Cargando…
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...
Autores principales: | , , , , , , |
---|---|
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 |
_version_ | 1783573068987236352 |
---|---|
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. |
format | Online Article Text |
id | pubmed-7439939 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Lippincott Williams & Wilkins |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT xietian geneticriskscoresforcomplexdiseasetraitsinyouth AT wangbin geneticriskscoresforcomplexdiseasetraitsinyouth AT nolteiljam geneticriskscoresforcomplexdiseasetraitsinyouth AT vandermostpeterj geneticriskscoresforcomplexdiseasetraitsinyouth AT oldehinkelalbertinej geneticriskscoresforcomplexdiseasetraitsinyouth AT hartmancatharinaa geneticriskscoresforcomplexdiseasetraitsinyouth AT sniederharold geneticriskscoresforcomplexdiseasetraitsinyouth |