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Longer time to peak glucose during the oral glucose tolerance test increases cardiovascular risk score and diabetes prevalence
INTRODUCTION: The pattern of glucose levels during an oral glucose tolerance test (OGTT) may be useful for predicting diabetes or cardiovascular disease (CVD). Our aim was to determine whether the time to peak glucose during the OGTT is associated with CVD risk scores and diabetes. METHODS: Individu...
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Public Library of Science
2017
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720677/ https://www.ncbi.nlm.nih.gov/pubmed/29216249 http://dx.doi.org/10.1371/journal.pone.0189047 |
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author | Lin, Yi-Chun Chen, Harn-Shen |
author_facet | Lin, Yi-Chun Chen, Harn-Shen |
author_sort | Lin, Yi-Chun |
collection | PubMed |
description | INTRODUCTION: The pattern of glucose levels during an oral glucose tolerance test (OGTT) may be useful for predicting diabetes or cardiovascular disease (CVD). Our aim was to determine whether the time to peak glucose during the OGTT is associated with CVD risk scores and diabetes. METHODS: Individuals with impaired fasting glucose (IFG) were enrolled in this observational study. Participants were grouped by the measured time to peak glucose (30, 60, 90 and 120 min) during the 75g OGTT. The primary outcome was 10-year CVD risk scores (using the Framingham risk score calculator). Secondary outcomes evaluated effect of time to peak glucose on prevalence of diabetes and indicators of glucose homeostasis. RESULTS: A total of 125 patients with IFG underwent OGTTs. Framingham 10-year risk score for the 90-min group was 1.7 times higher than for the 60-min group (6.98±6.56% vs. 4.05±4.60%, P = 0.023). Based on multivariate linear regression, time to peak glucose at 90 min was associated with a higher Framingham risk score than 60-min group (β coefficient: 2.043, 95% confidence interval: 0.067–6.008, P = 0.045). The percentages of patients with HbA(1c) ≥6.5%, isolated post-challenge hyperglycemia (IPH) and diabetes (combined IPH and HbA(1c) ≥6.5%) were significantly increased with longer times to peak glucose. Prevalence of diabetes was higher in the 90-min group than in the 60-min group (31.5% vs. 5.7%, P = 0.001). CONCLUSIONS: In subjects with IFG, those with a longer time to peak glucose had a higher Framingham 10-year risk score and were associated with a greater likelihood of IPH and diabetes. |
format | Online Article Text |
id | pubmed-5720677 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-57206772017-12-15 Longer time to peak glucose during the oral glucose tolerance test increases cardiovascular risk score and diabetes prevalence Lin, Yi-Chun Chen, Harn-Shen PLoS One Research Article INTRODUCTION: The pattern of glucose levels during an oral glucose tolerance test (OGTT) may be useful for predicting diabetes or cardiovascular disease (CVD). Our aim was to determine whether the time to peak glucose during the OGTT is associated with CVD risk scores and diabetes. METHODS: Individuals with impaired fasting glucose (IFG) were enrolled in this observational study. Participants were grouped by the measured time to peak glucose (30, 60, 90 and 120 min) during the 75g OGTT. The primary outcome was 10-year CVD risk scores (using the Framingham risk score calculator). Secondary outcomes evaluated effect of time to peak glucose on prevalence of diabetes and indicators of glucose homeostasis. RESULTS: A total of 125 patients with IFG underwent OGTTs. Framingham 10-year risk score for the 90-min group was 1.7 times higher than for the 60-min group (6.98±6.56% vs. 4.05±4.60%, P = 0.023). Based on multivariate linear regression, time to peak glucose at 90 min was associated with a higher Framingham risk score than 60-min group (β coefficient: 2.043, 95% confidence interval: 0.067–6.008, P = 0.045). The percentages of patients with HbA(1c) ≥6.5%, isolated post-challenge hyperglycemia (IPH) and diabetes (combined IPH and HbA(1c) ≥6.5%) were significantly increased with longer times to peak glucose. Prevalence of diabetes was higher in the 90-min group than in the 60-min group (31.5% vs. 5.7%, P = 0.001). CONCLUSIONS: In subjects with IFG, those with a longer time to peak glucose had a higher Framingham 10-year risk score and were associated with a greater likelihood of IPH and diabetes. Public Library of Science 2017-12-07 /pmc/articles/PMC5720677/ /pubmed/29216249 http://dx.doi.org/10.1371/journal.pone.0189047 Text en © 2017 Lin, Chen http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Lin, Yi-Chun Chen, Harn-Shen Longer time to peak glucose during the oral glucose tolerance test increases cardiovascular risk score and diabetes prevalence |
title | Longer time to peak glucose during the oral glucose tolerance test increases cardiovascular risk score and diabetes prevalence |
title_full | Longer time to peak glucose during the oral glucose tolerance test increases cardiovascular risk score and diabetes prevalence |
title_fullStr | Longer time to peak glucose during the oral glucose tolerance test increases cardiovascular risk score and diabetes prevalence |
title_full_unstemmed | Longer time to peak glucose during the oral glucose tolerance test increases cardiovascular risk score and diabetes prevalence |
title_short | Longer time to peak glucose during the oral glucose tolerance test increases cardiovascular risk score and diabetes prevalence |
title_sort | longer time to peak glucose during the oral glucose tolerance test increases cardiovascular risk score and diabetes prevalence |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720677/ https://www.ncbi.nlm.nih.gov/pubmed/29216249 http://dx.doi.org/10.1371/journal.pone.0189047 |
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