Polygenic hazard score models for the prediction of Alzheimer's free survival using the lasso for Cox's proportional hazards model

IF 1.7 4区 医学 Q3 GENETICS & HEREDITY
Georg Hahn, Dmitry Prokopenko, Julian Hecker, Sharon M. Lutz, Kristina Mullin, Rudolph E. Tanzi, Stacia DeSantis, Christoph Lange
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Abstract

The prediction of the susceptibility of an individual to a certain disease is an important and timely research area. An established technique is to estimate the risk of an individual with the help of an integrated risk model, that is, a polygenic risk score with added epidemiological covariates. However, integrated risk models do not capture any time dependence, and may provide a point estimate of the relative risk with respect to a reference population. The aim of this work is twofold. First, we explore and advocate the idea of predicting the time-dependent hazard and survival (defined as disease-free time) of an individual for the onset of a disease. This provides a practitioner with a much more differentiated view of absolute survival as a function of time. Second, to compute the time-dependent risk of an individual, we use published methodology to fit a Cox's proportional hazard model to data from a genetic SNP study of time to Alzheimer's disease (AD) onset, using the lasso to incorporate further epidemiological variables such as sex, APOE (apolipoprotein E, a genetic risk factor for AD) status, 10 leading principal components, and selected genomic loci. We apply the lasso for Cox's proportional hazards to a data set of 6792 AD patients (composed of 4102 cases and 2690 controls) and 87 covariates. We demonstrate that fitting a lasso model for Cox's proportional hazards allows one to obtain more accurate survival curves than with state-of-the-art (likelihood-based) methods. Moreover, the methodology allows one to obtain personalized survival curves for a patient, thus giving a much more differentiated view of the expected progression of a disease than the view offered by integrated risk models. The runtime to compute personalized survival curves is under a minute for the entire data set of AD patients, thus enabling it to handle datasets with 60,000–100,000 subjects in less than 1 h.

利用考克斯比例危险模型的套索,建立预测阿尔茨海默氏症患者自由生存期的多基因危险评分模型。
预测个人对某种疾病的易感性是一个重要而及时的研究领域。一种成熟的技术是借助综合风险模型来估计个体的风险,即多基因风险评分加上流行病学协变量。然而,综合风险模型无法捕捉任何时间依赖性,只能提供相对于参照人群的相对风险点估算值。这项工作有两个目的。首先,我们探索并倡导预测个体发病时与时间相关的危险性和生存期(定义为无病时间)。这为从业者提供了一个更有区别的绝对生存时间函数。其次,为了计算个体的时间相关风险,我们使用已公布的方法,对阿尔茨海默病(AD)发病时间的遗传 SNP 研究数据拟合 Cox 比例危险模型,并使用套索法纳入更多流行病学变量,如性别、APOE(载脂蛋白 E,AD 的遗传风险因素)状态、10 个主要主成分和选定的基因组位点。我们在一个包含 6792 例 AD 患者(由 4102 例病例和 2690 例对照组成)和 87 个协变量的数据集上应用了 lasso 的 Cox 比例危险度模型。我们证明,与最先进的(基于似然法的)方法相比,拟合 Cox 比例危险度的套索模型可以获得更准确的生存曲线。此外,该方法还能获得患者的个性化生存曲线,因此,与综合风险模型相比,该方法能提供更有区别的疾病预期进展情况。对整个 AD 患者数据集而言,计算个性化生存曲线的运行时间不到一分钟,因此可以在 1 小时内处理 60,000 至 100,000 个受试者的数据集。
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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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