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. 2024 Sep 30;13(9):1521-1528.
doi: 10.21037/tp-24-172. Epub 2024 Sep 13.

Predictive value of immune-related parameters in severe Mycoplasma pneumoniae pneumonia in children

Affiliations

Predictive value of immune-related parameters in severe Mycoplasma pneumoniae pneumonia in children

Chaoyue Jiang et al. Transl Pediatr. .

Abstract

Background: The severity of Mycoplasma pneumoniae pneumonia (MPP) is strongly correlated with the extent of the host's immune-inflammatory response. In order to diagnose the severity of MPP early, this study sought to explore the predictive value of immune-related parameters in severe MPP (sMPP) in admitted children.

Methods: We performed a database analysis consisting of patients diagnosed at our medical centers with MPP between 2021 and 2023. We included pediatric patients and examined the association between complete blood cell count (CBC), lymphocyte subsets and the severity of MPP. Binary logistic regression was performed to identify the independent risk factors of sMPP. Receiver operating characteristic (ROC) curves were used to estimate discriminant ability.

Results: A total of 245 MPP patients were included in the study, with 131 males and 114 females, median aged 6.0 [interquartile range (IQR), 4.0-8.0] years, predominantly located in 2023, and accounted for 64.5%. Among them, 79 pediatric patients were diagnosed as sMPP. The parameters of CBC including white blood cell (WBC) counts, neutrophil counts, monocyte counts, platelet counts, and neutrophil-to-lymphocyte ratio (NLR), were higher in the sMPP group (all P<0.05). The parameters of lymphocyte subsets including CD3+ T cell ratio (CD3+%) and CD3+CD8+ T cell ratio (CD3+CD8+%), were lower in the sMPP group (all P<0.05). And CD3-CD19+ B cell ratio (CD3-CD19+%) was higher in the sMPP group. Logistic regression analysis showed that age, CD3-CD19+%, and monocyte counts were identified as independent risk factors for the development of sMPP (all P<0.001). The three factors were applied in constructing a prediction model that was tested with 0.715 of the area under the ROC curve (AUC). The AUC of the prediction model for children aged ≤5 years was 0.823 and for children aged >5 years was 0.693.

Conclusions: The predictive model formulated by age, CD3-CD19+%, and monocyte counts may play an important role in the early diagnosis of sMPP in admitted children, especially in children aged ≤5 years.

Keywords: Mycoplasma pneumoniae pneumonia (MPP); pediatrics; risk factor; severity prediction.

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Conflict of interest statement

Conflicts of Interest: All authors have completed the ICMJE uniform disclosure form (available at https://tp.amegroups.com/article/view/10.21037/tp-24-172/coif). The authors have no conflicts of interest to declare.

Figures

Figure 1
Figure 1
The number of sMPP and nsMPP cases in 2021–2023. MPP, Mycoplasma pneumoniae pneumonia; sMPP, severe Mycoplasma pneumoniae pneumonia; nsMPP, non-severe Mycoplasma pneumoniae pneumonia.
Figure 2
Figure 2
ROC curves of the combined index of age + CD3CD19+% + monocyte counts for predicting sMPP. (A) ROC curves for children of all ages. The AUC was 0.715, with sensitivity 72.2% and specificity 63.3%. (B) ROC curves for children aged ≤5 years. The AUC was 0.823, with sensitivity 84.0% and specificity 77.9%. (C) ROC curves for children aged >5 years. The AUC was 0.693, with sensitivity 72.2% and specificity 61.8%. ROC, receiver operating characteristic; AUC, area under the ROC curve; CI, confidence interval; CD3CD19+%, CD3CD19+ B cell ratio; sMPP, severe Mycoplasma pneumoniae pneumonia.

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References

    1. Ding G, Zhang X, Vinturache A, et al. Challenges in the treatment of pediatric Mycoplasma pneumoniae pneumonia. Eur J Pediatr 2024;183:3001-11. 10.1007/s00431-024-05519-1 - DOI - PubMed
    1. Jain S, Williams DJ, Arnold SR, et al. Community-acquired pneumonia requiring hospitalization among U.S. children. N Engl J Med 2015;372:835-45. 10.1056/NEJMoa1405870 - DOI - PMC - PubMed
    1. Gao LW, Yin J, Hu YH, et al. The epidemiology of paediatric Mycoplasma pneumoniae pneumonia in North China: 2006 to 2016. Epidemiol Infect 2019;147:e192. 10.1017/S0950268819000839 - DOI - PMC - PubMed
    1. Hu J, Ye Y, Chen X, et al. Insight into the Pathogenic Mechanism of Mycoplasma pneumoniae. Curr Microbiol 2022;80:14. 10.1007/s00284-022-03103-0 - DOI - PMC - PubMed
    1. Saraya T, Kurai D, Nakagaki K, et al. Novel aspects on the pathogenesis of Mycoplasma pneumoniae pneumonia and therapeutic implications. Front Microbiol 2014;5:410. 10.3389/fmicb.2014.00410 - DOI - PMC - PubMed

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