肺炎支原体,内皮细胞特异性分子 -1,肝素结合蛋白,早期诊断,预后 ," /> 肺炎支原体,内皮细胞特异性分子 -1,肝素结合蛋白,早期诊断,预后 ,"/> Mycoplasma pneumoniae,Endothelial cell specific molecule-1,Heparin-binding protein,Early diagnosis, Prognosis ,"/> <div> <span style="font-size:14px;line-height:2;">血清内皮细胞特异性分子 -1、肝素结合蛋白在肺炎支原体感染患儿预后评估中的价值</span> </div>
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发育医学电子杂志  2026, Vol. 14 Issue (3): 216-222    DOI: 10.3969/j.issn.2095-5340.2026.03.007
  生长发育   论著 |
血清内皮细胞特异性分子 -1、肝素结合蛋白在肺炎支原体感染患儿预后评估中的价值
李佳  徐丹 刘宇 赵悦含  李蕾 吴迪
首都医科大学附属北京友谊医院儿科,北京 100050;2. 衡水市第二人民医院 外三科,河北 衡水 053000
Value of serum endothelial cell specific molecular-1 and heparin-binding protein in the prognostic evaluation of Mycoplasma pneumoniae infection in children
Li Jia , Xu Dan, Liu Yu, et al.
1. Department of Pediatrics, Beijing Friendship Hospital, Capital Medical University, Beijing 100050, China; 2. Department of the Third Surgery, Hengshui Second People's Hospital, Hengshui, Hebei 053000, China
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摘要 
目的  探究血清内皮细胞特异性分子 -1(endothelial cell specific molecule-1,ESM-1)与肝素结合蛋白(heparin-binding protein,HBP)在儿童肺炎支原体(Mycoplasma pneumoniae,MP)感染预后评估中的价值。方法 采用前瞻性研究方法,选取 2022 年 1 月至 2023 年 1 月于首都医科大学附属北京友谊医院就诊的 168 例 MP 患儿作为 MP 组,根据治疗后是否痊愈将患儿分为预后良好组(n=112)和预后不良组(n=56)。基于随机数字表法选取同期于该院体检的 150 例健康儿童作为对照组,记录所有研究对象的年龄、身体质量指数等一般资料。采用酶联免疫吸附试验(enzyme-inked immunosorbent assay,ELISA)法检测血清 ESM-1、HBP 的表达水平。采用多因素 Logistic 回归分析探讨 MP 患儿发生预后不良的影响因素;采用 Pearson 法评价预后不良 MP 患儿血清中 ESM-1 与 HBP 表达水平的相关性;绘制受试者工作特征(receiver operating characteristic,ROC)曲线,分析血清 ESM-1、HBP 的表达水平对 MP 患儿预后不良的诊断价值,并采用 Delong 检验比较曲线下面积(area under the curve,AUC)的差异。统计学方法采用独立样本 t 检验、χ 2 检验。结果 MP 组患儿血清中 ESM-1、HBP 的表达水平显著高于对照组[(4.81±1.42) μg/L 与(3.69±1.13) μg/L,(24.47±7.31) μg/L 与(18.74±6.11) μg/L,t 值分别为 7.720、7.534,
P 值均 <0.001];预后不良组患儿血清中超敏 C- 反应蛋白(hypersensitive C-reaction protein,hs-CRP)、降钙素原(procalcitonin,PCT)、乳酸脱氢酶(lactate dehydrogenase,LDH)、ESM-1、HBP 的表达水平显著高于预后良好组[(25.34±7.56) mg/L 与(21.28±6.32) mg/L,(8.66±2.61) μg/L 与(6.21±1.93) μg/L,(345.72±103.25) U/L 与(267.21±83.14) U/L、(5.78±1.56) μg/L 与(4.32±1.14) μg/L,(29.16±7.11) μg/L 与(22.13±6.24) μg/L,t 值分别为 3.672、6.870、5.312、6.892、6.567,P 值均 <0.001]。多因素 Logistic 回归分析结果显示,血清中 hs-CRP、ESM-1、HBP 的表达水平是 MP 患儿预后不良的独立危险因素(OR 值分别为 1.546、1.587、1.826,P 值均 <0.05);Pearson 相关性分析结果显示,预后不良患儿血清中 ESM-1与 HBP 的表达水平呈正相关(r=0.445,P<0.001);ROC 曲线分析结果显示,ESM-1、HBP 单独及联合诊断 MP 患儿预后不良的 AUC 值分别为 0.791、0.820、0.880,两者联合诊断优于 ESM-1、HBP 单独诊断(Z 值分别为 2.889、2.084,P 值均 <0.05)。结论 血清 ESM-1 和 HBP 在 MP 患儿预后评估中具有较高的价值,可作为早期诊断及预后评估的有效指标。
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关键词:  肺炎支原体')" href="#">    
Abstract: 
Objective To explore the value of serum endothelial cell specific molecule-1 (ESM-1) and heparin binding protein (HBP) in prognostic evaluation of Mycoplasma pneumoniae (MP) infection in children. Methods A prospective study was conducted. A total of 168 children with MP admitted to Beijing Friendship Hospital, Capital Medical University from January 2022 to January 2023 were enrolled as the MP group. Based on treatment outcomes, they were divided into the favorable prognosis group (n=112) and the poor prognosis group (n=56). During the same period, 150 healthy children who underwent physical examinations at the hospital were selected as the control group by using a random number table method. The general data including age and body mass index were recorded for all participants. The expression levels of serum ESM-1 and HBP were detected using enzyme-linked immunosorbent assay (ELISA). Multivariate Logistic regression analysis was performed to explore the influencing factors of poor prognosis in children with MP
