Gao X Raymond, Huang Hua, Kim Heejin
Department of Ophthalmology and Visual Sciences, University of Illinois at Chicago, Chicago, IL, USA.
Departments of Ophthalmology and Visual Science and Biomedical Informatics, Division of Human Genetics, The Ohio State University, Columbus, OH, USA.
Transl Vis Sci Technol. 2019 Apr 4;8(2):10. doi: 10.1167/tvst.8.2.10. eCollection 2019 Apr.
Elevated intraocular pressure (IOP) is an important risk factor for glaucoma. We constructed polygenic risk scores (PRSs) for IOP using the UK Biobank (UKB) data set to test whether the PRSs are associated with IOP and whether using them improves glaucoma prediction.
We conducted this study using 435,678 European participants from the UKB. We constructed weighted and unweighted PRSs using single nucleotide polymorphisms (SNPs) derived from the UKB data and previously reported IOP SNPs. We examined the associations of the PRSs with IOP and primary open-angle glaucoma (POAG) using linear and logistic regression, respectively. To quantify the discriminatory ability of the PRSs on POAG, we used the area under the receiver operating characteristic curve (AUC).
The weighted PRS was significantly associated with IOP ( ∼ 10), after adjusting for age and sex. The PRS explained an additional 4% of variance in IOP. The weighted PRS was also significantly associated with POAG ( = 1.8 × 10). Subjects in the top quintile of the IOP PRS were 6.34 (95% confidence interval [CI]: 4.82-8.33; = 2.1 × 10) times more likely to have POAG, compared to those in the bottom category. The weighted PRS improved the discriminatory power for POAG (AUC increased by 5%, = 6.2 × 10) when added to the other covariates. The unweighted PRS exhibited similar results.
We determined that IOP PRSs are significantly associated with IOP and improve the prediction of POAG.
PRSs help reduce the burden of glaucoma by early detection of genetically susceptible individuals.
眼压升高是青光眼的一个重要危险因素。我们利用英国生物银行(UKB)数据集构建了眼压的多基因风险评分(PRSs),以测试PRSs是否与眼压相关,以及使用它们是否能改善青光眼预测。
我们使用来自UKB的435,678名欧洲参与者进行了这项研究。我们使用从UKB数据中得出的单核苷酸多态性(SNPs)和先前报道的眼压SNPs构建了加权和未加权的PRSs。我们分别使用线性回归和逻辑回归研究了PRSs与眼压和原发性开角型青光眼(POAG)的关联。为了量化PRSs对POAG的鉴别能力,我们使用了受试者工作特征曲线下面积(AUC)。
在调整年龄和性别后,加权PRS与眼压显著相关(~10)。PRS解释了眼压额外4%的方差。加权PRS也与POAG显著相关(=1.8×10)。与最低类别相比,眼压PRS最高五分位数的受试者患POAG的可能性高6.34倍(95%置信区间[CI]:4.82 - 8.33;=2.1×10)。当添加到其他协变量中时,加权PRS提高了对POAG的鉴别能力(AUC增加了5%,=6.2×10)。未加权的PRS也表现出类似的结果。
我们确定眼压PRSs与眼压显著相关,并改善了POAG的预测。
PRSs有助于通过早期检测遗传易感个体来减轻青光眼负担。