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Identification of metabolic markers predictive of prediabetes in a Korean population
Prediabetes (PD) is a high-risk state of developing type 2 diabetes, and cardiovascular and metabolic diseases. Metabolomics-based biomarker studies can provide advanced opportunities for prediction of PD over the conventional methods. Here, we aimed to identify metabolic markers and verify their ab...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738529/ https://www.ncbi.nlm.nih.gov/pubmed/33319826 http://dx.doi.org/10.1038/s41598-020-78961-4 |
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author | Lee, Heun-Sik Park, Tae-Joon Kim, Jeong-Min Yun, Jun Ho Yu, Ho-Yeong Kim, Yeon-Jung Kim, Bong-Jo |
author_facet | Lee, Heun-Sik Park, Tae-Joon Kim, Jeong-Min Yun, Jun Ho Yu, Ho-Yeong Kim, Yeon-Jung Kim, Bong-Jo |
author_sort | Lee, Heun-Sik |
collection | PubMed |
description | Prediabetes (PD) is a high-risk state of developing type 2 diabetes, and cardiovascular and metabolic diseases. Metabolomics-based biomarker studies can provide advanced opportunities for prediction of PD over the conventional methods. Here, we aimed to identify metabolic markers and verify their abilities to predict PD, as compared to the performance of the traditional clinical risk factor (CRF) and previously reported metabolites in other population-based studies. Targeted metabolites quantification was performed in 1723 participants in the Korea Association REsource (KARE) cohort, from which 500 normal individuals were followed up for 6 years. We selected 12 significant metabolic markers, including five amino acids, four glycerophospholipids, two sphingolipids, and one acylcarnitine, at baseline, resulting in a predicted incidence of PD with an area under the curve (AUC) of 0.71 during follow-up. The performance of these metabolic markers compared to that of fasting glucose was significantly higher in obese patients (body mass index: BMI ≥ 25 kg/m(2), 0.79 vs. 0.58, P < 0.001). The combination with metabolic markers, CRF, and fasting glucose yielded the best prediction performance (AUC = 0.86). Our results revealed that metabolic markers were not only associated with the risk of PD, but also improved the prediction performance in combination with conventional approaches. |
format | Online Article Text |
id | pubmed-7738529 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-77385292020-12-17 Identification of metabolic markers predictive of prediabetes in a Korean population Lee, Heun-Sik Park, Tae-Joon Kim, Jeong-Min Yun, Jun Ho Yu, Ho-Yeong Kim, Yeon-Jung Kim, Bong-Jo Sci Rep Article Prediabetes (PD) is a high-risk state of developing type 2 diabetes, and cardiovascular and metabolic diseases. Metabolomics-based biomarker studies can provide advanced opportunities for prediction of PD over the conventional methods. Here, we aimed to identify metabolic markers and verify their abilities to predict PD, as compared to the performance of the traditional clinical risk factor (CRF) and previously reported metabolites in other population-based studies. Targeted metabolites quantification was performed in 1723 participants in the Korea Association REsource (KARE) cohort, from which 500 normal individuals were followed up for 6 years. We selected 12 significant metabolic markers, including five amino acids, four glycerophospholipids, two sphingolipids, and one acylcarnitine, at baseline, resulting in a predicted incidence of PD with an area under the curve (AUC) of 0.71 during follow-up. The performance of these metabolic markers compared to that of fasting glucose was significantly higher in obese patients (body mass index: BMI ≥ 25 kg/m(2), 0.79 vs. 0.58, P < 0.001). The combination with metabolic markers, CRF, and fasting glucose yielded the best prediction performance (AUC = 0.86). Our results revealed that metabolic markers were not only associated with the risk of PD, but also improved the prediction performance in combination with conventional approaches. Nature Publishing Group UK 2020-12-15 /pmc/articles/PMC7738529/ /pubmed/33319826 http://dx.doi.org/10.1038/s41598-020-78961-4 Text en © The Author(s) 2020 Open Access This 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/. |
spellingShingle | Article Lee, Heun-Sik Park, Tae-Joon Kim, Jeong-Min Yun, Jun Ho Yu, Ho-Yeong Kim, Yeon-Jung Kim, Bong-Jo Identification of metabolic markers predictive of prediabetes in a Korean population |
title | Identification of metabolic markers predictive of prediabetes in a Korean population |
title_full | Identification of metabolic markers predictive of prediabetes in a Korean population |
title_fullStr | Identification of metabolic markers predictive of prediabetes in a Korean population |
title_full_unstemmed | Identification of metabolic markers predictive of prediabetes in a Korean population |
title_short | Identification of metabolic markers predictive of prediabetes in a Korean population |
title_sort | identification of metabolic markers predictive of prediabetes in a korean population |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7738529/ https://www.ncbi.nlm.nih.gov/pubmed/33319826 http://dx.doi.org/10.1038/s41598-020-78961-4 |
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