infection. Pearson method was used to evaluate the correlation between serum ESM-1 and HBP expression levels in children with poor prognosis. Receiver operating characteristic (ROC) curves were plotted to analyze the diagnostic value of serum ESM-1 and HBP expression levels for poor prognosis in children with MP infection, and the Delong test was applied to compare the differences in the area under the curve (AUC). Statistical analysis was performed using the independent sample t-test and χ2 test. Results The serum expression levels of ESM-1 and HBP in the MP group were significantly higher than those in the control group[(4.81±1.42) μg/L vs (3.69±1.13) μg/L, (24.47±7.31) μg/L vs (18.74±6.11) μg/L, t values were 7.720, 7.534, all P<0.001]. The serum expression levels of high-sensitivity C-reactive protein (hs-CRP), procalcitonin (PCT), lactate dehydrogenase (LDH), ESM-1, and HBP in the poor prognosis group were significantly higher than those in the favorable prognosis group[(25.34±7.56) mg/L vs (21.28±6.32) mg/L, (8.66±2.61) μg/L vs (6.21±1.93) μg/L, (345.72±103.25) U/L vs (267.21±83.14) U/L, (5.78±1.56) μg/L vs (4.32±1.14) μg/L, (29.16±7.11) μg/L vs (22.13±6.24) μg/L, t values were 3.672, 6.870, 5.312, 6.892, 6.567, all P<0.001]. Multivariate Logistic regression analysis showed that the serum expression levels of hs-CRP, ESM-1, and HBP were independent risk factors for poor prognosis in children with MP (OR values were 1.546, 1.587, 1.826, respectively, all P<0.05). Pearson correlation analysis showed that the serum expression levels of ESM-1 was positively correlated with HBP in children with poor prognosi, (r=0.445, P<0.001). ROC curve analysis showed that the AUC values for ESM-1 alone, HBP alone, and their combination in predicting poor prognosis in children with MP was 0.791, 0.820, and 0.880, respectively. The combined diagnosis of ESM-1 and HBP was superior to either ESM-1 alone or HBP alone (Z values were 2.889, 2.084, respectively, all P<0.05). Conclusion Serum ESM-1 and HBP have high value in prognosis evaluation of MP children, and can be used as effective indicators for early diagnosis and prognosis evaluation.
Key words:  Mycoplasma pneumoniae')" href="#">
收稿日期:  2025-12-25                出版日期:  2026-05-30      发布日期:  2026-05-30      期的出版日期:  2026-05-30
基金资助: 
河北省医学科学研究重点课题计划项目(20240471)
通讯作者:  李佳    E-mail:  996834920@qq.com
引用本文:    
李佳 徐丹 刘宇 赵悦含 李蕾 吴迪.
血清内皮细胞特异性分子 -1、肝素结合蛋白在肺炎支原体感染患儿预后评估中的价值
[J]. 发育医学电子杂志, 2026, 14(3): 216-222.
Li Jia , Xu Dan, Liu Yu, et al..
Value of serum endothelial cell specific molecular-1 and heparin-binding protein in the prognostic evaluation of Mycoplasma pneumoniae infection in children
. Journal of Developmental Medicine(Electronic Version), 2026, 14(3): 216-222.
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