Network medicine analysis of COPD multimorbidities

Background: Patients with chronic obstructive pulmonary disease (COPD) often suffer concomitant disorders that worsen significantly their health status and vital prognosis. The pathogenic mechanisms underlying COPD multimorbidities are not completely understood, thus the exploration of potential mol...

Descripción completa

Detalles Bibliográficos
Autores: Grosdidier, Solene, Ferrer, Antoni, Faner, Rosa, Pinero, Janet, Roca, Josep, García-Cosío, Borja, Agusti, Alvar, Gea, Joaquim, Sanz, Ferran, Furlong, Laura I.
Tipo de recurso: artículo
Fecha de publicación:2014
País:España
Institución:Conselleria de Salut i Consum del Govern de les Illes Balears
Repositorio:Docusalut
Idioma:inglés
OAI Identifier:oai:docusalut.com:20.500.13003/11124
Acceso en línea:https://hdl.handle.net/20.500.13003/11124
Access Level:acceso abierto
Palabra clave:Protein Interaction Maps
Pulmonary Disease, Chronic Obstructive
Smoke
Gene Expression Regulation
Humans
Smoking
Health Status
Prognosis
Gene Regulatory Networks
Risk Factors
Signal Transduction
Comorbidity
Systems Biology
Prevalence
Systems Integration
Redes Reguladoras de Genes
Pronóstico
Estado de Salud
Humanos
Biología de Sistemas
Factores de Riesgo
Enfermedad Pulmonar Obstructiva Crónica
Fumar
Regulación de la Expresión Génica
Mapas de Interacción de Proteínas
Prevalencia
Comorbilidad
Integración de Sistemas
Humo
Transducción de Señal
Diseasome
Systems biology
Network medicine
Multimorbidity
COPD
Tobacco chemicals
Descripción
Sumario:Background: Patients with chronic obstructive pulmonary disease (COPD) often suffer concomitant disorders that worsen significantly their health status and vital prognosis. The pathogenic mechanisms underlying COPD multimorbidities are not completely understood, thus the exploration of potential molecular and biological linkages between COPD and their associated diseases is of great interest. Methods: We developed a novel, unbiased, integrative network medicine approach for the analysis of the diseasome, interactome, the biological pathways and tobacco smoke exposome, which has been applied to the study of 16 prevalent COPD multimorbidities identified by clinical experts. Results: Our analyses indicate that all COPD multimorbidities studied here are related at the molecular and biological level, sharing genes, proteins and biological pathways. By inspecting the connections of COPD with their associated diseases in more detail, we identified known biological pathways involved in COPD, such as inflammation, endothelial dysfunction or apoptosis, serving as a proof of concept of the methodology. More interestingly, we found previously overlooked biological pathways that might contribute to explain COPD multimorbidities, such as hemostasis in COPD multimorbidities other than cardiovascular disorders, and cell cycle pathway in the association of COPD with depression. Moreover, we also observed similarities between COPD multimorbidities at the pathway level, suggesting common biological mechanisms for different COPD multimorbidities. Finally, chemicals contained in the tobacco smoke target an average of 69% of the identified proteins participating in COPD multimorbidities. Conclusions: The network medicine approach presented here allowed the identification of plausible molecular links between COPD and comorbid diseases, and showed that many of them are targets of the tobacco exposome, proposing new areas of research for understanding the molecular underpinning of COPD multimorbidities.