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首页> 外文期刊>Journal of biomedical informatics. >Data driven linear algebraic methods for analysis of molecular pathways: Application to disease progression in shock/trauma
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Data driven linear algebraic methods for analysis of molecular pathways: Application to disease progression in shock/trauma

机译:数据驱动的线性代数方法分析分子途径:在休克/创伤疾病进展中的应用

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Motivation: Although trauma is the leading cause of death for those below 45. years of age, there is a dearth of information about the temporal behavior of the underlying biological mechanisms in those who survive the initial trauma only to later suffer from syndromes such as multiple organ failure. Levels of serum cytokines potentially affect the clinical outcomes of trauma; understanding how cytokine levels modulate intra-cellular signaling pathways can yield insights into molecular mechanisms of disease progression and help to identify targeted therapies. However, developing such analyses is challenging since it necessitates the integration and interpretation of large amounts of heterogeneous, quantitative and qualitative data. Here we present the Pathway Semantics Algorithm (PSA), an algebraic process of node and edge analyses of evoked biological pathways over time for in silico discovery of biomedical hypotheses, using data from a prospective controlled clinical study of the role of cytokines in multiple organ failure (MOF) at a major US trauma center. A matrix algebra approach was used in both the PSA node and PSA edge analyses with different matrix configurations and computations based on the biomedical questions to be examined. In the edge analysis, a percentage measure of crosstalk called XTALK was also developed to assess cross-pathway interference. Results: In the node/molecular analysis of the first 24. h from trauma, PSA uncovered seven molecules evoked computationally that differentiated outcomes of MOF or non-MOF (NMOF), of which three molecules had not been previously associated with any shock/trauma syndrome. In the edge/molecular interaction analysis, PSA examined four categories of functional molecular interaction relationships - activation, expression, inhibition, and transcription - and found that the interaction patterns and crosstalk changed over time and outcome. The PSA edge analysis suggests that a diagnosis, prognosis or therapy based on molecular interaction mechanisms may be most effective within a certain time period and for a specific functional relationship.
机译:动机:尽管对于45岁以下的人来说,创伤是主要的死亡原因,但对于那些在最初的创伤中幸存下来,后来又患有多种疾病的人而言,缺乏有关潜在生物学机制的暂时性行为的信息不足器官衰竭。血清细胞因子水平可能影响创伤的临床结果;了解细胞因子水平如何调节细胞内信号通路可以深入了解疾病进展的分子机制,并有助于确定靶向疗法。但是,由于需要对大量异类,定量和定性数据进行整合和解释,因此开展此类分析具有挑战性。在这里,我们使用来自细胞因子在多器官衰竭中作用的前瞻性对照临床研究的数据,介绍了路径语义算法(PSA),它是随着时间的推移在计算机上发现生物医学假设的节点和边缘分析诱发生物路径的代数过程。 (MOF)在美国一家主要的创伤中心。基于要检查的生物医学问题,在PSA节点和PSA边缘分析中都使用了矩阵代数方法,具有不同的矩阵配置和计算。在边缘分析中,还开发了一种称为XTALK的串扰百分比度量来评估交叉路径干扰。结果:在创伤后头24小时的节点/分子分析中,PSA发现了7个分子,这些分子在计算上引起了MOF或非MOF(NMOF)的不同结局,其中三个分子以前未曾与任何电击/创伤相关综合症。在边缘/分子相互作用分析中,PSA检查了四类功能性分子相互作用关系-激活,表达,抑制和转录-并发现相互作用模式和串扰随时间和结果而变化。 PSA边缘分析表明,基于分子相互作用机制的诊断,预后或疗法在特定时间段内和特定功能关系上可能最有效。

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