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Genetic Variation in FADS Genes and Plasma Cholesterol Levels in 2-Year-Old Infants: KOALA Birth Cohort Study

OBJECTIVE: Single nucleotide polymorphisms (SNPs) in genes involved in fatty acid metabolism (FADS1 FADS2 gene cluster) are associated with plasma lipid levels. We aimed to investigate whether these associations are already present early in life and compare the relative contribution of FADS SNPs vs...

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Autores principales: Moltó-Puigmartí, Carolina, Jansen, Eugène, Heinrich, Joachim, Standl, Marie, Mensink, Ronald P., Plat, Jogchum, Penders, John, Mommers, Monique, Koppelman, Gerard H., Postma, Dirkje S., Thijs, Carel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648514/
https://www.ncbi.nlm.nih.gov/pubmed/23667444
http://dx.doi.org/10.1371/journal.pone.0061671
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author Moltó-Puigmartí, Carolina
Jansen, Eugène
Heinrich, Joachim
Standl, Marie
Mensink, Ronald P.
Plat, Jogchum
Penders, John
Mommers, Monique
Koppelman, Gerard H.
Postma, Dirkje S.
Thijs, Carel
author_facet Moltó-Puigmartí, Carolina
Jansen, Eugène
Heinrich, Joachim
Standl, Marie
Mensink, Ronald P.
Plat, Jogchum
Penders, John
Mommers, Monique
Koppelman, Gerard H.
Postma, Dirkje S.
Thijs, Carel
author_sort Moltó-Puigmartí, Carolina
collection PubMed
description OBJECTIVE: Single nucleotide polymorphisms (SNPs) in genes involved in fatty acid metabolism (FADS1 FADS2 gene cluster) are associated with plasma lipid levels. We aimed to investigate whether these associations are already present early in life and compare the relative contribution of FADS SNPs vs traditional (non-genetic) factors as determinants of plasma lipid levels. METHODS: Information on infants’ plasma total cholesterol levels, genotypes of five FADS SNPs (rs174545, rs174546, rs174556, rs174561, and rs3834458), anthropometric data, maternal characteristics, and breastfeeding history was available for 521 2-year-old children from the KOALA Birth Cohort Study. For 295 of these 521 children, plasma HDLc and non-HDLc levels were also known. Multivariable linear regression analysis was used to study the associations of genetic and non-genetic determinants with cholesterol levels. RESULTS: All FADS SNPs were significantly associated with total cholesterol levels. Heterozygous and homozygous for the minor allele children had about 4% and 8% lower total cholesterol levels than major allele homozygotes. In addition, homozygous for the minor allele children had about 7% lower HDLc levels. This difference reached significance for the SNPs rs174546 and rs3834458. The associations went in the same direction for non-HDLc, but statistical significance was not reached. The percentage of total variance of total cholesterol levels explained by FADS SNPs was relatively low (lower than 3%) but of the same order as that explained by gender and the non-genetic determinants together. CONCLUSIONS: FADS SNPs are associated with plasma total cholesterol and HDLc levels in preschool children. This brings a new piece of evidence to explain how blood lipid levels may track from childhood to adulthood. Moreover, the finding that these SNPs explain a similar amount of variance in total cholesterol levels as the non-genetic determinants studied reveals the potential importance of investigating the effects of genetic variations in early life.
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spelling pubmed-36485142013-05-10 Genetic Variation in FADS Genes and Plasma Cholesterol Levels in 2-Year-Old Infants: KOALA Birth Cohort Study Moltó-Puigmartí, Carolina Jansen, Eugène Heinrich, Joachim Standl, Marie Mensink, Ronald P. Plat, Jogchum Penders, John Mommers, Monique Koppelman, Gerard H. Postma, Dirkje S. Thijs, Carel PLoS One Research Article OBJECTIVE: Single nucleotide polymorphisms (SNPs) in genes involved in fatty acid metabolism (FADS1 FADS2 gene cluster) are associated with plasma lipid levels. We aimed to investigate whether these associations are already present early in life and compare the relative contribution of FADS SNPs vs traditional (non-genetic) factors as determinants of plasma lipid levels. METHODS: Information on infants’ plasma total cholesterol levels, genotypes of five FADS SNPs (rs174545, rs174546, rs174556, rs174561, and rs3834458), anthropometric data, maternal characteristics, and breastfeeding history was available for 521 2-year-old children from the KOALA Birth Cohort Study. For 295 of these 521 children, plasma HDLc and non-HDLc levels were also known. Multivariable linear regression analysis was used to study the associations of genetic and non-genetic determinants with cholesterol levels. RESULTS: All FADS SNPs were significantly associated with total cholesterol levels. Heterozygous and homozygous for the minor allele children had about 4% and 8% lower total cholesterol levels than major allele homozygotes. In addition, homozygous for the minor allele children had about 7% lower HDLc levels. This difference reached significance for the SNPs rs174546 and rs3834458. The associations went in the same direction for non-HDLc, but statistical significance was not reached. The percentage of total variance of total cholesterol levels explained by FADS SNPs was relatively low (lower than 3%) but of the same order as that explained by gender and the non-genetic determinants together. CONCLUSIONS: FADS SNPs are associated with plasma total cholesterol and HDLc levels in preschool children. This brings a new piece of evidence to explain how blood lipid levels may track from childhood to adulthood. Moreover, the finding that these SNPs explain a similar amount of variance in total cholesterol levels as the non-genetic determinants studied reveals the potential importance of investigating the effects of genetic variations in early life. Public Library of Science 2013-05-08 /pmc/articles/PMC3648514/ /pubmed/23667444 http://dx.doi.org/10.1371/journal.pone.0061671 Text en © 2013 Moltó-Puigmartí 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, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Moltó-Puigmartí, Carolina
Jansen, Eugène
Heinrich, Joachim
Standl, Marie
Mensink, Ronald P.
Plat, Jogchum
Penders, John
Mommers, Monique
Koppelman, Gerard H.
Postma, Dirkje S.
Thijs, Carel
Genetic Variation in FADS Genes and Plasma Cholesterol Levels in 2-Year-Old Infants: KOALA Birth Cohort Study
title Genetic Variation in FADS Genes and Plasma Cholesterol Levels in 2-Year-Old Infants: KOALA Birth Cohort Study
title_full Genetic Variation in FADS Genes and Plasma Cholesterol Levels in 2-Year-Old Infants: KOALA Birth Cohort Study
title_fullStr Genetic Variation in FADS Genes and Plasma Cholesterol Levels in 2-Year-Old Infants: KOALA Birth Cohort Study
title_full_unstemmed Genetic Variation in FADS Genes and Plasma Cholesterol Levels in 2-Year-Old Infants: KOALA Birth Cohort Study
title_short Genetic Variation in FADS Genes and Plasma Cholesterol Levels in 2-Year-Old Infants: KOALA Birth Cohort Study
title_sort genetic variation in fads genes and plasma cholesterol levels in 2-year-old infants: koala birth cohort study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3648514/
https://www.ncbi.nlm.nih.gov/pubmed/23667444
http://dx.doi.org/10.1371/journal.pone.0061671
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