基因表达数据的主成分分析:心房颤动病例

F. Censi, G. Calcagnini, P. Bartolini, A. Giuliani
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引用次数: 1

摘要

心房颤动(AF)是最常见的持续性心律失常。房颤还与广泛的结构、收缩和电生理重构有关,这些重构可以维持房颤本身。了解这些重塑过程的分子事件对于开发新的靶向治疗干预措施至关重要。本文采用以基因表达值为统计单位,以患者为变量的矩阵提取主成分,对永久性房颤患者和对照组的微阵列数据进行分析。这些数据来自美国国立卫生研究院(National Institute of Health)的公共功能基因组数据库(称为Gene Expression Omnibus, GEO)。对记录#GSE2240的数据进行分析,包括右心房心肌(附件)样本。数据涉及两个Affymetrix平台U133A和U133B。从30例接受心脏直视手术或冠状动脉旁路移植术的患者中获得右心房附件。其中,10名患者患有永久性房颤,20名患者没有房颤病史。永久性房颤患者和对照组之间基因表达谱的差异与数据变异性的很小一部分有关。然而,就因子负荷和评分而言,分析如此微小的差异,成功地将患者与对照组区分开来,并提供了与心肌组织和炎症过程相关的AF状况的机制观点。
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Principal component analysis of gene expression data: The case of atrial fibrillation
Atrial fibrillation (AF) is the most common persistent cardiac arrhythmia. AF is also associated with extensive structural, contractile, and electrophysiological remodeling, which can sustain AF itself. The understanding of the molecular events of these remodeling processes is essential for the development of new targeted therapeutic interventions. In this paper microarray data related to permanent AF patients and controls were analyzed using the principal components extracted from a matrix having gene expression values as statistical units and patients as variables. The data were obtained from the public functional genomics data repository of the National Institute of Health (called Gene Expression Omnibus, GEO). Data from record #GSE2240 have been analyzed, consisting of samples of right atrial myocardium (appendage). Data were related to two Affymetrix platforms U133A and U133B. Right atrial appendages were obtained from 30 patients undergoing open heart surgery for valve repair or coronary artery bypass grafting. Of these, 10 patients had permanent AF and 20 patients had no history of AF. The differences in gene expression profiles between permanent AF patients and controls are related to a very small part of the data variability. However, the analysis of such a small difference in terms of factor loadings and scores, succeed in discriminating patients from controls and in offering a mechanistic view relating AF condition to both cardiac muscle organization and inflammatory processes.
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