Aykan Umit, Akdemir M Orcun, Yildirim Ozlem, Varlibas Figen
Department of Ophthalmology, Near East University, Faculty of Medicine Nicosia Cyprus.
Department of Ophthalmology, Bulent Ecevit University, Faculty of Medicine Zonguldak Turkey.
Neuroophthalmology. 2013 Nov 19;37(6):239-246. doi: 10.3109/01658107.2013.830627. eCollection 2013.
We compared the visual field performances of patients with mild Alzheimer disease (AD) with normal subjects and detected visual field impairment attributable to the magnocellular pathway using frequency doubling technology-Matrix (FDT-Matrix). We recruited 43 patients with mild AD (mean age: 68.0 ± 7.2 years) and 33 controls who are visually and cognitively normal (mean age: 64.1 ± 6.4 years). All participants had at least two reliable FDT-Matrix 30-2 tests. Reliability indices, global indices (mean deviation and pattern standard deviation), and glaucoma hemifield test results were measured with FDT-Matrix. The mean test duration was significantly longer in patient group compared with controls ( = 0.002). Among the reliability indices, false negatives were higher in patient group than controls ( = 0.003). There were statistically significant differences in mean deviation and pattern standard deviation values ( < 0.0001 and < 0.0001, respectively) and glaucoma hemifield test results ( < 0.001) between the patient and the control group. Our results imply that the pathogenesis of cognitive deterioration may not only be confined to the cortical area but also to the magnocellular pathway. We underline that FDT testing can be useful for the identification of early impairment and the follow-up of patients with AD.
我们比较了轻度阿尔茨海默病(AD)患者与正常受试者的视野表现,并使用频率加倍技术 - 矩阵(FDT - 矩阵)检测了归因于大细胞通路的视野损害。我们招募了43例轻度AD患者(平均年龄:68.0 ± 7.2岁)和33名视力和认知正常的对照者(平均年龄:64.1 ± 6.4岁)。所有参与者至少进行了两次可靠的FDT - 矩阵30 - 2测试。使用FDT - 矩阵测量可靠性指标、整体指标(平均偏差和模式标准偏差)以及青光眼半视野测试结果。与对照组相比,患者组的平均测试持续时间明显更长(P = 0.002)。在可靠性指标中,患者组的假阴性率高于对照组(P = 0.003)。患者组和对照组之间在平均偏差和模式标准偏差值(分别为P < 0.0001和P < 0.0001)以及青光眼半视野测试结果(P < 0.001)方面存在统计学显著差异。我们的结果表明,认知衰退的发病机制可能不仅局限于皮质区域,还涉及大细胞通路。我们强调FDT测试对于识别早期损害以及AD患者的随访可能是有用的。