BACKGROUND: Advanced glycation endproducts (AGEs) may play a role in the development of coronary artery calcification (CAC) in type 1 diabetes (T1DM). We studied plasma AGEs in association with T1DM and CAC, and whether or not the latter association could be explained by low-grade inflammation (LGI) or endothelial dysfunction (ED). METHODS: We studied 165 individuals with and 169 without T1DM. CAC was quantified in a CAC score based on CT-scanning. Plasma levels of protein-bound pentosidine, Nϵ-(carboxymethyl)lysine (CML) and Nϵ-(carboxyethyl)lysine (CEL) were measured with HPLC/UPLC with fluorescence detection or tandem-mass spectrometry. Tetrahydropyrimidine (THP) was measured with ELISA, as were HsCRP, and sVCAM-1 and vWF, as markers for LGI and ED, respectively. Associations were analyzed with ANCOVA and adjusted for age, sex, BMI, waist-to-hip ratio, smoking, blood pressure, lipid profile, eGFR and T1DM. RESULTS: Individuals with T1DM had higher plasma levels of pentosidine, CML and THP compared with controls; means (95% CI) were 0.69 (0.65-0.73) vs. 0.51 (0.48-0.54) nmol/mmol LYS, pâ<â0.001; 105 (102-107) vs. 93 (90-95) nmol/mmol LYS, pâ<â0.001; and 126 (118-134) vs. 113 (106-120) U/mL, pâ=â0.03, respectively. Levels of pentosidine were higher in individuals with T1DM with a moderate to high compared with a low CAC score, means (95% CI) were 0.81 (0.70-0.93) vs. 0.67 (0.63-0.71) nmol/mmol LYS, pâ=â0.03, respectively. This difference was not attenuated by adjustment for LGI or ED. CONCLUSIONS: We found a positive association between pentosidine and CAC in T1DM. These results may indicate that AGEs are possibly involved in the development of CAC in individuals with T1DM.
Plasma levels of advanced glycation endproducts are associated with type 1 diabetes and coronary artery calcification.
血浆中晚期糖基化终产物的水平与 1 型糖尿病和冠状动脉钙化有关
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作者:van Eupen Marcelle G A, Schram Miranda T, Colhoun Helen M, Scheijen Jean L J M, Stehouwer Coen D A, Schalkwijk Casper G
| 期刊: | Cardiovascular Diabetology | 影响因子: | 10.600 |
| 时间: | 2013 | 起止号: | 2013 Oct 17; 12:149 |
| doi: | 10.1186/1475-2840-12-149 | 研究方向: | 代谢 |
| 疾病类型: | 糖尿病 | ||
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