Department of Biomedicine and Prevention, Genetics Section, University of Rome "Tor Vergata", Via Montpellier 1, 00133, Rome, Italy.
Acta Diabetol. 2013 Dec;50(6):867-72. doi: 10.1007/s00592-013-0469-7. Epub 2013 Mar 27.
MicroRNAs are small single-stranded molecules that have emerged as important genomic regulators in different pathways. Different studies have shown that they are implicated in the metabolism and glucose homeostasis, and therefore, they could also be involved in the pathogenesis of metabolic disorders such as type 2 diabetes (T2DM). The aim of this study was to verify whether genetic variations in candidate microRNA (miRNA or miR) genes could contribute to T2DM susceptibility. We have selected 13 miRNAs as candidate loci according to literature data and to a computational analysis. MicroRNA genes were analyzed by direct sequencing in a cohort of 163 Italian T2DM patients and 185 healthy controls. We identified 6 novel variants never described before and 9 SNPs already described in databases. Five newly identified variants were found only in the cases group. We performed a case/control association study to test the associations of particular alleles/genotypes of identified SNPs with the disease. Two polymorphisms were associated with T2DM susceptibility: in particular, the G allele of rs895819 in hsa-mir-27a has shown a significantly protective effect (OR = 0.58 and P = 0.008), while the G allele of rs531564 in hsa-mir-124a appears to be a risk allele (OR = 2.15, P = 0.008). This is the first report indicating that genetic polymorphisms in miRNA regions could contribute to T2DM susceptibility.
微小 RNA 是小的单链分子,已成为不同途径中重要的基因组调节因子。不同的研究表明,它们与代谢和葡萄糖稳态有关,因此,它们也可能参与代谢紊乱的发病机制,如 2 型糖尿病 (T2DM)。本研究旨在验证候选微小 RNA (miRNA 或 miR) 基因的遗传变异是否可能导致 T2DM 易感性。我们根据文献数据和计算分析选择了 13 个 miRNA 作为候选基因座。在 163 名意大利 T2DM 患者和 185 名健康对照者的队列中,通过直接测序分析了微小 RNA 基因。我们确定了 6 个以前从未描述过的新变体和 9 个数据库中已描述的 SNP。仅在病例组中发现了 5 个新鉴定的变体。我们进行了病例/对照关联研究,以测试鉴定 SNP 的特定等位基因/基因型与疾病的关联。有两个多态性与 T2DM 易感性相关:特别是 hsa-mir-27a 中的 rs895819 的 G 等位基因显示出显著的保护作用(OR = 0.58,P = 0.008),而 hsa-mir-124a 中的 rs531564 的 G 等位基因似乎是风险等位基因(OR = 2.15,P = 0.008)。这是第一个表明 miRNA 区域的遗传多态性可能导致 T2DM 易感性的报告。