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Is ambient air pollution associated with onset of sudden infant death syndrome: a case-crossover study in the UK

OBJECTIVES: Air pollution has been associated with increased mortality and morbidity in several studies with indications that its effect could be more severe in children. This study examined the relationship between short-term variations in criteria air pollutants and occurrence of sudden infant dea...

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Autores principales: Litchfield, Ian J, Ayres, Jon G, Jaakkola, Jouni J K, Mohammed, Nuredin I
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898297/
https://www.ncbi.nlm.nih.gov/pubmed/29654005
http://dx.doi.org/10.1136/bmjopen-2017-018341
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author Litchfield, Ian J
Ayres, Jon G
Jaakkola, Jouni J K
Mohammed, Nuredin I
author_facet Litchfield, Ian J
Ayres, Jon G
Jaakkola, Jouni J K
Mohammed, Nuredin I
author_sort Litchfield, Ian J
collection PubMed
description OBJECTIVES: Air pollution has been associated with increased mortality and morbidity in several studies with indications that its effect could be more severe in children. This study examined the relationship between short-term variations in criteria air pollutants and occurrence of sudden infant death syndrome (SIDS). DESIGN: We used a case-crossover study design which is widely applied in air pollution studies and particularly useful for estimating the risk of a rare acute outcome associated with short-term exposure. SETTING: The study used data from the West Midlands region in the UK. PARTICIPANTS: We obtained daily time series data on SIDS mortality (ICD-9: 798.0 or ICD-10: R95) for the period 1996–2006 with a total of 211 SIDS events. PRIMARY OUTCOME MEASURES: Daily counts of SIDS events. RESULTS: For an IQR increase in previous day pollutant concentration, the percentage increases (95% CI) in SIDS were 16 (6 to 27) for PM(10), 1 (−7 to 10) for SO(2), 5 (−4 to 14) for CO, −17 (−27 to –6) for O(3), 16 (2 to 31) for NO(2) and 2 (−3 to 8) for NO after controlling for average temperature and national holidays. PM(10) and NO(2) showed relatively consistent association which persisted across different lag structures and after adjusting for copollutants. CONCLUSIONS: The results indicated ambient air pollutants, particularly PM(10) and NO(2), may show an association with increased SIDS mortality. Thus, future studies are recommended to understand possible mechanistic explanations on the role of air pollution on SIDS incidence and the ways in which we might reduce pollution exposure among infants.
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spelling pubmed-58982972018-04-16 Is ambient air pollution associated with onset of sudden infant death syndrome: a case-crossover study in the UK Litchfield, Ian J Ayres, Jon G Jaakkola, Jouni J K Mohammed, Nuredin I BMJ Open Epidemiology OBJECTIVES: Air pollution has been associated with increased mortality and morbidity in several studies with indications that its effect could be more severe in children. This study examined the relationship between short-term variations in criteria air pollutants and occurrence of sudden infant death syndrome (SIDS). DESIGN: We used a case-crossover study design which is widely applied in air pollution studies and particularly useful for estimating the risk of a rare acute outcome associated with short-term exposure. SETTING: The study used data from the West Midlands region in the UK. PARTICIPANTS: We obtained daily time series data on SIDS mortality (ICD-9: 798.0 or ICD-10: R95) for the period 1996–2006 with a total of 211 SIDS events. PRIMARY OUTCOME MEASURES: Daily counts of SIDS events. RESULTS: For an IQR increase in previous day pollutant concentration, the percentage increases (95% CI) in SIDS were 16 (6 to 27) for PM(10), 1 (−7 to 10) for SO(2), 5 (−4 to 14) for CO, −17 (−27 to –6) for O(3), 16 (2 to 31) for NO(2) and 2 (−3 to 8) for NO after controlling for average temperature and national holidays. PM(10) and NO(2) showed relatively consistent association which persisted across different lag structures and after adjusting for copollutants. CONCLUSIONS: The results indicated ambient air pollutants, particularly PM(10) and NO(2), may show an association with increased SIDS mortality. Thus, future studies are recommended to understand possible mechanistic explanations on the role of air pollution on SIDS incidence and the ways in which we might reduce pollution exposure among infants. BMJ Publishing Group 2018-04-12 /pmc/articles/PMC5898297/ /pubmed/29654005 http://dx.doi.org/10.1136/bmjopen-2017-018341 Text en © Article author(s) (or their employer(s) unless otherwise stated in the text of the article) 2018. All rights reserved. No commercial use is permitted unless otherwise expressly granted. This is an Open Access article distributed in accordance with the terms of the Creative Commons Attribution (CC BY 4.0) license, which permits others to distribute, remix, adapt and build upon this work, for commercial use, provided the original work is properly cited. See: http://creativecommons.org/licenses/by/4.0/
spellingShingle Epidemiology
Litchfield, Ian J
Ayres, Jon G
Jaakkola, Jouni J K
Mohammed, Nuredin I
Is ambient air pollution associated with onset of sudden infant death syndrome: a case-crossover study in the UK
title Is ambient air pollution associated with onset of sudden infant death syndrome: a case-crossover study in the UK
title_full Is ambient air pollution associated with onset of sudden infant death syndrome: a case-crossover study in the UK
title_fullStr Is ambient air pollution associated with onset of sudden infant death syndrome: a case-crossover study in the UK
title_full_unstemmed Is ambient air pollution associated with onset of sudden infant death syndrome: a case-crossover study in the UK
title_short Is ambient air pollution associated with onset of sudden infant death syndrome: a case-crossover study in the UK
title_sort is ambient air pollution associated with onset of sudden infant death syndrome: a case-crossover study in the uk
topic Epidemiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5898297/
https://www.ncbi.nlm.nih.gov/pubmed/29654005
http://dx.doi.org/10.1136/bmjopen-2017-018341
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