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Landscape of the relationship between. type 2 diabetes and coronary heart disease through an integrated gene network analysis

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单位: [1]Ningbo Univ, Sch Med, Zhejiang Prov Key Lab Pathophysiol, Ningbo 315211, Zhejiang, Peoples R China [2]Ningbo Univ, Sch Med, Ctr Diabet, Ningbo 315211, Zhejiang, Peoples R China [3]Ningbo Univ, Affiliated Hosp, Ningbo 315211, Zhejiang, Peoples R China [4]Huazhong Univ Sci & Technol,Tone Med Coll,Tongji Hosp,Inst Hypertens,Wuhan 430074,Peoples R China [5]Huazhong Univ Sci & Technol,Tone Med Coll,Tongji Hosp,Dept Internal Med,Wuhan 430074,Peoples R China
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关键词: Type 2 diabetes Coronary artery disease Genome-wide association Network analysis Protein-protein interaction Pathway Hub

摘要:
Type 2 diabetes (T2D) and coronary artery disease (CAD) are closely related chronic diseases with high prevalence and morbidity. However, a comprehensive comparison of the two diseases is lacking. Recent genomewide association studies (GWAS) have identified a handful of single nucleotide polymorphisms (SNPs) that are significantly associated with the risk of T2D and CAD. These most significant findings may help interpret the pathogenesis of T2D and CAD. However, tremendous results from these GWAS are ignored. Here we revisited the raw datasets of these GWAS and performed an integrated gene network analysis to unveil the relationship between T2D and CAD by combining multiple datasets including protein-protein interaction (PPI) database, publication libraries, and pathway datasets. Our results showed that majority of genes were involved in the first module (1122 genes in T2D and 895 in CAD). Four pathways were found to be common in both T2D and CAD, including regulation of actin cytoskeleton, calcium signaling pathway, MAPK signaling pathway and focal adhesion (all P <0.00001). MAX which was involved in small cell lung cancer pathway was a hub gene unique to T2D (OR = 1.2, P = 0.006) but not in CAD. In contrast, three hub genes including PLEKHG5 (T2D: OR = 1, P = 1; CAD: OR = 1.12, P = 0.006), TIAM1 (T2D: OR = 1, P = 1; CAD: OR = 1.48, P = 0.004) and AKAP13 (T2D: OR = 1, P = 1; CAD: OR =. 1.38, P = 0.001) were hub genes unique to CAD. Moreover, for some hub genes (such as SMAD3) that were susceptible to both T2D and CAD, their associated polymorphisms were unique to each of the two diseases. Our findings might provide a landscape of the relationship between T2D and CAD. (c) 2014 Elsevier B.V. All rights reserved.

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出版当年[2013]版:
大类 | 4 区 生物
小类 | 4 区 遗传学
最新[2025]版:
大类 | 3 区 生物学
小类 | 3 区 遗传学
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出版当年[2012]版:
Q3 GENETICS & HEREDITY
最新[2023]版:
Q2 GENETICS & HEREDITY

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第一作者单位: [1]Ningbo Univ, Sch Med, Zhejiang Prov Key Lab Pathophysiol, Ningbo 315211, Zhejiang, Peoples R China
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