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Temporal changes in serum uric acid and risk for metabolic syndrome: a longitudinal cohort study

BACKGROUND: Studies suggested elevated serum uric acid (SUA) levels are associated with metabolic syndrome (MetS). However, it remains unclear whether baseline SUA and temporal changes predict MetS. The study aimed to investigate the association of baseline SUA and its temporal longitudinal changes...

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Autores principales: Feng, Xuan, Guo, Yi, Tu, Huakang, Li, Shu, Chen, Chen, Sun, Mingxi, Wang, Sicong, Li, Bohan, Wu, Xifeng, Song, Zhenya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258088/
https://www.ncbi.nlm.nih.gov/pubmed/35794651
http://dx.doi.org/10.1186/s13098-022-00861-6
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author Feng, Xuan
Guo, Yi
Tu, Huakang
Li, Shu
Chen, Chen
Sun, Mingxi
Wang, Sicong
Li, Bohan
Wu, Xifeng
Song, Zhenya
author_facet Feng, Xuan
Guo, Yi
Tu, Huakang
Li, Shu
Chen, Chen
Sun, Mingxi
Wang, Sicong
Li, Bohan
Wu, Xifeng
Song, Zhenya
author_sort Feng, Xuan
collection PubMed
description BACKGROUND: Studies suggested elevated serum uric acid (SUA) levels are associated with metabolic syndrome (MetS). However, it remains unclear whether baseline SUA and temporal changes predict MetS. The study aimed to investigate the association of baseline SUA and its temporal longitudinal changes with subsequent risk of MetS. METHODS: We conducted a retrospective longitudinal cohort study among 44,176 healthy participants aged 18 years and older without MetS at enrollment. The baseline levels and longitudinal changes of SUA were categorized by gender-specific quintiles. Participants were followed to identify newly developed MetS. We employed Cox model to investigate the relationship between SUA and MetS in men and women separately. RESULTS: During a median follow-up of 2.4 years, 5461 (12.36%) participants developed MetS. After adjustment of demographic, major clinical factors, a higher level of baseline SUA was associated with a significant higher risk of MetS. The corresponding HRs (95% CIs) comparing participants at extreme quintiles were 2.59 (2.32, 2.88) in men and 2.87 (2.41, 3.43) in women. Larger longitudinal absolute increase in SUA was also related to an increases risk of MetS (top vs bottom quintile, 1.70 [1.53, 1.89] in men and 1.94 [1.65, 2.28] in women), regardless the level of baseline SUA. Similarly, the HRs about SUA longitudinal percentage changes were 1.74 (1.56, 1.94) in men and 2.01 (1.69, 2.39) in women, respectively. Moreover, we observed the highest risk of MetS among participants with both higher baseline SUA and larger longitudinal increase in SUA. CONCLUSION: Higher baseline SUA and larger temporal increase in SUA independently predicted risk of MetS, highlighting the importance of longitudinal SUA monitoring and management for primary prevention of MetS in the general population.
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spelling pubmed-92580882022-07-07 Temporal changes in serum uric acid and risk for metabolic syndrome: a longitudinal cohort study Feng, Xuan Guo, Yi Tu, Huakang Li, Shu Chen, Chen Sun, Mingxi Wang, Sicong Li, Bohan Wu, Xifeng Song, Zhenya Diabetol Metab Syndr Research BACKGROUND: Studies suggested elevated serum uric acid (SUA) levels are associated with metabolic syndrome (MetS). However, it remains unclear whether baseline SUA and temporal changes predict MetS. The study aimed to investigate the association of baseline SUA and its temporal longitudinal changes with subsequent risk of MetS. METHODS: We conducted a retrospective longitudinal cohort study among 44,176 healthy participants aged 18 years and older without MetS at enrollment. The baseline levels and longitudinal changes of SUA were categorized by gender-specific quintiles. Participants were followed to identify newly developed MetS. We employed Cox model to investigate the relationship between SUA and MetS in men and women separately. RESULTS: During a median follow-up of 2.4 years, 5461 (12.36%) participants developed MetS. After adjustment of demographic, major clinical factors, a higher level of baseline SUA was associated with a significant higher risk of MetS. The corresponding HRs (95% CIs) comparing participants at extreme quintiles were 2.59 (2.32, 2.88) in men and 2.87 (2.41, 3.43) in women. Larger longitudinal absolute increase in SUA was also related to an increases risk of MetS (top vs bottom quintile, 1.70 [1.53, 1.89] in men and 1.94 [1.65, 2.28] in women), regardless the level of baseline SUA. Similarly, the HRs about SUA longitudinal percentage changes were 1.74 (1.56, 1.94) in men and 2.01 (1.69, 2.39) in women, respectively. Moreover, we observed the highest risk of MetS among participants with both higher baseline SUA and larger longitudinal increase in SUA. CONCLUSION: Higher baseline SUA and larger temporal increase in SUA independently predicted risk of MetS, highlighting the importance of longitudinal SUA monitoring and management for primary prevention of MetS in the general population. BioMed Central 2022-07-06 /pmc/articles/PMC9258088/ /pubmed/35794651 http://dx.doi.org/10.1186/s13098-022-00861-6 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis 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/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Feng, Xuan
Guo, Yi
Tu, Huakang
Li, Shu
Chen, Chen
Sun, Mingxi
Wang, Sicong
Li, Bohan
Wu, Xifeng
Song, Zhenya
Temporal changes in serum uric acid and risk for metabolic syndrome: a longitudinal cohort study
title Temporal changes in serum uric acid and risk for metabolic syndrome: a longitudinal cohort study
title_full Temporal changes in serum uric acid and risk for metabolic syndrome: a longitudinal cohort study
title_fullStr Temporal changes in serum uric acid and risk for metabolic syndrome: a longitudinal cohort study
title_full_unstemmed Temporal changes in serum uric acid and risk for metabolic syndrome: a longitudinal cohort study
title_short Temporal changes in serum uric acid and risk for metabolic syndrome: a longitudinal cohort study
title_sort temporal changes in serum uric acid and risk for metabolic syndrome: a longitudinal cohort study
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9258088/
https://www.ncbi.nlm.nih.gov/pubmed/35794651
http://dx.doi.org/10.1186/s13098-022-00861-6
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