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A Comparison of Statistical Methods for the Discovery of Genetic Risk Factors Using Longitudinal Family Study Designs

机译:纵向家族研究设计发现遗传危险因素的统计方法比较

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摘要

The etiology of immune-related diseases or traits is often complex, involving many genetic and environmental factors and their interactions. While methodological approaches focusing on an outcome measured at one time point have succeeded in identifying genetic factors involved in immune-related traits, they fail to capture complex disease mechanisms that fluctuate over time. It is increasingly recognized that longitudinal studies, where an outcome is measured at multiple time points, have great potential to shed light on complex disease mechanisms involving genetic factors. However, longitudinal data require specialized statistical methods, especially in family studies where multiple sources of correlation in the data must be modeled. Using simulated data with known genetic effects, we examined the performance of different analytical methods for investigating associations between genetic factors and longitudinal phenotypes in twin data. The simulations were modeled on data from the Québec Newborn Twin Study, an ongoing population-based longitudinal study of twin births with multiple phenotypes, such as cortisol levels and body mass index, collected multiple times in infancy and early childhood and with sequencing data on immune-related genes and pathways. We compared approaches that we classify as (1) family-based methods applied to summaries of the observations over time, (2) longitudinal-based methods with simplifications of the familial correlation, and (3) Bayesian family-based method with simplifications of the temporal correlation. We found that for estimation of the genetic main and interaction effects, all methods gave estimates close to the true values and had similar power. If heritability estimation is desired, approaches of type (1) also provide heritability estimates close to the true value. Our work shows that the simpler approaches are likely adequate to detect genetic effects; however, interpretation of these effects is more challenging.
机译:免疫相关疾病或特征的病因通常很复杂,涉及许多遗传和环境因素及其相互作用。尽管侧重于某一时间点的结果的方法论方法已经成功地确定了与免疫相关性状有关的遗传因素,但它们未能捕获随时间波动的复杂疾病机制。人们越来越认识到,在多个时间点测量结果的纵向研究具有很大的潜力,可以阐明涉及遗传因素的复杂疾病机制。但是,纵向数据需要专门的统计方法,尤其是在家庭研究中,必须对数据中的多个相关源进行建模。使用具有已知遗传效应的模拟数据,我们研究了调查双胞胎数据中遗传因素与纵向表型之间关联的不同分析方法的性能。模拟是基于魁北克新生儿双胞胎研究的数据而进行的,魁北克新生儿双胞胎是一项正在进行的基于人口的纵向研究,对双胞胎具有多种表型,例如皮质醇水平和体重指数,在婴儿期和幼儿期进行了多次采集,并具有免疫测序数据相关基因和途径。我们比较了归类为(1)随时间推移适用于观察结果摘要的基于家庭的方法,(2)简化了家庭相关性的基于纵向的方法以及(3)简化了家庭关系的基于贝叶斯基于家庭的方法的方法。时间相关。我们发现,对于遗传主链和相互作用效应的估计,所有方法均给出了接近真实值的估计,并且具有相似的功效。如果需要进行遗传力估算,则类型(1)的方法还可以提供接近真实值的遗传力估算值。我们的工作表明,更简单的方法可能足以检测遗传效应。然而,对这些影响的解释更具挑战性。

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