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Genetic Risk Scores for Complex Disease Traits in Youth

BACKGROUND: For most disease-related traits the magnitude of the contribution of genetic factors in adolescents remains unclear. METHODS: Twenty continuous traits related to anthropometry, cardiovascular and renal function, metabolism, and inflammation were selected from the ongoing prospective Trac...

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Autores principales: Xie, Tian, Wang, Bin, Nolte, Ilja M., van der Most, Peter J., Oldehinkel, Albertine J., Hartman, Catharina A., Snieder, Harold
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Lippincott Williams & Wilkins 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439939/
https://www.ncbi.nlm.nih.gov/pubmed/32527150
http://dx.doi.org/10.1161/CIRCGEN.119.002775
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author Xie, Tian
Wang, Bin
Nolte, Ilja M.
van der Most, Peter J.
Oldehinkel, Albertine J.
Hartman, Catharina A.
Snieder, Harold
author_facet Xie, Tian
Wang, Bin
Nolte, Ilja M.
van der Most, Peter J.
Oldehinkel, Albertine J.
Hartman, Catharina A.
Snieder, Harold
author_sort Xie, Tian
collection PubMed
description BACKGROUND: For most disease-related traits the magnitude of the contribution of genetic factors in adolescents remains unclear. METHODS: Twenty continuous traits related to anthropometry, cardiovascular and renal function, metabolism, and inflammation were selected from the ongoing prospective Tracking Adolescents’ Individual Lives Survey cohort in the Netherlands with measurements of up to 5 waves from age 11 to 22 years (n=1354, 47.6% males) and all traits available at the third wave (mean age [SD]=16.22 [0.66]). For each trait, unweighted and weighted genetic risk scores (GRSs) were generated based on significantly associated single nucleotide polymorphisms identified from literature. The variance explained by the GRSs in adolescents were estimated by linear regression after adjustment for covariates. RESULTS: Except for ALT (alanine transaminase), all GRSs were significantly associated with their traits. The trait variance explained by the GRSs was highest for lipoprotein[a] (39.59%) and varied between 0.09% (ALT) and 18.49% (LDL [low-density lipoprotein]) for the other traits. For most traits, the variances explained in adolescents were comparable with or slightly smaller than those in adults. Significant increases of trait levels (except ALT) and increased risks for overweight/obesity (odds ratio, 6.41 [95% CI, 2.95–15.56]) and hypertension (odds ratio, 2.86 [95% CI, 1.39–6.17]) were found in individuals in the top GRS decile compared with those at the bottom decile. CONCLUSIONS: Variances explained by adult-based GRSs for disease-related traits in adolescents, although still relatively modest, were comparable with or slightly smaller than in adults offering promise for improved risk prediction at early ages.
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spelling pubmed-74399392020-09-04 Genetic Risk Scores for Complex Disease Traits in Youth Xie, Tian Wang, Bin Nolte, Ilja M. van der Most, Peter J. Oldehinkel, Albertine J. Hartman, Catharina A. Snieder, Harold Circ Genom Precis Med Original Articles BACKGROUND: For most disease-related traits the magnitude of the contribution of genetic factors in adolescents remains unclear. METHODS: Twenty continuous traits related to anthropometry, cardiovascular and renal function, metabolism, and inflammation were selected from the ongoing prospective Tracking Adolescents’ Individual Lives Survey cohort in the Netherlands with measurements of up to 5 waves from age 11 to 22 years (n=1354, 47.6% males) and all traits available at the third wave (mean age [SD]=16.22 [0.66]). For each trait, unweighted and weighted genetic risk scores (GRSs) were generated based on significantly associated single nucleotide polymorphisms identified from literature. The variance explained by the GRSs in adolescents were estimated by linear regression after adjustment for covariates. RESULTS: Except for ALT (alanine transaminase), all GRSs were significantly associated with their traits. The trait variance explained by the GRSs was highest for lipoprotein[a] (39.59%) and varied between 0.09% (ALT) and 18.49% (LDL [low-density lipoprotein]) for the other traits. For most traits, the variances explained in adolescents were comparable with or slightly smaller than those in adults. Significant increases of trait levels (except ALT) and increased risks for overweight/obesity (odds ratio, 6.41 [95% CI, 2.95–15.56]) and hypertension (odds ratio, 2.86 [95% CI, 1.39–6.17]) were found in individuals in the top GRS decile compared with those at the bottom decile. CONCLUSIONS: Variances explained by adult-based GRSs for disease-related traits in adolescents, although still relatively modest, were comparable with or slightly smaller than in adults offering promise for improved risk prediction at early ages. Lippincott Williams & Wilkins 2020-06-11 /pmc/articles/PMC7439939/ /pubmed/32527150 http://dx.doi.org/10.1161/CIRCGEN.119.002775 Text en © 2020 The Authors. Circulation: Genomic and Precision Medicine is published on behalf of the American Heart Association, Inc., by Wolters Kluwer Health, Inc. This is an open access article under the terms of the Creative Commons Attribution Non-Commercial-NoDerivs (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use, distribution, and reproduction in any medium, provided that the original work is properly cited, the use is noncommercial, and no modifications or adaptations are made.
spellingShingle Original Articles
Xie, Tian
Wang, Bin
Nolte, Ilja M.
van der Most, Peter J.
Oldehinkel, Albertine J.
Hartman, Catharina A.
Snieder, Harold
Genetic Risk Scores for Complex Disease Traits in Youth
title Genetic Risk Scores for Complex Disease Traits in Youth
title_full Genetic Risk Scores for Complex Disease Traits in Youth
title_fullStr Genetic Risk Scores for Complex Disease Traits in Youth
title_full_unstemmed Genetic Risk Scores for Complex Disease Traits in Youth
title_short Genetic Risk Scores for Complex Disease Traits in Youth
title_sort genetic risk scores for complex disease traits in youth
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7439939/
https://www.ncbi.nlm.nih.gov/pubmed/32527150
http://dx.doi.org/10.1161/CIRCGEN.119.002775
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