Developing and validating a comprehensive polygenic risk score to enhance keratoconus risk prediction.

IF 3.1 2区 生物学 Q3 BIOCHEMISTRY & MOLECULAR BIOLOGY Human molecular genetics Pub Date : 2024-11-13 DOI:10.1093/hmg/ddae157
Weixiong He, Urmo Võsa, Teele Palumaa, Jue-Sheng Ong, Santiago Diaz Torres, Alex W Hewitt, David A Mackey, Puya Gharahkhani, Tõnu Esko, Stuart MacGregor
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Abstract

Purpose: This study aimed to develop and validate a comprehensive polygenic risk score (PRS) for keratoconus, enhancing the predictive accuracy for identifying individuals at increased risk, which is crucial for preventing keratoconus-associated visual impairment such as post-Laser-assisted in situ keratomileusis (LASIK) ectasia.

Methods: We applied a multi-trait analysis approach (MTAG) to genome-wide association study data on keratoconus and quantitative keratoconus-related traits and used this to construct PRS models for keratoconus risk using several PRS methodologies. We evaluated the predictive performance of the PRSs in two biobanks: Estonian Biobank (EstBB; 375 keratoconus cases and 17 902 controls) and UK Biobank (UKB: 34 keratoconus cases and 1000 controls). Scores were compared using the area under the curve (AUC) and odds ratios (ORs) for various PRS models.

Results: The PRS models demonstrated significant predictive capabilities in EstBB, with the SBayesRC model achieving the highest OR of 2.28 per standard deviation increase in PRS, with a model containing age, sex and PRS showing good predictive accuracy (AUC = 0.72). In UKB, we found that adding the best-performing PRS to a model containing corneal measurements increased the AUC from 0.84 to 0.88 (P = 0.012 for difference), with an OR of 4.26 per standard deviation increase in the PRS. These models showed improved predictive capability compared to previous keratoconus PRS.

Conclusion: The PRS models enhanced prediction of keratoconus risk, even with corneal measurements, showing potential for clinical use to identify individuals at high risk of keratoconus, and potentially help reduce the risk of post-LASIK ectasia.

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开发并验证综合多基因风险评分,加强角膜病风险预测。
目的:本研究旨在开发和验证角膜病的综合多基因风险评分(PRS),提高识别风险增加个体的预测准确性,这对于预防激光辅助原位角膜磨镶术(LASIK)后异位症等角膜病相关视力损伤至关重要:我们将多性状分析方法(MTAG)应用于有关角膜病和角膜病相关定量性状的全基因组关联研究数据,并使用几种 PRS 方法构建了角膜病风险 PRS 模型。我们在两个生物库中评估了 PRS 的预测性能:爱沙尼亚生物库(EstBB;375 例角膜病病例和 17902 例对照)和英国生物库(UKB:34 例角膜病病例和 1000 例对照)。使用各种 PRS 模型的曲线下面积(AUC)和几率比(ORs)对得分进行比较:PRS模型在EstBB中表现出了显著的预测能力,其中SBayesRC模型的OR值最高,PRS每增加一个标准差,OR值就增加2.28,而包含年龄、性别和PRS的模型则表现出了良好的预测准确性(AUC = 0.72)。在 UKB 中,我们发现将表现最好的 PRS 添加到包含角膜测量值的模型中,可将 AUC 从 0.84 提高到 0.88(差异 P = 0.012),PRS 每增加一个标准差的 OR 为 4.26。与之前的角膜塑形镜 PRS 相比,这些模型显示出更强的预测能力:PRS模型提高了对角膜病风险的预测能力,即使角膜测量结果也是如此,显示了临床应用于识别角膜病高风险人群的潜力,并有可能帮助降低LASIK术后异位的风险。
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来源期刊
Human molecular genetics
Human molecular genetics 生物-生化与分子生物学
CiteScore
6.90
自引率
2.90%
发文量
294
审稿时长
2-4 weeks
期刊介绍: Human Molecular Genetics concentrates on full-length research papers covering a wide range of topics in all aspects of human molecular genetics. These include: the molecular basis of human genetic disease developmental genetics cancer genetics neurogenetics chromosome and genome structure and function therapy of genetic disease stem cells in human genetic disease and therapy, including the application of iPS cells genome-wide association studies mouse and other models of human diseases functional genomics computational genomics In addition, the journal also publishes research on other model systems for the analysis of genes, especially when there is an obvious relevance to human genetics.
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