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Quantile-Dependent Expressivity of Serum Uric Acid Concentrations

OBJECTIVE: “Quantile-dependent expressivity” occurs when the effect size of a genetic variant depends upon whether the phenotype (e.g., serum uric acid) is high or low relative to its distribution. Analyses were performed to test whether serum uric acid heritability is quantile-specific and whether...

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Autor principal: Williams, Paul T.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448993/
https://www.ncbi.nlm.nih.gov/pubmed/34545327
http://dx.doi.org/10.1155/2021/3889278
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author Williams, Paul T.
author_facet Williams, Paul T.
author_sort Williams, Paul T.
collection PubMed
description OBJECTIVE: “Quantile-dependent expressivity” occurs when the effect size of a genetic variant depends upon whether the phenotype (e.g., serum uric acid) is high or low relative to its distribution. Analyses were performed to test whether serum uric acid heritability is quantile-specific and whether this could explain some reported gene-environment interactions. METHODS: Serum uric acid concentrations were analyzed from 2151 sibships and 12,068 offspring-parent pairs from the Framingham Heart Study. Quantile-specific heritability from offspring-parent regression slopes (β(OP), h(2) = 2β(OP)/(1 + r(spouse))) and full-sib regression slopes (β(FS), h(2) = {(1 + 8r(spouse)β(FS))(0.5) − 1}/(2r(spouse))) was robustly estimated by quantile regression with nonparametric significance assigned from 1000 bootstrap samples. RESULTS: Quantile-specific h(2) (±SE) increased with increasing percentiles of the offspring's sex- and age-adjusted uric acid distribution when estimated from β(OP) (P(trend) = 0.001): 0.34 ± 0.03 at the 10(th), 0.36 ± 0.03 at the 25(th), 0.41 ± 0.03 at the 50(th), 0.46 ± 0.04 at the 75(th), and 0.49 ± 0.05 at the 90(th) percentile and when estimated from β(FS) (P(trend) = 0.006). This is consistent with the larger genetic effect size of (1) the SLC2A9 rs11722228 polymorphism in gout patients vs. controls, (2) the ABCG2 rs2231142 polymorphism in men vs. women, (3) the SLC2A9 rs13113918 polymorphism in obese patients prior to bariatric surgery vs. two-year postsurgery following 29 kg weight loss, (4) the ABCG2 rs6855911 polymorphism in obese vs. nonobese women, and (5) the LRP2 rs2544390 polymorphism in heavier drinkers vs. abstainers. Quantile-dependent expressivity may also explain the larger genetic effect size of an SLC2A9/PKD2/ABCG2 haplotype for high vs. low intakes of alcohol, chicken, or processed meats. CONCLUSIONS: Heritability of serum uric acid concentrations is quantile-specific.
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spelling pubmed-84489932021-09-19 Quantile-Dependent Expressivity of Serum Uric Acid Concentrations Williams, Paul T. Int J Genomics Research Article OBJECTIVE: “Quantile-dependent expressivity” occurs when the effect size of a genetic variant depends upon whether the phenotype (e.g., serum uric acid) is high or low relative to its distribution. Analyses were performed to test whether serum uric acid heritability is quantile-specific and whether this could explain some reported gene-environment interactions. METHODS: Serum uric acid concentrations were analyzed from 2151 sibships and 12,068 offspring-parent pairs from the Framingham Heart Study. Quantile-specific heritability from offspring-parent regression slopes (β(OP), h(2) = 2β(OP)/(1 + r(spouse))) and full-sib regression slopes (β(FS), h(2) = {(1 + 8r(spouse)β(FS))(0.5) − 1}/(2r(spouse))) was robustly estimated by quantile regression with nonparametric significance assigned from 1000 bootstrap samples. RESULTS: Quantile-specific h(2) (±SE) increased with increasing percentiles of the offspring's sex- and age-adjusted uric acid distribution when estimated from β(OP) (P(trend) = 0.001): 0.34 ± 0.03 at the 10(th), 0.36 ± 0.03 at the 25(th), 0.41 ± 0.03 at the 50(th), 0.46 ± 0.04 at the 75(th), and 0.49 ± 0.05 at the 90(th) percentile and when estimated from β(FS) (P(trend) = 0.006). This is consistent with the larger genetic effect size of (1) the SLC2A9 rs11722228 polymorphism in gout patients vs. controls, (2) the ABCG2 rs2231142 polymorphism in men vs. women, (3) the SLC2A9 rs13113918 polymorphism in obese patients prior to bariatric surgery vs. two-year postsurgery following 29 kg weight loss, (4) the ABCG2 rs6855911 polymorphism in obese vs. nonobese women, and (5) the LRP2 rs2544390 polymorphism in heavier drinkers vs. abstainers. Quantile-dependent expressivity may also explain the larger genetic effect size of an SLC2A9/PKD2/ABCG2 haplotype for high vs. low intakes of alcohol, chicken, or processed meats. CONCLUSIONS: Heritability of serum uric acid concentrations is quantile-specific. Hindawi 2021-09-02 /pmc/articles/PMC8448993/ /pubmed/34545327 http://dx.doi.org/10.1155/2021/3889278 Text en Copyright © 2021 Paul T. Williams. https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Williams, Paul T.
Quantile-Dependent Expressivity of Serum Uric Acid Concentrations
title Quantile-Dependent Expressivity of Serum Uric Acid Concentrations
title_full Quantile-Dependent Expressivity of Serum Uric Acid Concentrations
title_fullStr Quantile-Dependent Expressivity of Serum Uric Acid Concentrations
title_full_unstemmed Quantile-Dependent Expressivity of Serum Uric Acid Concentrations
title_short Quantile-Dependent Expressivity of Serum Uric Acid Concentrations
title_sort quantile-dependent expressivity of serum uric acid concentrations
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8448993/
https://www.ncbi.nlm.nih.gov/pubmed/34545327
http://dx.doi.org/10.1155/2021/3889278
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