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Published on: August 7, 2017
Alterations in Serum-Free Amino Acid Profiles in Childhood Asthma
Joanna Matysiak1, Agnieszka Klupczynska2, Kacper Packi2
1Faculty of Health Sciences, The President Stanisław Wojciechowski State University of Applied Sciences in Kalisz, 62-800 Kalisz, Poland.
Insights
Researchers identified specific amino acids (AAs) as potential biomarkers for childhood asthma. Altered levels of taurine, L-valine, and others may aid in early diagnosis and personalized treatment strategies for pediatric asthma.
Area of Science:
- Biochemistry
- Pediatric Pulmonology
- Metabolomics
Background:
- Childhood asthma diagnosis is challenging, relying on clinical signs and response to treatment.
- Novel biomarkers are crucial for differentiating asthma phenotypes and personalizing therapy.
- Amino acids (AAs) are fundamental metabolites with potential roles in disease pathogenesis.
Purpose of the Study:
- To identify metabolomic-based biomarkers for childhood asthma among serum-free amino acids.
- To investigate the role of proteinogenic and non-proteinogenic AAs in pediatric asthma.
- To explore potential diagnostic markers for early asthma detection.
Main Methods:
- Analysis of a wide panel of serum-free amino acids in asthmatic children and healthy controls.
- Utilized high-performance liquid chromatography with tandem mass spectrometry (LC-MS/MS) for AA quantification.
- Employed uni- and multivariate statistical analyses to interpret the metabolomic data.
Main Results:
- Asthmatic children showed decreased serum concentrations of taurine, L-valine, and DL-β-aminoisobutyric acid.
- Elevated levels of ƴ-amino-n-butyric acid and L-arginine were observed in asthmatic children.
- These specific AA alterations suggest a role in the pathogenesis of childhood asthma.
Conclusions:
- Specific serum amino acid profiles may serve as novel biomarkers for childhood asthma.
- Findings contribute to the understanding of asthma pathogenesis and personalized medicine.
- Potential for integrating these biomarkers into clinical practice for improved diagnosis and treatment.
Abstract:
Asthma often begins in childhood, although making an early diagnosis is difficult. Clinical manifestations, the exclusion of other causes of bronchial obstruction, and responsiveness to anti-inflammatory therapy are the main tool of diagnosis. However, novel, precise, and functional biochemical markers are needed in the differentiation of asthma phenotypes, endotypes, and creating personalized therapy. The aim of the study was to search for metabolomic-based asthma biomarkers among free amino acids (AAs). A wide panel of serum-free AAs in asthmatic children, covering both proteinogenic and non-proteinogenic AAs, were analyzed. The examination included two groups of individuals between 3 and 18 years old: asthmatic children and the control group consisted of children with neither asthma nor allergies. High-performance liquid chromatography combined with tandem mass spectrometry (LC-MS/MS technique) was used for AA measurements. The data were analyzed by applying uni- and multivariate statistical tests. The obtained results indicate the decreased serum concentration of taurine, L-valine, DL-β-aminoisobutyric acid, and increased levels of ƴ-amino-n-butyric acid and L-arginine in asthmatic children when compared to controls. The altered concentration of these AAs can testify to their role in the pathogenesis of childhood asthma. The authors' results should contribute to the future introduction of new diagnostic markers into clinical practice.
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