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一种探索生物状态差异的差异网络方法:在糖尿病前期中的应用。

A differential network approach to exploring differences between biological states: an application to prediabetes.

机构信息

Epidemiology and Biostatistics, Imperial College London, London, United Kingdom.

出版信息

PLoS One. 2011;6(9):e24702. doi: 10.1371/journal.pone.0024702. Epub 2011 Sep 27.

Abstract

BACKGROUND

Variations in the pattern of molecular associations are observed during disease development. The comprehensive analysis of molecular association patterns and their changes in relation to different physiological conditions can yield insight into the biological basis of disease-specific phenotype variation.

METHODOLOGY

Here, we introduce a formal statistical method for the differential analysis of molecular associations via network representation. We illustrate our approach with extensive data on lipoprotein subclasses measured by NMR spectroscopy in 4,406 individuals with normal fasting glucose, and 531 subjects with impaired fasting glucose (prediabetes). We estimate the pair-wise association between measures using shrinkage estimates of partial correlations and build the differential network based on this measure of association. We explore the topological properties of the inferred network to gain insight into important metabolic differences between individuals with normal fasting glucose and prediabetes.

CONCLUSIONS/SIGNIFICANCE: Differential networks provide new insights characterizing differences in biological states. Based on conventional statistical methods, few differences in concentration levels of lipoprotein subclasses were found between individuals with normal fasting glucose and individuals with prediabetes. By performing the differential analysis of networks, several characteristic changes in lipoprotein metabolism known to be related to diabetic dyslipidemias were identified. The results demonstrate the applicability of the new approach to identify key molecular changes inaccessible to standard approaches.

摘要

背景

在疾病发展过程中观察到分子关联模式的变化。全面分析分子关联模式及其与不同生理状态的变化,可以深入了解疾病特异性表型变异的生物学基础。

方法

在这里,我们引入了一种通过网络表示形式对分子关联进行差异分析的正式统计方法。我们用通过 NMR 光谱测量的 4406 名空腹血糖正常和 531 名空腹血糖受损(糖尿病前期)个体的脂蛋白亚类的广泛数据来说明我们的方法。我们使用偏相关的收缩估计来估计措施之间的成对关联,并基于该关联度量构建差异网络。我们探索推断网络的拓扑性质,以深入了解空腹血糖正常和糖尿病前期个体之间重要的代谢差异。

结论/意义:差异网络提供了新的见解,可用于描述生物状态的差异。基于传统的统计方法,在空腹血糖正常的个体和糖尿病前期的个体之间,脂蛋白亚类的浓度水平几乎没有差异。通过对网络进行差异分析,确定了几种与糖尿病脂代谢紊乱相关的脂蛋白代谢的特征变化。结果表明,该新方法适用于识别标准方法无法获得的关键分子变化。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/df7a/3181317/c41f4e5d29b6/pone.0024702.g001.jpg

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