Association of glycemic variability with oxidative stress and AGE accumulation in type 2 diabetes

Oxidative stress and advanced glycation end products (AGEs) could promote vascular aging in type 2 diabetes mellitus (T2DM), but their relationship with glycemic variability remains unclear. We conducted a cross-sectional study of 68 patients with T2DM who underwent continuous glucose monitoring (CGM). Short-, intermediate-, and long-term glycemic variability were assessed using the % coefficient of variation of glucose (%CV), mean of daily differences (MODD), and HbA1c variability over the prior 2 years, respectively. Oxidative stress was measured by the diacron-reactive oxygen metabolites (d-ROMs) test, and AGE accumulation by skin autofluorescence (SAF). Multivariate analyses identified female sex, %CV, MODD, and nephropathy stage as independent correlates of d-ROMs (adjusted R<sup>2</sup> = 0.436). Duration of diabetes, MODD, urinary albumin-to-creatinine ratio, and macroangiopathy were independently associated with SAF (adjusted R<sup>2</sup> = 0.265). This study suggests that short- and intermediate-term glycemic variability correlate with oxidative stress and AGE accumulation, which may be associated with vascular complications in T2DM.

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Publication Details

Journal
Scientific Reports
Published
2025-12-11
DOI
https://doi.org/10.1038/s41598-025-31845-x
Citations
1
Primary Topic
Advanced Glycation End Products research
Type
article
Field-Weighted Citation Impact
1.32
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Association of glycemic variability with oxidative stress and AGE accumulation in type 2 diabetes

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Scientific Reports
Advanced Glycation End Products research
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article

Association of glycemic variability with oxidative stress and AGE accumulation in type 2 diabetes

Michishige Terasaki, Tomoyasu Fukui, Makoto Ohara, Nobuaki Takehana, Noriyuki Takahashi, Yusaku Mori, Naoya Osaka, Sho-ichi Yamagishi, Hiroe Sugita
article en
1 citations

Abstract

Oxidative stress and advanced glycation end products (AGEs) could promote vascular aging in type 2 diabetes mellitus (T2DM), but their relationship with glycemic variability remains unclear. We conducted a cross-sectional study of 68 patients with T2DM who underwent continuous glucose monitoring (CGM). Short-, intermediate-, and long-term glycemic variability were assessed using the % coefficient of variation of glucose (%CV), mean of daily differences (MODD), and HbA1c variability over the prior 2 years, respectively. Oxidative stress was measured by the diacron-reactive oxygen metabolites (d-ROMs) test, and AGE accumulation by skin autofluorescence (SAF). Multivariate analyses identified female sex, %CV, MODD, and nephropathy stage as independent correlates of d-ROMs (adjusted R<sup>2</sup> = 0.436). Duration of diabetes, MODD, urinary albumin-to-creatinine ratio, and macroangiopathy were independently associated with SAF (adjusted R<sup>2</sup> = 0.265). This study suggests that short- and intermediate-term glycemic variability correlate with oxidative stress and AGE accumulation, which may be associated with vascular complications in T2DM.

Scientific ReportsVol. 16(1)
SHOWA Medical University (JP)
Openalex Percentile: Top 13%
Advanced Glycation End Products research
1.32
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