dc.contributor.author
Enríquez Rodríguez, Cesar Jesse
dc.contributor.author
Agranovich, Bella
dc.contributor.author
Pascual Guàrdia, Sergi
dc.contributor.author
Faner, Rosa
dc.contributor.author
Camps Ubach, Ramon
dc.contributor.author
Castro Acosta, Ady Angélica
dc.contributor.author
López Campos, José Luis
dc.contributor.author
Peces Barba, Germán
dc.contributor.author
Seijo Maceiras, Luis Miguel
dc.contributor.author
Caguana, Oswaldo Antonio
dc.contributor.author
Rodríguez Chiaradia, Diego Agustín
dc.contributor.author
Barreiro, Esther
dc.contributor.author
Monsó, Eduard
dc.contributor.author
Cosío, Borja G.
dc.contributor.author
Abramovich, Ifat
dc.contributor.author
Agustí García-Navarro, Àlvar
dc.contributor.author
Casadevall, Carme
dc.contributor.author
Gea Guiral, Joaquim
dc.contributor.author
BIOMEPOC Group
dc.date.issued
2026-02-26T15:15:24Z
dc.date.issued
2026-02-26T15:15:24Z
dc.date.issued
2025-07-02
dc.date.issued
2026-02-26T15:15:24Z
dc.identifier
https://hdl.handle.net/2445/227544
dc.description.abstract
Chronic Obstructive Pulmonary Disease (COPD) is a complex condition with high mortality. Early identification of patients at increased risk of death remains a major clinical challenge. This pilot study aimed to explore whether plasma metabolomic profiling could aid in the prediction of long-term (7-year) mortality and provide insight into potential underlying mechanisms. Plasma samples from 54 randomly selected stable COPD patients were analyzed using both untargeted and semi-targeted LC-MS approaches. After excluding patients with unclear death data, non-COPD-related deaths and metabolomic outliers, 41 individuals were included in the final analysis. During follow-up, 13 patients (32%) died, and 28 survived. Univariate analysis identified 12 metabolites—mainly amino acids—that differed significantly between the two groups. Functional analysis suggested a significant disruption in energy production pathways. Predictive models developed using machine learning algorithms, consisting of either ten metabolites alone or nine metabolites plus FEV1, achieved high accuracy for 7-year mortality prediction, with the latter model performing slightly better. Internal validation was conducted using five-fold cross-validation. While exploratory, these findings support the hypothesis that early metabolic alterations, particularly in energy pathways, may contribute to long-term mortality risk in stable COPD patients, and could complement traditional prognostic markers such as FEV1.
dc.format
application/pdf
dc.relation
Reproducció del document publicat a: https://doi.org/10.3390/ijms26136373
dc.relation
International Journal of Molecular Sciences, 2025, vol. 26, num.13
dc.relation
https://doi.org/10.3390/ijms26136373
dc.rights
cc-by (c) César Jessé Enríquez-Rodríguez et al., 2025
dc.rights
http://creativecommons.org/licenses/by/4.0/
dc.rights
info:eu-repo/semantics/openAccess
dc.subject
Malalties pulmonars obstructives cròniques
dc.subject
Trastorns del metabolisme
dc.subject
Chronic obstructive pulmonary diseases
dc.subject
Disorders of metabolism
dc.title
Metabolomic signatures predict seven-year mortality in clinically stable COPD patients
dc.type
info:eu-repo/semantics/article
dc.type
info:eu-repo/semantics/publishedVersion