全血细胞计数来源的免疫炎症指标与不同年龄段儿童肺炎支原体肺炎重症化的关系
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军委后勤保障部卫生局面上项目(21JSZ05).


Relationship between immunoinflammatory indicators derived from complete blood count and severity of Mycoplasma pneumoniae pneumonia in children of different ages
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Supported by General Program of Health Bureau of General Logistics Support Department of Military Commission (21JSZ05).

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    摘要:

    目的 探讨9种全血细胞计数来源的免疫炎症指标与不同年龄段儿童肺炎支原体肺炎(MPP)重症化的关系。方法 选择2023年7月1日至2024年12月31日在海军军医大学第一附属医院儿科病房住院治疗的2 132例MPP患儿为研究对象,分为重症MPP(SMPP)组和非重症MPP(NSMPP)组,按照年龄、性别1∶1匹配后根据年龄将患儿分为1~6岁、>6~16岁2个亚组进行分析,收集并比较各组的基本资料、实验室检查结果及全血细胞计数来源的免疫炎症指标。采用单因素和多因素Cox比例风险回归模型分析SMPP的影响因素,利用ROC曲线评估差异有统计学意义的指标对SMPP的预测价值。结果 SMPP患儿220例,占MPP的10.3%。1~6岁患儿中,与NSMPP组相比,SMPP组患儿的住院时间长,血小板(PLT)计数、血小板与淋巴细胞比值(PLR)、中性粒细胞与淋巴细胞比值、衍生的中性粒细胞与淋巴细胞比值和系统性免疫炎症指数高(均P<0.05),其中PLR是患儿进展至SMPP的独立危险因素(OR=1.010,95%CI 1.003~1.018,P=0.007),PLR预测SMPP的AUC为0.635(95%CI 0.560~0.711,P<0.001),最佳截断值为125.04,此时对应的灵敏度为57.7%、特异度为70.2%;以最佳截断值为界将所有患儿分为低PLR组和高PLR组,高PLR组的重症率高于低PLR组[65.9% (60/91)vs 37.6%(44/117),P<0.001],以四分位数为界将所有患儿分为Q1~Q4组,Q4组的重症率(71.2%,37/52)高于Q1~Q3组(均P<0.05)。>6~16岁患儿中,与NSMPP组相比,SMPP组患儿的PLT和PLR高(均P<0.05),但都不是患儿进展至SMPP的独立危险因素(均P>0.05);以最佳截断值(137.03)为界将所有患儿分为低PLR组和高PLR组,高PLR组的重症率高于低PLR组[57.0%(77/135)vs 40.2%(39/97),P=0.011],以四分位数为界将所有患儿分为Q1~Q4组,Q4组的重症率(65.5%,38/58)高于Q1~Q3组(均P<0.05)。结论 全血细胞计数来源的免疫炎症指标,尤其是PLR,对于预测不同年龄段MPP患儿的重症化具有一定的应用价值。

    Abstract:

    Objective To investigate the relationship between 9 immunoinflammatory indicators derived from complete blood count and the severity of Mycoplasma pneumoniae pneumonia (MPP) in children of different ages. Methods Totally 2 132 children with MPP who were hospitalized in the Department of Pediatrics of The First Affiliated Hospital of Naval Medical University from Jul. 1, 2023, to Dec. 31, 2024 were enrolled, and were assigned to severe MPP (SMPP) or non-severe MPP (NSMPP) groups. According to age and gender 1∶1 matching, the children were assigned to 2 subgroups according to age (1-6 years old and >6-16 years old). The basic data, laboratory examination and immunoinflammatory indicators from complete blood count of each group were collected and compared. The influencing factors of SMPP were analyzed by univariate and multivariate Cox proportional hazards regression models. Receiver operating characteristic curves were used to analyze the predictive value of indicators that showed statistically significant differences for SMPP. Results There were 220 patients with SMPP, accounting for 10.3% of MPP. In children aged 1-6 years, compared with the NSMPP group, the SMPP group had a longer hospital stay, higher platelet (PLT) count, platelet-to-lymphocyte ratio (PLR), neutrophil-to-lymphocyte ratio, derived neutrophil-to-lymphocyte ratio and systemic immune-inflammation index (all P<0.05). PLR was an independent risk factor for SMPP (odds ratio=1.010, 95% confidence interval [CI]1.003-1.018, P=0.007). The area under curve predicted by PLR for SMPP was 0.635 (95%CI 0.560-0.711, P<0.001), the best cut-off value was 125.04, and the corresponding sensitivity and specificity were 57.7% and 70.2%, respectively. All the children were assigned to low PLR group or high PLR group using the best cut-off value as the boundary, and the severe disease rate in the high PLR group was significantly higher than that in the low PLR group (65.9%[60/91] vs 37.6%[44/117], P<0.001). All the children were assigned to Q1-Q4 groups by quartile, and the severe disease rate of the Q4 group (71.2%, 37/52) was significantly higher than that of the Q1-Q3 group (all P<0.05). In children aged >6-16 years, compared with the NSMPP group, the PLT and PLR in the SMPP group were higher (both P<0.05), but neither was an independent risk factor. All the children were assigned to low PLR group or high PLR group using the best cut-off value (137.03) as the boundary, and the severe disease rate in the high PLR group was significantly higher than that in the low PLR group (57.0%[77/135] vs 40.2%[39/97], P=0.011). All the children were assigned to Q1-Q4 groups by quartile, and the severe disease rate of the Q4 group (65.5%, 38/58) was significantly higher than that of the Q1-Q3 group (all P<0.05). Conclusion The immunoinflammatory indicators derived from complete blood count, especially PLR, have certain application value in predicting the severity of MPP children in different ages.

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  • 收稿日期:2025-02-13
  • 最后修改日期:2025-06-04
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  • 在线发布日期: 2025-11-25
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