BMC Endocrine Disorders · 2021 · 12 citations · 15 references
MedicineBiochemistryEndocrinologyDiabetologyGlycobiologyMetabolic RegulationAdipose TissueDiabetes MellitusDiabetes Mellitus BiochemistryGlycemic ControlAbdominal Visceral FatBlood Glucose RegulationGlucose Metabolism BiomarkersGlycemic BiomarkersImpaired Glucose ToleranceOxidative Stress In DiabetesOxidative Stress In Metabolic DisordersOxidative Stress Injury
Abstract Background This study aimed to investigate the differences in oxidative stress (OS) levels represented by 8-iso-prostaglandin F 2α (8-iso-PGF 2α ) and analyze its correlation with the intra-abdominal fat (IAF) area and the glycolipid index. Methods We recruited a total of 160 eligible subjects. According to the blood glucose levels and the T2DM duration, subjects were divided into three groups: Type 2 Diabetes (T2DM) group, Prediabetic group, and Normal glucose-tolerance (NC) group, containing 66, 41, 53 patients, respectively. T2DM groups were additionally divided into a new-onset T2DM group including 29 patients and a non-new-onset T2DM group including 37 patients. General clinical data and biochemical indicators were collected. Intra-abdominal fat (IAF) was measured by MRI. 8-iso-PGF 2α was measured by ELISA. Results Compared with the NC group, levels of systolic blood pressure (SBP), waist-to-hip ratio (WHR), FBG, 2 h postprandial glycemia(2hPG), 2 h insulin (2 h INS), IAF area, HOMA-IR, and 8-iso-PGF 2α increased, and high-density lipoprotein cholesterol (HDL-C) decreased in T2DM groups and Prediabetic group ( P < 0.05). The 2 h INS level was the highest in the Prediabetic group; 2hPG, and IAF area were the highest in the new-onset T2DM group; WHR, FBG, HOMA-IR and 8-iso-PGF 2α were the highest in the non-new-onset T2DM group. Multiple stepwise regression analysis identified IAF area and FBG as the strongest and independent determinant of 8-iso-PGF 2α ( P < 0.01). Conclusions In various glycometabolism populations, 8-iso-PGF2α is significantly correlated with FBG and IAF, this suggests that high blood glucose and abdominal obesity can increase the damage related to the OS in vivo.
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