Cargando…

Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Tromsø Study

BACKGROUND: Elevated uric acid (UA) is associated with the presence of the metabolic syndrome (MetS). In a prospective cohort study, we assessed whether baseline and longitudinal change in UA were risk factors for development of MetS and its individual components. METHODS: We included 3087 women and...

Descripción completa

Detalles Bibliográficos
Autores principales: Norvik, Jon V., Storhaug, Hilde M., Ytrehus, Kirsti, Jenssen, Trond G., Zykova, Svetlana N., Eriksen, Bjørn O., Solbu, Marit D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862215/
https://www.ncbi.nlm.nih.gov/pubmed/27165776
http://dx.doi.org/10.1186/s12872-016-0265-8
_version_ 1782431329340620800
author Norvik, Jon V.
Storhaug, Hilde M.
Ytrehus, Kirsti
Jenssen, Trond G.
Zykova, Svetlana N.
Eriksen, Bjørn O.
Solbu, Marit D.
author_facet Norvik, Jon V.
Storhaug, Hilde M.
Ytrehus, Kirsti
Jenssen, Trond G.
Zykova, Svetlana N.
Eriksen, Bjørn O.
Solbu, Marit D.
author_sort Norvik, Jon V.
collection PubMed
description BACKGROUND: Elevated uric acid (UA) is associated with the presence of the metabolic syndrome (MetS). In a prospective cohort study, we assessed whether baseline and longitudinal change in UA were risk factors for development of MetS and its individual components. METHODS: We included 3087 women and 2996 men who had UA measured in the population based Tromsø Study 1994–95. The participants were stratified according to body mass index (BMI). Endpoints were MetS and each component of the syndrome after 7 years, according to the revised National Cholesterol Education Program’s Adult Treatment Panel III (NCEP-ATP III) definition. RESULTS: Multiple logistic regression analyses showed that higher baseline UA was associated with higher odds of developing elevated blood pressure in overweight subjects (BMI ≥ 25 kg/m(2), odds ratio [OR] per 59 μmol/L UA increase 1.44, 95 % confidence interval [CI] = 1.17–1.77, P = 0.001), but not in normal-weight subjects (BMI < 25 kg/m(2), P for interaction = 0.04). Overweight also modified the association between baseline UA and the development of elevated fasting glucose (P for interaction = 0.01). UA was a predictor of MetS in all subjects (OR per 59 μmol/L UA increase 1.29, 95 % CI 1.18–1.41, P < 0.001). Furthermore, longitudinal UA change was independently associated with the development of MetS in all subjects (OR per 59 μmol/L UA increase over 7 years 1.28, 95 % CI 1.16–1.42, P < 0.001). CONCLUSION: Increased levels of baseline UA independently predicted development of elevated blood pressure and higher fasting glycemia in the overweight, but not the normal-weight subjects. Baseline UA and longitudinal increase in UA over 7 years was associated with the development of MetS in all subjects. Whether increased UA should be treated differently in normal-weight and overweight persons needs further study.
format Online
Article
Text
id pubmed-4862215
institution National Center for Biotechnology Information
language English
publishDate 2016
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-48622152016-05-11 Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Tromsø Study Norvik, Jon V. Storhaug, Hilde M. Ytrehus, Kirsti Jenssen, Trond G. Zykova, Svetlana N. Eriksen, Bjørn O. Solbu, Marit D. BMC Cardiovasc Disord Research Article BACKGROUND: Elevated uric acid (UA) is associated with the presence of the metabolic syndrome (MetS). In a prospective cohort study, we assessed whether baseline and longitudinal change in UA were risk factors for development of MetS and its individual components. METHODS: We included 3087 women and 2996 men who had UA measured in the population based Tromsø Study 1994–95. The participants were stratified according to body mass index (BMI). Endpoints were MetS and each component of the syndrome after 7 years, according to the revised National Cholesterol Education Program’s Adult Treatment Panel III (NCEP-ATP III) definition. RESULTS: Multiple logistic regression analyses showed that higher baseline UA was associated with higher odds of developing elevated blood pressure in overweight subjects (BMI ≥ 25 kg/m(2), odds ratio [OR] per 59 μmol/L UA increase 1.44, 95 % confidence interval [CI] = 1.17–1.77, P = 0.001), but not in normal-weight subjects (BMI < 25 kg/m(2), P for interaction = 0.04). Overweight also modified the association between baseline UA and the development of elevated fasting glucose (P for interaction = 0.01). UA was a predictor of MetS in all subjects (OR per 59 μmol/L UA increase 1.29, 95 % CI 1.18–1.41, P < 0.001). Furthermore, longitudinal UA change was independently associated with the development of MetS in all subjects (OR per 59 μmol/L UA increase over 7 years 1.28, 95 % CI 1.16–1.42, P < 0.001). CONCLUSION: Increased levels of baseline UA independently predicted development of elevated blood pressure and higher fasting glycemia in the overweight, but not the normal-weight subjects. Baseline UA and longitudinal increase in UA over 7 years was associated with the development of MetS in all subjects. Whether increased UA should be treated differently in normal-weight and overweight persons needs further study. BioMed Central 2016-05-10 /pmc/articles/PMC4862215/ /pubmed/27165776 http://dx.doi.org/10.1186/s12872-016-0265-8 Text en © Norvik et al. 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research Article
Norvik, Jon V.
Storhaug, Hilde M.
Ytrehus, Kirsti
Jenssen, Trond G.
Zykova, Svetlana N.
Eriksen, Bjørn O.
Solbu, Marit D.
Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Tromsø Study
title Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Tromsø Study
title_full Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Tromsø Study
title_fullStr Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Tromsø Study
title_full_unstemmed Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Tromsø Study
title_short Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Tromsø Study
title_sort overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: the tromsø study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4862215/
https://www.ncbi.nlm.nih.gov/pubmed/27165776
http://dx.doi.org/10.1186/s12872-016-0265-8
work_keys_str_mv AT norvikjonv overweightmodifiesthelongitudinalassociationbetweenuricacidandsomecomponentsofthemetabolicsyndromethetromsøstudy
AT storhaughildem overweightmodifiesthelongitudinalassociationbetweenuricacidandsomecomponentsofthemetabolicsyndromethetromsøstudy
AT ytrehuskirsti overweightmodifiesthelongitudinalassociationbetweenuricacidandsomecomponentsofthemetabolicsyndromethetromsøstudy
AT jenssentrondg overweightmodifiesthelongitudinalassociationbetweenuricacidandsomecomponentsofthemetabolicsyndromethetromsøstudy
AT zykovasvetlanan overweightmodifiesthelongitudinalassociationbetweenuricacidandsomecomponentsofthemetabolicsyndromethetromsøstudy
AT eriksenbjørno overweightmodifiesthelongitudinalassociationbetweenuricacidandsomecomponentsofthemetabolicsyndromethetromsøstudy
AT solbumaritd overweightmodifiesthelongitudinalassociationbetweenuricacidandsomecomponentsofthemetabolicsyndromethetromsøstudy