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The Effect of an Infant Formula Supplemented with AA and DHA on Fatty Acid Levels of Infants with Different FADS Genotypes: The COGNIS Study
Polymorphisms in the fatty acid desaturase (FADS) genes influence the arachidonic (AA) and docosahexaenoic (DHA) acid concentrations (crucial in early life). Infants with specific genotypes may require different amounts of these fatty acids (FAs) to maintain an adequate status. The aim of this study...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470942/ https://www.ncbi.nlm.nih.gov/pubmed/30871048 http://dx.doi.org/10.3390/nu11030602 |
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author | Salas Lorenzo, Isabel Chisaguano Tonato, Aida M. de la Garza Puentes, Andrea Nieto, Ana Herrmann, Florian Dieguez, Estefanía Castellote, Ana I. López-Sabater, M. Carmen Rodríguez-Palmero, Maria Campoy, Cristina |
author_facet | Salas Lorenzo, Isabel Chisaguano Tonato, Aida M. de la Garza Puentes, Andrea Nieto, Ana Herrmann, Florian Dieguez, Estefanía Castellote, Ana I. López-Sabater, M. Carmen Rodríguez-Palmero, Maria Campoy, Cristina |
author_sort | Salas Lorenzo, Isabel |
collection | PubMed |
description | Polymorphisms in the fatty acid desaturase (FADS) genes influence the arachidonic (AA) and docosahexaenoic (DHA) acid concentrations (crucial in early life). Infants with specific genotypes may require different amounts of these fatty acids (FAs) to maintain an adequate status. The aim of this study was to determine the effect of an infant formula supplemented with AA and DHA on FAs of infants with different FADS genotypes. In total, 176 infants from the COGNIS study were randomly allocated to the Standard Formula (SF; n = 61) or the Experimental Formula (EF; n = 70) group, the latter supplemented with AA and DHA. Breastfed infants were added as a reference group (BF; n = 45). FAs and FADS polymorphisms were analyzed from cheek cells collected at 3 months of age. FADS minor allele carriership in formula fed infants, especially those supplemented, was associated with a declined desaturase activity and lower AA and DHA levels. Breastfed infants were not affected, possibly to the high content of AA and DHA in breast milk. The supplementation increased AA and DHA levels, but mostly in major allele carriers. In conclusion, infant FADS genotype could contribute to narrow the gap of AA and DHA concentrations between breastfed and formula fed infants. |
format | Online Article Text |
id | pubmed-6470942 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-64709422019-04-25 The Effect of an Infant Formula Supplemented with AA and DHA on Fatty Acid Levels of Infants with Different FADS Genotypes: The COGNIS Study Salas Lorenzo, Isabel Chisaguano Tonato, Aida M. de la Garza Puentes, Andrea Nieto, Ana Herrmann, Florian Dieguez, Estefanía Castellote, Ana I. López-Sabater, M. Carmen Rodríguez-Palmero, Maria Campoy, Cristina Nutrients Article Polymorphisms in the fatty acid desaturase (FADS) genes influence the arachidonic (AA) and docosahexaenoic (DHA) acid concentrations (crucial in early life). Infants with specific genotypes may require different amounts of these fatty acids (FAs) to maintain an adequate status. The aim of this study was to determine the effect of an infant formula supplemented with AA and DHA on FAs of infants with different FADS genotypes. In total, 176 infants from the COGNIS study were randomly allocated to the Standard Formula (SF; n = 61) or the Experimental Formula (EF; n = 70) group, the latter supplemented with AA and DHA. Breastfed infants were added as a reference group (BF; n = 45). FAs and FADS polymorphisms were analyzed from cheek cells collected at 3 months of age. FADS minor allele carriership in formula fed infants, especially those supplemented, was associated with a declined desaturase activity and lower AA and DHA levels. Breastfed infants were not affected, possibly to the high content of AA and DHA in breast milk. The supplementation increased AA and DHA levels, but mostly in major allele carriers. In conclusion, infant FADS genotype could contribute to narrow the gap of AA and DHA concentrations between breastfed and formula fed infants. MDPI 2019-03-12 /pmc/articles/PMC6470942/ /pubmed/30871048 http://dx.doi.org/10.3390/nu11030602 Text en © 2019 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Salas Lorenzo, Isabel Chisaguano Tonato, Aida M. de la Garza Puentes, Andrea Nieto, Ana Herrmann, Florian Dieguez, Estefanía Castellote, Ana I. López-Sabater, M. Carmen Rodríguez-Palmero, Maria Campoy, Cristina The Effect of an Infant Formula Supplemented with AA and DHA on Fatty Acid Levels of Infants with Different FADS Genotypes: The COGNIS Study |
title | The Effect of an Infant Formula Supplemented with AA and DHA on Fatty Acid Levels of Infants with Different FADS Genotypes: The COGNIS Study |
title_full | The Effect of an Infant Formula Supplemented with AA and DHA on Fatty Acid Levels of Infants with Different FADS Genotypes: The COGNIS Study |
title_fullStr | The Effect of an Infant Formula Supplemented with AA and DHA on Fatty Acid Levels of Infants with Different FADS Genotypes: The COGNIS Study |
title_full_unstemmed | The Effect of an Infant Formula Supplemented with AA and DHA on Fatty Acid Levels of Infants with Different FADS Genotypes: The COGNIS Study |
title_short | The Effect of an Infant Formula Supplemented with AA and DHA on Fatty Acid Levels of Infants with Different FADS Genotypes: The COGNIS Study |
title_sort | effect of an infant formula supplemented with aa and dha on fatty acid levels of infants with different fads genotypes: the cognis study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6470942/ https://www.ncbi.nlm.nih.gov/pubmed/30871048 http://dx.doi.org/10.3390/nu11030602 |
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