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Plasma Branched-Chain Amino Acids and Risk of Incident Type 2 Diabetes: Results from the PREVEND Prospective Cohort Study

Plasma branched-chain amino acids (BCAAs) are linked to metabolic disease, but their relevance for prediction of type 2 diabetes development is unclear. We determined the association of plasma BCAAs with type 2 diabetes risk in the prevention of renal and vascular end-stage disease (PREVEND) cohort....

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Autores principales: Flores-Guerrero, Jose L., Osté, Maryse C. J., Kieneker, Lyanne M., Gruppen, Eke G., Wolak-Dinsmore, Justyna, Otvos, James D., Connelly, Margery A., Bakker, Stephan J. L., Dullaart, Robin P. F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306832/
https://www.ncbi.nlm.nih.gov/pubmed/30518023
http://dx.doi.org/10.3390/jcm7120513
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author Flores-Guerrero, Jose L.
Osté, Maryse C. J.
Kieneker, Lyanne M.
Gruppen, Eke G.
Wolak-Dinsmore, Justyna
Otvos, James D.
Connelly, Margery A.
Bakker, Stephan J. L.
Dullaart, Robin P. F.
author_facet Flores-Guerrero, Jose L.
Osté, Maryse C. J.
Kieneker, Lyanne M.
Gruppen, Eke G.
Wolak-Dinsmore, Justyna
Otvos, James D.
Connelly, Margery A.
Bakker, Stephan J. L.
Dullaart, Robin P. F.
author_sort Flores-Guerrero, Jose L.
collection PubMed
description Plasma branched-chain amino acids (BCAAs) are linked to metabolic disease, but their relevance for prediction of type 2 diabetes development is unclear. We determined the association of plasma BCAAs with type 2 diabetes risk in the prevention of renal and vascular end-stage disease (PREVEND) cohort. The BCAAs were measured by means of nuclear magnetic resonance spectroscopy. We evaluated the prospective associations of BCAAs with type 2 diabetes in 6244 subjects. The BCAAs were positively associated with HOMA-IR after multivariable adjustment (p < 0.0001). During median follow-up for 7.5 years, 301 cases of type 2 diabetes were ascertained. The Kaplan-Meier plot demonstrated that patients in the highest BCAA quartile presented a higher risk (p log-rank < 0.001). Cox regression analyses revealed a positive association between BCAA and type 2 diabetes; the hazard ratio (HR) for the highest quartile was 6.15 (95% CI: 4.08, 9.24, p < 0.0001). After adjustment for multiple clinical and laboratory variables, the association remained (HR 2.80 (95% CI: 1.72, 4.53), p < 0.0001). C-statistics, Net reclassification improvement, and −2 log likelihood were better after adding BCAAs to the traditional risk model (p = 0.01 to <0.001). In conclusions, high concentrations of BCAAs associate with insulin resistance and with increased risk of type 2 diabetes. This association is independent of multiple risk factors, HOMA-IR and β cell function.
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spelling pubmed-63068322019-01-02 Plasma Branched-Chain Amino Acids and Risk of Incident Type 2 Diabetes: Results from the PREVEND Prospective Cohort Study Flores-Guerrero, Jose L. Osté, Maryse C. J. Kieneker, Lyanne M. Gruppen, Eke G. Wolak-Dinsmore, Justyna Otvos, James D. Connelly, Margery A. Bakker, Stephan J. L. Dullaart, Robin P. F. J Clin Med Article Plasma branched-chain amino acids (BCAAs) are linked to metabolic disease, but their relevance for prediction of type 2 diabetes development is unclear. We determined the association of plasma BCAAs with type 2 diabetes risk in the prevention of renal and vascular end-stage disease (PREVEND) cohort. The BCAAs were measured by means of nuclear magnetic resonance spectroscopy. We evaluated the prospective associations of BCAAs with type 2 diabetes in 6244 subjects. The BCAAs were positively associated with HOMA-IR after multivariable adjustment (p < 0.0001). During median follow-up for 7.5 years, 301 cases of type 2 diabetes were ascertained. The Kaplan-Meier plot demonstrated that patients in the highest BCAA quartile presented a higher risk (p log-rank < 0.001). Cox regression analyses revealed a positive association between BCAA and type 2 diabetes; the hazard ratio (HR) for the highest quartile was 6.15 (95% CI: 4.08, 9.24, p < 0.0001). After adjustment for multiple clinical and laboratory variables, the association remained (HR 2.80 (95% CI: 1.72, 4.53), p < 0.0001). C-statistics, Net reclassification improvement, and −2 log likelihood were better after adding BCAAs to the traditional risk model (p = 0.01 to <0.001). In conclusions, high concentrations of BCAAs associate with insulin resistance and with increased risk of type 2 diabetes. This association is independent of multiple risk factors, HOMA-IR and β cell function. MDPI 2018-12-04 /pmc/articles/PMC6306832/ /pubmed/30518023 http://dx.doi.org/10.3390/jcm7120513 Text en © 2018 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Flores-Guerrero, Jose L.
Osté, Maryse C. J.
Kieneker, Lyanne M.
Gruppen, Eke G.
Wolak-Dinsmore, Justyna
Otvos, James D.
Connelly, Margery A.
Bakker, Stephan J. L.
Dullaart, Robin P. F.
Plasma Branched-Chain Amino Acids and Risk of Incident Type 2 Diabetes: Results from the PREVEND Prospective Cohort Study
title Plasma Branched-Chain Amino Acids and Risk of Incident Type 2 Diabetes: Results from the PREVEND Prospective Cohort Study
title_full Plasma Branched-Chain Amino Acids and Risk of Incident Type 2 Diabetes: Results from the PREVEND Prospective Cohort Study
title_fullStr Plasma Branched-Chain Amino Acids and Risk of Incident Type 2 Diabetes: Results from the PREVEND Prospective Cohort Study
title_full_unstemmed Plasma Branched-Chain Amino Acids and Risk of Incident Type 2 Diabetes: Results from the PREVEND Prospective Cohort Study
title_short Plasma Branched-Chain Amino Acids and Risk of Incident Type 2 Diabetes: Results from the PREVEND Prospective Cohort Study
title_sort plasma branched-chain amino acids and risk of incident type 2 diabetes: results from the prevend prospective cohort study
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6306832/
https://www.ncbi.nlm.nih.gov/pubmed/30518023
http://dx.doi.org/10.3390/jcm7120513
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