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Trans Am Ophthalmol Soc. 1990;88:163-73; discussion 173-8.
2
The long-term effects of visible light on the eye.可见光对眼睛的长期影响。
Arch Ophthalmol. 1992 Jan;110(1):99-104. doi: 10.1001/archopht.1992.01080130101035.
3
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4
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5
Risk of age-related macular degeneration in eyes with macular drusen or hyperpigmentation: the Blue Mountains Eye Study cohort.存在黄斑玻璃膜疣或色素沉着的眼睛发生年龄相关性黄斑变性的风险:蓝山眼研究队列
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Exposure to sunlight and other risk factors for age-related macular degeneration.暴露于阳光及其他与年龄相关性黄斑变性的风险因素。
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Lipofuscin, Its Origin, Properties, and Contribution to Retinal Fluorescence as a Potential Biomarker of Oxidative Damage to the Retina.脂褐素,其起源、特性以及作为视网膜氧化损伤潜在生物标志物对视网膜荧光的贡献。
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本文引用的文献

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Epidemiologic investigation of occupational carcinogenesis using a serially additive expected dose model.使用系列累加预期剂量模型对职业致癌作用进行的流行病学调查。
Am J Epidemiol. 1980 Dec;112(6):787-97. doi: 10.1093/oxfordjournals.aje.a113051.
2
Action spectrum for retinal injury from near-ultraviolet radiation in the aphakic monkey.无晶状体猴近紫外线辐射所致视网膜损伤的作用光谱。
Am J Ophthalmol. 1982 Mar;93(3):299-306. doi: 10.1016/0002-9394(82)90529-3.
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Senile macular degeneration: a case-control study.老年性黄斑变性:一项病例对照研究。
Am J Epidemiol. 1983 Aug;118(2):213-27. doi: 10.1093/oxfordjournals.aje.a113629.
4
Three major pathologic processes caused by light in the primate retina: a search for mechanisms.灵长类视网膜中由光引起的三种主要病理过程:机制探寻
Trans Am Ophthalmol Soc. 1982;80:517-79.
5
Classification of human senile cataractous change by the American Cooperative Cataract Research Group (CCRG) method: III. The association of nuclear color (sclerosis) with extent of cataract formation, age, and visual acuity.采用美国白内障研究协作组(CCRG)方法对人类老年性白内障变化进行分类:III. 核颜色(硬化)与白内障形成程度、年龄及视力的相关性
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Eye protective techniques for bright light.强光下的眼部防护技术
Ophthalmology. 1983 Aug;90(8):937-44. doi: 10.1016/s0161-6420(83)80021-9.
7
Senile macular degeneration: review of epidemiologic features.老年性黄斑变性:流行病学特征综述
Am J Epidemiol. 1983 Aug;118(2):132-51. doi: 10.1093/oxfordjournals.aje.a113624.
8
Sun gazing as the cause of foveomacular retinitis.凝视太阳作为中心凹黄斑部视网膜病变的病因。
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9
Photic maculopathy in rhesus monkey. A light and electron microscopic study.
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10
Relationship of senile macular degeneration to ocular pigmentation.老年性黄斑变性与眼部色素沉着的关系。
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可见光与年龄相关性黄斑变性风险

Visible light and risk of age-related macular degeneration.

作者信息

Taylor H R, Muñoz B, West S, Bressler N M, Bressler S B, Rosenthal F S

机构信息

Dana Center for Preventive Ophthalmology, Wilmer Institute, Johns Hopkins University, Baltimore, Maryland.

出版信息

Trans Am Ophthalmol Soc. 1990;88:163-73; discussion 173-8.

PMID:2095019
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1298584/
Abstract

Sunlight exposure has been suggested as a cause of AMD. To examine this, we collected detailed histories of ocular sun exposure in 838 watermen who work on the Chesapeake Bay. The presence and severity of AMD was assessed in stereo macular photographs. Macular changes were classified into four grades of increasing severity ranging from the presence of 5 or more drusen (AMD-1) to extensive geographic atrophy or disciform scars (AMD-4). Previously, we found no association between AMD and ocular exposure to either UV-B (290 to 320 nm) or two bands of UV-A (320 to 340 nm and 340 to 400 nm). We have undertaken further analysis to determine whether ocular exposure to violet light (400 to 450 nm), blue light (400 to 500 nm), or all visible light (400 to 700 nm) was associated with AMD. Ocular exposure was estimated using model computations of ambient irradiance and estimates of the ratio of ocular to ambient exposure. Compared to age-matched controls, established cases (AMD-4), but not milder cases, had significantly higher exposure to both blue and visible light over the preceding 20 years (Wilcoxon sign rank test, P = 0.027). There was no difference in exposure at younger ages. These data suggest that high levels of exposure to blue and visible light late in life may be important in causing AMD.

摘要

阳光照射被认为是年龄相关性黄斑变性(AMD)的一个病因。为了对此进行研究,我们收集了838名在切萨皮克湾工作的渔民详细的眼部阳光照射史。通过立体黄斑照片评估AMD的存在及严重程度。黄斑变化被分为四个严重程度递增的等级,从存在5个或更多的玻璃膜疣(AMD-1)到广泛的地图状萎缩或盘状瘢痕(AMD-4)。此前,我们发现AMD与眼部暴露于紫外线B(290至320纳米)或两个紫外线A波段(320至340纳米和340至400纳米)之间没有关联。我们进一步进行了分析,以确定眼部暴露于紫光(400至450纳米)、蓝光(400至500纳米)或所有可见光(400至700纳米)是否与AMD有关。眼部暴露量通过环境辐照度的模型计算以及眼部与环境暴露比率的估计值来估算。与年龄匹配的对照组相比,确诊病例(AMD-4),而非病情较轻的病例,在过去20年中蓝光和可见光的暴露量显著更高(Wilcoxon符号秩检验,P = 0.027)。年轻时的暴露量没有差异。这些数据表明,晚年高水平暴露于蓝光和可见光可能在AMD的发病中起重要作用。