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Pregnancy exposures and risk of childhood asthma admission in a population birth cohort
BACKGROUND: There is increasing interest in the potential for in utero exposures to affect the risk of asthma. We used population data to explore the associations between perinatal conditions and the risk of hospital admission with asthma between the 2nd and 5th birthday. METHODS: The study populati...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Blackwell Publishing Ltd
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263424/ https://www.ncbi.nlm.nih.gov/pubmed/21929593 http://dx.doi.org/10.1111/j.1399-3038.2011.01206.x |
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author | Algert, Charles S Bowen, Jennifer R Lain, Samantha L Allen, Hugh D Vivian-Taylor, Josephine M Roberts, Christine L |
author_facet | Algert, Charles S Bowen, Jennifer R Lain, Samantha L Allen, Hugh D Vivian-Taylor, Josephine M Roberts, Christine L |
author_sort | Algert, Charles S |
collection | PubMed |
description | BACKGROUND: There is increasing interest in the potential for in utero exposures to affect the risk of asthma. We used population data to explore the associations between perinatal conditions and the risk of hospital admission with asthma between the 2nd and 5th birthday. METHODS: The study population was 240,511 singleton infants born during 2001–2003. Birth records and longitudinally linked hospital admissions were used to identify asthma admissions and to model potential risk factors. RESULTS: A total of 7245 children (3.0%) had one or more childhood admissions with asthma. In utero infectious exposures associated with childhood asthma were maternal antenatal admission with a urinary tract infection (UTI) [adjusted odds ratio (aOR) = 1.49, 95% confidence interval (1.23–1.79)] and pre-term pre-labor rupture of membranes (PROM) [aOR = 1.23 (1.04–1.45)]. There was no evidence that gestational age at time of first antenatal UTI admission (<28, ≥28 wks) affected the risk of asthma (homogeneity test p = 0.6). Pre-term birth was a risk factor for asthma admission, with the risk decreasing by 5.3% with each extra week of gestation. Autumn and winter conceptions were associated with an increased risk of childhood asthma admission: winter aOR = 1.15 (1.08–1.23), autumn aOR = 1.09 (1.02–1.16). CONCLUSIONS: As in utero exposure to both UTI and PROM carry an increased risk of childhood asthma admission, this suggests that the immune system response generally is the relevant factor rather than a specific organism. The season-associated risk is consistent with early pregnancy exposures such as the winter flu season or low vitamin D. |
format | Online Article Text |
id | pubmed-3263424 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Blackwell Publishing Ltd |
record_format | MEDLINE/PubMed |
spelling | pubmed-32634242012-01-23 Pregnancy exposures and risk of childhood asthma admission in a population birth cohort Algert, Charles S Bowen, Jennifer R Lain, Samantha L Allen, Hugh D Vivian-Taylor, Josephine M Roberts, Christine L Pediatr Allergy Immunol Original Articles BACKGROUND: There is increasing interest in the potential for in utero exposures to affect the risk of asthma. We used population data to explore the associations between perinatal conditions and the risk of hospital admission with asthma between the 2nd and 5th birthday. METHODS: The study population was 240,511 singleton infants born during 2001–2003. Birth records and longitudinally linked hospital admissions were used to identify asthma admissions and to model potential risk factors. RESULTS: A total of 7245 children (3.0%) had one or more childhood admissions with asthma. In utero infectious exposures associated with childhood asthma were maternal antenatal admission with a urinary tract infection (UTI) [adjusted odds ratio (aOR) = 1.49, 95% confidence interval (1.23–1.79)] and pre-term pre-labor rupture of membranes (PROM) [aOR = 1.23 (1.04–1.45)]. There was no evidence that gestational age at time of first antenatal UTI admission (<28, ≥28 wks) affected the risk of asthma (homogeneity test p = 0.6). Pre-term birth was a risk factor for asthma admission, with the risk decreasing by 5.3% with each extra week of gestation. Autumn and winter conceptions were associated with an increased risk of childhood asthma admission: winter aOR = 1.15 (1.08–1.23), autumn aOR = 1.09 (1.02–1.16). CONCLUSIONS: As in utero exposure to both UTI and PROM carry an increased risk of childhood asthma admission, this suggests that the immune system response generally is the relevant factor rather than a specific organism. The season-associated risk is consistent with early pregnancy exposures such as the winter flu season or low vitamin D. Blackwell Publishing Ltd 2011-12 /pmc/articles/PMC3263424/ /pubmed/21929593 http://dx.doi.org/10.1111/j.1399-3038.2011.01206.x Text en © 2011 John Wiley & Sons A/S http://creativecommons.org/licenses/by/2.5/ Re-use of this article is permitted in accordance with the Creative Commons Deed, Attribution 2.5, which does not permit commercial exploitation. |
spellingShingle | Original Articles Algert, Charles S Bowen, Jennifer R Lain, Samantha L Allen, Hugh D Vivian-Taylor, Josephine M Roberts, Christine L Pregnancy exposures and risk of childhood asthma admission in a population birth cohort |
title | Pregnancy exposures and risk of childhood asthma admission in a population birth cohort |
title_full | Pregnancy exposures and risk of childhood asthma admission in a population birth cohort |
title_fullStr | Pregnancy exposures and risk of childhood asthma admission in a population birth cohort |
title_full_unstemmed | Pregnancy exposures and risk of childhood asthma admission in a population birth cohort |
title_short | Pregnancy exposures and risk of childhood asthma admission in a population birth cohort |
title_sort | pregnancy exposures and risk of childhood asthma admission in a population birth cohort |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3263424/ https://www.ncbi.nlm.nih.gov/pubmed/21929593 http://dx.doi.org/10.1111/j.1399-3038.2011.01206.x |
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