在分析基因与体力活动的相互作用时,从极端暴露中选择个体的前景。

IF 1.1 4区 生物学 Q4 GENETICS & HEREDITY
Human Heredity Pub Date : 2018-01-01 Epub Date: 2019-06-05 DOI:10.1159/000499711
Oyomoare L Osazuwa-Peters, Karen Schwander, R J Waken, Lisa de las Fuentes, Tuomas O Kilpeläinen, Ruth J F Loos, Susan B Racette, Yun Ju Sung, D C Rao
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引用次数: 0

摘要

背景:以较低的四分位数作为分界点的二分法常用于协调不同研究中的异质性体力活动(PA)测量。然而,这可能会造成分类错误,并阻碍新位点的发现:本研究旨在评估从暴露极值(SIEE)中选择个体作为减少此类误分类的替代方法的性能:方法:针对弗雷明汉心脏研究(Framingham Heart Study)中的收缩压和舒张压,我们利用SIEE和其他两种二分法得出的三个PA变量进行了全基因组关联研究和基因-PA相互作用分析。我们比较了检测到的基因位点数量以及与使用定量 PA 变量发现的基因位点的重叠情况。此外,我们还进行了模拟研究,以评估偏倚、误诊率(FDR)和暴露组中协同/拮抗遗传效应下的功率,以及存在/不存在测量误差的情况:在实证分析中,SIEE 的表现既不是最好的,也不是最差的。在大多数模拟方案中,SIEE 的 FDR 和功率都一直优于其他方案。特别是在以拮抗效应和测量误差为特征的情景中,SIEE 的偏差最小,功率最大:结论:SIEE 的前景似乎仅限于检测具有拮抗效应的位点。结论:SIEE 的前景似乎仅限于检测具有拮抗效应的位点,要评估 SIEE 的全部优势还需要进一步的研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions.

The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions.

The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions.

The Promise of Selecting Individuals from the Extremes of Exposure in the Analysis of Gene-Physical Activity Interactions.

Background: Dichotomization using the lower quartile as cutoff is commonly used for harmonizing heterogeneous physical activity (PA) measures across studies. However, this may create misclassification and hinder discovery of new loci.

Objectives: This study aimed to evaluate the performance of selecting individuals from the extremes of the exposure (SIEE) as an alternative approach to reduce such misclassification.

Method: For systolic and diastolic blood pressure in the Framingham Heart Study, we performed a genome-wide association study with gene-PA interaction analysis using three PA variables derived by SIEE and two other dichotomization approaches. We compared number of loci detected and overlap with loci found using a quantitative PA variable. In addition, we performed simulation studies to assess bias, false discovery rates (FDR), and power under synergistic/antagonistic genetic effects in exposure groups and in the presence/absence of measurement error.

Results: In the empirical analysis, SIEE's performance was neither the best nor the worst. In most simulation scenarios, SIEE was consistently outperformed in terms of FDR and power. Particularly, in a scenario characterized by antagonistic effects and measurement error, SIEE had the least bias and highest power.

Conclusion: SIEE's promise appears limited to detecting loci with antagonistic effects. Further studies are needed to evaluate SIEE's full advantage.

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来源期刊
Human Heredity
Human Heredity 生物-遗传学
CiteScore
2.50
自引率
0.00%
发文量
12
审稿时长
>12 weeks
期刊介绍: Gathering original research reports and short communications from all over the world, ''Human Heredity'' is devoted to methodological and applied research on the genetics of human populations, association and linkage analysis, genetic mechanisms of disease, and new methods for statistical genetics, for example, analysis of rare variants and results from next generation sequencing. The value of this information to many branches of medicine is shown by the number of citations the journal receives in fields ranging from immunology and hematology to epidemiology and public health planning, and the fact that at least 50% of all ''Human Heredity'' papers are still cited more than 8 years after publication (according to ISI Journal Citation Reports). Special issues on methodological topics (such as ‘Consanguinity and Genomics’ in 2014; ‘Analyzing Rare Variants in Complex Diseases’ in 2012) or reviews of advances in particular fields (‘Genetic Diversity in European Populations: Evolutionary Evidence and Medical Implications’ in 2014; ‘Genes and the Environment in Obesity’ in 2013) are published every year. Renowned experts in the field are invited to contribute to these special issues.
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