Literature DB >> 24720446

Increased plasma levels of the methylglyoxal in patients with newly diagnosed type 2 diabetes 2.

Xiang Kong1, Ming-zhe Ma, Kai Huang, Li Qin, Hong-mei Zhang, Zhen Yang, Xiao-yong Li, Qing Su.   

Abstract

BACKGROUND: Methylglyoxal (MG) is a reactive-dicarbonyl that is thought to contribute to the development of diabetes either as a precursor for advanced glycation end products or as a direct toxin. The present study was designed to determine plasma MG level in patients with newly diagnosed type 2 diabetes mellitus (T2DM) and to evaluate the relationship between MG and other parameters, such as oxidative stress and metabolic indices.
METHODS: Methylglyoxal was measured by high-performance liquid chromatographic/tandem mass spectrometry in plasma from 48 subjects with newly diagnosed T2DM. The relationship between two variables was analyzed using Spearman's correlation analysis. Multiple stepwise linear regression analysis was used to assess the association of plasma MG and other parameters.
RESULTS: Plasma MG level in patients with newly diagnosed T2DM (65.2 ± 19.2 ng/mL) were significantly higher than that in control individuals (40.1 ± 11.1 ng/mL, P < 0.05). The plasma level of MG was positively correlated with the glycosylated hemoglobin A1c (HbA1c, r = 0.670, P < 0.01) and malondialdehyde (MDA, r = 0.694, P < 0.01). Multiple linear regression analysis revealed that both HbA1c and MDA are significant independent determinants of plasma MG level.
CONCLUSIONS: These findings suggest that increased plasma MG level is associated with the elevation of HbA1c and MDA in newly diagnosed T2DM patients.
© 2014 Ruijin Hospital, Shanghai Jiaotong University School of Medicine and Wiley Publishing Asia Pty Ltd.

Entities:  

Keywords:  glycosylated hemoglobin A1c; methylglyoxal; oxidative stress; type 2 diabetes mellitus; 关键词:糖化血红蛋白A1c,甲基乙二醛,氧化应激,2型糖尿病

Mesh:

Substances:

Year:  2014        PMID: 24720446     DOI: 10.1111/1753-0407.12160

Source DB:  PubMed          Journal:  J Diabetes        ISSN: 1753-0407            Impact factor:   4.006


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