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全血基因共表达网络提示哮喘人群肥胖中多个相互关联的分子途径

Gene Coexpression Networks in Whole Blood Implicate Multiple Interrelated Molecular Pathways in Obesity in People with Asthma.

机构信息

Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts, USA.

Division of Environmental Health, Department of Preventive Medicine, Keck School of Medicine, University of Southern California, Los Angeles, California, USA.

出版信息

Obesity (Silver Spring). 2018 Dec;26(12):1938-1948. doi: 10.1002/oby.22341. Epub 2018 Oct 25.

Abstract

OBJECTIVE

Asthmatic children who develop obesity through adolescence have poorer disease outcomes compared with those who do not. This study aimed to characterize the biology of childhood asthma complicated by adult obesity.

METHODS

Gene expression networks are powerful statistical tools for characterizing human disease that leverage the putative coregulatory relationships of genes to infer relevant biological pathways. Weighted gene coexpression network analysis of gene expression data was performed in whole blood from 514 adult asthmatic subjects. Then, module preservation and association replication analyses were performed in 418 subjects from two independent asthma cohorts (one pediatric and one adult).

RESULTS

A multivariate model was identified in which three gene coexpression network modules were associated with incident obesity in the discovery cohort (each P < 0.05). Two module memberships were enriched for genes in pathways related to platelets, integrins, extracellular matrix, smooth muscle, NF-κB signaling, and Hedgehog signaling. The network structures of each of the obesity modules were significantly preserved in both replication cohorts (permutation P = 9.999E-05). The corresponding module gene sets were significantly enriched for differential expression in subjects with obesity in both replication cohorts (each P < 0.05).

CONCLUSIONS

The gene coexpression network profiles thus implicate multiple interrelated pathways in the biology of an important endotype of asthma with obesity.

摘要

目的

与不肥胖的青少年哮喘患者相比,在青春期肥胖的哮喘儿童的疾病结局更差。本研究旨在描述肥胖合并成年期哮喘的儿童的生物学特征。

方法

基因表达网络是一种强大的统计学工具,可用于描述人类疾病,利用基因的假定核心调控关系来推断相关的生物学途径。对 514 例成年哮喘患者的全血基因表达数据进行加权基因共表达网络分析。然后,在两个独立的哮喘队列(一个儿科队列和一个成人队列)的 418 例患者中进行模块保存和关联复制分析。

结果

在发现队列中,有一个多变量模型确定了三个与肥胖发生相关的基因共表达网络模块(每个 P 值均小于 0.05)。两个模块成员与与血小板、整合素、细胞外基质、平滑肌、NF-κB 信号和 Hedgehog 信号相关的通路中的基因丰富相关。每个肥胖模块的网络结构在两个复制队列中均显著保存(置换 P 值为 9.999E-05)。在两个复制队列中,肥胖组中相应的模块基因集均存在差异表达,且差异显著(每个 P 值均小于 0.05)。

结论

基因共表达网络谱因此表明,与肥胖合并哮喘的重要表型相关的多个相互关联的途径涉及生物学机制。

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