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Association of maternal serum lipids at late gestation with the risk of neonatal macrosomia in women without diabetes mellitus

BACKGROUND: Macrosomia is a serious public health problem worldwide due to its increasing prevalence and adverse influences on maternal and neonatal outcomes. Maternal dyslipidemia exerts potential and adverse impacts on pregnant women and newborns. However, the association between maternal serum li...

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Autores principales: Wang, Xiangxiang, Guan, Qingbo, Zhao, Jiajun, Yang, Feifei, Yuan, Zhongshang, Yin, Yongchao, Fang, Rui, Liu, Lingwei, Zuo, Changting, Gao, Ling
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896067/
https://www.ncbi.nlm.nih.gov/pubmed/29642923
http://dx.doi.org/10.1186/s12944-018-0707-7
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author Wang, Xiangxiang
Guan, Qingbo
Zhao, Jiajun
Yang, Feifei
Yuan, Zhongshang
Yin, Yongchao
Fang, Rui
Liu, Lingwei
Zuo, Changting
Gao, Ling
author_facet Wang, Xiangxiang
Guan, Qingbo
Zhao, Jiajun
Yang, Feifei
Yuan, Zhongshang
Yin, Yongchao
Fang, Rui
Liu, Lingwei
Zuo, Changting
Gao, Ling
author_sort Wang, Xiangxiang
collection PubMed
description BACKGROUND: Macrosomia is a serious public health problem worldwide due to its increasing prevalence and adverse influences on maternal and neonatal outcomes. Maternal dyslipidemia exerts potential and adverse impacts on pregnant women and newborns. However, the association between maternal serum lipids and the risk of macrosomia has not yet been clearly elucidated. We explored the association between the maternal lipids profile at late gestation and the risk of having macrosomia among women without diabetes mellitus (DM). METHODS: The medical records of 5407 pregnant women giving birth to single live babies at term were retrospectively analyzed. Subjects with DM, hypertension, thyroid disorders and fetal malformation were excluded. Maternal fasting serum lipids were measured during late pregnancy. Logistic regression analysis was used to analyze the variables associated with the risk of macrosomia. RESULTS: Maternal serum triglyceride (TG) and high-density lipoprotein cholesterol (HDL-C) levels were related to macrosomia; each 1 mmol/L increase in TG resulted in a 27% increase in macrosomia risk, while each 1 mmol/L increase in HDL-C level resulted in a 37% decrease in macrosomia risk, even after adjusting for potential confounders. Notably, the risk of macrosomia increased progressively with increased maternal serum TG levels and decreased HDL-C levels. Compared with women with serum TG levels < 2.5 mmol/L, women with TG levels greater than 3.92 mmol/L had an approximately 2.8-fold increased risk of macrosomia. Compared with women with serum HDL-C levels above 2.23 mmol/L, women with HDL-C levels of less than 1.62 mmol/L had a 1.9-fold increased risk of giving birth to an infan with macrosomia. In addition, a higher risk of macrosomia was observed in women with simultaneous hypertriglyceridemia and low serum HDL-C levels (odds ratio [OR] 2.400, 95% confidence interval [CI]: 1.760–3.274) compared to those with hypertriglyceridemia or low serum HDL-C alone (OR 2.074, 95% CI: 1.609–2.673 and OR 1.363, 95% CI: 1.028–1.809, respectively). CONCLUSIONS: Maternal serum TG levels and HDL-C levels at late gestation are independent predictors of macrosomia in women without DM. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12944-018-0707-7) contains supplementary material, which is available to authorized users.
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spelling pubmed-58960672018-04-20 Association of maternal serum lipids at late gestation with the risk of neonatal macrosomia in women without diabetes mellitus Wang, Xiangxiang Guan, Qingbo Zhao, Jiajun Yang, Feifei Yuan, Zhongshang Yin, Yongchao Fang, Rui Liu, Lingwei Zuo, Changting Gao, Ling Lipids Health Dis Research BACKGROUND: Macrosomia is a serious public health problem worldwide due to its increasing prevalence and adverse influences on maternal and neonatal outcomes. Maternal dyslipidemia exerts potential and adverse impacts on pregnant women and newborns. However, the association between maternal serum lipids and the risk of macrosomia has not yet been clearly elucidated. We explored the association between the maternal lipids profile at late gestation and the risk of having macrosomia among women without diabetes mellitus (DM). METHODS: The medical records of 5407 pregnant women giving birth to single live babies at term were retrospectively analyzed. Subjects with DM, hypertension, thyroid disorders and fetal malformation were excluded. Maternal fasting serum lipids were measured during late pregnancy. Logistic regression analysis was used to analyze the variables associated with the risk of macrosomia. RESULTS: Maternal serum triglyceride (TG) and high-density lipoprotein cholesterol (HDL-C) levels were related to macrosomia; each 1 mmol/L increase in TG resulted in a 27% increase in macrosomia risk, while each 1 mmol/L increase in HDL-C level resulted in a 37% decrease in macrosomia risk, even after adjusting for potential confounders. Notably, the risk of macrosomia increased progressively with increased maternal serum TG levels and decreased HDL-C levels. Compared with women with serum TG levels < 2.5 mmol/L, women with TG levels greater than 3.92 mmol/L had an approximately 2.8-fold increased risk of macrosomia. Compared with women with serum HDL-C levels above 2.23 mmol/L, women with HDL-C levels of less than 1.62 mmol/L had a 1.9-fold increased risk of giving birth to an infan with macrosomia. In addition, a higher risk of macrosomia was observed in women with simultaneous hypertriglyceridemia and low serum HDL-C levels (odds ratio [OR] 2.400, 95% confidence interval [CI]: 1.760–3.274) compared to those with hypertriglyceridemia or low serum HDL-C alone (OR 2.074, 95% CI: 1.609–2.673 and OR 1.363, 95% CI: 1.028–1.809, respectively). CONCLUSIONS: Maternal serum TG levels and HDL-C levels at late gestation are independent predictors of macrosomia in women without DM. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12944-018-0707-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-04-11 /pmc/articles/PMC5896067/ /pubmed/29642923 http://dx.doi.org/10.1186/s12944-018-0707-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Wang, Xiangxiang
Guan, Qingbo
Zhao, Jiajun
Yang, Feifei
Yuan, Zhongshang
Yin, Yongchao
Fang, Rui
Liu, Lingwei
Zuo, Changting
Gao, Ling
Association of maternal serum lipids at late gestation with the risk of neonatal macrosomia in women without diabetes mellitus
title Association of maternal serum lipids at late gestation with the risk of neonatal macrosomia in women without diabetes mellitus
title_full Association of maternal serum lipids at late gestation with the risk of neonatal macrosomia in women without diabetes mellitus
title_fullStr Association of maternal serum lipids at late gestation with the risk of neonatal macrosomia in women without diabetes mellitus
title_full_unstemmed Association of maternal serum lipids at late gestation with the risk of neonatal macrosomia in women without diabetes mellitus
title_short Association of maternal serum lipids at late gestation with the risk of neonatal macrosomia in women without diabetes mellitus
title_sort association of maternal serum lipids at late gestation with the risk of neonatal macrosomia in women without diabetes mellitus
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5896067/
https://www.ncbi.nlm.nih.gov/pubmed/29642923
http://dx.doi.org/10.1186/s12944-018-0707-7
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