胰腺结石蛋白/再生蛋白(PSP/reg)作为预测2型糖尿病微血管并发症的生化标志物

Abrar Albadr, N. Haddad
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引用次数: 0

摘要

背景:2型糖尿病(T2DM)以胰岛素抵抗(IR)和功能β (β)细胞质量进行性下降为特征,部分原因是β细胞凋亡率增加。胰石蛋白/再生蛋白(PSP/reg)主要由胰腺产生,在胰腺疾病中急剧升高。β细胞在凋亡过程中刺激邻近存活细胞中PSP/reg基因的表达,随后这些细胞分泌PSP/reg蛋白,这可能在细胞再生中起作用。目的:分析2型糖尿病患者血清PSP/reg蛋白水平及其与微血管并发症的关系。对象与方法:150名参与者(男性64人,女性86人;年龄40-70岁),包括伴有或不伴有微血管并发症的T2DM患者以及健康对照者。测定随机血糖(RBG)、糖化血红蛋白(HbA1c)、血脂、尿素、肌酐(Cr)等生化指标。采用酶联免疫吸附试验(ELISA)测定血清PSP/reg蛋白水平。结果:伴有微血管并发症的T2DM患者血清PSP/reg蛋白水平明显高于对照组(p<0.001)和无微血管并发症的T2DM患者(p<0.001)。PSP/reg蛋白与2型糖尿病病程(p<0.001)、RBG (p<0.001)和HbA1c (p<0.001)相关。微血管并发症出现的曲线下面积(AUC)为0.973。结论:PSP/reg蛋白可作为预测T2DM微血管并发症的生化指标。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Pancreatic Stone Protein/ regenerating Protein (PSP/reg) as a Biochemical Marker for prediction of Microvascular Complications of Type 2 Diabetes Mellitus
Background: Type 2 diabetes mellitus (T2DM) characterized by insulin resistance (IR) and progressive decline in functional beta (β) cell mass partially due to increased β cell apoptosis rate. Pancreatic stone protein /regenerating protein (PSP/reg) is produced mainly by the pancreas and elevated drastically during pancreatic disorder. Beta cells are experiencing apoptosis that stimulate the expression of PSP/reg gene in surviving neighboring cells, and that PSP/reg protein is subsequently secreted from these cells which could play a role in their regeneration. Objectives: To analyze serum levels of PSP/reg protein in T2DM patients and evaluate its correlation with the microvascular complications of the disease. Subjects and Methods: One hundred fifty participants (64 males, 86 females; aged 40–70 years) include T2DM patients with and without microvascular complications as well as healthy controls were enrolled in this study. Biochemical parameters like random blood glucose (RBG), glycated hemoglobin (HbA1c), lipid profile, urea and creatinine (Cr) were measured. Serum values of PSP/reg protein were measured by enzyme- linked immunosorbent assay (ELISA). Results: Serum levels of PSP/reg protein were found significantly elevated in T2DM patients with microvascular complications compared with those of controls (p<0.001) and T2DM patients without microvascular complications (p< 0.001).PSP/reg protein is correlated with type 2 DM duration (p<0.001), RBG (p<0.001), and HbA1c (p<0.001). The area under the curve (AUC) for the presence of microvascular complications was 0.973. Conclusion: PSP/reg protein may be used as biochemical marker to predict microvascular complications of T2DM.  
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CiteScore
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