Literature DB >> 24681829

Advanced glycation end products are associated with arterial stiffness in type 1 diabetes.

Gemma Llauradó1, Victòria Ceperuelo-Mallafré2, Carme Vilardell2, Rafael Simó2, Pilar Gil2, Albert Cano2, Joan Vendrell2, José-Miguel González-Clemente3.   

Abstract

The aim of this study was to investigate the relationship between advanced glycation end products (AGEs) and arterial stiffness (AS) in subjects with type 1 diabetes without clinical cardiovascular events. A set of 68 patients with type 1 diabetes and 68 age- and sex-matched healthy subjects were evaluated. AGEs were assessed using serum concentrations of N-carboxy-methyl-lysine (CML) and using skin autofluorescence. AS was assessed by aortic pulse wave velocity (aPWV), using applanation tonometry. Patients with type 1 diabetes had higher serum concentrations of CML (1.18 vs 0.96 μg/ml; P=0.008) and higher levels of skin autofluorescence (2.10 vs 1.70; P<0.001) compared with controls. These differences remained significant after adjustment for classical cardiovascular risk factors. Skin autofluorescence was positively associated with aPWV in type 1 diabetes (r=0.370; P=0.003). No association was found between CML and aPWV. Skin autofluorescence was independently and significantly associated with aPWV in subjects with type 1 diabetes (β=0.380; P<0.001) after adjustment for classical cardiovascular risk factors. Additional adjustments for HbA1c, disease duration, and low-grade inflammation did not change these results. In conclusion, skin accumulation of autofluorescent AGEs is associated with AS in subjects with type 1 diabetes and no previous cardiovascular events. These findings indicate that determination of tissue AGE accumulation may be a useful marker for AS in type 1 diabetes.
© 2014 Society for Endocrinology.

Entities:  

Keywords:  advanced glycation end products; arterial stiffness; arteriosclerosis; pulse wave velocity; skin autofluorescence; type 1 diabetes mellitus

Mesh:

Substances:

Year:  2014        PMID: 24681829     DOI: 10.1530/JOE-13-0407

Source DB:  PubMed          Journal:  J Endocrinol        ISSN: 0022-0795            Impact factor:   4.286


  27 in total

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