Quantification of Drusen in Macular Degeneration
黄斑变性中玻璃膜疣的量化
基本信息
- 批准号:6420119
- 负责人:
- 金额:$ 14.97万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2002
- 资助国家:美国
- 起止时间:2002-02-01 至 2004-01-31
- 项目状态:已结题
- 来源:
- 关键词:angiogenesis biomarker cataract clinical research computer program /software digital imaging disease /disorder proneness /risk eye disorder diagnosis eye fundus photography eye laser surgery human data longitudinal human study macular degeneration macular drusen nutrition pathologic process photocoagulation therapy vitamins
项目摘要
DESCRIPTION: (Applicant's Abstract) Age-related macular degeneration (AMD) is
the most common cause of blindness in the United Sates in Americans over the
age of 50. Drusen are by-products of rod and cone metabolism and their presence
in the ocular fundus is a clinical sign of AMD. It is known that patients whose
eyes harbor drusen are at special risk of visual loss from AMD. In a
prospective, multi-centered trial, the Age-Related Eye Disease Study (AREDS),
some 5000 patients have been enrolled and followed at six-month intervals to
determine risk factors for AMD as well as to measure the influence of certain
multivitamins and micronutrients on the progression of macular degeneration and
cataract. In another prospective, randomized, controlled trial, the
Prophylactic Treatment of AMD Trial (PTAMD), patients with multiple large
drusen have been enrolled to determine whether a minimal laser treatment
applied one time provides any benefit with respect to lowering rates of visual
loss and rates of development of choroidal neovascularization (CNVM). During
the PTAMD and AREDS trials, photographs of the fundi of each participant have
been taken at least annually in the form of Ektachrome color slides. These
slides are evaluated by human readers in a Reading Center and the extent of the
drusen is categorized accordingly.
The applicant proposes to perform a quantitative analysis on the color slides
of the macula of all patients who have been enrolled into the PTAMD and AREDS
trials at the Pittsburgh site, as well as other patients who have AMD and have
been followed similarly for a minimum of three years. The original slides will
be digitized onto CD disks for permanent archiving, and will be analyzed using
a specially-written computer algorithm which semi-automatically detects drusen
in digital images. Once detected, quantitative measurements of the area of
drusen extent and size of each drusen are generated for each image. This method
is more precise than characterizing drusen using traditional long and more
subjective protocols, and may be valuable in determining the risks of a given
patient developing choroidal neovascularization and visual loss before such
events occur. That is, such continuous quantitative data may, when analyzed,
provide a more accurate and sensitive assessment of risk compared to
conventional measurement techniques.
描述:(申请人的摘要)视网膜相关性黄斑变性(AMD)是
美国最常见的致盲原因是
50岁玻璃疣是视杆细胞和视锥细胞代谢的副产物,
是AMD的临床体征。据了解,
患有玻璃疣的眼睛有因AMD而导致视力丧失的特殊风险。中
前瞻性、多中心试验,眼动相关眼病研究(AREDS),
大约5000名患者被招募,并每隔6个月进行一次随访,
确定AMD的风险因素,以及测量某些因素的影响,
多种维生素和微量营养素对黄斑变性进展的影响,
白内障在另一项前瞻性随机对照试验中,
预防性治疗AMD试验(PTAMD),多个大的
玻璃疣已经登记,以确定是否有最小的激光治疗,
施用一次提供了关于降低视觉损害率的任何益处。
脉络膜新生血管(CNVM)的损失和发展速率。期间
在PTAMD和AREDS试验中,每个参与者的眼底照片
至少每年以Ektachrome彩色幻灯片的形式拍摄。这些
幻灯片由人类读者在阅读中心评估,
玻璃疣被相应地分类。
申请人建议对彩色载玻片进行定量分析
所有入组PTAMD和AREDS的患者的黄斑
在匹兹堡的试验,以及其他患有AMD的患者,
至少三年的类似跟踪。原始幻灯片将
数字化到CD盘上永久存档,并将使用
一种专门编写的计算机算法,
在数字图像中。一旦被检测到,
为每个图像生成每个玻璃疣的玻璃疣程度和大小。该方法
比使用传统的长时间和更长的时间来表征玻璃疣更精确,
主观协议,并可能是有价值的,在确定风险的给定
患者在此之前发生脉络膜新生血管和视力丧失
事件发生。也就是说,当分析时,
提供更准确和敏感的风险评估,
传统测量技术。
项目成果
期刊论文数量(0)
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科研奖励数量(0)
会议论文数量(0)
专利数量(0)
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THOMAS R FRIBERG其他文献
THOMAS R FRIBERG的其他文献
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{{ truncateString('THOMAS R FRIBERG', 18)}}的其他基金
Quantification of Drusen in Macular Degeneration
黄斑变性中玻璃膜疣的量化
- 批准号:
6620653 - 财政年份:2002
- 资助金额:
$ 14.97万 - 项目类别:
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