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miRNA Signatures of Insulin Resistance in Obesity.
Jones, Angela; Danielson, Kirsty M; Benton, Miles C; Ziegler, Olivia; Shah, Ravi; Stubbs, Richard S; Das, Saumya; Macartney-Coxson, Donia.
Afiliação
  • Jones A; Biomarkers Group, Institute of Environmental Science and Research, Wellington, New Zealand.
  • Danielson KM; Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Benton MC; Biomarkers Group, Institute of Environmental Science and Research, Wellington, New Zealand.
  • Ziegler O; Genomics Research Centre, Institute of Health and Biomedical Innovation, Queensland University of Technology, Brisbane, Queensland, Australia.
  • Shah R; Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Stubbs RS; Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
  • Das S; The Wakefield Clinic, Wellington, New Zealand.
  • Macartney-Coxson D; Cardiovascular Research Center, Massachusetts General Hospital, Boston, Massachusetts, USA.
Obesity (Silver Spring) ; 25(10): 1734-1744, 2017 10.
Article em En | MEDLINE | ID: mdl-28834285
ABSTRACT

OBJECTIVE:

Extracellular microRNAs (miRNAs) represent functional biomarkers for obesity and related disorders; this study investigated plasma miRNAs in insulin resistance phenotypes in obesity.

METHODS:

One hundred seventy-five miRNAs were analyzed in females with obesity (insulin sensitivity, n = 11; insulin resistance, n = 19; type 2 diabetes, n = 15) and without obesity (n = 12). Correlations between miRNA level and clinical parameters and levels of 15 miRNAs in a murine obesity model were investigated.

RESULTS:

One hundred six miRNAs were significantly (adjusted P ≤ 0.05) different between controls and at least one obesity phenotype, including miRNAs with the following attributes previously reported roles in obesity and altered circulating levels (e.g., miR-122, miR-192); known roles in obesity but no reported changes in circulating levels (e.g., miR-378a); and no current reported role in, or association with, obesity (e.g., miR-28-5p, miR-374b, miR-32). The miRNAs in the latter group were found to be associated with extracellular vesicles. Forty-eight miRNAs showed significant correlations with clinical parameters; stepwise regression retained let-7b, miR-144-5p, miR-34a, and miR-532-5p in a model predictive of insulin resistance (R2 = 0.57, P = 7.5 × 10-8 ). Both miR-378a and miR-122 were perturbed in metabolically relevant tissues in a murine model of obesity.

CONCLUSIONS:

This study expands on the role of extracellular miRNAs in insulin-resistant phenotypes of obesity and identifies candidate miRNAs not previously associated with obesity.
Assuntos

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Resistência à Insulina / MicroRNAs / Diabetes Mellitus Tipo 2 / Obesidade Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: Obesity (Silver Spring) Assunto da revista: CIENCIAS DA NUTRICAO / FISIOLOGIA / METABOLISMO Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Nova Zelândia

Texto completo: 1 Bases de dados: MEDLINE Assunto principal: Resistência à Insulina / MicroRNAs / Diabetes Mellitus Tipo 2 / Obesidade Tipo de estudo: Prognostic_studies Limite: Adult / Female / Humans / Middle aged Idioma: En Revista: Obesity (Silver Spring) Assunto da revista: CIENCIAS DA NUTRICAO / FISIOLOGIA / METABOLISMO Ano de publicação: 2017 Tipo de documento: Article País de afiliação: Nova Zelândia