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Anti-sRAGE autoimmunity in obesity: Downturn after bariatric surgery is independent of previous diabetic status

Authors :
R. Caiazzo
Eric Boulanger
Pierre Fontaine
Maïté Daroux
M. Lambert
Jean-Baptiste Beuscart
Nicolas Grossin
Rodrigo Lorenzi
Alexandre Patrice
Marie Pigeyre
S. Dubucquoi
François Pattou
Source :
Diabetes & Metabolism. 40:356-362
Publication Year :
2014
Publisher :
Elsevier BV, 2014.

Abstract

Morbid obesity increases the risk of cardiovascular disease (CVD). The receptor for advanced glycation end-products (RAGE) is implicated in proinflammatory processes that underlie CVD. Its soluble form (sRAGE) has been proposed as a vascular biomarker. Recently, anti-sRAGE autoantibodies were described and found to be increased in diseases where RAGE is overexpressed. This study aimed to investigate serum levels of anti-sRAGE autoantibodies in morbidly obese patients.After exclusion based on specific criteria, 150 subjects (50 normoglycemics, 50 glucose-intolerants and 50 diabetics) were randomly recruited from a cohort of 750 obese patients (ABOS). Serum sRAGE and anti-sRAGE autoantibodies were measured before bariatric surgery. Sixty-nine patients were followed for up to 1year after gastric bypass, and their levels of sRAGE and anti-sRAGE autoantibodies measured. The control group consisted of healthy blood donors.Compared with controls, baseline levels of sRAGE and anti-sRAGE autoantibodies were significantly higher in all obese patients independently of glucose regulation (P0.001). At 1year after gastric bypass, sRAGE and anti-sRAGE were decreased (P0.001). The decrease in anti-sRAGE autoantibodies was correlated with an increase in high-density lipoprotein (HDL; P=0.02).Independently of previous diabetic status, morbid obesity increases sRAGE and anti-sRAGE levels. Weight loss after gastric bypass is followed by a decrease in both titres. The decrease in anti-sRAGE correlates with an increase in HDL.

Details

ISSN :
12623636
Volume :
40
Database :
OpenAIRE
Journal :
Diabetes & Metabolism
Accession number :
edsair.doi.dedup.....69c9d0f3b98c1e89195228bb81ffa50b
Full Text :
https://doi.org/10.1016/j.diabet.2014.04.008