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Etiological Subgroups of Small-for-Gestational-Age: Differential Neurodevelopmental Outcomes

OBJECTIVES: It remains unclear why substantial variations in neurodevelopmental outcomes exist within small-for-gestational-age (SGA) children. We prospectively compared 5-y neurodevelopmental outcomes across SGA etiological subgroups. METHODS: Children born SGA (N = 1050) from U.S. Early Childhood...

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Autores principales: Li, Xiuhong, Eiden, Rina D., Epstein, Leonard H., Shenassa, Edmond D., Xie, Chuanbo, Wen, Xiaozhong
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976943/
https://www.ncbi.nlm.nih.gov/pubmed/27501456
http://dx.doi.org/10.1371/journal.pone.0160677
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author Li, Xiuhong
Eiden, Rina D.
Epstein, Leonard H.
Shenassa, Edmond D.
Xie, Chuanbo
Wen, Xiaozhong
author_facet Li, Xiuhong
Eiden, Rina D.
Epstein, Leonard H.
Shenassa, Edmond D.
Xie, Chuanbo
Wen, Xiaozhong
author_sort Li, Xiuhong
collection PubMed
description OBJECTIVES: It remains unclear why substantial variations in neurodevelopmental outcomes exist within small-for-gestational-age (SGA) children. We prospectively compared 5-y neurodevelopmental outcomes across SGA etiological subgroups. METHODS: Children born SGA (N = 1050) from U.S. Early Childhood Longitudinal Study-Birth Cohort (2001–2007) was divided into etiological subgroups by each of 7 well-established prenatal risk factors. We fit linear regression models to compare 5-y reading, math, gross motor and fine motor scores across SGA subgroups, adjusting for socio-demographic confounders. RESULTS: Compared to singleton SGA subgroup, multiple-birth SGA subgroup had lower mean reading (adjusted mean difference, -4.08 [95% confidence interval, -6.10, -2.06]) and math (-2.22 [-3.61, -0.84]) scores. These disadvantages in reading and math existed only among multiple-birth SGA subgroup without ovulation stimulation (reading, -4.50 [-6.64, -2.36]; math, -2.91 [-4.37, -1.44]), but not among those with ovulation stimulation (reading, -2.33 [-6.24, 1.57]; math 0.63 [-1.86, 3.12]). Compared to singleton SGA subgroup without maternal smoking and inadequate gestational weight gain, singleton SGA subgroup with co-occurrence of maternal smoking and inadequate gestational weight gain (GWG) had lower mean reading (-4.81 [-8.50, -1.12]) and math (-2.95 [-5.51, -0.38]) scores. These differences were not mediated by Apgar score. CONCLUSIONS: Multiple-birth SGA subgroups (vs. singleton SGA) or singleton SGA subgroup with co-occurrence of smoking and inadequate GWG (vs. singleton SGA subgroup without maternal smoking and inadequate gestational weight gain) have poorer cognitive development up to 5 y.
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spelling pubmed-49769432016-08-25 Etiological Subgroups of Small-for-Gestational-Age: Differential Neurodevelopmental Outcomes Li, Xiuhong Eiden, Rina D. Epstein, Leonard H. Shenassa, Edmond D. Xie, Chuanbo Wen, Xiaozhong PLoS One Research Article OBJECTIVES: It remains unclear why substantial variations in neurodevelopmental outcomes exist within small-for-gestational-age (SGA) children. We prospectively compared 5-y neurodevelopmental outcomes across SGA etiological subgroups. METHODS: Children born SGA (N = 1050) from U.S. Early Childhood Longitudinal Study-Birth Cohort (2001–2007) was divided into etiological subgroups by each of 7 well-established prenatal risk factors. We fit linear regression models to compare 5-y reading, math, gross motor and fine motor scores across SGA subgroups, adjusting for socio-demographic confounders. RESULTS: Compared to singleton SGA subgroup, multiple-birth SGA subgroup had lower mean reading (adjusted mean difference, -4.08 [95% confidence interval, -6.10, -2.06]) and math (-2.22 [-3.61, -0.84]) scores. These disadvantages in reading and math existed only among multiple-birth SGA subgroup without ovulation stimulation (reading, -4.50 [-6.64, -2.36]; math, -2.91 [-4.37, -1.44]), but not among those with ovulation stimulation (reading, -2.33 [-6.24, 1.57]; math 0.63 [-1.86, 3.12]). Compared to singleton SGA subgroup without maternal smoking and inadequate gestational weight gain, singleton SGA subgroup with co-occurrence of maternal smoking and inadequate gestational weight gain (GWG) had lower mean reading (-4.81 [-8.50, -1.12]) and math (-2.95 [-5.51, -0.38]) scores. These differences were not mediated by Apgar score. CONCLUSIONS: Multiple-birth SGA subgroups (vs. singleton SGA) or singleton SGA subgroup with co-occurrence of smoking and inadequate GWG (vs. singleton SGA subgroup without maternal smoking and inadequate gestational weight gain) have poorer cognitive development up to 5 y. Public Library of Science 2016-08-08 /pmc/articles/PMC4976943/ /pubmed/27501456 http://dx.doi.org/10.1371/journal.pone.0160677 Text en © 2016 Li 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 (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Li, Xiuhong
Eiden, Rina D.
Epstein, Leonard H.
Shenassa, Edmond D.
Xie, Chuanbo
Wen, Xiaozhong
Etiological Subgroups of Small-for-Gestational-Age: Differential Neurodevelopmental Outcomes
title Etiological Subgroups of Small-for-Gestational-Age: Differential Neurodevelopmental Outcomes
title_full Etiological Subgroups of Small-for-Gestational-Age: Differential Neurodevelopmental Outcomes
title_fullStr Etiological Subgroups of Small-for-Gestational-Age: Differential Neurodevelopmental Outcomes
title_full_unstemmed Etiological Subgroups of Small-for-Gestational-Age: Differential Neurodevelopmental Outcomes
title_short Etiological Subgroups of Small-for-Gestational-Age: Differential Neurodevelopmental Outcomes
title_sort etiological subgroups of small-for-gestational-age: differential neurodevelopmental outcomes
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4976943/
https://www.ncbi.nlm.nih.gov/pubmed/27501456
http://dx.doi.org/10.1371/journal.pone.0160677
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