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Fetuin-A in Infants Born Small- or Large-for-Gestational-Age
Fetuin-A is a multifunctional glycoprotein that has been implicated in insulin resistance and bone metabolism. We assessed whether fetuin-A is associated with poor or excessive fetal growth. In the Shanghai Birth Cohort, we conducted a nested case-control study of 60 trios of small-for-gestational-a...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561389/ https://www.ncbi.nlm.nih.gov/pubmed/33117283 http://dx.doi.org/10.3389/fendo.2020.567955 |
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author | Wang, Wen-Juan Wang, Shufan Yang, Meng-Nan Dong, Yu He, Hua Fang, Fang Huang, Rong Yu, Xiao-Gang Zhang, Guang-Hui Zhao, Xia Zheng, Tao Huang, Xiao-Yi Zhang, Jun Ouyang, Fengxiu Luo, Zhong-Cheng |
author_facet | Wang, Wen-Juan Wang, Shufan Yang, Meng-Nan Dong, Yu He, Hua Fang, Fang Huang, Rong Yu, Xiao-Gang Zhang, Guang-Hui Zhao, Xia Zheng, Tao Huang, Xiao-Yi Zhang, Jun Ouyang, Fengxiu Luo, Zhong-Cheng |
author_sort | Wang, Wen-Juan |
collection | PubMed |
description | Fetuin-A is a multifunctional glycoprotein that has been implicated in insulin resistance and bone metabolism. We assessed whether fetuin-A is associated with poor or excessive fetal growth. In the Shanghai Birth Cohort, we conducted a nested case-control study of 60 trios of small-for-gestational-age (SGA, birth weight <10th percentile), optimal-for-gestational-age (OGA, 25–75th, the reference) and large-for-gestational-age (LGA, >90th percentile) infants matched by sex and gestational age. Cord plasma concentrations of fetuin-A and fetal growth factors [insulin, proinsulin, insulin-like growth factor (IGF)-I and IGF-II] were measured. Cord plasma fetuin-A concentrations were higher in SGA (809.4 ± 306.9 μg/ml, P = 0.026) and LGA (924.2 ± 375.9 μg/ml, P < 0.001) relative to OGA (680.7 ± 262.1 μg/ml) newborns, and were not correlated to insulin, proinsulin, IGF-I and IGF-II (all P > 0.2). Higher fetuin-A concentrations were associated with increased risks of SGA [OR = 1.67 (1.08–2.58) per SD increment, P = 0.024] and LGA [OR = 2.36 (1.53–3.66), P < 0.001]. Adjusting for maternal and neonatal characteristics and fetal growth factors, the elevated risk changed little for LGA [adjusted OR = 2.28 (1.29–4.01), P = 0.005], but became non-significant for SGA (P = 0.202). Our study is the first to demonstrate that fetuin-A may be involved in excessive fetal growth. This association is independent of fetal growth factors. |
format | Online Article Text |
id | pubmed-7561389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-75613892020-10-27 Fetuin-A in Infants Born Small- or Large-for-Gestational-Age Wang, Wen-Juan Wang, Shufan Yang, Meng-Nan Dong, Yu He, Hua Fang, Fang Huang, Rong Yu, Xiao-Gang Zhang, Guang-Hui Zhao, Xia Zheng, Tao Huang, Xiao-Yi Zhang, Jun Ouyang, Fengxiu Luo, Zhong-Cheng Front Endocrinol (Lausanne) Endocrinology Fetuin-A is a multifunctional glycoprotein that has been implicated in insulin resistance and bone metabolism. We assessed whether fetuin-A is associated with poor or excessive fetal growth. In the Shanghai Birth Cohort, we conducted a nested case-control study of 60 trios of small-for-gestational-age (SGA, birth weight <10th percentile), optimal-for-gestational-age (OGA, 25–75th, the reference) and large-for-gestational-age (LGA, >90th percentile) infants matched by sex and gestational age. Cord plasma concentrations of fetuin-A and fetal growth factors [insulin, proinsulin, insulin-like growth factor (IGF)-I and IGF-II] were measured. Cord plasma fetuin-A concentrations were higher in SGA (809.4 ± 306.9 μg/ml, P = 0.026) and LGA (924.2 ± 375.9 μg/ml, P < 0.001) relative to OGA (680.7 ± 262.1 μg/ml) newborns, and were not correlated to insulin, proinsulin, IGF-I and IGF-II (all P > 0.2). Higher fetuin-A concentrations were associated with increased risks of SGA [OR = 1.67 (1.08–2.58) per SD increment, P = 0.024] and LGA [OR = 2.36 (1.53–3.66), P < 0.001]. Adjusting for maternal and neonatal characteristics and fetal growth factors, the elevated risk changed little for LGA [adjusted OR = 2.28 (1.29–4.01), P = 0.005], but became non-significant for SGA (P = 0.202). Our study is the first to demonstrate that fetuin-A may be involved in excessive fetal growth. This association is independent of fetal growth factors. Frontiers Media S.A. 2020-09-30 /pmc/articles/PMC7561389/ /pubmed/33117283 http://dx.doi.org/10.3389/fendo.2020.567955 Text en Copyright © 2020 Wang, Wang, Yang, Dong, He, Fang, Huang, Yu, Zhang, Zhao, Zheng, Huang, Zhang, Ouyang and Luo. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Endocrinology Wang, Wen-Juan Wang, Shufan Yang, Meng-Nan Dong, Yu He, Hua Fang, Fang Huang, Rong Yu, Xiao-Gang Zhang, Guang-Hui Zhao, Xia Zheng, Tao Huang, Xiao-Yi Zhang, Jun Ouyang, Fengxiu Luo, Zhong-Cheng Fetuin-A in Infants Born Small- or Large-for-Gestational-Age |
title | Fetuin-A in Infants Born Small- or Large-for-Gestational-Age |
title_full | Fetuin-A in Infants Born Small- or Large-for-Gestational-Age |
title_fullStr | Fetuin-A in Infants Born Small- or Large-for-Gestational-Age |
title_full_unstemmed | Fetuin-A in Infants Born Small- or Large-for-Gestational-Age |
title_short | Fetuin-A in Infants Born Small- or Large-for-Gestational-Age |
title_sort | fetuin-a in infants born small- or large-for-gestational-age |
topic | Endocrinology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7561389/ https://www.ncbi.nlm.nih.gov/pubmed/33117283 http://dx.doi.org/10.3389/fendo.2020.567955 |
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