Department of Biochemistry, Meram Faculty of Medicine, Necmettin Erbakan University, Konya, Turkey.
Obes Facts. 2012;5(5):700-9. doi: 10.1159/000343954. Epub 2012 Oct 18.
We have measured ischemia-modified albumin (IMA), total antioxidant status (TAS), total oxidant status (TOS) and high-sensitivity C-reactive protein (hsCRP) levels in obese and normal-weight subjects to investigate if IMA can be used as a biomarker of oxidative stress and inflammation and if IMA was an independent determinant of obesity or not.
The study was performed on 92 obese subjects (20 male, 72 female) aged 38 ± 11 years and 78 normal-weight controls (19 male, 59 female) aged 37 ± 11 years. Serum lipids, IMA, TAS, TOS, and hsCRP levels of the subjects were measured.
IMA (p < 0.05), TOS (p < 0.001), and hsCRP (p < 0.001) levels of the obese subjects were significantly higher, whereas TAS levels were significantly lower (p < 0.05) than those of the controls after adjustment for age and gender. In the linear regression analysis, waist circumference (r² = 0.139, p < 0.01), BMI (r² = 0.136, p < 0.01) and insulin (r² = 0.120, p < 0.05) were shown to be significant independent determinants of IMA levels.
We have found that oxidative stress and inflammation were increased and antioxidative defense was decreased, which resulted in increased levels of IMA, a biomarker of ischemia, in obese subjects. Also, obesity and insulin were found to be independent determinants of IMA. Thus, obese subjects are under high risk of ischemia, and IMA may be used as a biomarker of oxidative stress and ischemia. Further larger investigations are needed to confirm this opinion.
我们测量了肥胖和正常体重受试者的缺血修饰白蛋白(IMA)、总抗氧化状态(TAS)、总氧化状态(TOS)和高敏 C 反应蛋白(hsCRP)水平,以研究 IMA 是否可用作氧化应激和炎症的生物标志物,以及 IMA 是否是肥胖的独立决定因素。
该研究纳入了 92 名肥胖受试者(20 名男性,72 名女性),年龄为 38 ± 11 岁,以及 78 名正常体重对照组受试者(19 名男性,59 名女性),年龄为 37 ± 11 岁。测量了受试者的血清脂质、IMA、TAS、TOS 和 hsCRP 水平。
肥胖受试者的 IMA(p < 0.05)、TOS(p < 0.001)和 hsCRP(p < 0.001)水平显著升高,而 TAS 水平显著降低(p < 0.05),经年龄和性别校正后,与对照组相比。在线性回归分析中,腰围(r² = 0.139,p < 0.01)、BMI(r² = 0.136,p < 0.01)和胰岛素(r² = 0.120,p < 0.05)被证明是 IMA 水平的显著独立决定因素。
我们发现肥胖受试者的氧化应激和炎症增加,抗氧化防御减少,导致缺血标志物 IMA 水平升高。此外,肥胖和胰岛素被发现是 IMA 的独立决定因素。因此,肥胖患者存在较高的缺血风险,IMA 可能作为氧化应激和缺血的生物标志物。需要进一步的大规模研究来证实这一观点。