Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.

Previous genome wide association studies (GWAS) identified associations of multiple common variants with diastolic and systolic blood pressure traits in adults. However, the contribution of these loci to variations of blood pressure in early life is unclear. We assessed the child and parental contri...

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Main Authors: Sébastien Robiou-du-Pont, Sonia S Anand, Katherine M Morrison, Sarah D McDonald, Stephanie A Atkinson, Koon K Teo, David Meyre
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2017-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC5646805?pdf=render
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spelling doaj-0427a3f289f847128578c3dd74c41bfc2020-11-25T01:10:56ZengPublic Library of Science (PLoS)PLoS ONE1932-62032017-01-011210e018621810.1371/journal.pone.0186218Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.Sébastien Robiou-du-PontSonia S AnandKatherine M MorrisonSarah D McDonaldStephanie A AtkinsonKoon K TeoDavid MeyrePrevious genome wide association studies (GWAS) identified associations of multiple common variants with diastolic and systolic blood pressure traits in adults. However, the contribution of these loci to variations of blood pressure in early life is unclear. We assessed the child and parental contributions of 33 GWAS single-nucleotide polymorphisms (SNPs) for blood pressure in 1,525 participants (515 children, 406 mothers and 237 fathers) of the Family Atherosclerosis Monitoring In early life (FAMILY) study followed-up for 5 years. Two genotype scores for systolic (29 SNPs) and diastolic (24 SNPs) blood pressure were built. Linear mixed-effect regressions showed significant association between rs1378942 in CSK and systolic blood pressure (β = 0.98±0.46, P = 3.4×10-2). The child genotype scores for diastolic and systolic blood pressure were not associated in children. Nominally significant parental genetic effects were found between the SNPs rs11191548 (CYP17A1) (paternal, β = 2.78±1.49, P = 6.1×10-2 for SBP and β = 3.60±1.24, P = 3.7×10-3 for DBP), rs17367504 (MTHFR) (paternal, β = 2.42±0.93, P = 9.3×10-3 for SBP and β = 1.89±0.80, P = 1.8×10-2 for DBP and maternal, β = -1.32±0.60, P = 2.9×10-2 and β = -1.97±0.77, P = 1.0×10-2, for SBP and DBP respectively) and child blood pressure. Our study supports the view that adult GWAS loci have a limited impact on blood pressure during the five first years of life. The parental genetic effects observed on blood pressure in children may suggest epigenetic mechanisms in the transmission of the risk of hypertension. Further replication is needed to confirm our results.http://europepmc.org/articles/PMC5646805?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Sébastien Robiou-du-Pont
Sonia S Anand
Katherine M Morrison
Sarah D McDonald
Stephanie A Atkinson
Koon K Teo
David Meyre
spellingShingle Sébastien Robiou-du-Pont
Sonia S Anand
Katherine M Morrison
Sarah D McDonald
Stephanie A Atkinson
Koon K Teo
David Meyre
Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.
PLoS ONE
author_facet Sébastien Robiou-du-Pont
Sonia S Anand
Katherine M Morrison
Sarah D McDonald
Stephanie A Atkinson
Koon K Teo
David Meyre
author_sort Sébastien Robiou-du-Pont
title Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.
title_short Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.
title_full Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.
title_fullStr Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.
title_full_unstemmed Parental and offspring contribution of genetic markers of adult blood pressure in early life: The FAMILY study.
title_sort parental and offspring contribution of genetic markers of adult blood pressure in early life: the family study.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2017-01-01
description Previous genome wide association studies (GWAS) identified associations of multiple common variants with diastolic and systolic blood pressure traits in adults. However, the contribution of these loci to variations of blood pressure in early life is unclear. We assessed the child and parental contributions of 33 GWAS single-nucleotide polymorphisms (SNPs) for blood pressure in 1,525 participants (515 children, 406 mothers and 237 fathers) of the Family Atherosclerosis Monitoring In early life (FAMILY) study followed-up for 5 years. Two genotype scores for systolic (29 SNPs) and diastolic (24 SNPs) blood pressure were built. Linear mixed-effect regressions showed significant association between rs1378942 in CSK and systolic blood pressure (β = 0.98±0.46, P = 3.4×10-2). The child genotype scores for diastolic and systolic blood pressure were not associated in children. Nominally significant parental genetic effects were found between the SNPs rs11191548 (CYP17A1) (paternal, β = 2.78±1.49, P = 6.1×10-2 for SBP and β = 3.60±1.24, P = 3.7×10-3 for DBP), rs17367504 (MTHFR) (paternal, β = 2.42±0.93, P = 9.3×10-3 for SBP and β = 1.89±0.80, P = 1.8×10-2 for DBP and maternal, β = -1.32±0.60, P = 2.9×10-2 and β = -1.97±0.77, P = 1.0×10-2, for SBP and DBP respectively) and child blood pressure. Our study supports the view that adult GWAS loci have a limited impact on blood pressure during the five first years of life. The parental genetic effects observed on blood pressure in children may suggest epigenetic mechanisms in the transmission of the risk of hypertension. Further replication is needed to confirm our results.
url http://europepmc.org/articles/PMC5646805?pdf=render
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