 和 BA18)、双侧旁中央小叶(BA5)、右侧中央前回(BA6)、右侧额中回(BA9)、右侧颞下回(BA20)、右侧角回(BA39)、左侧楔前叶(BA7)、左侧颞中回(BA21)和颞上回(BA22)。相反,患者在最受损区域附近的 BA39 表现出 GM 密度增加。此外,在 POAG 的晚期,一些 GM 密度降低区域与双眼平均缺损(MD)和疾病持续时间(r 从-0.761 到-0.458)有关。
我们的研究结果表明,POAG 不同阶段存在不同的发病机制。在 POAG 的晚期,视路背侧和腹侧的视觉相关皮质出现萎缩和变性,但在 VBM 中未发现 POAG 的早期阶段存在这种情况。这种 GM 密度变化可能与 POAG 的发病机制有关。