Jie Li, Cillian Hourican, Pashupati P. Mishra, Binisha H. Mishra, Mika Kähönen, Olli T. Raitakari, Reijo Laaksonen, Mika Ala-Korpela, Liisa Keltikangas-Järvinen, Markus Juonala, Terho Lehtimäki, Jos A. Bosch, Rick Quax
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This dataset\nassesses CVD and depression, along with related risk factors and two omics of\nbiomarkers: metabolites and lipids. Instead of directly correlating CVD-related\nphenotypes and depressive symptoms, we extended the notion of bipartite\nnetworks to create a multipartite network that connects these phenotype and\nsymptom variables to intermediate biological variables. Projecting from these\nintermediate variables results in a weighted multilayer network, where each\nlink between CVD and depression variables is marked by its `layer' (i.e.,\nmetabolome or lipidome). Using this projection method, we identified potential\nmediating biomarkers that connect CVD to depression. These biomarkers thus may\nplay significant roles in the biological pathways of CVD-depression\ncomorbidity. 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引用次数: 0
摘要
心血管疾病(CVD)与抑郁症之间存在着明显的合并症,这种合并症可高度预测不良的临床结果。然而,其潜在的生物学途径仍然难以破解,这可能是由于它与多种机制之间的非线性关联。互信息为分析这种错综复杂的关系提供了一个框架。在这项研究中,我们提出了一种基于互信息相关性的多方投影方法,以构建多层疾病网络。我们将该方法应用于 "芬兰青年研究"(Young Finns Study)的一个波次的横断面数据集。该数据集评估了心血管疾病和抑郁症,以及相关的风险因素和两个全息生物标志物:代谢物和血脂。我们没有直接将心血管疾病相关表型和抑郁症状联系起来,而是扩展了双分型网络的概念,创建了一个多分型网络,将这些表型和症状变量与中间生物变量联系起来。从这些中间变量进行投影,就会产生一个加权多层网络,其中心血管疾病和抑郁症变量之间的每个链接都以其 "层"(即代谢组或脂质组)为标记。利用这种预测方法,我们确定了连接心血管疾病和抑郁症的潜在中介生物标志物。因此,这些生物标志物可能在心血管疾病-抑郁症的生物学路径中发挥重要作用。我们的方法可以推广到任何数量的omics层和疾病表型,提供了一个真正系统级的导致合并症的生物通路概览。
Multilayer Network of Cardiovascular Diseases and Depression via Multipartite Projection
There is a significant comorbidity between cardiovascular diseases (CVD) and
depression that is highly predictive of poor clinical outcome. Yet, its
underlying biological pathways remain challenging to decipher, presumably due
to its non-linear associations across multiple mechanisms. Mutual information
provides a framework to analyze such intricacies. In this study, we proposed a
multipartite projection method based on mutual information correlations to
construct multilayer disease networks. We applied the method to a
cross-sectional dataset from a wave of the Young Finns Study. This dataset
assesses CVD and depression, along with related risk factors and two omics of
biomarkers: metabolites and lipids. Instead of directly correlating CVD-related
phenotypes and depressive symptoms, we extended the notion of bipartite
networks to create a multipartite network that connects these phenotype and
symptom variables to intermediate biological variables. Projecting from these
intermediate variables results in a weighted multilayer network, where each
link between CVD and depression variables is marked by its `layer' (i.e.,
metabolome or lipidome). Using this projection method, we identified potential
mediating biomarkers that connect CVD to depression. These biomarkers thus may
play significant roles in the biological pathways of CVD-depression
comorbidity. Additionally, the projected network highlights sex and BMI as the
most important risk factors, or confounders, associated with the comorbidity.
Our method can generalize to any number of omics layers and disease phenotypes,
offering a truly system-level overview of biological pathways contributing to
comorbidity.