Advanced Glycation Endproducts: A Marker of Long-term Exposure to Glycemia

Author:

Klonoff David C.1ORCID,Aaron Rachel E.2ORCID,Tian Tiffany2ORCID,DuNova Ashley Y.2ORCID,Pandey Ambarish3ORCID,Rhee Connie4,Fleming G. Alexander5ORCID,Sacks David B.6ORCID,Pop-Busui Rodica7ORCID,Kerr David8ORCID

Affiliation:

1. Diabetes Research Institute, Mills-Peninsula Medical Center, San Mateo, CA, USA

2. Diabetes Technology Society, Burlingame, CA, USA

3. Division of Cardiology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, TX, USA

4. VA Greater Los Angeles Healthcare System, UCLA, Los Angeles, CA, USA

5. Kinexum, Harpers Ferry, WV, USA

6. National Institutes of Health, Bethesda, MD, USA

7. University of Michigan, Ann Arbor, MI, USA

8. Sutter Health Center for Health Systems Research, Santa Barbara, CA, USA

Abstract

This article examines the importance of advanced glycation endproducts (AGEs) and summarizes the structure of AGEs, pathological changes associated with AGEs, the contribution of AGEs to metabolic memory, and the value of AGEs as a predictor of diabetic complications and cardiovascular disease in people with and without diabetes. As a practical focus, skin autofluorescence (SAF) is examined as an attractive approach for estimating AGE burden. The measurement of AGEs may be of significant value to specific individuals and groups, including Black and Hispanic/Latino Americans, as they appear to have higher concentrations of hemoglobin A1c (HbA1c) than would be predicted by other metrics of mean glycemia. We hypothesize that if the amount of glycation of HbA1c is greater than expected from measured glucose levels, and if AGEs are accumulating, then this accumulation of AGEs might account for the increased rate of complications of diabetes in populations with high rates of vascular disease and other complications. Thus, identifying and modifying the burden of AGEs based on measurement of AGEs by SAF may turn out to be a worthwhile metric to determine individuals who are at high risk for the complications of diabetes as well as others without diabetes at risk of vascular disease. We conclude that available evidence supports SAF as both a clinical measurement and as a means of evaluating interventions aimed at reducing the risks of vascular disease and diabetic complications.

Publisher

SAGE Publications

Reference80 articles.

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