首页> 美国卫生研究院文献>Cell Stress Chaperones >Data mining-based statistical analysis of biological data uncovers hidden significance: clustering Hashimoto’s thyroiditis patients based on the response of their PBMC with IL-2 and IFN-γ secretion to stimulation with Hsp60
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Data mining-based statistical analysis of biological data uncovers hidden significance: clustering Hashimoto’s thyroiditis patients based on the response of their PBMC with IL-2 and IFN-γ secretion to stimulation with Hsp60

机译:基于数据挖掘的生物数据统计分析发现了隐藏的意义:基于桥本甲状腺炎患者的IL-2和IFN-γ分泌的PBMC对Hsp60刺激的反应将其聚类

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摘要

The pathogenesis of Hashimoto’s thyroiditis includes autoimmunity involving thyroid antigens, autoantibodies, and possibly cytokines. It is unclear what role plays Hsp60, but our recent data indicate that it may contribute to pathogenesis as an autoantigen. Its role in the induction of cytokine production, pro- or anti-inflammatory, was not elucidated, except that we found that peripheral blood mononucleated cells (PBMC) from patients or from healthy controls did not respond with cytokine production upon stimulation by Hsp60 in vitro with patterns that would differentiate patients from controls with statistical significance. This “negative” outcome appeared when the data were pooled and analyzed with conventional statistical methods. We re-analyzed our data with non-conventional statistical methods based on data mining using the classification and regression tree learning algorithm and clustering methodology. The results indicate that by focusing on IFN-γ and IL-2 levels before and after Hsp60 stimulation of PBMC in each patient, it is possible to differentiate patients from controls. A major general conclusion is that when trying to identify disease markers such as levels of cytokines and Hsp60, reference to standards obtained from pooled data from many patients may be misleading. The chosen biomarker, e.g., production of IFN-γ and IL-2 by PBMC upon stimulation with Hsp60, must be assessed before and after stimulation and the results compared within each patient and analyzed with conventional and data mining statistical methods.
机译:桥本甲状腺炎的发病机制包括涉及甲状腺抗原,自身抗体和可能的细胞因子的自身免疫。尚不清楚Hsp60发挥什么作用,但我们最近的数据表明它可能作为自身抗原促成发病机理。没有阐明其在诱导细胞因子产生(促炎或抗炎)中的作用,除了我们发现患者或健康对照组的外周血单核细胞(PBMC)在体外受Hsp60刺激后对细胞因子产生没有反应具有可以将患者与具有统计学意义的对照区分开的模式。当对数据进行汇总并使用常规统计方法进行分析时,就会出现这种“负面”结果。我们使用分类和回归树学习算法以及聚类方法,基于基于数据挖掘的非常规统计方法对数据进行了重新分析。结果表明,通过关注每个患者中Hsp60刺激PBMC之前和之后的IFN-γ和IL-2水平,可以将患者与对照组区分开。一个主要的一般性结论是,当试图确定疾病标志物(例如细胞因子和Hsp60的水平)时,参考从许多患者的汇总数据中获得的标准可能会产生误导。在刺激前后,必须评估所选的生物标志物,例如,PBMC在受Hsp60刺激后由PBMC产生的IFN-γ和IL-2,并在每个患者中比较结果,并用常规和数据挖掘统计方法进行分析。

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