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Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men

There is substantial genetic predisposition to bladder cancer (BC). Recently, blood pressure (BP) was positively associated with BC risk in men, but the potential interaction with genetic susceptibility for BC is unknown. We investigated a weighted genetic risk score (wGRS) of 18 BC genetic variants...

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Autores principales: Teleka, Stanley, Orho-Melander, Marju, Liedberg, Fredrik, Melander, Olle, Jirström, Karin, Stocks, Tanja
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622916/
https://www.ncbi.nlm.nih.gov/pubmed/36316463
http://dx.doi.org/10.1038/s41598-022-23225-6
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author Teleka, Stanley
Orho-Melander, Marju
Liedberg, Fredrik
Melander, Olle
Jirström, Karin
Stocks, Tanja
author_facet Teleka, Stanley
Orho-Melander, Marju
Liedberg, Fredrik
Melander, Olle
Jirström, Karin
Stocks, Tanja
author_sort Teleka, Stanley
collection PubMed
description There is substantial genetic predisposition to bladder cancer (BC). Recently, blood pressure (BP) was positively associated with BC risk in men, but the potential interaction with genetic susceptibility for BC is unknown. We investigated a weighted genetic risk score (wGRS) of 18 BC genetic variants, BP, and their interaction, in relation to incident urothelial cancer (UC, n = 385) risk in 10,576 men. We used Cox regression, the likelihood ratio test, and the relative excess risk for interaction to calculate hazard ratios (HR) of UC, multiplicative interaction and additive interaction respectively. There was evidence of a positive additive interaction between SBP and the wGRS in relation to aggressive (P = 0.02) but not non-aggressive (P = 0.60) UC. The HR of aggressive UC was for SBP ≥ 140 mmHg and the upper 50% of the wGRS combined 1.72 (95% CI 1.03–2.87) compared to the counterpart group. Additionally, the 20-year risk of aggressive UC in 60 year-old men was 0.78% in the low SBP/low wGRS group and 1.33% in the high SBP/high wGRS group. Our findings support a potential additive interaction between the wGRS and SBP on aggressive UC among men. If replicated, the findings on interaction may provide biological and public health insight to prevent aggressive UC.
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spelling pubmed-96229162022-11-02 Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men Teleka, Stanley Orho-Melander, Marju Liedberg, Fredrik Melander, Olle Jirström, Karin Stocks, Tanja Sci Rep Article There is substantial genetic predisposition to bladder cancer (BC). Recently, blood pressure (BP) was positively associated with BC risk in men, but the potential interaction with genetic susceptibility for BC is unknown. We investigated a weighted genetic risk score (wGRS) of 18 BC genetic variants, BP, and their interaction, in relation to incident urothelial cancer (UC, n = 385) risk in 10,576 men. We used Cox regression, the likelihood ratio test, and the relative excess risk for interaction to calculate hazard ratios (HR) of UC, multiplicative interaction and additive interaction respectively. There was evidence of a positive additive interaction between SBP and the wGRS in relation to aggressive (P = 0.02) but not non-aggressive (P = 0.60) UC. The HR of aggressive UC was for SBP ≥ 140 mmHg and the upper 50% of the wGRS combined 1.72 (95% CI 1.03–2.87) compared to the counterpart group. Additionally, the 20-year risk of aggressive UC in 60 year-old men was 0.78% in the low SBP/low wGRS group and 1.33% in the high SBP/high wGRS group. Our findings support a potential additive interaction between the wGRS and SBP on aggressive UC among men. If replicated, the findings on interaction may provide biological and public health insight to prevent aggressive UC. Nature Publishing Group UK 2022-10-31 /pmc/articles/PMC9622916/ /pubmed/36316463 http://dx.doi.org/10.1038/s41598-022-23225-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) .
spellingShingle Article
Teleka, Stanley
Orho-Melander, Marju
Liedberg, Fredrik
Melander, Olle
Jirström, Karin
Stocks, Tanja
Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men
title Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men
title_full Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men
title_fullStr Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men
title_full_unstemmed Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men
title_short Interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men
title_sort interaction between blood pressure and genetic risk score for bladder cancer, and risk of urothelial carcinoma in men
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9622916/
https://www.ncbi.nlm.nih.gov/pubmed/36316463
http://dx.doi.org/10.1038/s41598-022-23225-6
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