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Correlation of the plasma sphingoid base profile with results from oral glucose tolerance tests in gestational diabetes mellitus

Oral glucose tolerance test (OGTT) is usually insufficient to accurately predict the risk for type 2 diabetes mellitus (T2DM), it is therefore necessary to identify an additional biomarker that would most likely improve the accuracy of OGTT. The current OGTT was performed in 53 volunteers after inge...

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Autores principales: Khan, Abad, Hornemann, Thorsten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Leibniz Research Centre for Working Environment and Human Factors 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491909/
https://www.ncbi.nlm.nih.gov/pubmed/28694753
http://dx.doi.org/10.17179/excli2017-171
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author Khan, Abad
Hornemann, Thorsten
author_facet Khan, Abad
Hornemann, Thorsten
author_sort Khan, Abad
collection PubMed
description Oral glucose tolerance test (OGTT) is usually insufficient to accurately predict the risk for type 2 diabetes mellitus (T2DM), it is therefore necessary to identify an additional biomarker that would most likely improve the accuracy of OGTT. The current OGTT was performed in 53 volunteers after ingestion of 75 g glucose in 250 ml water to each volunteer. Similarly the sphingoid base profile of these volunteers was explored using liquid-chromatography linked with mass spectrometer (LC-MS) and correlated with the different time-points glucose values of OGTT as well as with total area under the curve (tAUC), incremental area under the curve (iAUC), and positive incremental area under the curve (pAUC). The findings showed that 1-deoxysphinganine (1-deoxySA) was significantly positively correlated with the 1-hour, 2-hour, and 3-hour plasma glucose level as well as with total, incremental, and positive incremental AUC while 1-deoxysphingosine (1-deoxySO) was correlated only with 1-hour, 2-hour glucose levels and tAUC of OGTT. The C18SAdiene was negatively correlated with all-time points glucose values and AUCs followed by negative correlation of C18SO, C16SO and C17SO with 2-hour glucose and tAUC of OGTT. The ratios of 1-deoxySA and 1-deoxySO with respect to C18SAdiene have shown significant correlation with 2-hour and AUCs. These ratios were higher in subjects with gestational diabetes in comparison with normal subjects. These findings underlined that 1-deoxysphingolipids (1-deoxySLs) and their ratios with C18SAdiene could be significantly correlated with the glucose load of OGTT and might be used as predictive biomarkers along with OGTT for the risk assessment of diabetes.
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spelling pubmed-54919092017-07-10 Correlation of the plasma sphingoid base profile with results from oral glucose tolerance tests in gestational diabetes mellitus Khan, Abad Hornemann, Thorsten EXCLI J Original Article Oral glucose tolerance test (OGTT) is usually insufficient to accurately predict the risk for type 2 diabetes mellitus (T2DM), it is therefore necessary to identify an additional biomarker that would most likely improve the accuracy of OGTT. The current OGTT was performed in 53 volunteers after ingestion of 75 g glucose in 250 ml water to each volunteer. Similarly the sphingoid base profile of these volunteers was explored using liquid-chromatography linked with mass spectrometer (LC-MS) and correlated with the different time-points glucose values of OGTT as well as with total area under the curve (tAUC), incremental area under the curve (iAUC), and positive incremental area under the curve (pAUC). The findings showed that 1-deoxysphinganine (1-deoxySA) was significantly positively correlated with the 1-hour, 2-hour, and 3-hour plasma glucose level as well as with total, incremental, and positive incremental AUC while 1-deoxysphingosine (1-deoxySO) was correlated only with 1-hour, 2-hour glucose levels and tAUC of OGTT. The C18SAdiene was negatively correlated with all-time points glucose values and AUCs followed by negative correlation of C18SO, C16SO and C17SO with 2-hour glucose and tAUC of OGTT. The ratios of 1-deoxySA and 1-deoxySO with respect to C18SAdiene have shown significant correlation with 2-hour and AUCs. These ratios were higher in subjects with gestational diabetes in comparison with normal subjects. These findings underlined that 1-deoxysphingolipids (1-deoxySLs) and their ratios with C18SAdiene could be significantly correlated with the glucose load of OGTT and might be used as predictive biomarkers along with OGTT for the risk assessment of diabetes. Leibniz Research Centre for Working Environment and Human Factors 2017-04-18 /pmc/articles/PMC5491909/ /pubmed/28694753 http://dx.doi.org/10.17179/excli2017-171 Text en Copyright © 2017 Khan et al. http://creativecommons.org/licenses/by/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution Licence (http://creativecommons.org/licenses/by/4.0/) You are free to copy, distribute and transmit the work, provided the original author and source are credited.
spellingShingle Original Article
Khan, Abad
Hornemann, Thorsten
Correlation of the plasma sphingoid base profile with results from oral glucose tolerance tests in gestational diabetes mellitus
title Correlation of the plasma sphingoid base profile with results from oral glucose tolerance tests in gestational diabetes mellitus
title_full Correlation of the plasma sphingoid base profile with results from oral glucose tolerance tests in gestational diabetes mellitus
title_fullStr Correlation of the plasma sphingoid base profile with results from oral glucose tolerance tests in gestational diabetes mellitus
title_full_unstemmed Correlation of the plasma sphingoid base profile with results from oral glucose tolerance tests in gestational diabetes mellitus
title_short Correlation of the plasma sphingoid base profile with results from oral glucose tolerance tests in gestational diabetes mellitus
title_sort correlation of the plasma sphingoid base profile with results from oral glucose tolerance tests in gestational diabetes mellitus
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5491909/
https://www.ncbi.nlm.nih.gov/pubmed/28694753
http://dx.doi.org/10.17179/excli2017-171
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