Marrow adipose tissue spectrum in obesity and type 2 diabetes mellitus

Author:

de Araújo Iana M1,Salmon Carlos E G2,Nahas Andressa K3,Nogueira-Barbosa Marcello H1,Elias Jorge1,de Paula Francisco J A1

Affiliation:

1. 1Department of Internal MedicineRibeirao Preto Medical School

2. 2Department of PhysicsFaculty of Philosophy, Sciences and Arts of Ribeirao Preto

3. 3Department of EpidemiologySchool of Public Health, USP, Ribeirão Preto, Sao Paulo,, Brazil

Abstract

ObjectiveTo assess the association of bone mass and marrow adipose tissue (MAT) with other fat depots, insulin resistance, bone remodeling markers, adipokines and glucose control in type 2 diabetes and obesity.Design and methodsThe study groups comprised 24 controls (C), 26 obese (O) and 28 type 2 diabetes. Dual-energy X-ray absorptiometry was used to determine bone mineral density (BMD). Blood samples were collected for biochemical measurements.1H Magnetic resonance spectroscopy was used to assess MAT in the L3 vertebra, and abdominal magnetic resonance imaging was used to assess intrahepatic lipids in visceral (VAT) and subcutaneous adipose tissue. Regression analysis models were used to test the association between parameters.ResultsAt all sites tested, BMD was higher in type 2 diabetes than in O and C subjects. The C group showed lower VAT values than the type 2 diabetes group and lower IHL than the O and type 2 diabetes groups. However, MAT was similar in the 3 groups. Osteocalcin and C-terminal telopeptide of type 1 collagen were lower in type 2 diabetes than those in C and O subjects. Moreover, at all sites, BMD was negatively associated with osteocalcin. No association was observed between MAT and VAT. No relationship was observed among MAT and HOMA-IR, leptin, adiponectin or Pref-1, but MAT was positively associated with glycated hemoglobin.ConclusionsMAT is not a niche for fat accumulation under conditions of energy surplus and type 2 diabetes, also is not associated with VAT or insulin resistance. MAT is associated with glycated hemoglobin.

Publisher

Bioscientifica

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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