Cargando…

Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases

BACKGROUND: Obesity during childhood can lead to increased risk of adverse cardiometabolic diseases such as type 2 diabetes and coronary artery disease during adult life. Evidence for strong genetic correlations between child and adult body mass index (BMI) suggest the possibility of shared genetic...

Descripción completa

Detalles Bibliográficos
Autores principales: Tekola-Ayele, Fasil, Lee, Anthony, Workalemahu, Tsegaselassie, Sánchez-Pozos, Katy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449964/
https://www.ncbi.nlm.nih.gov/pubmed/30947744
http://dx.doi.org/10.1186/s40246-019-0202-x
_version_ 1783408959473844224
author Tekola-Ayele, Fasil
Lee, Anthony
Workalemahu, Tsegaselassie
Sánchez-Pozos, Katy
author_facet Tekola-Ayele, Fasil
Lee, Anthony
Workalemahu, Tsegaselassie
Sánchez-Pozos, Katy
author_sort Tekola-Ayele, Fasil
collection PubMed
description BACKGROUND: Obesity during childhood can lead to increased risk of adverse cardiometabolic diseases such as type 2 diabetes and coronary artery disease during adult life. Evidence for strong genetic correlations between child and adult body mass index (BMI) suggest the possibility of shared genetic effects. We performed a test for pleiotropy (shared genetics) and functional enrichment of single nucleotide polymorphisms (SNPs) associated with childhood BMI and 15 adult cardiometabolic traits using a unified statistical approach that integrates pleiotropy and functional annotation data. RESULTS: Pleiotropic genetic effects were significantly abundant in 13 out of 15 childhood BMI-adult cardiometabolic trait tests (P < 3.3 × 10(−3)). SNPs associated with both childhood BMI and adult traits were more likely to be functionally deleterious than SNPs associated with neither trait. Genetic variants associated with increased childhood obesity tend to increase risk of cardiometabolic diseases in adulthood. We replicated 39 genetic loci that are known to be associated with childhood BMI and adult traits (coronary artery disease, HDL cholesterol, myocardial infarction, triglycerides, total cholesterol, type 2 diabetes, BMI, waist circumference, and waist-to-hip ratio) in previous genome-wide association studies. We also found a novel association of rs12446632 near GPRC5B, which is highly expressed in adipose tissue and the central nervous system, with adult HDL cholesterol. CONCLUSIONS: This study found significant pleiotropic genetic effects and enrichment of functional annotations in genetic variants that were jointly associated with childhood obesity and adult cardiometabolic diseases. The findings provide new avenues to disentangle the genetic basis of life course associations between childhood obesity and adult cardiometabolic diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40246-019-0202-x) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-6449964
institution National Center for Biotechnology Information
language English
publishDate 2019
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-64499642019-04-16 Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases Tekola-Ayele, Fasil Lee, Anthony Workalemahu, Tsegaselassie Sánchez-Pozos, Katy Hum Genomics Primary Research BACKGROUND: Obesity during childhood can lead to increased risk of adverse cardiometabolic diseases such as type 2 diabetes and coronary artery disease during adult life. Evidence for strong genetic correlations between child and adult body mass index (BMI) suggest the possibility of shared genetic effects. We performed a test for pleiotropy (shared genetics) and functional enrichment of single nucleotide polymorphisms (SNPs) associated with childhood BMI and 15 adult cardiometabolic traits using a unified statistical approach that integrates pleiotropy and functional annotation data. RESULTS: Pleiotropic genetic effects were significantly abundant in 13 out of 15 childhood BMI-adult cardiometabolic trait tests (P < 3.3 × 10(−3)). SNPs associated with both childhood BMI and adult traits were more likely to be functionally deleterious than SNPs associated with neither trait. Genetic variants associated with increased childhood obesity tend to increase risk of cardiometabolic diseases in adulthood. We replicated 39 genetic loci that are known to be associated with childhood BMI and adult traits (coronary artery disease, HDL cholesterol, myocardial infarction, triglycerides, total cholesterol, type 2 diabetes, BMI, waist circumference, and waist-to-hip ratio) in previous genome-wide association studies. We also found a novel association of rs12446632 near GPRC5B, which is highly expressed in adipose tissue and the central nervous system, with adult HDL cholesterol. CONCLUSIONS: This study found significant pleiotropic genetic effects and enrichment of functional annotations in genetic variants that were jointly associated with childhood obesity and adult cardiometabolic diseases. The findings provide new avenues to disentangle the genetic basis of life course associations between childhood obesity and adult cardiometabolic diseases. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40246-019-0202-x) contains supplementary material, which is available to authorized users. BioMed Central 2019-04-04 /pmc/articles/PMC6449964/ /pubmed/30947744 http://dx.doi.org/10.1186/s40246-019-0202-x Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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 Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Primary Research
Tekola-Ayele, Fasil
Lee, Anthony
Workalemahu, Tsegaselassie
Sánchez-Pozos, Katy
Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases
title Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases
title_full Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases
title_fullStr Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases
title_full_unstemmed Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases
title_short Shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases
title_sort shared genetic underpinnings of childhood obesity and adult cardiometabolic diseases
topic Primary Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6449964/
https://www.ncbi.nlm.nih.gov/pubmed/30947744
http://dx.doi.org/10.1186/s40246-019-0202-x
work_keys_str_mv AT tekolaayelefasil sharedgeneticunderpinningsofchildhoodobesityandadultcardiometabolicdiseases
AT leeanthony sharedgeneticunderpinningsofchildhoodobesityandadultcardiometabolicdiseases
AT workalemahutsegaselassie sharedgeneticunderpinningsofchildhoodobesityandadultcardiometabolicdiseases
AT sanchezpozoskaty sharedgeneticunderpinningsofchildhoodobesityandadultcardiometabolicdiseases