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Age-specific Mycoplasma pneumoniae pneumonia-associated myocardial damage in children
Cheng-Mei Li1, Li Gu, Shao-Jun Yin
1Department of Paediatrics, Tenth People's Hospital, Tongji University, Shanghai, China.
Insights
Mycoplasma pneumoniae pneumonia (MPP) causes significant myocardial damage in children, particularly those aged 13-36 months and 7-14 years. This highlights potential age-specific immune responses to the infection.
Area of Science:
- Pediatric Cardiology
- Infectious Diseases
- Immunology
Background:
- Mycoplasma pneumoniae pneumonia (MPP) is a common childhood respiratory infection.
- Myocardial damage can be a complication of MPP, but its age-specific incidence is not well understood.
Purpose of the Study:
- To quantify Mycoplasma pneumoniae-associated myocardial damage in children with pneumonia.
- To investigate age-specific differences in MPP-related cardiac injury.
Main Methods:
- Children (0-14 years) with pneumonia and elevated serum creatine kinase isoenzyme-MB (CK-MB) were enrolled.
- Participants were tested for Mycoplasma pneumoniae immunoglobulin M (IgM) and stratified into four age groups.
- Age-specific myocardial damage was analyzed based on M. pneumoniae IgM status.
Main Results:
- Children positive for M. pneumoniae IgM showed higher fever incidence and median serum CK-MB levels.
- Significantly greater myocardial damage (higher CK-MB) was observed in M. pneumoniae IgM-positive children aged 13-36 months and 72 months-14 years.
- No significant difference in myocardial damage was found in the 37-71 months age group.
Conclusions:
- Mycoplasma pneumoniae infection is linked to increased myocardial damage in specific pediatric age groups (13-36 months and 72 months-14 years).
- Findings suggest that immune responses to M. pneumoniae may vary with age, influencing cardiac involvement.
Objective:
To measure Mycoplasma pneumoniae pneumonia (MPP)-associated myocardial damage in different age groups of children with pneumonia.
Methods:
Children aged 0-14 years with pneumonia and myocardial damage (serum creatine kinase isoenzyme-MB [CK-MB] concentration >25 U/l) were enrolled in the study. The children were classified as Mycoplasma pneumoniae immunoglobulin M positive (M. pneumoniae IgM+) or negative (M. pneumoniae IgM-) based on a serological test. Children were stratified into four age groups in order to analyse age-specific MPP-associated myocardial damage.
Results:
The incidence of fever was significantly higher in children who were M. pneumoniae IgM+ compared with M. pneumoniae IgM- children. The median serum CK-MB concentration was significantly higher in children who were M. pneumoniae IgM+ compared with those who were M. pneumoniae IgM-. Children who were M. pneumoniae IgM+ in the 13-36 months and 72 months-14 years age groups had significantly higher median serum CK-MB concentrations than those who were M. pneumoniae IgM- in the same age group.
Conclusions:
M. pneumoniae infection was associated with greater myocardial damage in children aged 13-36 months and 72 months-14 years. This suggests age-specific immune responses to M. pneumoniae.
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