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Published on: August 7, 2017
Reduced Steroid Metabolites Identify Infection-Prone Children in Two Independent Pre-Birth Cohorts
Nicole Prince1, Min Kim2, Rachel S Kelly1
1Channing Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA 02115, USA.
Insights
Lower levels of steroid metabolites in children are linked to increased respiratory infections. This finding could help identify children prone to infections early in life.
Area of Science:
- Pediatrics
- Metabolomics
- Immunology
Background:
- Recurrent respiratory infections pose significant risks to infant health.
- Identifying children susceptible to infections early is crucial but lacks established methods.
Purpose of the Study:
- To explore the association between steroid metabolites and respiratory infection incidence in early childhood.
- To identify potential metabolomic biomarkers for early infection proneness.
Main Methods:
- Analysis of plasma samples from two pre-birth cohorts (VITAL and COPSAC) at ages 1 and 6 years.
- Quantification of 18 steroid metabolites across various classes.
- Poisson regression to assess links between steroid metabolites and respiratory infection counts.
Main Results:
- Reduced levels of steroid metabolites (androgenic, corticosteroid, pregnenolone, progestin classes) were observed in children with higher infection rates.
- These patterns remained consistent and significant at age 6 years.
Conclusions:
- Steroid metabolite profiles may serve as indicators for identifying children prone to infections.
- Further clinical evaluation is recommended to establish their utility as a screening tool.
Abstract:
Recurrent respiratory infections are a leading cause of morbidity and mortality in early life, but there is no broadly accepted means to identify infection-prone children during this highly vulnerable period. In this study, we investigated associations between steroid metabolites and incident respiratory infections in two pre-birth cohorts to identify novel metabolomic signatures of early infection proneness. Children from the Vitamin D Antenatal Asthma Reduction Trial and the Copenhagen Prospective Studies on Asthma in Childhood were included, and profiling was performed on plasma samples collected at ages 1 and 6 years. Both cohorts recorded incidence of lower respiratory infections, upper respiratory infections, ear infections, and colds. Poisson regression analysis assessed the associations between 18 steroid metabolites and the total number of respiratory infections that occurred in offspring during follow-up. We found that steroid metabolites across androgenic, corticosteroid, pregnenolone, and progestin classes were reduced in children that suffered more infections, and these patterns persisted at age 6 years, generally reflecting consistency in direction of effect and significance. Our analysis suggested steroid metabolite measurement may be useful in screening for infection proneness during this critical developmental period. Future studies should clinically evaluate their potential utility as a clinical screening tool.
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