Circulating miRNA expression in long-standing type 1 diabetes mellitus

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作者
Paula Morales-Sánchez
Carmen Lambert
Jessica Ares-Blanco
Lorena Suárez-Gutiérrez
Elsa Villa-Fernández
Ana Victoria Garcia
Miguel García-Villarino
Juan Ramón Tejedor
Mario F. Fraga
Edelmiro Menéndez Torre
Pedro Pujante
Elías Delgado
机构
[1] Health Research Institute of the Principality of Asturias (ISPA),Endocrinology, Nutrition, Diabetes and Obesity Group (ENDO)
[2] Instituto de Salud Carlos III,Centre for Biomedical Network Research on Rare Diseases (CIBERER)
[3] University of Barcelona,Endocrinology and Nutrition Department
[4] Asturias Central University Hospital,Medicine Department
[5] University of Oviedo,Nanomaterials and Nanotechnology Research Center (CINN
[6] Health Research Institute of Asturias (ISPA),CSIC)
[7] Institute of Oncology of Asturias (IUOPA),Department of Organisms and Systems Biology (B.O.S)
[8] University of Oviedo,undefined
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Type 1 diabetes is a chronic autoimmune disease which results in inefficient regulation of glucose homeostasis and can lead to different vascular comorbidities through life. In this study we aimed to analyse the circulating miRNA expression profile of patients with type 1 diabetes, and with no other associated pathology. For this, fasting plasma was obtained from 85 subjects. Next generation sequencing analysis was firstly performed to identify miRNAs that were differentially expressed between groups (20 patients vs. 10 controls). hsa-miR-1-3p, hsa-miR-200b-3p, hsa-miR-9-5p, and hsa-miR-1200 expression was also measured by Taqman RT-PCR to validate the observed changes (34 patients vs. 21 controls). Finally, through a bioinformatic approach, the main pathways affected by the target genes of these miRNAs were studied. Among the studied miRNAs, hsa-miR-1-3p expression was found significantly increased in patients with type 1 diabetes compared to controls, and positively correlated with glycated haemoglobin levels. Additionally, by using a bioinformatic approach, we could observe that changes in hsa-miR-1-3p directly affect genes involved in vascular development and cardiovascular pathologies. Our results suggest that, circulating hsa-miR-1-3p in plasma, together with glycaemic control, could be used as prognostic biomarkers in type 1 diabetes, helping to prevent the development of vascular complications in these patients.
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