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妊娠期糖尿病患者血清晚期糖基化终产物及其受体介导的氧化应激与围产期结局的相关性

Correlation between serum advanced glycation end-products and their receptor-mediated oxidative stress and perinatal outcomes in gestational diabetes mellitus.

作者信息

Zhang Ying, Li Teng, Wang Zhi-Heng, Liu Yun

机构信息

Department of Laboratory Medicine, Obstetrics and Gynecology Hospital of Fudan University, Shanghai 200011, China.

Department of Interventional Radiology, The People's Hospital of Weifang City, Weifang 261041, Shandong Province, China.

出版信息

World J Diabetes. 2025 Jun 15;16(6):104177. doi: 10.4239/wjd.v16.i6.104177.

Abstract

BACKGROUND

Gestational diabetes mellitus (GDM) is one of the most prevalent metabolic disorders of pregnancy. Advanced glycation end-products (AGEs) are a complex and highly heterogeneous group of compounds formed from amino acids and reducing sugars. High-AGE diet exposure during pregnancy may cause adverse effects.

AIM

To investigate the expression levels of AGE and AGE receptor (RAGE) in the serum and placenta of pregnant women with GDM and to assess the association of their mediated oxidative stress response with perinatal outcomes.

METHODS

This study retrospectively analyzed the clinical data of 126 pregnant women with GDM who gave birth in the Obstetrics Department of Obstetrics and Gynecology Hospital of Fudan University from January 2023 to January 2024. A total of 85 pregnant women of similar age without GDM during the same period were selected as the control group. Fasting blood glucose, glycated hemoglobin, AGEs, soluble RAGE (sRAGE), and oxidative stress were compared in both groups. Postpartum placental tissue was collected to identify RAGE protein expression. Participants with GDM were categorized based on perinatal outcomes into normal ( = 89) and adverse perinatal outcome groups ( = 37), and differences in serum AGE-RAGE levels and oxidative stress were analyzed. The influencing factors of adverse perinatal outcomes were analyzed using logistic regression.

RESULTS

The GDM group demonstrated notably higher serum AGE ( = 8.955) and malondialdehyde (MDA) levels ( = 14.14) and lower sRAGE ( = 16.37) and superoxide dismutase (SOD) levels ( = 18.50) than the control group at 24-28 weeks of gestation and before delivery ( < 0.0001). Serum AGE levels were positively correlated with MDA and negatively related to SOD at 24-28 weeks of pregnancy (SOD: = 0.393, MDA: = 0.424, < 0.0001) and before delivery (SOD: = 0.443, MDA: = 0.492, < 0.0001), whereas AGE was inversely associated with sRAGE in the GDM group ( = -0.495, < 0.0001). Serum AGE levels were significantly higher ( = 9.225, < 0.0001) and the sRAGE level ( = 3.563, < 0.0001) was significantly lower in participants with adverse perinatal outcomes than those with normal perinatal outcomes in the GDM group. Logistic regression analysis revealed AGE level as a risk factor (OR = 1.056, P < 0.0001) and sRAGE level (OR = 0.949, < 0.0001) as a protective factor for adverse perinatal outcomes in GDM.

CONCLUSION

High serum AGE level is a risk factor for adverse perinatal outcomes in GDM, whereas high sRAGE levels are protective. AGEs and RAGE may be associated with oxidative stress in pregnant women with GDM.

摘要

背景

妊娠期糖尿病(GDM)是妊娠期最常见的代谢紊乱之一。晚期糖基化终产物(AGEs)是由氨基酸和还原糖形成的一组复杂且高度异质的化合物。孕期高AGE饮食暴露可能会产生不良影响。

目的

研究GDM孕妇血清和胎盘中AGE及AGE受体(RAGE)的表达水平,并评估其介导的氧化应激反应与围产期结局的相关性。

方法

本研究回顾性分析了2023年1月至2024年1月在复旦大学附属妇产科医院产科分娩的126例GDM孕妇的临床资料。选取同期85例年龄相仿的非GDM孕妇作为对照组。比较两组的空腹血糖、糖化血红蛋白、AGEs、可溶性RAGE(sRAGE)和氧化应激情况。收集产后胎盘组织以鉴定RAGE蛋白表达。将GDM患者根据围产期结局分为正常组(=89)和围产期不良结局组(=37),分析血清AGE-RAGE水平和氧化应激的差异。采用逻辑回归分析围产期不良结局的影响因素。

结果

在妊娠24 - 28周及分娩前,GDM组血清AGE水平(=8.955)和丙二醛(MDA)水平(=14.14)显著高于对照组,而sRAGE水平(=16.37)和超氧化物歧化酶(SOD)水平(=18.50)显著低于对照组(<0.0001)。妊娠24 - 28周时(SOD:=0.393,MDA:=0.424,<0.0001)及分娩前(SOD:=0.443,MDA:=0.492,<0.0001),血清AGE水平与MDA呈正相关,与SOD呈负相关,而在GDM组中AGE与sRAGE呈负相关(=-0.495,<0.0001)。GDM组中围产期不良结局患者的血清AGE水平显著更高(=9.225,<(0.0001)),sRAGE水平显著更低(=3.563,<0.0001)。逻辑回归分析显示,AGE水平是GDM围产期不良结局的危险因素(OR = 1.056,P < 0.0001),sRAGE水平是保护因素(OR = 0.949,<0.0001)。

结论

高血清AGE水平是GDM围产期不良结局的危险因素,而高sRAGE水平具有保护作用。AGEs和RAGE可能与GDM孕妇的氧化应激有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f75b/12179900/7c3d1ea9a13d/wjd-16-6-104177-g001.jpg

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