Wang Mingjie, He Limei, Chang Yuandi, Yan Zhaoli
Department of Endocrinology, Affiliated Hospital of Inner Mongolia Medical University, Hohhot, China.
Department of Internal Medicine, The First Hospital of Inner Mongolia Prison Administration, Hohhot, Inner Mongolia, China.
Front Endocrinol (Lausanne). 2025 May 23;16:1534490. doi: 10.3389/fendo.2025.1534490. eCollection 2025.
This study aimed to determine potential serum biomarkers of type 2 diabetes (T2DM) through proteomic data analysis and protein association assessment.
This study included 80 patients with obesity, 76 patients with newly diagnosed T2DM combined with obesity, and 73 healthy controls. Proteomics analysis was used to investigate changes in protein abundance in the serum across the three groups. Correlations were analyzed using logistic regression, Pearson's correlation, and Spearman's correlation. Group comparisons for non-normally distributed continuous or categorical variables were performed using the Mann-Whitney U test, Kruskal-Wallis test, χ test, or Fisher's exact probability test, as appropriate. Logistic regression analysis was employed to identify independent predictors, and correlations were evaluated using Pearson or Spearman tests based on data distribution. Receiver operating characteristic (ROC) curve analysis was employed to determine the predictive value of the differential proteins for the diagnosis of obesity and T2DM.
In this study, two-dimensional gel electrophoresis was used to analyze three groups. Several proteins were differentially expressed, with α2-macroglobulin (α2-MG) showing significant up-regulation in the obesity and T2DM + obesity groups compared to the control group. ELISA verification showed higher α2-MG levels in the obesity (2.746±0.391 g/L) and T2DM + obesity (3.261±0.400 g/L) groups than in the control group (1.376±0.229 g/L) (P<0.05). For predicting obesity and T2DM combined with obesity, α2-MG (AUC=0.873 and 0.601 respectively) were significant predictors.
Serum a2-MG levels are elevated in obese individuals and those with T2DM. It shows high sensitivity and specificity for predicting obesity and T2DM, suggesting its potential as a biomarker for T2DM diagnosis. However, further large-scale studies are needed to confirm its clinical utility.
本研究旨在通过蛋白质组数据分析和蛋白质关联评估来确定2型糖尿病(T2DM)潜在的血清生物标志物。
本研究纳入80例肥胖患者、76例新诊断的T2DM合并肥胖患者和73例健康对照。采用蛋白质组学分析研究三组血清中蛋白质丰度的变化。使用逻辑回归、Pearson相关性分析和Spearman相关性分析进行相关性分析。对于非正态分布的连续或分类变量,根据情况使用Mann-Whitney U检验、Kruskal-Wallis检验、χ检验或Fisher精确概率检验进行组间比较。采用逻辑回归分析确定独立预测因子,并根据数据分布使用Pearson或Spearman检验评估相关性。采用受试者工作特征(ROC)曲线分析来确定差异蛋白对肥胖和T2DM诊断的预测价值。
在本研究中,使用二维凝胶电泳分析三组。几种蛋白质存在差异表达,与对照组相比,α2-巨球蛋白(α2-MG)在肥胖组和T2DM +肥胖组中显著上调。ELISA验证显示肥胖组(2.746±0.391 g/L)和T2DM +肥胖组(3.261±0.400 g/L)的α2-MG水平高于对照组(1.376±0.229 g/L)(P<0.05)。对于预测肥胖和T2DM合并肥胖,α2-MG(AUC分别为0.873和0.601)是显著的预测因子。
肥胖个体和T2DM患者血清α2-MG水平升高。它在预测肥胖和T2DM方面显示出高敏感性和特异性,表明其作为T2DM诊断生物标志物的潜力。然而,需要进一步的大规模研究来证实其临床实用性。