Cargando…
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...
Autores principales: | , , , , , , , , , |
---|---|
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 |
_version_ | 1784741464473862144 |
---|---|
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. |
format | Online Article Text |
id | pubmed-9258088 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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 |
work_keys_str_mv | AT fengxuan temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy AT guoyi temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy AT tuhuakang temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy AT lishu temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy AT chenchen temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy AT sunmingxi temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy AT wangsicong temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy AT libohan temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy AT wuxifeng temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy AT songzhenya temporalchangesinserumuricacidandriskformetabolicsyndromealongitudinalcohortstudy |