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Chromium exposure and incidence of metabolic syndrome among American young adults over a 23-year follow-up: the CARDIA Trace Element Study

Studies suggest that chromium deficiency is associated with elevated levels of fasting blood glucose, circulating insulin, cholesterol and triglycerides, and decreased proportion of lean body mass. However, data directly relating chromium levels to metabolic syndrome (MetS) risk are lacking. A total...

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Autores principales: Bai, Jianling, Xun, Pengcheng, Morris, Steve, Jacobs, David R., Liu, Kiang, He, Ka
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614983/
https://www.ncbi.nlm.nih.gov/pubmed/26489690
http://dx.doi.org/10.1038/srep15606
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author Bai, Jianling
Xun, Pengcheng
Morris, Steve
Jacobs, David R.
Liu, Kiang
He, Ka
author_facet Bai, Jianling
Xun, Pengcheng
Morris, Steve
Jacobs, David R.
Liu, Kiang
He, Ka
author_sort Bai, Jianling
collection PubMed
description Studies suggest that chromium deficiency is associated with elevated levels of fasting blood glucose, circulating insulin, cholesterol and triglycerides, and decreased proportion of lean body mass. However, data directly relating chromium levels to metabolic syndrome (MetS) risk are lacking. A total of 3,648 American adults from the Coronary Artery Risk Development in Young Adults (CARDIA) study, aged 20–32 years, were prospectively examined for the incidence of MetS and its five components from 1987–88 to 2010–11. Baseline toenail chromium levels were measured with instrumental neutron-activation analysis. Incident MetS was defined by the NCEP-ATP III criteria. During the 23-year follow-up, 878 incident MetS cases were identified. Baseline toenail chromium was inversely associated with incidence of MetS as well as its blood lipid components. The multivariable-adjusted hazard ratio (HR) (95% confidence interval [CI]) of MetS comparing the highest to the lowest quartiles of toenail chromium levels was 0.80 (0.66–0.98; P(linear trend) = 0.006). The adjusted HRs were 0.82 (0.68–0.98; P(trend) = 0.045) for having abnormal triglycerides levels and 0.75 (0.64–0.88; P(trend)  = 0.030) for having abnormal HDL cholesterol levels. Toenail chromium levels were inversely and longitudinally associated with incidence of MetS in American young adults. This inverse association was mainly explained by its relation to blood lipids.
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spelling pubmed-46149832015-10-29 Chromium exposure and incidence of metabolic syndrome among American young adults over a 23-year follow-up: the CARDIA Trace Element Study Bai, Jianling Xun, Pengcheng Morris, Steve Jacobs, David R. Liu, Kiang He, Ka Sci Rep Article Studies suggest that chromium deficiency is associated with elevated levels of fasting blood glucose, circulating insulin, cholesterol and triglycerides, and decreased proportion of lean body mass. However, data directly relating chromium levels to metabolic syndrome (MetS) risk are lacking. A total of 3,648 American adults from the Coronary Artery Risk Development in Young Adults (CARDIA) study, aged 20–32 years, were prospectively examined for the incidence of MetS and its five components from 1987–88 to 2010–11. Baseline toenail chromium levels were measured with instrumental neutron-activation analysis. Incident MetS was defined by the NCEP-ATP III criteria. During the 23-year follow-up, 878 incident MetS cases were identified. Baseline toenail chromium was inversely associated with incidence of MetS as well as its blood lipid components. The multivariable-adjusted hazard ratio (HR) (95% confidence interval [CI]) of MetS comparing the highest to the lowest quartiles of toenail chromium levels was 0.80 (0.66–0.98; P(linear trend) = 0.006). The adjusted HRs were 0.82 (0.68–0.98; P(trend) = 0.045) for having abnormal triglycerides levels and 0.75 (0.64–0.88; P(trend)  = 0.030) for having abnormal HDL cholesterol levels. Toenail chromium levels were inversely and longitudinally associated with incidence of MetS in American young adults. This inverse association was mainly explained by its relation to blood lipids. Nature Publishing Group 2015-10-22 /pmc/articles/PMC4614983/ /pubmed/26489690 http://dx.doi.org/10.1038/srep15606 Text en Copyright © 2015, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Bai, Jianling
Xun, Pengcheng
Morris, Steve
Jacobs, David R.
Liu, Kiang
He, Ka
Chromium exposure and incidence of metabolic syndrome among American young adults over a 23-year follow-up: the CARDIA Trace Element Study
title Chromium exposure and incidence of metabolic syndrome among American young adults over a 23-year follow-up: the CARDIA Trace Element Study
title_full Chromium exposure and incidence of metabolic syndrome among American young adults over a 23-year follow-up: the CARDIA Trace Element Study
title_fullStr Chromium exposure and incidence of metabolic syndrome among American young adults over a 23-year follow-up: the CARDIA Trace Element Study
title_full_unstemmed Chromium exposure and incidence of metabolic syndrome among American young adults over a 23-year follow-up: the CARDIA Trace Element Study
title_short Chromium exposure and incidence of metabolic syndrome among American young adults over a 23-year follow-up: the CARDIA Trace Element Study
title_sort chromium exposure and incidence of metabolic syndrome among american young adults over a 23-year follow-up: the cardia trace element study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4614983/
https://www.ncbi.nlm.nih.gov/pubmed/26489690
http://dx.doi.org/10.1038/srep15606
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