Turku Centre for Biotechnology, University of Turku and Åbo Akademi University, Turku, FI-20520, Finland.
Department of Computer Science, Aalto University School of Science, Aalto, FI-00076, Finland.
Sci Rep. 2018 Apr 12;8(1):5883. doi: 10.1038/s41598-018-24019-5.
Children develop rapidly during the first years of life, and understanding the sources and associated levels of variation in the serum proteome is important when using serum proteins as markers for childhood diseases. The aim of this study was to establish a reference model for the evolution of a healthy serum proteome during early childhood. Label-free quantitative proteomics analyses were performed for 103 longitudinal serum samples collected from 15 children at birth and between the ages of 3-36 months. A flexible Gaussian process-based probabilistic modelling framework was developed to evaluate the effects of different variables, including age, living environment and individual variation, on the longitudinal expression profiles of 266 reliably identified and quantified serum proteins. Age was the most dominant factor influencing approximately half of the studied proteins, and the most prominent age-associated changes were observed already during the first year of life. High inter-individual variability was also observed for multiple proteins. These data provide important details on the maturing serum proteome during early life, and evaluate how patterns detected in cord blood are conserved in the first years of life. Additionally, our novel modelling approach provides a statistical framework to detect associations between covariates and non-linear time series data.
儿童在生命的最初几年中迅速发育,了解血清蛋白质组中变异的来源和相关水平对于将血清蛋白作为儿童疾病的标志物非常重要。本研究旨在建立一个健康的血清蛋白质组在幼儿期的演变参考模型。对从 15 名儿童出生时和 3-36 个月之间收集的 103 个纵向血清样本进行了无标记定量蛋白质组学分析。开发了一种灵活的基于高斯过程的概率建模框架,以评估不同变量(包括年龄、生活环境和个体差异)对 266 种可靠鉴定和定量的血清蛋白的纵向表达谱的影响。年龄是影响大约一半研究蛋白的最主要因素,并且在生命的第一年中就观察到了最明显的与年龄相关的变化。多个蛋白质也表现出高个体间变异性。这些数据提供了关于生命早期成熟的血清蛋白质组的重要细节,并评估了在脐带血中检测到的模式如何在生命的最初几年中得以保留。此外,我们的新建模方法提供了一个统计框架,用于检测协变量和非线性时间序列数据之间的关联。