Department of Ophthalmology, University of Washington, Seattle, WA, USA.
Kaiser Permanente Washington Health Research Institute, Seattle, WA, USA.
J Alzheimers Dis. 2019;68(2):647-655. doi: 10.3233/JAD-181087.
The aging eye offers unique opportunities to study and understand the aging brain, in particular related to Alzheimer's disease (AD) and dementia. However, little is known about relationships between eye diseases and dementia-related neurodegeneration.
To determine the potential association between three age-related eye diseases and AD and dementia-related neuropathology.
We reviewed autopsy data from the prospective longitudinal Adult Changes in Thought (ACT) cohort. ICD-9 codes were used to identify diagnoses of diabetic retinopathy, glaucoma, and age-related macular degeneration. Multivariate regression models were used to determine odds ratios (OR) of neuropathology features associated with dementia, including Braak stage, Consortium to Establish a Registry for AD (CERAD score), Lewy bodies, hippocampal sclerosis, and microvascular brain injury, in addition to quantitative paired helical filament (PHF)-tau levels for people with and without each eye condition. We also evaluated interactions between eye conditions and dementia related neuropathologic findings were evaluated.
676 autopsies were included. Diabetic retinopathy was significantly associated with increased risk of deep cerebral microinfarcts (OR = 1.91 [95% confidence interval (CI) 1.11, 3.27], p = 0.02). No other significant association or interaction between eye diseases and neuropathology was found. When PHF-tau quantity was evaluated in 124 decedents, the OR for the association between PHF-tau in the occipital cortex and glaucoma was 1.36 (95% CI 0.91, 2.03, p = 0.13). No statistical correction was made for multiple comparisons.
Increased risk of deep cerebral microinfarcts was found in participants diagnosed with diabetic retinopathy. Eye diseases such as glaucoma may increase susceptibility to neurofibrillary tangles in the occipital cortex.
衰老的眼睛为研究和了解衰老的大脑提供了独特的机会,特别是与阿尔茨海默病(AD)和痴呆有关的大脑。然而,人们对眼部疾病与痴呆相关的神经退行性变之间的关系知之甚少。
确定三种与年龄相关的眼部疾病与 AD 和痴呆相关神经病理学之间的潜在关联。
我们回顾了前瞻性纵向成人思想变化(ACT)队列的尸检数据。使用国际疾病分类第 9 版(ICD-9)代码来确定糖尿病性视网膜病变、青光眼和年龄相关性黄斑变性的诊断。使用多变量回归模型来确定与痴呆相关的神经病理学特征的优势比(OR),包括 Braak 分期、阿尔茨海默病建立登记册联盟(CERAD 评分)、路易体、海马硬化和微血管脑损伤,以及有和没有每种眼部疾病的人的定量配对螺旋丝(PHF)-tau 水平。我们还评估了眼部疾病与痴呆相关神经病理学发现之间的相互作用。
纳入 676 例尸检。糖尿病性视网膜病变与深部脑微梗死的风险增加显著相关(OR = 1.91 [95%置信区间(CI)1.11,3.27],p = 0.02)。未发现其他眼部疾病与神经病理学之间存在显著关联或相互作用。当评估 124 名死者的 PHF-tau 量时,青光眼与枕叶皮质 PHF-tau 之间关联的 OR 为 1.36(95% CI 0.91,2.03,p = 0.13)。未对多次比较进行统计校正。
诊断为糖尿病性视网膜病变的参与者中发现深部脑微梗死的风险增加。青光眼等眼部疾病可能会增加枕叶皮质神经原纤维缠结的易感性。