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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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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