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Comparison of Levels of Three Tobacco Smoke Exposure Biomarkers in Children of Smokers
Objectives: Cotinine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), and N-oxides are biomarkers of tobacco smoke exposure (TSE) used to assess short- and longer-term TSE. The objective of this study was to assess the associations between these TSE biomarkers, sociodemographics, parental smok...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622785/ https://www.ncbi.nlm.nih.gov/pubmed/34831559 http://dx.doi.org/10.3390/ijerph182211803 |
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author | Mahabee-Gittens, E. Melinda Matt, Georg E. Ding, Lili Merianos, Ashley L. |
author_facet | Mahabee-Gittens, E. Melinda Matt, Georg E. Ding, Lili Merianos, Ashley L. |
author_sort | Mahabee-Gittens, E. Melinda |
collection | PubMed |
description | Objectives: Cotinine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), and N-oxides are biomarkers of tobacco smoke exposure (TSE) used to assess short- and longer-term TSE. The objective of this study was to assess the associations between these TSE biomarkers, sociodemographics, parental smoking, and child TSE patterns among 0–17-year-olds. Methods: A convenience sample of 179 pediatric patients (mean (SD) age = 7.9 (4.3) years) who lived with ≥1 smoker and who had parental assessments completed and urine samples analyzed for the three TSE biomarkers of interest were included. Biomarker levels were log-transformed, univariate regression models were built and Pearson correlations were assessed. Results: In total, 100% of children had detectable levels of cotinine and >96% had detectable NNAL and N-oxide levels. The geometric means of cotinine, NNAL, and N-oxide levels were 10.1 ng/mL, 25.3 pg/mL, and 22.9 pg/mL, respectively. The mean (SD) number of daily cigarettes smoked by parents was 10.6 (6.0) cigarettes. Child age negatively correlated with urinary cotinine (r = −0.202, p = 0.007) and log NNAL levels (r = −0.275, p < 0.001). The highest log-cotinine levels were in children who were younger, of African American race, and whose parents had a lower education, an annual income ≤USD15,000, and no smoking bans. The highest log-NNAL and N-oxide levels were in children whose parents had a lower education, had no smoking bans, and were around higher numbers of cigarettes. Conclusion: Children of smokers who were younger, African American, and had no smoking bans had the highest TSE biomarker levels. Targeted interventions are needed to reduce TSE levels among high-risk children. |
format | Online Article Text |
id | pubmed-8622785 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-86227852021-11-27 Comparison of Levels of Three Tobacco Smoke Exposure Biomarkers in Children of Smokers Mahabee-Gittens, E. Melinda Matt, Georg E. Ding, Lili Merianos, Ashley L. Int J Environ Res Public Health Article Objectives: Cotinine, 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL), and N-oxides are biomarkers of tobacco smoke exposure (TSE) used to assess short- and longer-term TSE. The objective of this study was to assess the associations between these TSE biomarkers, sociodemographics, parental smoking, and child TSE patterns among 0–17-year-olds. Methods: A convenience sample of 179 pediatric patients (mean (SD) age = 7.9 (4.3) years) who lived with ≥1 smoker and who had parental assessments completed and urine samples analyzed for the three TSE biomarkers of interest were included. Biomarker levels were log-transformed, univariate regression models were built and Pearson correlations were assessed. Results: In total, 100% of children had detectable levels of cotinine and >96% had detectable NNAL and N-oxide levels. The geometric means of cotinine, NNAL, and N-oxide levels were 10.1 ng/mL, 25.3 pg/mL, and 22.9 pg/mL, respectively. The mean (SD) number of daily cigarettes smoked by parents was 10.6 (6.0) cigarettes. Child age negatively correlated with urinary cotinine (r = −0.202, p = 0.007) and log NNAL levels (r = −0.275, p < 0.001). The highest log-cotinine levels were in children who were younger, of African American race, and whose parents had a lower education, an annual income ≤USD15,000, and no smoking bans. The highest log-NNAL and N-oxide levels were in children whose parents had a lower education, had no smoking bans, and were around higher numbers of cigarettes. Conclusion: Children of smokers who were younger, African American, and had no smoking bans had the highest TSE biomarker levels. Targeted interventions are needed to reduce TSE levels among high-risk children. MDPI 2021-11-10 /pmc/articles/PMC8622785/ /pubmed/34831559 http://dx.doi.org/10.3390/ijerph182211803 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Mahabee-Gittens, E. Melinda Matt, Georg E. Ding, Lili Merianos, Ashley L. Comparison of Levels of Three Tobacco Smoke Exposure Biomarkers in Children of Smokers |
title | Comparison of Levels of Three Tobacco Smoke Exposure Biomarkers in Children of Smokers |
title_full | Comparison of Levels of Three Tobacco Smoke Exposure Biomarkers in Children of Smokers |
title_fullStr | Comparison of Levels of Three Tobacco Smoke Exposure Biomarkers in Children of Smokers |
title_full_unstemmed | Comparison of Levels of Three Tobacco Smoke Exposure Biomarkers in Children of Smokers |
title_short | Comparison of Levels of Three Tobacco Smoke Exposure Biomarkers in Children of Smokers |
title_sort | comparison of levels of three tobacco smoke exposure biomarkers in children of smokers |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8622785/ https://www.ncbi.nlm.nih.gov/pubmed/34831559 http://dx.doi.org/10.3390/ijerph182211803 |
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