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Retina/RPE genes altered in aging as candidates for AMD

Retina/RPE genes altered in aging as candidates for AMD
视网膜/RPE 基因在衰老过程中发生改变,成为 AMD 的候选基因
批准号:
6626120
负责人:
SEPIDEH ZAREPARSI
金额:
$4.81万
依托单位国家:
美国
项目类别:
财政年份:
2002
资助国家:
美国
项目状态:
未结题
起止时间:
2002-03-19 至

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中文摘要
翻译
描述(由申请人提供):年龄相关性黄斑变性(AMD)是
英文摘要
DESCRIPTION (provided by applicant): Age-related macular degeneration (AMD) is the leading cause of irreversible vision loss among the elderly. The etiology of AMD is complex and appears to involve both a genetic and an environmental component. The specific cause(s) of AMD are not known. Advancing age is perhaps the most important risk factor. Thus it is essential to understand how age-related changes in the retina, retinal pigment epithelium (RPE) and Bruch's membrane predispose some individuals to subsequent development of AMD. Several cellular pathways are likely involved in the pathobiology of AMD. Two pathways that have specifically been suggested to play a role in AMD pathogenesis are: oxidative stress and lipid/cholesterol metabolism. The goal of this proposal is to identify candidate genes and examine their contribution to AMD susceptibility. The hypotheses of this study are a) aging of the retina and the RPE is characterized by changes in gene expression, and b) genes whose expression levels are altered during aging may include genes that specifically contribute to AMD susceptibility. The specific aims are: 1) To examine gene expression profiles in human retina and RPE during aging. Expression profiles will be compared between young adults and elderly controls. In particular, age-related changes in expression of genes involved in response to oxidative stress and lipid/cholesterol metabolism will be analyzed. 2) To identify candidate genes and examine their contribution to AMD. Associations between AMD susceptibility and genes, whose expression levels were found to change consistently during aging, will be explored in 641 AMD patients and 112 controls.
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Retina/RPE genes altered in aging as candidates for AMD
Retina/RPE genes altered in aging as candidates for AMD
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