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Association between early chronic methicillin-susceptible Staphylococcus aureus colonization and lung function in
Birce Sunman1, Ebru Yalcin1, Beste Ozsezen1
1Department of Pediatric Pulmonology, Hacettepe University Faculty of Medicine, Ihsan Dogramaci Children's Hospital, Ankara, Turkey.
Insights
Early methicillin-susceptible Staphylococcus aureus (MSSA) colonization in children with cystic fibrosis (CF) is linked to worse lung function and more frequent exacerbations by age 8. Further research is needed to confirm causality.
Area of Science:
- Pediatric Pulmonology
- Infectious Diseases in Cystic Fibrosis
- Microbiome and Health Outcomes
Background:
- Early-onset methicillin-susceptible Staphylococcus aureus (MSSA) colonization in children with cystic fibrosis (CF) may impact long-term health.
- Understanding the effects of early MSSA colonization is crucial for developing targeted interventions in CF care.
Purpose of the Study:
- To investigate the association between early chronic MSSA colonization and clinical outcomes at 8 years of age in children with CF.
- To compare lung function, nutritional status, and exacerbation frequency in early-onset versus late-onset MSSA colonization groups.
Main Methods:
- Retrospective cohort study of 52 children with CF and chronic MSSA colonization.
- Comparison of lung function (FEV1, FEF25-75, FVC), BMI, and exacerbation frequency at age 8.
- Groups defined by onset of chronic MSSA colonization: before age 4 (early) vs. age 4-6 (late).
Main Results:
- Children with early-onset MSSA colonization had significantly lower FEV1 and FEF25-75 at age 8 compared to the late-onset group.
- Exacerbation frequency between ages 6 and 8 was significantly higher in the early-onset MSSA colonization group.
- No significant difference in BMI was observed between the early-onset and late-onset groups at age 8.
Conclusions:
- Early chronic MSSA colonization in children with CF is associated with poorer lung function and increased exacerbations.
- The findings suggest a potential negative impact of early MSSA colonization on CF pulmonary outcomes.
- Further research is warranted to establish a definitive cause-and-effect relationship.
Background:
Our aim was to determine whether early chronic methicillin-susceptible Staphylococcus aureus (MSSA) colonization in children with cystic fibrosis (CF) is associated at 8 years of age with poorer lung function, poorer nutritional status, and increased exacerbation frequency.
Methods:
In this retrospective cohort study, a total of 52 children with chronic MSSA colonization were included. Of them, 26 were chronically colonized with MSSA before the age of 4 years (early onset), and 26 were chronically colonized from 4 years to 6 years of age (late-onset). At the age of 8 years, lung function, body mass index (BMI) as an indicator of nutritional status and frequency of pulmonary exacerbations were compared between two groups.
Results:
At 8 years of age, BMI was similar between the early-onset and late-onset groups (15.0 [min-max: 12.9-26.8] vs. 15.7 (min-max: 13.0-24.9), p = 0.327]. Percentage of forced expiratory volume in 1 s (FEV1) and forced expiratory flow between 25% and 75% of vital capacity (FEF25-75) in 8-year-old children were significantly lower in the early onset group compared to the late-onset group (98 [min-max: 44-139] vs. 106.5 [min-max: 82-131], p = 0.047; 84.9 ± 25.5 vs. -102.3 ± 26.3, respectively; p = 0.019], although the percentage of forced vital capacity did not differ significantly between two groups (93.5 [min-max: 45-131] vs. 103 [min-max: 84-119], respectively; p = 0.092). Exacerbation frequency between the ages of 6 and 8 years in the early onset group was higher compared to the late-onset group according to the Poisson regression model [1 (min-max:0-10) vs 0 (min-max:0-4), respectively; p = 0.044].
Conclusions:
Early chronic MSSA colonization is associated with poorer lung function and frequent exacerbations in children with CF. However, further studies are needed to reveal the cause-and-effect relationship between early chronic MSSA colonization and pulmonary outcome.
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