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首页> 外文期刊>Scientific reports. >A Two-Stage Whole-Genome Gene Expression Association Study of Young-Onset Hypertension in Han Chinese Population of Taiwan
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A Two-Stage Whole-Genome Gene Expression Association Study of Young-Onset Hypertension in Han Chinese Population of Taiwan

机译:台湾汉族人群年轻高血压的两阶段全基因组基因表达关联研究

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摘要

Hypertension is an important public health problem in the world. Since the intermediate position of the gene expression between genotype and phenotype makes it suitable to link genotype to phenotype, we carried out a two-stage whole-genome gene expression association study to find differentially expressed genes and pathways for hypertension. In the first stage, 126 cases and 149 controls were used to find out the differentially expressed genes. In the second stage, an independent set of samples (127 cases and 150 controls) was used to validate the results. Additionally, we conducted a gene set enrichment analysis (GSEA) to search for differentially affected pathways. A total of nine genes were implicated in the first stage (Bonferroni-corrected p-value??0.05). Among these genes, ZRANB1, FAM110A, PREP, ANKRD9 and LAMB2 were also differentially expressed in an existing database of hypertensive mouse model (GSE19817). A total of 16 pathways were identified by the GSEA. ZRANB1 and six pathways identified are related to TNF-α. Three pathways are related to interleukin, one to metabolic syndrome, and one to Hedgehog signaling. Identification of these genes and pathways suggest the importance of 1. inflammation, 2. visceral fat metabolism, and 3. adipocytes and osteocytes homeostasis in hypertension mechanisms and complications.
机译:高血压是世界上重要的公共卫生问题。由于基因表达在基因型和表型之间的中间位置使其适合于将基因型与表型联系起来,因此我们进行了一个两阶段的全基因组基因表达关联研究,以寻找差异表达的基因和高血压途径。在第一阶段,使用126例病例和149例对照来发现差异表达的基因。在第二阶段,使用一组独立的样本(127个病例和150个对照)来验证结果。此外,我们进行了基因集富集分析(GSEA),以寻找差异影响的途径。在第一阶段共涉及9个基因(Bonferroni校正的p值≥0.05)。在这些基因中,ZRANB1,FAM110A,PREP,ANKRD9和LAMB2在现有的高血压小鼠模型数据库(GSE19817)中也差异表达。 GSEA共鉴定了16条途径。 ZRANB1和确定的六个途径与TNF-α有关。三种途径与白介素有关,一种与代谢综合征有关,另一种与刺猬信号有关。这些基因和途径的鉴定表明1.炎症,2.内脏脂肪代谢和3.脂肪细胞和骨细胞稳态在高血压机制和并发症中的重要性。

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