| Literature DB >> 24784704 |
Emma Raitoharju1, Ilkka Seppälä2, Niku Oksala3, Leo-Pekka Lyytikäinen2, Olli Raitakari4, Jorma Viikari5, Mika Ala-Korpela6, Pasi Soininen7, Antti J Kangas7, Melanie Waldenberger8, Norman Klopp9, Thomas Illig9, Jaana Leiviskä10, Britt-Marie Loo10, Nina Hutri-Kähönen11, Mika Kähönen12, Reijo Laaksonen2, Terho Lehtimäki2.
Abstract
Since metabolic syndrome (MetS) is a collection of cardiovascular risk factors involving multiple signaling systems, we related the metabolic abnormalities associated with MetS with circulating microRNA profiles to pinpoint the affected signaling pathways. The blood microRNA profile, genome wide gene expression and serum NMR metabolomics were analyzed from 71 participants of the Young Finns Study. We found nine microRNAs that associated significantly with metabolites connected to MetS. MicroRNA-144-5p concentration correlated with glucose levels, hsa-1207-5p with glycosylated hemoglobin and hsa-miR-484 with metabolites related to insulin resistance. Hsa-miR-625-3p correlated with cholesterol levels, hsa-miR-1237-3p and hsa-miR-331-3p expression with certain fatty acids levels and hsa-miR-129-1-3p, -129-2-3p, and -1288-3p with glycerol levels. The down-regulated targets of miR-1207-5p and -129-2-3p were enriched in PI3K and MAPK pathways and 8 out of the 12 enriched pathways were down-regulated in individuals with MetS. In conclusion microRNAs associated with several aspects of MetS, possibly regulating glucose and lipid metabolism.Entities:
Keywords: Diabetes; MRNA expression; Metabolic syndrome; MicroRNA; NMR metabolomics
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Year: 2014 PMID: 24784704 DOI: 10.1016/j.mce.2014.04.013
Source DB: PubMed Journal: Mol Cell Endocrinol ISSN: 0303-7207 Impact factor: 4.102