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Low expression levels of miRNA-155 and miRNA-499a are associated with obesity in Type 2 diabetes.
Latini, Andrea; Benedittis, Giada De; Ciccacci, Cinzia; Novelli, Giuseppe; Spallone, Vincenza; Borgiani, Paola.
Afiliação
  • Latini A; Department of Biomedicine & Prevention, Genetics Section, University of Rome Tor Vergata, Rome, 00133, Italy.
  • Benedittis G; Department of Biomedicine & Prevention, Genetics Section, University of Rome Tor Vergata, Rome, 00133, Italy.
  • Ciccacci C; UniCamillus, Saint Camillus International University of Health Sciences, Rome, 00131, Italy.
  • Novelli G; Department of Biomedicine & Prevention, Genetics Section, University of Rome Tor Vergata, Rome, 00133, Italy.
  • Spallone V; IRCCS NEUROMED, Pozzilli, IS, 86077, Italy.
  • Borgiani P; School of Medicine, Department of Pharmacology, Reno University of Nevada, NV 89557, USA.
Epigenomics ; 16(2): 85-91, 2024 Jan.
Article em En | MEDLINE | ID: mdl-38221897
ABSTRACT
Background &

aims:

This study investigated a possible correlation between three circulating miRNAs, previously observed to be associated to diabetic polyneuropathy, and the obesity condition. Methods &

results:

The expression levels of miR-128a, miR-155 and miR499a were evaluated in 49 participants with Type 2 diabetes, divided into different groups based on the presence or absence of obesity and central obesity. The analyses revealed a significant decrease of miR-155 and miR-499a expression levels in obese subjects. In particular, the reduction appears to be even more significant in Type 2 diabetes subjects with central obesity.

Conclusion:

The results suggest that these miRNAs could be involved in obesity-driven pathogenetic mechanisms.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / Diabetes Mellitus Tipo 2 / MicroRNA Circulante Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: MicroRNAs / Diabetes Mellitus Tipo 2 / MicroRNA Circulante Idioma: En Ano de publicação: 2024 Tipo de documento: Article