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Maternal Smoking and Metabolic Health Biomarkers in Newborns
BACKGROUND: Maternal smoking has been associated with elevated risk of type 2 diabetes among the offspring in adulthood. The mechanisms underlying this fetal “programming” effect remain unclear. The present study sought to explore whether maternal smoking affects metabolic health biomarkers in fetus...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2015
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658089/ https://www.ncbi.nlm.nih.gov/pubmed/26599278 http://dx.doi.org/10.1371/journal.pone.0143660 |
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author | Fang, Fang Luo, Zhong-Cheng Dejemli, Anissa Delvin, Edgard Zhang, Jun |
author_facet | Fang, Fang Luo, Zhong-Cheng Dejemli, Anissa Delvin, Edgard Zhang, Jun |
author_sort | Fang, Fang |
collection | PubMed |
description | BACKGROUND: Maternal smoking has been associated with elevated risk of type 2 diabetes among the offspring in adulthood. The mechanisms underlying this fetal “programming” effect remain unclear. The present study sought to explore whether maternal smoking affects metabolic health biomarkers in fetuses/newborns. METHODS: In a prospective singleton pregnancy cohort (n = 248), we compared metabolic health biomarkers in the newborns of smoking and non-smoking mothers. Outcomes included cord plasma insulin, proinsulin, insulin-like growth factor I (IGF-I), IGF-II, leptin and adiponectin concentrations, glucose-to-insulin ratio (an indicator of insulin sensitivity) and proinsulin-to-insulin ratio (an indicator of β-cell function). RESULTS: Independent of maternal (glucose tolerance, age, ethnicity, parity, education, body mass index, alcohol use) and infant (sex, gestational age, birth weight z score, mode of delivery, cord blood glucose concentration) characteristics, the newborns of smoking mothers had lower IGF-I concentrations (mean: 6.7 vs. 8.4 nmol/L, adjusted p = 0.006), and marginally higher proinsulin-to-insulin ratios (0.94 vs. 0.72, adjusted p = 0.06) than the newborns of non-smoking mothers. Cord plasma insulin, proinsulin, IGF-II, leptin and adiponectin concentrations and glucose-to-insulin ratios were similar in the newborns of smoking and non-smoking mothers. CONCLUSIONS: Maternal smoking was associated with decreased fetal IGF-I levels, and borderline lower fetal β-cell function. Larger cohort studies are required to confirm the latter finding. The preliminary findings prompt the hypothesis that these early life metabolic changes may be involved in the impact of maternal smoking on future risk of metabolic syndrome related disorders in the offspring. |
format | Online Article Text |
id | pubmed-4658089 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2015 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-46580892015-12-02 Maternal Smoking and Metabolic Health Biomarkers in Newborns Fang, Fang Luo, Zhong-Cheng Dejemli, Anissa Delvin, Edgard Zhang, Jun PLoS One Research Article BACKGROUND: Maternal smoking has been associated with elevated risk of type 2 diabetes among the offspring in adulthood. The mechanisms underlying this fetal “programming” effect remain unclear. The present study sought to explore whether maternal smoking affects metabolic health biomarkers in fetuses/newborns. METHODS: In a prospective singleton pregnancy cohort (n = 248), we compared metabolic health biomarkers in the newborns of smoking and non-smoking mothers. Outcomes included cord plasma insulin, proinsulin, insulin-like growth factor I (IGF-I), IGF-II, leptin and adiponectin concentrations, glucose-to-insulin ratio (an indicator of insulin sensitivity) and proinsulin-to-insulin ratio (an indicator of β-cell function). RESULTS: Independent of maternal (glucose tolerance, age, ethnicity, parity, education, body mass index, alcohol use) and infant (sex, gestational age, birth weight z score, mode of delivery, cord blood glucose concentration) characteristics, the newborns of smoking mothers had lower IGF-I concentrations (mean: 6.7 vs. 8.4 nmol/L, adjusted p = 0.006), and marginally higher proinsulin-to-insulin ratios (0.94 vs. 0.72, adjusted p = 0.06) than the newborns of non-smoking mothers. Cord plasma insulin, proinsulin, IGF-II, leptin and adiponectin concentrations and glucose-to-insulin ratios were similar in the newborns of smoking and non-smoking mothers. CONCLUSIONS: Maternal smoking was associated with decreased fetal IGF-I levels, and borderline lower fetal β-cell function. Larger cohort studies are required to confirm the latter finding. The preliminary findings prompt the hypothesis that these early life metabolic changes may be involved in the impact of maternal smoking on future risk of metabolic syndrome related disorders in the offspring. Public Library of Science 2015-11-23 /pmc/articles/PMC4658089/ /pubmed/26599278 http://dx.doi.org/10.1371/journal.pone.0143660 Text en © 2015 Fang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Fang, Fang Luo, Zhong-Cheng Dejemli, Anissa Delvin, Edgard Zhang, Jun Maternal Smoking and Metabolic Health Biomarkers in Newborns |
title | Maternal Smoking and Metabolic Health Biomarkers in Newborns |
title_full | Maternal Smoking and Metabolic Health Biomarkers in Newborns |
title_fullStr | Maternal Smoking and Metabolic Health Biomarkers in Newborns |
title_full_unstemmed | Maternal Smoking and Metabolic Health Biomarkers in Newborns |
title_short | Maternal Smoking and Metabolic Health Biomarkers in Newborns |
title_sort | maternal smoking and metabolic health biomarkers in newborns |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4658089/ https://www.ncbi.nlm.nih.gov/pubmed/26599278 http://dx.doi.org/10.1371/journal.pone.0143660 |
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