Literature DB >> 33167075

Mapping IPF helps identify geographic regions at higher risk for disease development and potential triggers.

Jessica Germaine Shull1, Maria Teresa Pay2, Carla Lara Compte1, Miriam Olid2, Guadalupe Bermudo1, Karina Portillo3, Jacobo Sellarés4, Eva Balcells5, Vanesa Vicens-Zygmunt1, Lurdes Planas-Cerezales1, Diana Badenes-Bonet5,6,7, Rosana Blavia8, Pilar Rivera-Ortega1, Amalia Moreno9, Jordi Sans10, Damià Perich10, Silvia Barril11, Leonardo Esteban12, Laia Garcia-Bellmunt13, Jordi Esplugas14, Guillermo Suarez-Cuartin1, Jaume Bordas-Martinez1, Diego Castillo15, Rosa Jolis16, Inma Salvador17, Saioa Eizaguirre Anton18, Ana Villar19, Alejandro Robles-Perez20, M Josefa Cardona21, Enric Barbeta22, Maria Guadalupe Silveira23, Claudia Guevara24, Jordi Dorca1, Antoni Rosell3,7,25, Patricio Luburich1, Roger Llatjós1, Oriol Jorba2, Maria Molina-Molina1,7.   

Abstract

BACKGROUND AND
OBJECTIVE: The relationship between IPF development and environmental factors has not been completely elucidated. Analysing geographic regions of idiopathic pulmonary fibrosis (IPF) cases could help identify those areas with higher aggregation and investigate potential triggers. We hypothesize that cross-analysing location of IPF cases and areas of consistently high air pollution concentration could lead to recognition of environmental risk factors for IPF development.
METHODS: This retrospective study analysed epidemiological and clinical data from 503 patients registered in the Observatory IPF.cat from January 2017 to June 2019. Incident and prevalent IPF cases from the Catalan region of Spain were graphed based on their postal address. We generated maps of the most relevant air pollutant PM2.5 from the last 10 years using data from the CALIOPE air quality forecast system and observational data.
RESULTS: In 2018, the prevalence of IPF differed across provinces; from 8.1 cases per 100 000 habitants in Barcelona to 2.0 cases per 100 000 in Girona. The ratio of IPF was higher in some areas. Mapping PM2.5 levels illustrated that certain areas with more industry, traffic and shipping maintained markedly higher PM2.5 concentrations. Most of these locations correlated with higher aggregation of IPF cases. Compared with other risk factors, PM2.5 exposure was the most frequent.
CONCLUSION: In this retrospective study, prevalence of IPF is higher in areas of elevated PM2.5 concentration. Prospective studies with targeted pollution mapping need to be done in specific geographies to compile a broader profile of environmental factors involved in the development of pulmonary fibrosis.
© 2020 Asian Pacific Society of Respirology.

Entities:  

Keywords:  air pollution; early diagnosis; environmental risk factor; geographic region; idiopathic pulmonary fibrosis

Year:  2020        PMID: 33167075     DOI: 10.1111/resp.13973

Source DB:  PubMed          Journal:  Respirology        ISSN: 1323-7799            Impact factor:   6.424


  6 in total

1.  Harnessing PM2.5 Exposure Data to Predict Progression of Fibrotic Interstitial Lung Diseases Based on Telomere Length.

Authors:  Jessica Germaine Shull; Lurdes Planas-Cerezales; Carla Lara Compte; Rosario Perona; Maria Molina-Molina
Journal:  Front Med (Lausanne)       Date:  2022-05-12

2.  Astragaloside IV Protects from PM2.5-Induced Lung Injury by Regulating Autophagy via Inhibition of PI3K/Akt/mTOR Signaling in vivo and in vitro.

Authors:  Caixia Pei; Fei Wang; Demei Huang; Shihua Shi; Xiaomin Wang; Yilan Wang; Shuiqin Li; Yongcan Wu; Zhenxing Wang
Journal:  J Inflamm Res       Date:  2021-09-16

Review 3.  Molecular Mechanisms and Cellular Contribution from Lung Fibrosis to Lung Cancer Development.

Authors:  Anna Valeria Samarelli; Valentina Masciale; Beatrice Aramini; Georgina Pamela Coló; Roberto Tonelli; Alessandro Marchioni; Giulia Bruzzi; Filippo Gozzi; Dario Andrisani; Ivana Castaniere; Linda Manicardi; Antonio Moretti; Luca Tabbì; Giorgia Guaitoli; Stefania Cerri; Massimo Dominici; Enrico Clini
Journal:  Int J Mol Sci       Date:  2021-11-10       Impact factor: 5.923

Review 4.  Contemporary Concise Review 2021: Interstitial lung disease.

Authors:  Cormac McCarthy; Michael P Keane
Journal:  Respirology       Date:  2022-05-05       Impact factor: 6.175

Review 5.  Dissecting the Role of Mesenchymal Stem Cells in Idiopathic Pulmonary Fibrosis: Cause or Solution.

Authors:  Anna Valeria Samarelli; Roberto Tonelli; Irene Heijink; Aina Martin Medina; Alessandro Marchioni; Giulia Bruzzi; Ivana Castaniere; Dario Andrisani; Filippo Gozzi; Linda Manicardi; Antonio Moretti; Stefania Cerri; Riccardo Fantini; Luca Tabbì; Chiara Nani; Ilenia Mastrolia; Daniel J Weiss; Massimo Dominici; Enrico Clini
Journal:  Front Pharmacol       Date:  2021-07-05       Impact factor: 5.810

6.  Uncovering the Epidemiology of Idiopathic Pulmonary Fibrosis in the Veterans Affairs Health System.

Authors:  Robert M Tighe; Sachin Chaudhary
Journal:  Ann Am Thorac Soc       Date:  2022-02
  6 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.