Human Genetics Center and Department of Epidemiology, Human Genetics and Environmental Sciences, School of Public Health, The University of Texas Health Science Center at Houston, Houston, TX, USA.
Human Genome Sequencing Center, Baylor College of Medicine, Houston, TX, USA.
Hum Genet. 2018 Jan;137(1):85-94. doi: 10.1007/s00439-017-1858-8. Epub 2017 Dec 20.
The purpose of this study is to identify microRNA (miRNA) related polymorphism, including single nucleotide variants (SNVs) in mature miRNA-encoding sequences or in miRNA-target sites, and their association with cardiovascular disease (CVD) risk factors in African-American population. To achieve our objective, we examined 1900 African-Americans from the Atherosclerosis Risk in Communities study using SNVs identified from whole-genome sequencing data. A total of 971 SNVs found in 726 different mature miRNA-encoding sequences and 16,057 SNVs found in the three prime untranslated region (3'UTR) of 3647 protein-coding genes were identified and interrogated their associations with 17 CVD risk factors. Using single-variant-based approach, we found 5 SNVs in miRNA-encoding sequences to be associated with serum Lipoprotein(a) [Lp(a)], high-density lipoprotein (HDL) or triglycerides, and 2 SNVs in miRNA-target sites to be associated with Lp(a) and HDL, all with false discovery rates of 5%. Using a gene-based approach, we identified 3 pairs of associations between gene NSD1 and platelet count, gene HSPA4L and cardiac troponin T, and gene AHSA2 and magnesium. We successfully validated the association between a variant specific to African-American population, NR_039880.1:n.18A>C, in mature hsa-miR-4727-5p encoding sequence and serum HDL level in an independent sample of 2135 African-Americans. Our study provided candidate miRNAs and their targets for further investigation of their potential contribution to ethnic disparities in CVD risk factors.
本研究旨在确定与心血管疾病 (CVD) 风险因素相关的 miRNA(miRNA)相关多态性,包括成熟 miRNA 编码序列或 miRNA 靶位中的单核苷酸变异 (SNV)。为了实现我们的目标,我们使用全基因组测序数据鉴定的 SNV 检查了来自社区动脉粥样硬化风险研究的 1900 名非裔美国人。在 726 个不同成熟 miRNA 编码序列中发现了 971 个 SNV,在 3647 个蛋白质编码基因的 3'UTR 中发现了 16057 个 SNV,并研究了它们与 17 个 CVD 风险因素的关联。使用单变量方法,我们发现 miRNA 编码序列中的 5 个 SNV 与血清脂蛋白 (a) [Lp(a)]、高密度脂蛋白 (HDL) 或甘油三酯相关,miRNA 靶位中的 2 个 SNV 与 Lp(a) 和 HDL 相关,所有这些都具有 5%的错误发现率。使用基于基因的方法,我们鉴定了基因 NSD1 和血小板计数、基因 HSPA4L 和心肌肌钙蛋白 T 以及基因 AHSA2 和镁之间的 3 对关联。我们成功验证了特定于非裔美国人群体的变异 NR_039880.1:n.18A>C 在成熟 hsa-miR-4727-5p 编码序列中的关联与另一个独立的 2135 名非裔美国人样本中的血清 HDL 水平的关联。我们的研究为候选 miRNA 及其靶标提供了依据,以进一步研究它们对 CVD 风险因素的种族差异的潜在贡献。