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Glucose time series complexity as a predictor of type 2 diabetes

BACKGROUND: Complexity analysis of glucose profile may provide valuable information about the gluco‐regulatory system. We hypothesized that a complexity metric (detrended fluctuation analysis, DFA) may have a prognostic value for the development of type 2 diabetes in patients at risk. METHODS: A tot...

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Autores principales: Rodríguez de Castro, Carmen, Vigil, Luis, Vargas, Borja, García Delgado, Emilio, García Carretero, Rafael, Ruiz‐Galiana, Julián, Varela, Manuel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333459/
https://www.ncbi.nlm.nih.gov/pubmed/27253149
http://dx.doi.org/10.1002/dmrr.2831
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author Rodríguez de Castro, Carmen
Vigil, Luis
Vargas, Borja
García Delgado, Emilio
García Carretero, Rafael
Ruiz‐Galiana, Julián
Varela, Manuel
author_facet Rodríguez de Castro, Carmen
Vigil, Luis
Vargas, Borja
García Delgado, Emilio
García Carretero, Rafael
Ruiz‐Galiana, Julián
Varela, Manuel
author_sort Rodríguez de Castro, Carmen
collection PubMed
description BACKGROUND: Complexity analysis of glucose profile may provide valuable information about the gluco‐regulatory system. We hypothesized that a complexity metric (detrended fluctuation analysis, DFA) may have a prognostic value for the development of type 2 diabetes in patients at risk. METHODS: A total of 206 patients with any of the following risk factors (1) essential hypertension, (2) obesity or (3) a first‐degree relative with a diagnosis of diabetes were included in a survival analysis study for a diagnosis of new onset type 2 diabetes. At inclusion, a glucometry by means of a Continuous Glucose Monitoring System was performed, and DFA was calculated for a 24‐h glucose time series. Patients were then followed up every 6 months, controlling for the development of diabetes. RESULTS: In a median follow‐up of 18 months, there were 18 new cases of diabetes (58.5 cases/1000 patient‐years). DFA was a significant predictor for the development of diabetes, with ten events in the highest quartile versus one in the lowest (log‐rank test chi2 = 9, df = 1, p = 0.003), even after adjusting for other relevant clinical and biochemical variables. In a Cox model, the risk of diabetes development increased 2.8 times for every 0.1 DFA units. In a multivariate analysis, only fasting glucose, HbA(1c) and DFA emerged as significant factors. CONCLUSIONS: Detrended fluctuation analysis significantly performed as a harbinger of type 2 diabetes development in a high‐risk population. Complexity analysis may help in targeting patients who could be candidates for intensified treatment. Copyright © 2016 The Authors. Diabetes/Metabolism Research and Reviews Published by John Wiley & Sons Ltd.
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spelling pubmed-53334592017-03-16 Glucose time series complexity as a predictor of type 2 diabetes Rodríguez de Castro, Carmen Vigil, Luis Vargas, Borja García Delgado, Emilio García Carretero, Rafael Ruiz‐Galiana, Julián Varela, Manuel Diabetes Metab Res Rev Research Articles BACKGROUND: Complexity analysis of glucose profile may provide valuable information about the gluco‐regulatory system. We hypothesized that a complexity metric (detrended fluctuation analysis, DFA) may have a prognostic value for the development of type 2 diabetes in patients at risk. METHODS: A total of 206 patients with any of the following risk factors (1) essential hypertension, (2) obesity or (3) a first‐degree relative with a diagnosis of diabetes were included in a survival analysis study for a diagnosis of new onset type 2 diabetes. At inclusion, a glucometry by means of a Continuous Glucose Monitoring System was performed, and DFA was calculated for a 24‐h glucose time series. Patients were then followed up every 6 months, controlling for the development of diabetes. RESULTS: In a median follow‐up of 18 months, there were 18 new cases of diabetes (58.5 cases/1000 patient‐years). DFA was a significant predictor for the development of diabetes, with ten events in the highest quartile versus one in the lowest (log‐rank test chi2 = 9, df = 1, p = 0.003), even after adjusting for other relevant clinical and biochemical variables. In a Cox model, the risk of diabetes development increased 2.8 times for every 0.1 DFA units. In a multivariate analysis, only fasting glucose, HbA(1c) and DFA emerged as significant factors. CONCLUSIONS: Detrended fluctuation analysis significantly performed as a harbinger of type 2 diabetes development in a high‐risk population. Complexity analysis may help in targeting patients who could be candidates for intensified treatment. Copyright © 2016 The Authors. Diabetes/Metabolism Research and Reviews Published by John Wiley & Sons Ltd. John Wiley and Sons Inc. 2016-06-30 2017-02 /pmc/articles/PMC5333459/ /pubmed/27253149 http://dx.doi.org/10.1002/dmrr.2831 Text en Copyright © 2016 The Authors. Diabetes/Metabolism Research and Reviews Published by John Wiley & Sons Ltd. This is an open access article under the terms of the Creative Commons Attribution‐NonCommercial‐NoDerivs (http://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Research Articles
Rodríguez de Castro, Carmen
Vigil, Luis
Vargas, Borja
García Delgado, Emilio
García Carretero, Rafael
Ruiz‐Galiana, Julián
Varela, Manuel
Glucose time series complexity as a predictor of type 2 diabetes
title Glucose time series complexity as a predictor of type 2 diabetes
title_full Glucose time series complexity as a predictor of type 2 diabetes
title_fullStr Glucose time series complexity as a predictor of type 2 diabetes
title_full_unstemmed Glucose time series complexity as a predictor of type 2 diabetes
title_short Glucose time series complexity as a predictor of type 2 diabetes
title_sort glucose time series complexity as a predictor of type 2 diabetes
topic Research Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5333459/
https://www.ncbi.nlm.nih.gov/pubmed/27253149
http://dx.doi.org/10.1002/dmrr.2831
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