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Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study

Genetic information may help to identify individuals at increased risk for hypertension in early life, prior to the manifestation of elevated blood pressure (BP) values. We examined 369 Black and 832 White Bogalusa Heart Study (BHS) participants recruited in childhood and followed for approximately...

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Autores principales: Sun, Xiao, Pan, Yang, Zhang, Ruiyuan, De Anda-Duran, Ileana, Huang, Zhijie, Li, Changwei, Shi, Mengyao, Razavi, Alexander C., Bazzano, Lydia A., He, Jiang, Sofer, Tamar, Kelly, Tanika N.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408577/
https://www.ncbi.nlm.nih.gov/pubmed/36011384
http://dx.doi.org/10.3390/genes13081473
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author Sun, Xiao
Pan, Yang
Zhang, Ruiyuan
De Anda-Duran, Ileana
Huang, Zhijie
Li, Changwei
Shi, Mengyao
Razavi, Alexander C.
Bazzano, Lydia A.
He, Jiang
Sofer, Tamar
Kelly, Tanika N.
author_facet Sun, Xiao
Pan, Yang
Zhang, Ruiyuan
De Anda-Duran, Ileana
Huang, Zhijie
Li, Changwei
Shi, Mengyao
Razavi, Alexander C.
Bazzano, Lydia A.
He, Jiang
Sofer, Tamar
Kelly, Tanika N.
author_sort Sun, Xiao
collection PubMed
description Genetic information may help to identify individuals at increased risk for hypertension in early life, prior to the manifestation of elevated blood pressure (BP) values. We examined 369 Black and 832 White Bogalusa Heart Study (BHS) participants recruited in childhood and followed for approximately 37 years. The multi-ancestry genome-wide polygenic risk scores (PRSs) for systolic BP (SBP), diastolic BP (DBP), and hypertension were tested for an association with incident hypertension and stage 2 hypertension using Cox proportional hazards models. Race-stratified analyses were adjusted for baseline age, age2, sex, body mass index, genetic principal components, and BP. In Black participants, each standard deviation increase in SBP and DBP PRS conferred a 38% (p = 0.009) and 22% (p = 0.02) increased risk of hypertension and a 74% (p < 0.001) and 50% (p < 0.001) increased risk of stage 2 hypertension, respectively, while no association was observed with the hypertension PRSs. In Whites, each standard deviation increase in SBP, DBP, and hypertension PRS conferred a 24% (p < 0.05), 29% (p = 0.01), and 25% (p < 0.001) increased risk of hypertension, and a 27% (p = 0.08), 29% (0.01), and 42% (p < 0.001) increased risk of stage 2 hypertension, respectively. The addition of BP PRSs to the covariable-only models generally improved the C-statistics (p < 0.05). Multi-ancestry BP PRSs demonstrate the utility of genomic information in the early life prediction of hypertension.
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spelling pubmed-94085772022-08-26 Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study Sun, Xiao Pan, Yang Zhang, Ruiyuan De Anda-Duran, Ileana Huang, Zhijie Li, Changwei Shi, Mengyao Razavi, Alexander C. Bazzano, Lydia A. He, Jiang Sofer, Tamar Kelly, Tanika N. Genes (Basel) Article Genetic information may help to identify individuals at increased risk for hypertension in early life, prior to the manifestation of elevated blood pressure (BP) values. We examined 369 Black and 832 White Bogalusa Heart Study (BHS) participants recruited in childhood and followed for approximately 37 years. The multi-ancestry genome-wide polygenic risk scores (PRSs) for systolic BP (SBP), diastolic BP (DBP), and hypertension were tested for an association with incident hypertension and stage 2 hypertension using Cox proportional hazards models. Race-stratified analyses were adjusted for baseline age, age2, sex, body mass index, genetic principal components, and BP. In Black participants, each standard deviation increase in SBP and DBP PRS conferred a 38% (p = 0.009) and 22% (p = 0.02) increased risk of hypertension and a 74% (p < 0.001) and 50% (p < 0.001) increased risk of stage 2 hypertension, respectively, while no association was observed with the hypertension PRSs. In Whites, each standard deviation increase in SBP, DBP, and hypertension PRS conferred a 24% (p < 0.05), 29% (p = 0.01), and 25% (p < 0.001) increased risk of hypertension, and a 27% (p = 0.08), 29% (0.01), and 42% (p < 0.001) increased risk of stage 2 hypertension, respectively. The addition of BP PRSs to the covariable-only models generally improved the C-statistics (p < 0.05). Multi-ancestry BP PRSs demonstrate the utility of genomic information in the early life prediction of hypertension. MDPI 2022-08-18 /pmc/articles/PMC9408577/ /pubmed/36011384 http://dx.doi.org/10.3390/genes13081473 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Sun, Xiao
Pan, Yang
Zhang, Ruiyuan
De Anda-Duran, Ileana
Huang, Zhijie
Li, Changwei
Shi, Mengyao
Razavi, Alexander C.
Bazzano, Lydia A.
He, Jiang
Sofer, Tamar
Kelly, Tanika N.
Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study
title Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study
title_full Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study
title_fullStr Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study
title_full_unstemmed Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study
title_short Life-Course Associations between Blood Pressure-Related Polygenic Risk Scores and Hypertension in the Bogalusa Heart Study
title_sort life-course associations between blood pressure-related polygenic risk scores and hypertension in the bogalusa heart study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9408577/
https://www.ncbi.nlm.nih.gov/pubmed/36011384
http://dx.doi.org/10.3390/genes13081473
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