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Crosstalk between circulating microRNAs and chronotypical features in subjects with metabolic syndrome
Authors:Taís Silveira Assmann  Amanda Cuevas-Sierra  Francisca Salas-Pérez  José I Riezu-Boj  J Alfredo Martínez
Institution:1. Department of Nutrition, Food Science and Physiology;2. Center for Nutrition Research, University of Navarra , Pamplona, Spain;3. Center for Nutrition Research, University of Navarra , Pamplona, Spain;4. Centro De Investigación Biomédica En Red Fisiopatología De La Obesidad Y Nutrición (Ciberobn), Instituto De Salud Carlos III , Madrid, Spain;5. IdiSNA, Navarra Institute for Health Research , Pamplona, Spain;6. IdiSNA, Navarra Institute for Health Research , Pamplona, Spain;7. Madrid Institute of Advanced Studies (IMDEA Food), Food Institute , Madrid, Spain ORCID Iconhttps://orcid.org/0000-0001-5218-6941
Abstract:ABSTRACT

Circulating microRNAs (miRNAs) are valuable biomarkers that may provide important insight into the pathogenesis of metabolic syndrome (MetS). Moreover, there is an association between chronotypical characteristics and MetS predisposition. Considering that expression of some miRNAs is circadian-rhythm-dependent, the aim of this study was to investigate the circulating miRNA profile in subjects with and without MetS in association with chronotype. The expression of 86 metabolic syndrome-related miRNAs was investigated in the plasma of 21 subjects with MetS and in 82 subjects without MetS using miRCURY LNA miRNA PCR System technology. Chronotype was assessed using the Horne and Östberg Morningness-Eveningness Questionnaire. Bioinformatic analyses were performed to explore the target genes and biological pathways regulated by the selected miRNAs. Subjects with MetS were more often evening chronotype compared to non-MetS controls. Additionally, four miRNAs (miR-140-3p, miR-150-5p, miR-375, and miR-29 c-3p) demonstrated interaction with MetS and chronotype. Interestingly, the target genes of these four miRNAs participate in pathways related to the circadian clock. In conclusion, we identified four circulating miRNAs whose circulating levels could interact with MetS and chronotype.
Keywords:Circadian rhythm  microRNA  chronotype  miR-155-5p  miR-150-5p  miR-375  miR-140-3p  metabolic syndrome  clock genes
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