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Expression of MYD88 in Adipose Tissue of Obese People: Is There Some Role in the Development of Metabolic Syndrome?
Cuevas, Ada M; Lazo, Mariana; Zuñiga, Isabel; Carrasco, Fernando; Potter, Jim J; Alvarez, Veronica; Berry, Marcos; Maluenda, Fernando; Ferrario, Mario; Clark, Jeanne M.
Afiliação
  • Cuevas AM; 1 Center of Nutrition and Metabolic Diseases , Clinica Las Condes, Santiago, Chile .
  • Lazo M; 2 Division of General Internal Medicine, Department of Medicine, The Johns Hopkins University , Baltimore, Maryland.
  • Zuñiga I; 3 Department of Nutrition, Faculty of Medicine, University of Chile , Santiago, Chile .
  • Carrasco F; 1 Center of Nutrition and Metabolic Diseases , Clinica Las Condes, Santiago, Chile .
  • Potter JJ; 3 Department of Nutrition, Faculty of Medicine, University of Chile , Santiago, Chile .
  • Alvarez V; 4 Division of Gastroenterology and Hepatology, Department of Medicine, The Johns Hopkins University , Baltimore, Maryland.
  • Berry M; 1 Center of Nutrition and Metabolic Diseases , Clinica Las Condes, Santiago, Chile .
  • Maluenda F; 1 Center of Nutrition and Metabolic Diseases , Clinica Las Condes, Santiago, Chile .
  • Ferrario M; 1 Center of Nutrition and Metabolic Diseases , Clinica Las Condes, Santiago, Chile .
  • Clark JM; 1 Center of Nutrition and Metabolic Diseases , Clinica Las Condes, Santiago, Chile .
Metab Syndr Relat Disord ; 15(2): 80-85, 2017 03.
Article em En | MEDLINE | ID: mdl-28075222
ABSTRACT

BACKGROUND:

The mechanism leading to the development of metabolic complications in obese individuals is not fully understood. Thus, the objective of this study was to examine differences in insulin resistance, inflammation, cytokine and adipokine levels, and expression of selected genes across obese individuals with different number of metabolic syndrome (MetS) components.

METHODS:

Forty obese individuals who underwent bariatric surgery, divided in three groups based on the number of components of MetS, in addition to abdominal obesity (0, 1, and 2-3 additional components), were studied. Levels of inflammatory proteins, insulin resistance, cytokines, adipokines, and gene expression in subcutaneous (SAT) and visceral adipose tissue (VAT) were compared.

RESULTS:

There was a significantly higher expression of MYD88 in SAT among those with more components of MetS (P = 0.008). In SAT, but not in VAT, MYD88 expression was significantly correlated with toll-like receptor 4 expression (r = 0.7, P < 0.05). Expression of adipsin in SAT was also associated with the presence of more components of MetS, but with borderline statistical significance (P = 0.05). There were no significant differences in insulin resistance, inflammation, and cytokine and adipokine levels by the number of components of MetS.

CONCLUSIONS:

Our study suggests that MYD88 expression in SAT of obese subjects could be associated with the development of components of MetS.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tecido Adiposo / Síndrome Metabólica / Fator 88 de Diferenciação Mieloide / Obesidade Abdominal Tipo de estudo: Etiology_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Tecido Adiposo / Síndrome Metabólica / Fator 88 de Diferenciação Mieloide / Obesidade Abdominal Tipo de estudo: Etiology_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2017 Tipo de documento: Article