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Microvascular network alterations in the retina of patients with Alzheimer's disease

视网膜 微循环 医学 视网膜 心脏病学 优势比 内科学 眼科 阿尔茨海默病 病理 疾病 神经科学 心理学
作者
Carol Y. Cheung,Yi Ting Ong,M. Kamran Ikram,Shin Yeu Ong,Xiang Li,Saima Hilal,Joseree‐Ann S. Catindig,Narayanaswamy Venketasubramanian,Philip Yap,Dennis Seow,Christopher Chen,Tien Yin Wong
出处
期刊:Alzheimers & Dementia [Wiley]
卷期号:10 (2): 135-142 被引量:296
标识
DOI:10.1016/j.jalz.2013.06.009
摘要

Abstract Background Although cerebral small‐vessel disease has been implicated in the development of Alzheimer's disease (AD), the cerebral microcirculation is difficult to visualize directly in vivo. Because the retina provides a noninvasive window to assess the microcirculation, we determined whether quantitatively measured retinal microvascular parameters are associated with AD. Methods We conducted a case‐control study (case:control matching ≈ 1:2). Retinal photographs were analyzed using a computer program, and a spectrum of quantitative retinal microvascular parameters (caliber, fractal dimension, tortuosity, and bifurcation) were measured. Logistic regression models were used to compute the odds ratio (OR) and 95% confidence interval for AD adjusting for age, gender, ethnicity, smoking, hypertension, diabetes, hypercholesterolemia, and history of myocardial infarction. Results We included 136 demented patients with AD and 290 age‐gender‐race‐matched controls. Persons with narrower venular caliber (OR per standard deviation [SD] decrease, 2.01 [1.27–3.19]), decreased arteriolar and venular fractal dimension (OR per SD decrease 1.35 [1.08–1.68], 1.47 [1.17–1.84], respectively) and increased arteriolar and venular tortuosity (OR per SD increase, 1.84 [1.40–2.31], 1.94 [1.48–2.53], respectively) were more likely to have AD. These associations still persisted when only AD cases without a history of cerebrovascular disease were included. Conclusions Patients with AD have altered microvascular network in the retina (narrower retinal venules and a sparser and more tortuous retinal vessels) compared with matched nondemented controls. These changes in retinal microvasculature may reflect similar pathophysiological processes in cerebral microvasculature in the brains of patients with AD.
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