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Urinary Sodium Excretion Enhances the Effect of Alcohol on Blood Pressure
Alcohol consumption is linked to urinary sodium excretion and both of these traits are linked to hypertension and cardiovascular diseases (CVDs). The interplay between alcohol consumption and sodium on hypertension, and cardiovascular diseases (CVDs) is not well-described. Here, we used genetically...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319523/ https://www.ncbi.nlm.nih.gov/pubmed/35885821 http://dx.doi.org/10.3390/healthcare10071296 |
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author | Jiang, Xiyun Anasanti, Mila D. Drenos, Fotios Blakemore, Alexandra I. Pazoki, Raha |
author_facet | Jiang, Xiyun Anasanti, Mila D. Drenos, Fotios Blakemore, Alexandra I. Pazoki, Raha |
author_sort | Jiang, Xiyun |
collection | PubMed |
description | Alcohol consumption is linked to urinary sodium excretion and both of these traits are linked to hypertension and cardiovascular diseases (CVDs). The interplay between alcohol consumption and sodium on hypertension, and cardiovascular diseases (CVDs) is not well-described. Here, we used genetically predicted alcohol consumption and explored the relationships between alcohol consumption, urinary sodium, hypertension, and CVDs. Methods: We performed a comparative analysis among 295,189 participants from the prospective cohort of the UK Biobank (baseline data collected between 2006 and 2010). We created a genetic risk score (GRS) using 105 published genetic variants in Europeans that were associated with alcohol consumption. We explored the relationships between GRS, alcohol consumption, urinary sodium, blood pressure traits, and incident CVD. We used linear and logistic regression and Cox proportional hazards (PH) models and Mendelian randomization in our analysis. Results: The median follow-up time for composite CVD and stroke were 6.1 years and 7.1 years respectively. Our analyses showed that high alcohol consumption is linked to low urinary sodium excretion. Our results showed that high alcohol GRS was associated with high blood pressure and higher risk of stroke and supported an interaction effect between alcohol GRS and urinary sodium on stage 2 hypertension (P(interaction) = 0.03) and CVD (P(interaction) = 0.03), i.e., in the presence of high urinary sodium excretion, the effect of alcohol GRS on blood pressure may be enhanced. Conclusions: Our results show that urinary sodium excretion may offset the risk posed by genetic risk of alcohol consumption. |
format | Online Article Text |
id | pubmed-9319523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-93195232022-07-27 Urinary Sodium Excretion Enhances the Effect of Alcohol on Blood Pressure Jiang, Xiyun Anasanti, Mila D. Drenos, Fotios Blakemore, Alexandra I. Pazoki, Raha Healthcare (Basel) Article Alcohol consumption is linked to urinary sodium excretion and both of these traits are linked to hypertension and cardiovascular diseases (CVDs). The interplay between alcohol consumption and sodium on hypertension, and cardiovascular diseases (CVDs) is not well-described. Here, we used genetically predicted alcohol consumption and explored the relationships between alcohol consumption, urinary sodium, hypertension, and CVDs. Methods: We performed a comparative analysis among 295,189 participants from the prospective cohort of the UK Biobank (baseline data collected between 2006 and 2010). We created a genetic risk score (GRS) using 105 published genetic variants in Europeans that were associated with alcohol consumption. We explored the relationships between GRS, alcohol consumption, urinary sodium, blood pressure traits, and incident CVD. We used linear and logistic regression and Cox proportional hazards (PH) models and Mendelian randomization in our analysis. Results: The median follow-up time for composite CVD and stroke were 6.1 years and 7.1 years respectively. Our analyses showed that high alcohol consumption is linked to low urinary sodium excretion. Our results showed that high alcohol GRS was associated with high blood pressure and higher risk of stroke and supported an interaction effect between alcohol GRS and urinary sodium on stage 2 hypertension (P(interaction) = 0.03) and CVD (P(interaction) = 0.03), i.e., in the presence of high urinary sodium excretion, the effect of alcohol GRS on blood pressure may be enhanced. Conclusions: Our results show that urinary sodium excretion may offset the risk posed by genetic risk of alcohol consumption. MDPI 2022-07-13 /pmc/articles/PMC9319523/ /pubmed/35885821 http://dx.doi.org/10.3390/healthcare10071296 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 Jiang, Xiyun Anasanti, Mila D. Drenos, Fotios Blakemore, Alexandra I. Pazoki, Raha Urinary Sodium Excretion Enhances the Effect of Alcohol on Blood Pressure |
title | Urinary Sodium Excretion Enhances the Effect of Alcohol on Blood Pressure |
title_full | Urinary Sodium Excretion Enhances the Effect of Alcohol on Blood Pressure |
title_fullStr | Urinary Sodium Excretion Enhances the Effect of Alcohol on Blood Pressure |
title_full_unstemmed | Urinary Sodium Excretion Enhances the Effect of Alcohol on Blood Pressure |
title_short | Urinary Sodium Excretion Enhances the Effect of Alcohol on Blood Pressure |
title_sort | urinary sodium excretion enhances the effect of alcohol on blood pressure |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9319523/ https://www.ncbi.nlm.nih.gov/pubmed/35885821 http://dx.doi.org/10.3390/healthcare10071296 |
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