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      Cerebral magnetic resonance imaging of coincidental infarction and small vessel disease in retinal artery occlusion

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          Abstract

          There are several reports in the literature on the association between non-arteritic retinal artery occlusion (NA-RAO) and acute ischemic stroke. We investigated the burden of small vessel disease (SVD) and cerebral coincident infarction observed on cerebral magnetic resonance imaging (MRI) in patients with newly diagnosed NA-RAO. In this retrospective, observational, case-series study, consecutive patients with NA-RAO who underwent cerebral MRI within one month of diagnosis between September 2003 and October 2018 were included. The classification of NA-RAO was based on ophthalmologic and systemic examinations. We also investigated the co-incident infarction and burden of underlying SVD, which were categorized as white matter hyperintensity lesion (WMH), cerebral microbleeds (CMB), and silent lacunar infarction (SLI). Among the 272 patients enrolled in the study, 18% presented co-incident infarction and 73% had SVD, which included WMH (70%), CMB (14%), and SLI (30%). Co-incident infarction, WMH, and SLI significantly increased with age: co-incident infarction was observed in 8% of young (< 50 years) patients and 30% of old (≥ 70 years) patients. The embolic etiology of RAO (large artery atherosclerosis, cardioembolism, and undetermined etiology) was significantly associated with the prevalence of SVD (82%: 70%: 64%, P = 0.002) and co-incident infarction (30%: 19%: 8%; P = 0.009). Therefore, high co-incidence of acute cerebral infarction and underlying SVD burden warrant careful neurologic examination and appropriate brain imaging, followed by management of NA-RAO. Urgent brain imaging is particularly pertinent in elderly patients with NA-RAO.

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          MR signal abnormalities at 1.5 T in Alzheimer's dementia and normal aging.

          The type, frequency, and extent of MR signal abnormalities in Alzheimer's disease and normal aging are a subject of controversy. With a 1.5-MR unit we studied 12 Alzheimer patients, four subjects suffering from multiinfarct dementia and nine age-matched controls. Punctate or early confluent high-signal abnormalities in the deep white matter, noted in 60% of both Alzheimer patients and controls, were unrelated to the presence of hypertension or other vascular risk factors. A significant number of Alzheimer patients exhibited a more extensive smooth "halo" of periventricular hyperintensity when compared with controls (p = .024). Widespread deep white-matter hyperintensity (two patients) and extensive, irregular periventricular hyperintensity (three patients) were seen in multiinfarct dementia. Areas of high signal intensity affecting hippocampal and sylvian cortex were also present in five Alzheimer and two multiinfarct dementia patients, but absent in controls. Discrete, small foci of deep white-matter hyperintensity are not characteristic of Alzheimer's disease nor do they appear to imply a vascular cause for the dementing illness. The frequently observed "halo" of periventricular hyperintensity in Alzheimer's disease may be of diagnostic importance. High-signal abnormalities in specific cortical regions are likely to reflect disease processes localized to those structures.
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            Classification of subtype of acute ischemic stroke. Definitions for use in a multicenter clinical trial. TOAST. Trial of Org 10172 in Acute Stroke Treatment

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              Cerebral small vessel disease: from pathogenesis and clinical characteristics to therapeutic challenges.

              The term cerebral small vessel disease refers to a group of pathological processes with various aetiologies that affect the small arteries, arterioles, venules, and capillaries of the brain. Age-related and hypertension-related small vessel diseases and cerebral amyloid angiopathy are the most common forms. The consequences of small vessel disease on the brain parenchyma are mainly lesions located in the subcortical structures such as lacunar infarcts, white matter lesions, large haemorrhages, and microbleeds. Because lacunar infarcts and white matter lesions are easily detected by neuroimaging, whereas small vessels are not, the term small vessel disease is frequently used to describe the parenchyma lesions rather than the underlying small vessel alterations. This classification, however, restricts the definition of small vessel disease to ischaemic lesions and might be misleading. Small vessel disease has an important role in cerebrovascular disease and is a leading cause of cognitive decline and functional loss in the elderly. Small vessel disease should be a main target for preventive and treatment strategies, but all types of presentation and complications should be taken into account. Copyright 2010 Elsevier Ltd. All rights reserved.
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                Author and article information

                Contributors
                jck0097@gmail.com
                sejoon1@snu.ac.kr
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                13 January 2021
                13 January 2021
                2021
                : 11
                : 864
                Affiliations
                [1 ]GRID grid.412480.b, ISNI 0000 0004 0647 3378, Department of Ophthalmology, , Seoul National University College of Medicine, Seoul National University Bundang Hospital, ; 173-82 Gumi-ro, Bundang-gu, Seongnam-si, Gyeonggi-do 13620 South Korea
                [2 ]GRID grid.488451.4, ISNI 0000 0004 0570 3602, Department of Ophthalmology, , Kangdong Sacred Heart Hospital, ; Seoul, South Korea
                [3 ]GRID grid.412480.b, ISNI 0000 0004 0647 3378, Department of Radiology, , Seoul National University College of Medicine, Seoul National University Bundang Hospital, ; 173-82 Gumi-ro, Bundang-gu, Seongnam-si, Gyeonggi-do 13620 South Korea
                [4 ]GRID grid.412480.b, ISNI 0000 0004 0647 3378, Department of Neurology, , Seoul National University College of Medicine, Seoul National University Bundang Hospital, ; Seongnam, South Korea
                [5 ]GRID grid.412011.7, ISNI 0000 0004 1803 0072, Department of Ophthalmology, , Kangwon National University Hospital, ; Chuncheon, South Korea
                Article
                80014
                10.1038/s41598-020-80014-9
                7806736
                33441709
                4d2da6d0-c361-4479-ad88-990e94cbcb61
                © The Author(s) 2021

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 25 June 2020
                : 14 December 2020
                Funding
                Funded by: Institutional research fund from Seoul National University Bundang Hospital
                Award ID: 02-2012-067
                Award Recipient :
                Funded by: Research grant from Seoul National University Bundang Hospital
                Award ID: 13-2019-003
                Award Recipient :
                Categories
                Article
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                © The Author(s) 2021

                Uncategorized
                brain imaging,retinal diseases
                Uncategorized
                brain imaging, retinal diseases

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