首页|血清sKlotho、OPN水平与1型糖尿病儿童糖代谢紊乱及微血管并发症的相关性

血清sKlotho、OPN水平与1型糖尿病儿童糖代谢紊乱及微血管并发症的相关性

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目的 探讨 1 型糖尿病(T1DM)儿童血清分泌型Klotho(sKlotho)、骨桥蛋白(OPN)水平与糖代谢紊乱及微血管并发症的关系.方法 选择 2021 年 1 月至 2023 年 1 月诊治T1DM患儿 116 例为研究对象(TIDM组),根据是否存在微血管并发症分为并发症组 36 例和无并发症组 80 例.另选择同期拟行择期手术的 60 例腹股沟斜疝患儿为对照组.酶联免疫吸附实验检测各组血清sKlotho、OPN水平.Pearson分析T1DM患儿血清sKlotho、OPN与糖代谢指标[空腹血糖(FPG)、空腹胰岛素(FINS)、胰岛素抵抗指数(HOMA-IR)、糖化血红蛋白(HbA1c)]的相关性.多因素Logistic回归分析影响TIDM儿童微血管并发症发生的危险因素.受试者工作特征曲线(ROC)分析血清sKlotho、OPN对TIDM儿童微血管并发症发生的预测价值.结果 T1DM组血清sKlotho水平低于对照组,差异有统计学意义(t=42.141,P=0.000).T1DM组血清OPN水平,高于对照组差异有统计学意义(t=20.629,P=0.000).并发症组血清sKlotho水平低于无并发症组,而OPN水平高于无并发症组,差异具有统计学意义(均P<0.05).T1DM 患儿血清sKlotho与FPG、FINS、HOMA-IR、HbA1c呈显著负相关,血清OPN与FPG、FINS、HOMA-IR、HbA1c呈显著正相关(均P<0.05).sKlotho是影响T1DM 患儿微血管并发症发生的独立保护因素,OPN是影响T1DM 患儿微血管并发症发生的独立危险因素.血清sKlotho、OPN二者联合诊断T1DM患儿并发微血管并发症的曲线下面积为 0.850,大于两指标单独检测0.778、0.752,差异有统计学意义(Z=5.183、4.349,P均<0.001).结论 T1DM患儿血清sKlotho降低,OPN升高,两者与T1DM患儿糖代谢紊乱有关,两者联合有助于评估微血管并发症的发生.
Correlation analysis of serum sKlotho and OPN levels with glucose metabolism disorder and microvascular complications in children with type 1 diabetes mellitus
Objective To investigate the correlation of serum levels of secretory Klotho(sKlotho),and osteopontin(OPN)with glucose metabolism disorder and microvascular complications in children with type 1 diabetes mellitus(TIDM).Methods A total of 116 children with T1DM diagnosed and treated in our hospital from January 2021 to January 2023 were selected as the study subjects(TIDM group).According to the presence or absence of microvascular complications,they were divided into complication group(n=36)and non-complication group(n= 80).Another 60 children with indirect inguinal hernia managed by an elective surgery in our hospital during the same period were selected as the control group.The serum levels of sKlotho and OPN in each group were detected by enzyme linked immunosorbent assay(ELISA).Pearson correlation was performed to analyze the correlation of serum sKlotho and OPN with glucose metabolism indicators in children with T1DM,including fasting plasma glucose(FPG),fasting insulin(FINS),homeostatic model assessment for insulin resistance(HOMA-IR),and glycosylated hemoglobin(HbA1c).Multivariate logistic regression analysis was used to analyze the risk factors for microvascular complications in children with TIDM.The predictive value of serum sKlotho and OPN in the occurrence of microvascular complications in children with TIDM was analyzed by plotting the receiver operating characteristic(ROC)curve.Results The serum sKlotho level in T1DM group was significantly lower than that of control group(t = 42.141,P=0.000).The serum OPN level in T1DM group was significantly higher than that of control group(t=20.629,P=0.000).The serum sKlotho level in the complication group was significantly lower than that in the non-complication group,while the levels of OPN was significantly higher than those of the non-complication group(all P<0.05).In children with T1DM,serum sKlotho was significantly negatively correlated with FPG,FINS,HOMA-IR,and HbA1c,while serum OPN was significantly positively correlated with FPG,FINS,HOMA-IR,and HbA1c(all P<0.05).SKlotho was an independent protective factor for microvascular complications in children with T1DM,while OPN was an independent risk factor for it.The area under the curve(AUC)of the combined detection of serum sKlotho and OPN in diagnosing children with T1DM complicated with microvascular complications was 0.850,which was larger than that of the single detection(AUC=0.778,Z= 5.183;AUC= 0.752,Z= 4.349,respectively;both P<0.001).Conclusion The decrease of sKlotho and the increase of OPN are correlated with the disorder of glucose metabolism in children with T1DM.The combined detection of serum sKlotho and OPN contribute to predict the occurrence of microvascular complications.

childrentype 1 diabetesmicrovascular complicationsglucose metabolismKlothoosteopontin

王琦、邢晓婧、杨丽微

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154002 黑龙江省佳木斯市中心医院儿科

哈尔滨医科大学附属第六医院儿科

儿童 1型糖尿病 微血管并发症 糖代谢 Klotho 骨桥蛋白

黑龙江省医药卫生科研课题

2020155

2024

河北医药
河北省医学情报研究所

河北医药

CSTPCD
影响因子:1.075
ISSN:1002-7386
年,卷(期):2024.46(1)
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