TY - JOUR
T1 - Non-targeted integrative multi-omics approaches on sputum reveal potential diagnostic and monitoring biomarkers for respiratory diseases
AU - Mur, Luis
AU - Mironas, Adrian
AU - Paes, Rachel
AU - O'shea, Keiron
AU - Lewis, Keir
PY - 2017/9/6
Y1 - 2017/9/6
N2 - Introduction: In the era of personalised medicine post-genomic biomarkers could be employed to evaluate respiratory diseases. Particularly important targets are the rapid diagnosis, typing and staging of lung cancer (LC) and predicting exacerbations in patients with chronic obstructive pulmonary disease (COPD) which often occur as co-morbidities. In such approaches screens based on sputum, represent an attractive prospect.
Materials and Methods: Spontaneous sputum was collected from 155 patients and correlated with the corresponding clinic-radiological diagnosis (COPD, LC, controls derived from heavy smokers). Global DNA extractions were performed and consequently amplified for the 16S rRNA gene for identification of the microbial load as an indication of potential infection pressure/ relative immunological status. Mass-spectrometry (MS)-based technologies were employed to identify protein and metabolites within the sputum sample. The proteomic and metabolite profiles were analysed using multivariate statistical and machine-learning approaches to identify components that were associated with clinically relevant classes.
Results: Analysis of sputum revealed over 60 major classes of proteins differentially expressed and regulated across the disease spectrum. The microbial communities appear to fluctuate in number and also species across the investigated group and GOLD COPD classification with p<0.05. Interrogation of metabolite profiles showed distinctive biochemical changes within each patient group.
Conclusion: ‘Omic approaches based on sputum can differentiate a large variety of pulmonary diseases and offer diagnostic biomarkers.
AB - Introduction: In the era of personalised medicine post-genomic biomarkers could be employed to evaluate respiratory diseases. Particularly important targets are the rapid diagnosis, typing and staging of lung cancer (LC) and predicting exacerbations in patients with chronic obstructive pulmonary disease (COPD) which often occur as co-morbidities. In such approaches screens based on sputum, represent an attractive prospect.
Materials and Methods: Spontaneous sputum was collected from 155 patients and correlated with the corresponding clinic-radiological diagnosis (COPD, LC, controls derived from heavy smokers). Global DNA extractions were performed and consequently amplified for the 16S rRNA gene for identification of the microbial load as an indication of potential infection pressure/ relative immunological status. Mass-spectrometry (MS)-based technologies were employed to identify protein and metabolites within the sputum sample. The proteomic and metabolite profiles were analysed using multivariate statistical and machine-learning approaches to identify components that were associated with clinically relevant classes.
Results: Analysis of sputum revealed over 60 major classes of proteins differentially expressed and regulated across the disease spectrum. The microbial communities appear to fluctuate in number and also species across the investigated group and GOLD COPD classification with p<0.05. Interrogation of metabolite profiles showed distinctive biochemical changes within each patient group.
Conclusion: ‘Omic approaches based on sputum can differentiate a large variety of pulmonary diseases and offer diagnostic biomarkers.
UR - http://erj.ersjournals.com/lookup/doi/10.1183/1393003.congress-2017.PA375
U2 - 10.1183/1393003.congress-2017.PA375
DO - 10.1183/1393003.congress-2017.PA375
M3 - Article
SN - 0903-1936
VL - 50
JO - European Respiratory Journal
JF - European Respiratory Journal
IS - Supp 61
M1 - PA375
ER -