Literature DB >> 36258909

Assessment of Cystic Fibrosis Distribution Based on Air Pollution by Geographical Information System (GIS).

Maryam Hassanzad1, Parissa Farnia2, Poopak Farnia3, Mahdieh Arian4, Ali Valinejadi5, Hosseinali Ghaffaripour1, Noushin Baghaie1, Nima Hassanzad6, Leila Mohammadpour7, Ali Akbar Velayati2.   

Abstract

Background: It is widely accepted that concerns have been recently raised regarding the impact of air pollution on the health of children with cystic fibrosis (CF). Air pollution probably affects the exacerbation of CF and its laboratory findings. On the other hand, the World Health Organization (WHO) has asked all countries to update their data and reports on the distribution and prevalence of CF in different areas. The purpose of the present study was to investigate the distribution and prevalence of CF based on the levels of atmospheric pollutants, such as PM10, PM2.5, SO2, NO2, CO, and O3 in 22 zones of Tehran, and to report the abnormal laboratory findings that might indicate the exacerbation of CF. Materials and
Methods: The studied statistical population included children with CF referred to Masih Daneshvari Hospital from 2003 to 2020. Demographic data, location of living area, and laboratory findings were extracted from patient records. The geographic information system (GIS) was applied to indicate the distribution and dispersion of the disease. The information related to air pollutants was collected from all stations in Tehran during the studied period by the Department of Environment of Tehran Province, and the average levels were used for final reporting.
Results: The analysis results on 287 CF patients demonstrated that the risk of disease exacerbation significantly increased by the presence of air pollutants. In areas with multiple air pollutants, more laboratory findings were observed to be abnormal, and the lower survival rate for patients with CF was recorded. Investigating the CF distribution pattern based on climatic layers and above mean sea level (AMSL) indicated that distribution of the disease was higher in dry areas with lower AMSL and the higher volume of the atmospheric pollutants, which were primarily centralized in southern and central Tehran.
Conclusion: Environmental factors, such as air pollution, can be considered vital parameters, along with high-risk factors, such as pure and integrated race, migration, and mutation, influencing the prevalence and exacerbation of CF symptoms. Considering the higher prevalence of CF in deprived areas of Tehran, households' cultural and economic level appears to be a factor in the lack of diagnostic screening and prevention of CF in these areas. On the other hand, continuous monitoring of the air pollution caused by traffic and giving warnings to CF patients and their parents is particularly important. Copyright
© 2022 National Research Institute of Tuberculosis and Lung Disease.

Entities:  

Keywords:  Climatic processes; Cystic fibrosis; Disease mapping; Geographic information system; Medical informatics

Year:  2022        PMID: 36258909      PMCID: PMC9571236     

Source DB:  PubMed          Journal:  Tanaffos        ISSN: 1735-0344


  33 in total

1.  Public health education and practice using geographic information system technology.

Authors:  Mary E Riner; Cynthia Cunningham; Ann Johnson
Journal:  Public Health Nurs       Date:  2004 Jan-Feb       Impact factor: 1.462

2.  Mutation and new polymorphisms insight in introns 11 to 14a of CFTR gene of northern Iranian cystic fibrosis patients.

Authors:  Mohammad Reza Esmaeili Dooki; Reza Tabaripour; Razieh Rahimi; Haleh Akhavan-Niaki
Journal:  Gene       Date:  2015-03-28       Impact factor: 3.688

3.  Personal exposure to airborne particles and metals: results from the Particle TEAM study in Riverside, California.

Authors:  H Ozkaynak; J Xue; J Spengler; L Wallace; E Pellizzari; P Jenkins
Journal:  J Expo Anal Environ Epidemiol       Date:  1996 Jan-Mar

4.  Pulmonary exacerbations are associated with subsequent FEV1 decline in both adults and children with cystic fibrosis.

Authors:  Don B Sanders; Rachel C L Bittner; Margaret Rosenfeld; Gregory J Redding; Christopher H Goss
Journal:  Pediatr Pulmonol       Date:  2010-10-21

5.  Effect of residential proximity to major roadways on cystic fibrosis exacerbations.

Authors:  Mandeep S Jassal; Albert M Yu; Rajeev Bhatia; Thomas G Keens; Sally L Davidson Ward
Journal:  Int J Environ Health Res       Date:  2012-07-27       Impact factor: 3.411

6.  Traffic related air pollution and acute hospital admission for respiratory diseases in Drammen, Norway 1995-2000.

Authors:  Bente Oftedal; Per Nafstad; Per Magnus; Sonja Bjørkly; Anders Skrondal
Journal:  Eur J Epidemiol       Date:  2003       Impact factor: 8.082

7.  Global, regional, and national comparative risk assessment of 79 behavioural, environmental and occupational, and metabolic risks or clusters of risks, 1990-2015: a systematic analysis for the Global Burden of Disease Study 2015.

Authors: 
Journal:  Lancet       Date:  2016-10-08       Impact factor: 79.321

8.  Relations between depressive and anxious symptoms and quality of life in caregivers of children with cystic fibrosis.

Authors:  Kimberly A Driscoll; Karen Montag-Leifling; James D Acton; Avani C Modi
Journal:  Pediatr Pulmonol       Date:  2009-08

9.  Effect of temperature on cystic fibrosis lung disease and infections: a replicated cohort study.

Authors:  Joseph M Collaco; John McGready; Deanna M Green; Kathleen M Naughton; Christopher P Watson; Timothy Shields; Scott C Bell; Claire E Wainwright; Garry R Cutting
Journal:  PLoS One       Date:  2011-11-18       Impact factor: 3.240

10.  Ozone is associated with an increased risk of respiratory exacerbations in patients with cystic fibrosis.

Authors:  Sylvia C L Farhat; Marina B Almeida; Luiz Vicente R F Silva-Filho; Juliana Farhat; Joaquim C Rodrigues; Alfésio L F Braga
Journal:  Chest       Date:  2013-10       Impact factor: 9.410

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