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Similarities between acylcarnitine profiles in large for gestational age newborns and obesity

Large for gestational age (LGA) newborns have an increased risk of obesity, insulin resistance, and metabolic syndrome. Acylcarnitine profiles in obese children and adults are characterized by increased levels of C3, C5, and certain medium-chain (C12) and long-chain (C14:1 and C16) acylcarnitines. C...

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Autores principales: Sánchez-Pintos, Paula, de Castro, Maria-Jose, Roca, Iria, Rite, Segundo, López, Miguel, Couce, Maria-Luz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701125/
https://www.ncbi.nlm.nih.gov/pubmed/29176728
http://dx.doi.org/10.1038/s41598-017-15809-4
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author Sánchez-Pintos, Paula
de Castro, Maria-Jose
Roca, Iria
Rite, Segundo
López, Miguel
Couce, Maria-Luz
author_facet Sánchez-Pintos, Paula
de Castro, Maria-Jose
Roca, Iria
Rite, Segundo
López, Miguel
Couce, Maria-Luz
author_sort Sánchez-Pintos, Paula
collection PubMed
description Large for gestational age (LGA) newborns have an increased risk of obesity, insulin resistance, and metabolic syndrome. Acylcarnitine profiles in obese children and adults are characterized by increased levels of C3, C5, and certain medium-chain (C12) and long-chain (C14:1 and C16) acylcarnitines. C2 is also increased in insulin-resistant states. In this 1-year observational study of 2514 newborns (246 LGA newborns, 250 small for gestational age (GA) newborns, and 2018 appropriate for GA newborns), we analyzed and compared postnatal acylcarnitine profiles in LGA newborns with profiles described for obese individuals. Acylcarnitine analysis was performed by tandem mass spectrometry on dried-blood spots collected on day 3 of life. LGA newborns had higher levels of total short-chain acylcarnitines (p < 0.001), C2 (p < 0.01) and C3 (p < 0.001) acylcarnitines, and all C12, C14, and C16 acylcarnitines except C12:1. They also had a higher tendency towards carnitine insufficiency (p < 0.05) and carnitine deficiency (p < 0.001). No significant differences were observed between LGA newborns born to mothers with or without a history of gestational diabetes. This novel study describes a postnatal acylcarnitine profile in LGA with higher levels of C2, C3, total acylcarnitines, and total short-chain acylcarnitines that is characteristic of childhood and adult obesity and linked to an unhealthy metabolic phenotype.
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spelling pubmed-57011252017-11-30 Similarities between acylcarnitine profiles in large for gestational age newborns and obesity Sánchez-Pintos, Paula de Castro, Maria-Jose Roca, Iria Rite, Segundo López, Miguel Couce, Maria-Luz Sci Rep Article Large for gestational age (LGA) newborns have an increased risk of obesity, insulin resistance, and metabolic syndrome. Acylcarnitine profiles in obese children and adults are characterized by increased levels of C3, C5, and certain medium-chain (C12) and long-chain (C14:1 and C16) acylcarnitines. C2 is also increased in insulin-resistant states. In this 1-year observational study of 2514 newborns (246 LGA newborns, 250 small for gestational age (GA) newborns, and 2018 appropriate for GA newborns), we analyzed and compared postnatal acylcarnitine profiles in LGA newborns with profiles described for obese individuals. Acylcarnitine analysis was performed by tandem mass spectrometry on dried-blood spots collected on day 3 of life. LGA newborns had higher levels of total short-chain acylcarnitines (p < 0.001), C2 (p < 0.01) and C3 (p < 0.001) acylcarnitines, and all C12, C14, and C16 acylcarnitines except C12:1. They also had a higher tendency towards carnitine insufficiency (p < 0.05) and carnitine deficiency (p < 0.001). No significant differences were observed between LGA newborns born to mothers with or without a history of gestational diabetes. This novel study describes a postnatal acylcarnitine profile in LGA with higher levels of C2, C3, total acylcarnitines, and total short-chain acylcarnitines that is characteristic of childhood and adult obesity and linked to an unhealthy metabolic phenotype. Nature Publishing Group UK 2017-11-24 /pmc/articles/PMC5701125/ /pubmed/29176728 http://dx.doi.org/10.1038/s41598-017-15809-4 Text en © The Author(s) 2017 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Sánchez-Pintos, Paula
de Castro, Maria-Jose
Roca, Iria
Rite, Segundo
López, Miguel
Couce, Maria-Luz
Similarities between acylcarnitine profiles in large for gestational age newborns and obesity
title Similarities between acylcarnitine profiles in large for gestational age newborns and obesity
title_full Similarities between acylcarnitine profiles in large for gestational age newborns and obesity
title_fullStr Similarities between acylcarnitine profiles in large for gestational age newborns and obesity
title_full_unstemmed Similarities between acylcarnitine profiles in large for gestational age newborns and obesity
title_short Similarities between acylcarnitine profiles in large for gestational age newborns and obesity
title_sort similarities between acylcarnitine profiles in large for gestational age newborns and obesity
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5701125/
https://www.ncbi.nlm.nih.gov/pubmed/29176728
http://dx.doi.org/10.1038/s41598-017-15809-4
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