Fibrotic interstitial lung diseases and air pollution: a systematic literature review.


Journal

European respiratory review : an official journal of the European Respiratory Society
ISSN: 1600-0617
Titre abrégé: Eur Respir Rev
Pays: England
ID NLM: 9111391

Informations de publication

Date de publication:
30 Sep 2020
Historique:
received: 27 04 2020
accepted: 04 05 2020
entrez: 21 8 2020
pubmed: 21 8 2020
medline: 24 7 2021
Statut: epublish

Résumé

Air pollution is hypothesised to be a risk factor for interstitial lung diseases (ILD). This study systematically reviewed the literature regarding the impact of air pollution on idiopathic pulmonary fibrosis (IPF) and fibrotic interstitial lung diseases (ILD). A computer-assisted literature search of electronic databases was performed to identify studies focused on the association between ILDs and air pollution. Other inclusion criteria required that the article had to be: 1) original; 2) a prospective or retrospective study; and 3) fully published in English. Both randomised clinical trials and observational studies were considered. Only seven studies met the inclusion criteria. All studies investigated the relationship between pollution and IPF, except one that dealt with the relationship between pollution and hypersensitivity pneumonitis. Outcome measures included exacerbation of IPF, mortality, disease severity, prevalence of hypersensitivity pneumonitis, progression and incidence of IPF. On the whole, air pollution levels were negatively associated with outcomes in patients with IPF and fibrotic ILD outcome. The heterogeneity in the measurement and reporting of the end-points limited the performance of a quantitative synthesis of data. This systematic review provides supporting evidence linking exposure to air pollution to poor outcomes in patients with IPF and fibrotic ILD.

Sections du résumé

BACKGROUND BACKGROUND
Air pollution is hypothesised to be a risk factor for interstitial lung diseases (ILD). This study systematically reviewed the literature regarding the impact of air pollution on idiopathic pulmonary fibrosis (IPF) and fibrotic interstitial lung diseases (ILD).
METHODS METHODS
A computer-assisted literature search of electronic databases was performed to identify studies focused on the association between ILDs and air pollution. Other inclusion criteria required that the article had to be: 1) original; 2) a prospective or retrospective study; and 3) fully published in English. Both randomised clinical trials and observational studies were considered.
RESULTS RESULTS
Only seven studies met the inclusion criteria. All studies investigated the relationship between pollution and IPF, except one that dealt with the relationship between pollution and hypersensitivity pneumonitis. Outcome measures included exacerbation of IPF, mortality, disease severity, prevalence of hypersensitivity pneumonitis, progression and incidence of IPF. On the whole, air pollution levels were negatively associated with outcomes in patients with IPF and fibrotic ILD outcome. The heterogeneity in the measurement and reporting of the end-points limited the performance of a quantitative synthesis of data.
CONCLUSIONS CONCLUSIONS
This systematic review provides supporting evidence linking exposure to air pollution to poor outcomes in patients with IPF and fibrotic ILD.

Identifiants

pubmed: 32817115
pii: 29/157/200093
doi: 10.1183/16000617.0093-2020
pmc: PMC9488644
pii:
doi:

Types de publication

Journal Article Systematic Review

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

Copyright ©ERS 2020.

Déclaration de conflit d'intérêts

Conflict of interest: S. Harari reports grants and personal fees from Roche, outside the submitted work. Conflict of interest: G. Raghu has nothing to disclose. Conflict of interest: A. Caminati reports personal fees from Roche and Boehringer Ingelheim, outside the submitted work. Conflict of interest: M. Cruciani has nothing to disclose. Conflict of interest: M. Franchini has nothing to disclose. Conflict of interest: P. Mannucci has nothing to disclose.

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Auteurs

Sergio Harari (S)

U.O. di Pneumologia e Terapia Semi-Intensiva Respiratoria - Servizio di Fisiopatologia Respiratoria ed Emodinamica Polmonare, Ospedale San Giuseppe - MultiMedica IRCCS, Milan, Italy.
Dept of Medical Sciences, San Giuseppe Hospital MultiMedica IRCCS, Milan, Italy.
Dept of Clinical Sciences and Community Health, Università degli Studi di, Milan, Italy.
Both authors contributed equally.

Ganesh Raghu (G)

Center for Interstitial Lung Diseases, Dept of Medicine, University of Washington, Seattle, WA, USA.
Both authors contributed equally.

Antonella Caminati (A)

U.O. di Pneumologia e Terapia Semi-Intensiva Respiratoria - Servizio di Fisiopatologia Respiratoria ed Emodinamica Polmonare, Ospedale San Giuseppe - MultiMedica IRCCS, Milan, Italy lafitta@libero.it.

Mario Cruciani (M)

Italian National Blood Centre, National Institute of Health, Rome, Italy.
Infection Control Committee and Antibiotic Stewardship Programme, AULSS9 Scaligera, Verona, Italy.

Massimo Franchini (M)

Italian National Blood Centre, National Institute of Health, Rome, Italy.
Dept of Hematology and Transfusion Medicine, Carlo Poma Hospital, Mantua, Italy.

Piermannuccio Mannucci (P)

Scientific Direction, IRCCS Ca' Granda Maggiore Policlinico Hospital Foundation, Milan.

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