Age-Related Macular Degeneration and Its Genetic Risk: A Population-based Study.

IF 1.7 4区 医学 Q3 OPHTHALMOLOGY Current Eye Research Pub Date : 2024-08-18 DOI:10.1080/02713683.2024.2388692
Davide Garzone, Mohammed Aslam Imtiaz, Matthias M Mauschitz, N Ahmad Aziz, Frank G Holz, Monique M B Breteler, Robert P Finger
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Abstract

Purpose: Specific genetic factors might serve as markers for risk stratification of AMD progression, but their association with key features of AMD has not been fully elucidated. Thus, we investigated the association between overall and pathway-specific genetic risk scores (GRS) and lead loci (ARMS2, CFH) with AMD stages and features of high-risk nonlate AMD, including reticular pseudodrusen (RPD) and large drusen area (LDA).

Methods: We performed a cross-sectional analysis of data from the Rhineland Study, a population-based study in Bonn, Germany. We included 4016 individuals aged 50 years and older of European descent. GRS and pathway-specific subscores were constructed based on a large genome-wide association study of AMD. Subscores were generated based on gene-pathways associations (complement, extracellular matrix remodeling (ECM) and lipid metabolism). Associations were assessed using logistic and multinomial regression.

Results: The mean age of participants was 63.36 years and 1813 (45.1%) were men. The GRS was positive in 48.1% of individuals and increased, but did not fully overlap, across AMD stages. Pathway-specific subscores increased across AMD stages except for the ECM subscore, which only showed a trend for increasing in late AMD. Increasing overall GRS was associated with RPD and LDA (OR [95%CI] for RPD: 1.70 [1.33-2.15], for LDA: 1.64 [1.29-2.07]) among individuals with AMD. Similarly, higher complement and ECM subscores was associated with RPD, while for LDA, only an association with complement subscore was observed.

Conclusions: In a population-based setting, we confirmed higher genetic risk to be associated with more severe AMD and identified associations with high-risk features of intermediate AMD. Conjoint analyses suggested that high-risk features and late AMD might be differentially associated with genetic architecture in AMD, such as ECM remodeling. Incorporation of genetic information such as GRSs might improve AMD risk prediction strategies.

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老年性黄斑变性及其遗传风险:一项基于人群的研究。
目的:特定遗传因素可作为 AMD 进展风险分层的标记,但它们与 AMD 主要特征的关联尚未完全阐明。因此,我们研究了总体和通路特异性遗传风险评分(GRS)及主导基因位点(ARMS2、CFH)与 AMD 分期及高风险非晚期 AMD 特征(包括网状假皱纹(RPD)和大面积色素沉着(LDA))之间的关联:我们对莱茵兰研究(Rhineland Study)的数据进行了横断面分析。我们纳入了 4016 名 50 岁及以上的欧洲后裔。GRS和通路特异性子分数是根据一项大型AMD全基因组关联研究构建的。子分数是根据基因-途径关联(补体、细胞外基质重塑(ECM)和脂质代谢)生成的。采用逻辑回归和多项式回归对相关性进行了评估:参与者的平均年龄为 63.36 岁,1813 人(45.1%)为男性。48.1%的人的GRS呈阳性,在AMD的各个阶段,GRS均呈上升趋势,但并不完全重合。除 ECM 子分数(仅在 AMD 晚期呈上升趋势)外,各 AMD 阶段的通路特异性子分数均呈上升趋势。在 AMD 患者中,总体 GRS 的增加与 RPD 和 LDA 相关(RPD OR [95%CI]:1.70 [1.33-2.15],LDA:1.64 [1.29-2.07])。同样,较高的补体和 ECM 子分数与 RPD 相关,而对于 LDA,仅观察到与补体子分数相关:结论:在一个基于人群的环境中,我们证实了较高的遗传风险与较严重的 AMD 相关,并确定了与中度 AMD 高风险特征的关联。联合分析表明,高风险特征和晚期 AMD 可能与 AMD 的遗传结构(如 ECM 重塑)有不同的关联。纳入遗传信息(如遗传信息序列)可能会改善AMD风险预测策略。
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来源期刊
Current Eye Research
Current Eye Research 医学-眼科学
CiteScore
4.60
自引率
0.00%
发文量
163
审稿时长
12 months
期刊介绍: The principal aim of Current Eye Research is to provide rapid publication of full papers, short communications and mini-reviews, all high quality. Current Eye Research publishes articles encompassing all the areas of eye research. Subject areas include the following: clinical research, anatomy, physiology, biophysics, biochemistry, pharmacology, developmental biology, microbiology and immunology.
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