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正常眼压性青光眼的多基因风险预测

Polygenic Risk Prediction for Normal-Tension Glaucoma.

作者信息

Marzban Maryam, Diaz Torres Santiago, Yu Regina, He Weixiong, Mackey David A, Segrè Ayellet V, Wiggs Janey, MacGregor Stuart, Gharahkhani Puya

机构信息

QIMR Berghofer Medical Research Institute, Brisbane, Queensland, Australia.

The University of Western Australia, Centre for Ophthalmology and Visual Science, Perth, Western Australia, Australia.

出版信息

Invest Ophthalmol Vis Sci. 2025 Jul 1;66(9):4. doi: 10.1167/iovs.66.9.4.

Abstract

PURPOSE

Normal-tension glaucoma (NTG) is a subtype of glaucoma characterized by optic nerve damage in the setting of normal intraocular pressure. Polygenic risk scores (PRSs) have shown potential to assist with risk prediction in glaucoma, but to date no comprehensive studies have evaluated the predictive ability of PRSs for NTG.

METHODS

We utilized genome-wide association study (GWAS) summary data for NTG from a European cohort to estimate the variant weights and construct PRSs. The PRSs were computed using both the SBayesRC and clumping and thresholding (C+T) methods in 317 European ancestry NTG cases and 634 controls from the National Institutes of Health All of Us dataset. To validate our findings, we used the Genetics of Glaucoma (GOG) dataset for NTG cases (n = 89) and the QSkin Sun and Health Study (QSkin) dataset for controls (n = 267).

RESULTS

We applied the SBayesRC method, which incorporates genome functional annotation, to compare results across both studies. Logistic regression was performed to assess the association between PRSs and NTG. SBayesRC analysis demonstrated that the NTG PRS was significantly associated with NTG, yielding an odds ratio per standard deviation of 1.53 (95% confidence interval [CI], 1.32-1.77; P = 6.86 × 10⁻9) in the All of Us dataset and 1.83 (95% CI, 1.42-2.38; P = 4.01 × 10⁻6) in the combined GOG and QSkin dataset. The C+T method produced results similar to those for SBayesRC.

CONCLUSIONS

Despite the limited sample size of current NTG GWASs, our findings suggest that NTG-specific PRSs hold promise for risk prediction. Future large-scale GWASs for NTG may enable the development of clinically relevant PRSs, improving early detection and personalized risk assessment for this challenging phenotype.

摘要

目的

正常眼压性青光眼(NTG)是青光眼的一种亚型,其特征是在眼压正常的情况下发生视神经损伤。多基因风险评分(PRSs)已显示出有助于青光眼风险预测的潜力,但迄今为止,尚无全面研究评估PRSs对NTG的预测能力。

方法

我们利用来自欧洲队列的NTG全基因组关联研究(GWAS)汇总数据来估计变异权重并构建PRSs。在来自美国国立卫生研究院“我们所有人”数据集的317例欧洲血统NTG病例和634例对照中,使用SBayesRC和聚类与阈值设定(C+T)方法计算PRSs。为验证我们的发现,我们将青光眼遗传学(GOG)数据集用于NTG病例(n = 89),将QSkin阳光与健康研究(QSkin)数据集用于对照(n = 267)。

结果

我们应用纳入基因组功能注释的SBayesRC方法来比较两项研究的结果。进行逻辑回归以评估PRSs与NTG之间的关联。SBayesRC分析表明,NTG PRS与NTG显著相关,在“我们所有人”数据集中,每标准差的优势比为1.53(95%置信区间[CI],1.32 - 1.77;P = 6.86×10⁻⁹),在合并的GOG和QSkin数据集中为1.83(95%CI,1.42 - 2.38;P = 4.01×10⁻⁶)。C+T方法产生的结果与SBayesRC的结果相似。

结论

尽管当前NTG的GWAS样本量有限,但我们的发现表明,NTG特异性PRSs在风险预测方面具有前景。未来针对NTG的大规模GWAS可能会促成具有临床相关性的PRSs的开发,改善对这一具有挑战性表型的早期检测和个性化风险评估。

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