Department of Ecology and Evolutionary Biology, University of Arizona, Tucson.
Departments of Pathology and Biology, University of Washington, Seattle.
J Gerontol A Biol Sci Med Sci. 2020 Feb 14;75(3):466-472. doi: 10.1093/gerona/glz174.
Biomarkers are important tools for diagnosis, prognosis, and identification of the causal factors of physiological conditions. Biomarkers are typically identified by correlating biological measurements with the status of a condition in a sample of subjects. Cross-sectional studies sample subjects at a single timepoint, whereas longitudinal studies follow a cohort through time. Identifying biomarkers of aging is subject to unique challenges. Individuals who age faster have intrinsically higher mortality rates and so are preferentially lost over time, in a phenomenon known as cohort selection. In this article, we use simulations to show that cohort selection biases cross-sectional analysis away from identifying causal loci of aging, to the point where cross-sectional studies are less likely to identify loci that cause aging than if loci had been chosen at random. We go on to show this bias can be corrected by incorporating correlates of mortality identified from longitudinal studies, allowing cross-sectional studies to effectively identify the causal factors of aging.
生物标志物是诊断、预后和确定生理状况因果因素的重要工具。生物标志物通常通过将生物学测量与样本中某一状况的状态相关联来确定。横断面研究在单个时间点采集样本,而纵向研究则随着时间推移跟踪一个队列。确定衰老的生物标志物面临独特的挑战。衰老速度较快的个体固有死亡率较高,因此随着时间的推移,它们会被优先淘汰,这一现象称为队列选择。在本文中,我们使用模拟表明,队列选择会使横断面分析偏离衰老因果基因座的识别,以至于横断面研究识别导致衰老的基因座的可能性甚至低于随机选择基因座。我们进一步表明,通过纳入纵向研究中确定的死亡率相关因素,可以纠正这种偏差,使横断面研究能够有效地识别衰老的因果因素。