Can advanced glycation end‐products and their receptors be affected by weight loss? A systematic review

Summary Advanced glycation end products (AGEs) have been implicated in the pathogenesis of most chronic diseases. Therefore, identification of treatments that can attenuate the effects of these compounds and prevent cardiometabolic complications is of extreme public health interest. Recently, body w...

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Veröffentlicht in:Obesity reviews 2020-06, Vol.21 (6), p.e13000-n/a
Hauptverfasser: Tavares, Juliana F., Ribeiro, Priscila V. M., Coelho, Olívia G. L., Silva, Laís E. da, Alfenas, Rita C. G.
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Sprache:eng
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Zusammenfassung:Summary Advanced glycation end products (AGEs) have been implicated in the pathogenesis of most chronic diseases. Therefore, identification of treatments that can attenuate the effects of these compounds and prevent cardiometabolic complications is of extreme public health interest. Recently, body weight management interventions showed positive results on reducing serum AGE concentrations. Moreover, the soluble receptor for advanced glycation end products (sRAGE) is considered to be a novel biomarker to identify patients with obesity most likely to benefit from weight management interventions. This systematic review aimed to critically analyze papers evaluating the effects of weight loss on serum AGEs and its receptors in adults with excess body weight. MEDLINE, Cochrane, Scopus, and Lilacs databases were searched. Three studies evaluating the response of AGEs to energy‐restricted diets and six assessing sRAGE as the primary outcome were included. Energy‐restricted diets and bariatric surgery reduced serum AGE concentrations, but effects on endogenous secretory RAGE (esRAGE) and sRAGE concentrations are conflicting. These results may be associated with mechanisms related to changes in dietary intake and limiting endogenous AGE formation. Therefore, the role of energy‐restricted diets and bariatric surgery on lowering serum AGE concentrations, as well as its effects on AGEs receptors, deserves further investigation.
ISSN:1467-7881
1467-789X
DOI:10.1111/obr.13000