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Effect of insulin resistance on whole blood mRNA and microRNA expression affecting bone turnover.
Razny, Urszula; Polus, Anna; Goralska, Joanna; Zdzienicka, Anna; Gruca, Anna; Kapusta, Maria; Biela, Maria; Dembinska-Kiec, Aldona; Solnica, Bogdan; Malczewska-Malec, Malgorzata.
Afiliación
  • Razny U; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Polus A; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Goralska J; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Zdzienicka A; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Gruca A; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Kapusta M; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Biela M; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Dembinska-Kiec A; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Solnica B; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
  • Malczewska-Malec M; Department of Clinical Biochemistry, Jagiellonian University Medical College, Krakow, Poland.
Eur J Endocrinol ; 181(5): 525-537, 2019 Nov.
Article en En | MEDLINE | ID: mdl-31536965
ABSTRACT

OBJECTIVE:

To evaluate the effect of insulin resistance in obesity on the expression in whole blood of mRNA and miRNA affecting bone homeostasis as well as to estimate the influence of oral glucose load (OGTT) on serum osteocalcin concentration in obese individuals with and without insulin resistance.

DESIGN:

Cross-sectional study.

METHODS:

Carboxylated (cOC), undercarboxylated (ucOC) and total osteocalcin were measured by ELISA in the serum of obese subjects with insulin resistance (n = 41) and obese subjects without insulin resistance (n = 41) (control group) during OGTT. Analysis of gene expression (microarray) and miRNAs (real-time PCR) was performed in venous blood (representating samples) collected before OGTT from obese with insulin resistance and controls.

RESULTS:

Obese subjects with insulin resistance (higher HOMA-IR and lower oral glucose insulin sensitivity index) presented significantly increased expression of WNT signalling inhibitors (DKK1, DKK2, SOST, SFRP1) and downregulation of the key factor in WNT signalling - ß catenin participating in osteoblasts differentiation. Expression of miRNA involved in osteoblastogenesis was also inhibited (miR-29b, miR-181a, miR-210, miR-324-3p). During OGTT, contrary to the control group, subjects with insulin resistance presented suppression of cOC and total OC decrease after 1 and 2 h of oral glucose load.

CONCLUSIONS:

Obese subjects with insulin resistance may have defects in osteoblastogenesis that was demonstrated via key signalling molecules mRNA downregulation, and increased expression of WNT antagonists as well as inhibition of expression of miRNA participating in the regulation of osteoblast differentiation. Disturbed osteoblastogenesis in insulin-resistant subjects results in the suppression of blood carboxylated and total osteocalcin decrease during OGTT.
Asunto(s)

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Resistencia a la Insulina / ARN Mensajero / Remodelación Ósea / MicroARNs Tipo de estudio: Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Endocrinol Asunto de la revista: ENDOCRINOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Polonia

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Resistencia a la Insulina / ARN Mensajero / Remodelación Ósea / MicroARNs Tipo de estudio: Etiology_studies / Observational_studies / Prevalence_studies / Risk_factors_studies Límite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Eur J Endocrinol Asunto de la revista: ENDOCRINOLOGIA Año: 2019 Tipo del documento: Article País de afiliación: Polonia