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Indicators of iron status are correlated with adiponectin expression in adipose tissue of patients with morbid obesity.

Authors :
Pihan-Le Bars F
Bonnet F
Loréal O
Le Loupp AG
Ropert M
Letessier E
Prieur X
Bach K
Deugnier Y
Fromenty B
Cariou B
Source :
Diabetes & metabolism [Diabetes Metab] 2016 Apr; Vol. 42 (2), pp. 105-11. Date of Electronic Publication: 2015 Dec 08.
Publication Year :
2016

Abstract

Aim: The aim of this study was to assess interactions between glucose and iron homoeostasis in the adipose tissue (AT) of obese subjects.<br />Methods: A total of 46 obese patients eligible for bariatric surgery were recruited into the study. Anthropometric and biochemical characteristics were assessed, and biopsies of subcutaneous (SCAT) and visceral adipose tissue (VAT) performed. The mRNA levels of genes involved in iron and glucose homoeostasis were measured in their AT and compared with a pool of control samples.<br />Results: Gene expression of hepcidin (HAMP) was significantly increased in the SCAT and VAT of obese patients, while transferrin receptor (TFRC) expression was reduced, compared with non-obese controls, suggesting a higher iron load in obese patients. Also, mRNA levels of adiponectin (ADIPOQ) were decreased in both SCAT and VAT in obese patients, and correlated negatively with hepcidin expression, while adiponectin expression was positively correlated with TFRC expression in both SCAT and VAT. Interestingly, TFRC expression in VAT correlated negatively with several metabolic parameters, such as fasting blood glucose and LDL cholesterol.<br />Conclusion: Iron content appears to be increased in the SCAT and VAT of obese patients, and negatively correlated with adiponectin expression, which could be contributing to insulin resistance and the metabolic complications of obesity.<br /> (Copyright © 2015 Elsevier Masson SAS. All rights reserved.)

Details

Language :
English
ISSN :
1878-1780
Volume :
42
Issue :
2
Database :
MEDLINE
Journal :
Diabetes & metabolism
Publication Type :
Academic Journal
Accession number :
26677772
Full Text :
https://doi.org/10.1016/j.diabet.2015.10.007