首页|期刊导航|中国当代儿科杂志|多配体蛋白聚糖-1对早产儿坏死性小肠结肠炎的诊断价值:一项多中心前瞻性研究

多配体蛋白聚糖-1对早产儿坏死性小肠结肠炎的诊断价值:一项多中心前瞻性研究OA

Multicenter prospective study on the diagnostic value of syndecan-1 for necrotizing enterocolitis in preterm infants

中文摘要英文摘要

目的 探讨内皮糖萼损伤标志物多配体蛋白聚糖-1(syndecan-1,SDC-1)对早产儿坏死性小肠结肠炎(necrotizing enterocolitis,NEC)的临床诊断价值.方法 采用多中心、前瞻性研究设计,选取2025年2-7月陆军军医大学第一附属医院、四川省妇幼保健院及聊城市人民医院住院的Bell分期Ⅱ~Ⅲ期NEC早产儿为NEC组(38例),按1∶1比例选择同期非NEC早产儿为非NEC组(38例).收集两组患儿围产期资料以及血常规、SDC-1及超敏C反应蛋白(high-sensitivity C-reactive protein,hs-CRP)等指标的检测结果,采用多因素logistic回归分析评估早产儿NEC发生的危险因素,通过受试者操作特征曲线评估SDC-1对NEC的诊断价值.结果 NEC组中性粒细胞计数、SDC-1及hs-CRP水平显著高于非NEC组患儿(P<0.05),血小板计数显著低于非NEC组患儿(P<0.05).多因素logistic回归分析显示,SDC-1(OR=1.081,95%CI:1.028~1.137,P<0.05)及hs-CRP(OR=1.267,95%CI:1.051~1.527,P<0.05)水平升高是早产儿NEC发生的独立危险因素.受试者操作特征曲线分析显示,SDC-1(临界值为125 ng/mL)及hs-CRP(临界值为6.56 mg/L)诊断早产儿NEC的曲线下面积分别为0.882、0.863,两者联合对早产儿NEC诊断的曲线下面积为0.938,灵敏度和特异度分别为76.3%、97.4%.结论 SDC-1可作为诊断早产儿NEC的潜在生化标志物,但其临床应用价值仍需更大样本研究进一步验证.

Objective To investigate the clinical diagnostic value of the endothelial glycocalyx injury biomarker syndecan-1(SDC-1)for necrotizing enterocolitis(NEC)in preterm infants.Methods A multicenter,prospective study was conducted from February to July 2025 at the First Affiliated Hospital of Army Medical University,Sichuan Maternal and Child Health Hospital,and Liaocheng People's Hospital.Preterm infants with Bell stage Ⅱ-Ⅲ NEC were enrolled as the NEC group(n=38),and contemporaneous non-NEC preterm infants were selected in a 1∶1 ratio as the non-NEC group(n=38).Perinatal data and measurements of complete blood counts,SDC-1,and high-sensitivity C-reactive protein(hs-CRP)were collected.Multivariable logistic regression was used to evaluate risk factors for NEC.Receiver operating characteristic(ROC)curves were used to assess diagnostic performance of SDC-1.Results Neutrophil count,SDC-1,and hs-CRP levels were significantly higher in the NEC group than in the non-NEC group(P<0.05),while platelet count was significantly lower(P<0.05).Elevated SDC-1(OR=1.081,95%CI:1.028-1.137;P<0.05)and hs-CRP(OR=1.267,95%CI:1.051-1.527;P<0.05)were independent risk factors for NEC.ROC analysis showed that SDC-1(cutoff 125 ng/mL)and hs-CRP(cutoff 6.56 mg/L)yielded areas under the curve(AUCs)of 0.882 and 0.863,respectively.Their combination achieved an AUC of 0.938 with a sensitivity of 76.3%and a specificity of 97.4%.Conclusions SDC-1 is a potential biochemical biomarker for diagnosing NEC in preterm infants,but its clinical utility requires further validation in larger-sample studies.

尹显源;赵智慧;王钰;蔡娜;陈盛

陆军军医大学第一附属医院儿科,重庆 400038四川省妇幼保健院新生儿科,四川 成都 610000聊城市人民医院儿科,山东 聊城 252000陆军军医大学第一附属医院儿科,重庆 400038陆军军医大学第一附属医院儿科,重庆 400038

坏死性小肠结肠炎多配体蛋白聚糖-1超敏C反应蛋白早产儿

Necrotizing enterocolitisSyndecan-1High-sensitivity C-reactive proteinPreterm infant

《中国当代儿科杂志》 2026 (3)

277-284,8

国家自然科学基金项目(82301956、82170565)重庆市自然科学基金重点项目(2024NSCQ-KJFZZDX0018)重庆市科卫联合医学科研项目(2025MSXM037).

10.7499/j.issn.1008-8830.2508180

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