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遗传眼病风险评估(GRADE):前瞻性评估多基因风险评分预测青光眼和年龄相关性黄斑变性诊断的研究方案。

Genetic Risk Assessment of Degenerative Eye Disease (GRADE): study protocol of a prospective assessment of polygenic risk scores to predict diagnosis of glaucoma and age-related macular degeneration.

机构信息

Department of Ophthalmology, Flinders University, 1 Flinders Drive, 5042, Bedford Park, SA, Australia.

QIMR Berghofer Medical Research Institute, 4006, Herston, QLD, Australia.

出版信息

BMC Ophthalmol. 2023 Oct 24;23(1):431. doi: 10.1186/s12886-023-03143-5.

Abstract

BACKGROUND

Glaucoma and age-related macular degeneration (AMD) account for a substantial portion of global blindness. Both conditions are highly heritable, with recognised monogenic and polygenic inheritance patterns. Current screening guidelines lack decisive recommendations. Polygenic risk scores (PRS) allow for cost-effective broad population risk stratification for these conditions. The predictive potential of PRS could facilitate earlier diagnosis and treatment, and prevent unnecessary vision loss.

METHODS

The Genetic Risk Assessment of Degenerative Eye disease (GRADE) study is a prospective study designed to generate high-quality evidence about the feasibility of PRS to stratify individuals from the general population, enabling identification of those at highest risk of developing glaucoma or AMD. The targeted recruitment is 1000 individuals aged over 50 years, from which blood or saliva samples will be used for genotyping and an individual PRS for glaucoma and AMD will be derived. Individuals with PRS values in the bottom decile (n = 100), top decile (n = 100) and middle 80% (n = 100) for both glaucoma and AMD will undergo a detailed eye examination for glaucoma and/or AMD.

DISCUSSION

The primary objective will be to compare the prevalence of glaucoma and AMD cases between low, intermediate, and high PRS risk groups. We expect to find a higher prevalence of both diseases in the high PRS risk group, as compared to the middle and low risk groups. This prospective study will assess the clinical validity of a PRS for glaucoma and AMD in the general Australian population. Positive findings will support the implementation of PRS into clinical practice.

摘要

背景

青光眼和年龄相关性黄斑变性(AMD)占全球失明的很大一部分。这两种疾病都具有很强的遗传性,存在公认的单基因和多基因遗传模式。目前的筛查指南缺乏明确的建议。多基因风险评分(PRS)允许对这些疾病进行具有成本效益的广泛人群风险分层。PRS 的预测潜力可以促进早期诊断和治疗,并防止不必要的视力丧失。

方法

遗传性眼病风险评估(GRADE)研究是一项前瞻性研究,旨在生成关于 PRS 对来自普通人群的个体进行分层的可行性的高质量证据,从而识别出最有可能患上青光眼或 AMD 的个体。目标招募人数为 1000 名 50 岁以上的个体,从中采集血液或唾液样本进行基因分型,并得出青光眼和 AMD 的个体 PRS。PRS 值处于最低十分位数(n=100)、最高十分位数(n=100)和中间 80%(n=100)的个体将接受青光眼和/或 AMD 的详细眼部检查。

讨论

主要目标将是比较低、中、高 PRS 风险组中青光眼和 AMD 病例的患病率。我们预计高 PRS 风险组的两种疾病患病率都较高,与中低风险组相比。这项前瞻性研究将评估 PRS 对澳大利亚普通人群中青光眼和 AMD 的临床有效性。阳性发现将支持将 PRS 纳入临床实践。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6369/10594830/32aa8abd9008/12886_2023_3143_Figa_HTML.jpg

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