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Elevated Uric Acid Is Associated With New‐Onset Atrial Fibrillation: Results From the Swedish AMORIS Cohort

BACKGROUND: The role of uric acid is gaining increasing importance in the evaluation of cardiovascular disease, but its relationship with atrial fibrillation (AF) is unclear. This study aims to investigate the association between uric acid levels and risk of new‐onset AF. METHODS AND RESULTS: A tota...

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Autores principales: Ding, Mozhu, Viet, Ngoc Nguyen, Gigante, Bruna, Lind, Viktor, Hammar, Niklas, Modig, Karin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973652/
https://www.ncbi.nlm.nih.gov/pubmed/36633024
http://dx.doi.org/10.1161/JAHA.122.027089
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author Ding, Mozhu
Viet, Ngoc Nguyen
Gigante, Bruna
Lind, Viktor
Hammar, Niklas
Modig, Karin
author_facet Ding, Mozhu
Viet, Ngoc Nguyen
Gigante, Bruna
Lind, Viktor
Hammar, Niklas
Modig, Karin
author_sort Ding, Mozhu
collection PubMed
description BACKGROUND: The role of uric acid is gaining increasing importance in the evaluation of cardiovascular disease, but its relationship with atrial fibrillation (AF) is unclear. This study aims to investigate the association between uric acid levels and risk of new‐onset AF. METHODS AND RESULTS: A total of 339 604 individuals 30 to 60 years of age and free from cardiovascular disease at baseline (1985–1996) in the Swedish AMORIS (Apolipoprotein‐Mortality Risk) cohort were followed until December 31, 2019 for incident AF. Cox regression models were used to examine the association between uric acid and AF, adjusting for potential confounders and stratifying by incident cardiovascular disease. Over a mean follow‐up of 25.9 years, 46 516 incident AF cases occurred. Compared with the lowest uric acid quartile, each of the upper 3 quartiles were associated with an increased risk of AF in a dose–response manner. Adjusted hazard ratios were 1.09 (95% CI, 1.06–1.12) for second quartile, 1.19 (95% CI, 1.16–1.23) for third quartile, and 1.45 (95% CI, 1.41–1.49) for fourth quartile. The association was similar among individuals with and without incident hypertension, diabetes, heart failure, or coronary heart disease. The dose–response pattern was further supported in a subsample of individuals with repeated measurements of uric acid. CONCLUSIONS: Elevated uric acid was associated with an increased risk of AF, not only among people with cardiovascular disease and cardiovascular risk factors but also among those without. Future investigations are needed to examine whether lowering uric acid is relevant for AF prevention.
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spelling pubmed-99736522023-03-01 Elevated Uric Acid Is Associated With New‐Onset Atrial Fibrillation: Results From the Swedish AMORIS Cohort Ding, Mozhu Viet, Ngoc Nguyen Gigante, Bruna Lind, Viktor Hammar, Niklas Modig, Karin J Am Heart Assoc Original Research BACKGROUND: The role of uric acid is gaining increasing importance in the evaluation of cardiovascular disease, but its relationship with atrial fibrillation (AF) is unclear. This study aims to investigate the association between uric acid levels and risk of new‐onset AF. METHODS AND RESULTS: A total of 339 604 individuals 30 to 60 years of age and free from cardiovascular disease at baseline (1985–1996) in the Swedish AMORIS (Apolipoprotein‐Mortality Risk) cohort were followed until December 31, 2019 for incident AF. Cox regression models were used to examine the association between uric acid and AF, adjusting for potential confounders and stratifying by incident cardiovascular disease. Over a mean follow‐up of 25.9 years, 46 516 incident AF cases occurred. Compared with the lowest uric acid quartile, each of the upper 3 quartiles were associated with an increased risk of AF in a dose–response manner. Adjusted hazard ratios were 1.09 (95% CI, 1.06–1.12) for second quartile, 1.19 (95% CI, 1.16–1.23) for third quartile, and 1.45 (95% CI, 1.41–1.49) for fourth quartile. The association was similar among individuals with and without incident hypertension, diabetes, heart failure, or coronary heart disease. The dose–response pattern was further supported in a subsample of individuals with repeated measurements of uric acid. CONCLUSIONS: Elevated uric acid was associated with an increased risk of AF, not only among people with cardiovascular disease and cardiovascular risk factors but also among those without. Future investigations are needed to examine whether lowering uric acid is relevant for AF prevention. John Wiley and Sons Inc. 2023-01-12 /pmc/articles/PMC9973652/ /pubmed/36633024 http://dx.doi.org/10.1161/JAHA.122.027089 Text en © 2023 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.
spellingShingle Original Research
Ding, Mozhu
Viet, Ngoc Nguyen
Gigante, Bruna
Lind, Viktor
Hammar, Niklas
Modig, Karin
Elevated Uric Acid Is Associated With New‐Onset Atrial Fibrillation: Results From the Swedish AMORIS Cohort
title Elevated Uric Acid Is Associated With New‐Onset Atrial Fibrillation: Results From the Swedish AMORIS Cohort
title_full Elevated Uric Acid Is Associated With New‐Onset Atrial Fibrillation: Results From the Swedish AMORIS Cohort
title_fullStr Elevated Uric Acid Is Associated With New‐Onset Atrial Fibrillation: Results From the Swedish AMORIS Cohort
title_full_unstemmed Elevated Uric Acid Is Associated With New‐Onset Atrial Fibrillation: Results From the Swedish AMORIS Cohort
title_short Elevated Uric Acid Is Associated With New‐Onset Atrial Fibrillation: Results From the Swedish AMORIS Cohort
title_sort elevated uric acid is associated with new‐onset atrial fibrillation: results from the swedish amoris cohort
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9973652/
https://www.ncbi.nlm.nih.gov/pubmed/36633024
http://dx.doi.org/10.1161/JAHA.122.027089
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