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Antigen-Capture Enzyme-Linked Immunosorbent Assay for Specific Detection of Mycoplasma pneumoniae
Published on: February 24, 2023
Application value of systemic immune-inflammation index in predicting severe Mycoplasma pneumoniae pneumonia
Xiaocong Guo1,2,3, Honglin Luo3, Yaohui Song3
1Department of Clinical Laboratory, The Affiliated Traditional Chinese Medicine Hospital, Southwest Medical University, Luzhou, China.
Abstract:
Mycoplasma pneumoniae (MP) is the primary causative agent of community-acquired pneumonia. Severe mycoplasma pneumoniae pneumonia (SMPP) can result in multiorgan damage and even respiratory failure or death. This study aimed to evaluate the predictive value of the Systemic Immune-Inflammation Index (SII) for SMPP. This retrospective study included 254 hospitalized children with MP infections (SMPP group, n = 103; non-SMPP group, n = 151). Patient data, including complete blood count parameters (white blood cell, absolute neutrophil, absolute lymphocyte, absolute monocyte, and platelet counts), C-reactive protein (CRP), serum amyloid A (SAA), and other markers, were collected. Furthermore, the SII, Systemic Inflammation Response Index (SIRI), neutrophil/lymphocyte ratio (NLR), monocyte/lymphocyte ratio (MLR), and platelet/lymphocyte ratio (PLR) were calculated. T-tests and the Mann-Whitney U test were used to analyze differences between the groups. Logistic regression was applied to analyze the risk factors. Receiver operating characteristic (ROC) curves were plotted to evaluate the predictive performance of the SII and CRP for SMPP. The SMPP group exhibited significantly higher CRP and SAA levels, SII, NLR, MLR, PLR, and SIRI than the non-SMPP group (all P < 0.001). Logistic regression revealed that the SII (odds ratio [OR] = 1.006, 95% confidence interval [CI]: 1.001-1.010) and CRP (OR = 1.080, 95% CI: 1.041-1.120) were independent risk factors. ROC curve of the SII (area under the ROC curve = 0.883, sensitivity = 0.699, and specificity = 0.881) outperformed that of CRP. Thus, SII can serve as an effective biomarker for SMPP prediction. It can be a rapid and cost-effective method when combined with routine blood tests, thereby demonstrating considerable potential for clinical application.
Insights
The Systemic Immune-Inflammation Index (SII) effectively predicts severe Mycoplasma pneumoniae pneumonia (SMPP) in children. This simple blood test offers a rapid and cost-effective method for early detection and clinical application.
Area of Science:
- Pediatric Infectious Diseases
- Respiratory Medicine
- Clinical Immunology
- Biomarker Discovery
Background:
- Mycoplasma pneumoniae (MP) is a leading cause of community-acquired pneumonia.
- Severe MP pneumonia (SMPP) can lead to severe complications, including multiorgan damage and death.
- Accurate and early prediction of SMPP is crucial for timely intervention and improved patient outcomes.
Purpose of the Study:
- To evaluate the predictive value of the Systemic Immune-Inflammation Index (SII) for identifying severe Mycoplasma pneumoniae pneumonia (SMPP) in hospitalized children.
- To compare the predictive performance of SII against C-reactive protein (CRP) and other inflammatory markers.
Main Methods:
- A retrospective study involving 254 children with MP infections, categorized into SMPP (n=103) and non-SMPP (n=151) groups.
- Collection and analysis of complete blood count parameters, CRP, and serum amyloid A (SAA).
- Calculation of SII, SIRI, NLR, MLR, and PLR, followed by logistic regression and ROC curve analysis for predictive performance evaluation.
Main Results:
- The SMPP group showed significantly higher levels of CRP, SAA, SII, NLR, MLR, PLR, and SIRI compared to the non-SMPP group (P < 0.001).
- SII and CRP were identified as independent risk factors for SMPP.
- The SII demonstrated superior predictive performance (AUC=0.883) compared to CRP (AUC=0.779).
Conclusions:
- The Systemic Immune-Inflammation Index (SII) is an effective and independent biomarker for predicting severe Mycoplasma pneumoniae pneumonia in children.
- SII offers a rapid, cost-effective, and potentially valuable tool for clinical application when used with routine blood tests.
- Further research can explore the integration of SII into clinical guidelines for early SMPP detection and management.
