Background. Mycoplasma pneumoniae pneumonia (MPP) is the leading cause of community-acquired pneumonia in China and poses a significant threat to the health of children. This study aimed to evaluate the diagnostic value of leukocyte cell population data (CPD) and soluble cytokines in MPP to provide insights into its clinical diagnosis.
Methods. A total of 70 children with MPP confirmed via MP-DNA testing were enrolled in the MPP group. Simultaneously, 70 healthy children who underwent routine physical examinations were recruited as the control group. Peripheral blood leukocyte cell population parameters and serum soluble cytokine levels were collected from all participants. Through statistical analysis, the best combination of biomarkers for the early diagnosis of MPP was identified.
Results. The median age of patients with MPP was 7 (6–8) years, with a median fever duration of 6 (4.5–8.5) days. Statistically significant differences (p < 0.05) were observed between MPP and healthy control groups in a range of leukocyte CPD parameters. Among the leukocyte parameters, the side-scattered light distribution width index of the neutrophil area in the WDF scattergram (NE-WX) displayed the highest diagnostic performance, with an AUC of 0.846, sensitivity of 75.71%, and specificity of 87.14%. The side-scattered light intensity of the monocyte area in the WDF scattergram (MO-X), immature granulocyte percentage (IG%), and immature granulocyte count (IG) also demonstrated strong diagnostic values, with AUCs of 0.833, 0.818, and 0.807, respectively. Among the lymphocyte-related parameters, the side-scattered light distribution width index of the lymphocyte area in the WDF scattergram (LY-WX) and the fluorescence distribution width index of the lymphocyte area in the WDF scattergram (LY-WY) exhibited AUCs of 0.816 and 0.747, respectively, indicating good diagnostic ability. The MPP group exhibited significantly higher levels of soluble CD40 ligand (sCD40L), soluble interleukin-2 receptor alpha (sCD25), soluble triggering receptor expressed on myeloid cells-1 (sTREM-1), and soluble interleukin-6 receptor beta subunit (sCD130) than the control group (p < 0.05). Univariate and stepwise multivariable logistic regression analyses identified sCD25, sTREM-1, IG%, and MO-X as four independent risk factors for MPP. This combination of four markers achieved the best diagnostic performance, with an AUC of 0.996, significantly outperforming any single marker. The sensitivity and specificity of this combined model were 98.6%.
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