Predicting Lung Cancer in Korean Never-Smokers With Polygenic Risk Scores

IF 1.7 4区 医学 Q3 GENETICS & HEREDITY Genetic Epidemiology Pub Date : 2024-09-23 DOI:10.1002/gepi.22586
Juyeon Kim, Young Sik Park, Jin Hee Kim, Yun-Chul Hong, Young-Chul Kim, In-Jae Oh, Sun Ha Jee, Myung-Ju Ahn, Jong-Won Kim, Jae-Joon Yim, Sungho Won
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Abstract

In the last few decades, genome-wide association studies (GWAS) with more than 10,000 subjects have identified several loci associated with lung cancer and these loci have been used to develop novel risk prediction tools for cancer. The present study aimed to establish a lung cancer prediction model for Korean never-smokers using polygenic risk scores (PRSs); PRSs were calculated using a pruning-thresholding-based approach based on 11 genome-wide significant single nucleotide polymorphisms (SNPs). Overall, the odds ratios tended to increase as PRSs were larger, with the odds ratio of the top 5% PRSs being 1.71 (95% confidence interval: 1.31–2.23) using the 40%–60% percentile group as the reference, and the area under the curve (AUC) of the prediction model being of 0.76 (95% confidence interval: 0.747–0.774). The receiver operating characteristic (ROC) curves of the prediction model with and without PRSs as covariates were compared using DeLong's test, and a significant difference was observed. Our results suggest that PRSs can be valuable tools for predicting the risk of lung cancer.

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用多基因风险评分预测韩国从不吸烟者的肺癌发病率
在过去的几十年里,对超过 10,000 名受试者进行的全基因组关联研究(GWAS)发现了多个与肺癌相关的基因位点,这些基因位点已被用于开发新型癌症风险预测工具。本研究旨在利用多基因风险评分(PRSs)为韩国从不吸烟者建立一个肺癌预测模型;PRSs 是基于 11 个全基因组重要的单核苷酸多态性(SNPs),采用剪枝-阈值法计算得出的。总体而言,PRS越大,几率比越大,以40%-60%百分位数组为参照,前5% PRS的几率比为1.71(95%置信区间:1.31-2.23),预测模型的曲线下面积(AUC)为0.76(95%置信区间:0.747-0.774)。使用 DeLong 检验比较了以 PRS 为辅变量和不以 PRS 为辅变量的预测模型的接收器操作特征曲线(ROC),结果发现两者有显著差异。我们的研究结果表明,PRS 是预测肺癌风险的重要工具。
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来源期刊
Genetic Epidemiology
Genetic Epidemiology 医学-公共卫生、环境卫生与职业卫生
CiteScore
4.40
自引率
9.50%
发文量
49
审稿时长
6-12 weeks
期刊介绍: Genetic Epidemiology is a peer-reviewed journal for discussion of research on the genetic causes of the distribution of human traits in families and populations. Emphasis is placed on the relative contribution of genetic and environmental factors to human disease as revealed by genetic, epidemiological, and biologic investigations. Genetic Epidemiology primarily publishes papers in statistical genetics, a research field that is primarily concerned with development of statistical, bioinformatical, and computational models for analyzing genetic data. Incorporation of underlying biology and population genetics into conceptual models is favored. The Journal seeks original articles comprising either applied research or innovative statistical, mathematical, computational, or genomic methodologies that advance studies in genetic epidemiology. Other types of reports are encouraged, such as letters to the editor, topic reviews, and perspectives from other fields of research that will likely enrich the field of genetic epidemiology.
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