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Pathway-Based Genome-wide Association Studies Reveal That the Rac1 Pathway Is Associated with Plasma Adiponectin Levels

机译:基于通路的全基因组关联研究显示Rac1通路与血浆脂联素水平相关

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摘要

Pathway-based analysis as an alternative and effective approach to identify disease-related genes or loci has been verified. To decipher the genetic background of plasma adiponectin levels, we performed genome wide pathway-based association studies in extremely obese individuals and normal-weight controls. The modified Gene Set Enrichment Algorithm (GSEA) was used to perform the pathway-based analyses (the GenGen Program) in 746 European American females, which were collected from our previous GWAS in extremely obese (BMI > 35 kg/m2) and never-overweight (BMI<25 kg/m2) controls. Rac1 cell motility signaling pathway was associated with plasma adiponectin after false-discovery rate (FDR) correction (empirical P < 0.001, FDR = 0.008, family-wise error rate = 0.008). Other several Rac1-centered pathways, such as cdc42racPathway (empirical P < 0.001), hsa00603 (empirical P = 0.003) were among the top associations. The RAC1 pathway association was replicated by the ICSNPathway method, yielded a FDR = 0.002. Quantitative pathway analyses yielded similar results (empirical P = 0.001) for the Rac1 pathway, although it failed to pass the multiple test correction (FDR = 0.11). We further replicated our pathway associations in the ADIPOGen Consortium data by the GSA-SNP method. Our results suggest that Rac1 and related cell motility pathways might be associated with plasma adiponectin levels and biological functions of adiponectin.
机译:已经验证了基于途径的分析作为鉴定疾病相关基因或基因座的另一种有效途径。为了破译血浆脂联素水平的遗传背景,我们在极度肥胖的个体和体重正常的对照组中进行了基于全基因组途径的关联研究。改良的基因集富集算法(GSEA)用于对746名欧美女性进行基于路径的分析(GenGen程序),这些女性是从我们以前的GWAS中以超重肥胖(BMI> 35 kg / m 2)收集的)和永不超重(BMI <25 kg / m 2 )控件。假发现率(FDR)校正后,Rac1细胞运动信号通路与血浆脂联素相关(经验P <0.001,FDR = 0.008,家庭错误率= 0.008)。其他几个以Rac1为中心的途径,如cdc42racPathway(经验值P <0.001),hsa00603(经验值P = 0.003)是最重要的关联。通过ICSNPathway方法复制RAC1途径的关联,得出FDR = 0.002。尽管Rac1通路未通过多重检验校正(FDR = 0.11),但定量通路分析对Rac1通路产生了相似的结果(经验值P = 0.001)。我们通过GSA-SNP方法在ADIPOGen联盟数据中进一步复制了我们的途径关联。我们的结果表明,Rac1和相关的细胞运动途径可能与血浆脂联素水平和脂联素的生物学功能有关。

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