Ornek Diker Vesile, Serin Ozden, Yorulmaz Ertug Ebru, Baytekin Ozlem, Oguz Osman, Güvenen Güvenç
Mehmet Akif Ersoy T.C.S. Training and Research Hospital, Medical Biochemistry, Istanbul, Turkey.
Istanbul Taksim Egitim ve Aragtirma Hastanesi, Medical Biochemistry, Istanbul, Turkey.
J Med Biochem. 2025 Aug 21;44(5):1067-1073. doi: 10.5937/jomb0-57001.
Adipocytokines, along with macrophages infiltrating adipose tissue, contribute to chronic low-grade inflammation, which leads to insulin resistance and type 2 diabetes. Understanding insulin resistance in non-diabetic individuals and its cellular mechanisms is key for developing effective treatments and improving current protocols. This study aimed to investigate the levels of Retinol Binding Protein 4 (RBP4), Lipocalin-2, and high-sensitivity C-reactive protein (hsCRP) in individuals with impaired fasting glucose (IFG), impaired glucose tolerance (IGT), and type 2 diabetes mellitus (T2DM).
This prospective case-control study included individuals with IFG, IGT, and newly diagnosed T2DM. Routine laboratory tests, including fasting blood glucose, insulin, HbA1c, and lipid profiles, were collected and analysed. RBP4, Lipocalin-2, and hsCRP levels were measured using the ELISA method.
Significant differences were found in fasting blood glucose, insulin, triglycerides, total cholesterol, and HOMA-IR values among the study groups. hsCRP levels were significantly elevated in the IGT and T2DM groups compared to controls, while RBP4 and Lipocalin-2 levels showed no significant differences. A positive correlation was observed between hsCRP and HbA1c in the IFG group, as well as between hsCRP and Lipocalin-2 in the T2DM group.
This study demonstrates that hsCRP and Lipocalin-2 are associated with early glucose metabolism abnormalities and may serve as markers for insulin resistance and inflammation in prediabetes and T2DM. Future research is needed to clarify the roles of these biomarkers and their potential as therapeutic targets in diabetes prevention and treatment.
脂肪细胞因子与浸润脂肪组织的巨噬细胞共同导致慢性低度炎症,进而引发胰岛素抵抗和2型糖尿病。了解非糖尿病个体的胰岛素抵抗及其细胞机制是开发有效治疗方法和改进现有方案的关键。本研究旨在调查空腹血糖受损(IFG)、糖耐量受损(IGT)和2型糖尿病(T2DM)患者中视黄醇结合蛋白4(RBP4)、脂质运载蛋白2和高敏C反应蛋白(hsCRP)的水平。
这项前瞻性病例对照研究纳入了IFG、IGT和新诊断的T2DM患者。收集并分析了包括空腹血糖、胰岛素、糖化血红蛋白和血脂谱在内的常规实验室检查结果。采用酶联免疫吸附测定法(ELISA法)测量RBP4、脂质运载蛋白2和hsCRP水平。
研究组之间在空腹血糖、胰岛素、甘油三酯、总胆固醇和稳态模型评估胰岛素抵抗(HOMA-IR)值方面存在显著差异。与对照组相比,IGT和T2DM组的hsCRP水平显著升高,而RBP4和脂质运载蛋白2水平无显著差异。在IFG组中,hsCRP与糖化血红蛋白之间以及在T2DM组中hsCRP与脂质运载蛋白2之间观察到正相关。
本研究表明,hsCRP和脂质运载蛋白2与早期糖代谢异常相关,可能作为糖尿病前期和T2DM中胰岛素抵抗和炎症的标志物。需要进一步的研究来阐明这些生物标志物的作用及其作为糖尿病预防和治疗中治疗靶点的潜力。