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An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers

BACKGROUND: Gestational diabetes mellitus (GDM) represents the main metabolic alteration during pregnancy. The available methods for diagnosing GDM identify women when the disease is established, and pancreatic beta-cell insufficiency has occurred.The present study aimed to generate an early predict...

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Autores principales: Razo-Azamar, Melissa, Nambo-Venegas, Rafael, Meraz-Cruz, Noemí, Guevara-Cruz, Martha, Ibarra-González, Isabel, Vela-Amieva, Marcela, Delgadillo-Velázquez, Jaime, Santiago, Xanic Caraza, Escobar, Rafael Figueroa, Vadillo-Ortega, Felipe, Palacios-González, Berenice
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234027/
https://www.ncbi.nlm.nih.gov/pubmed/37264408
http://dx.doi.org/10.1186/s13098-023-01098-7
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author Razo-Azamar, Melissa
Nambo-Venegas, Rafael
Meraz-Cruz, Noemí
Guevara-Cruz, Martha
Ibarra-González, Isabel
Vela-Amieva, Marcela
Delgadillo-Velázquez, Jaime
Santiago, Xanic Caraza
Escobar, Rafael Figueroa
Vadillo-Ortega, Felipe
Palacios-González, Berenice
author_facet Razo-Azamar, Melissa
Nambo-Venegas, Rafael
Meraz-Cruz, Noemí
Guevara-Cruz, Martha
Ibarra-González, Isabel
Vela-Amieva, Marcela
Delgadillo-Velázquez, Jaime
Santiago, Xanic Caraza
Escobar, Rafael Figueroa
Vadillo-Ortega, Felipe
Palacios-González, Berenice
author_sort Razo-Azamar, Melissa
collection PubMed
description BACKGROUND: Gestational diabetes mellitus (GDM) represents the main metabolic alteration during pregnancy. The available methods for diagnosing GDM identify women when the disease is established, and pancreatic beta-cell insufficiency has occurred.The present study aimed to generate an early prediction model (under 18 weeks of gestation) to identify those women who will later be diagnosed with GDM. METHODS: A cohort of 75 pregnant women was followed during gestation, of which 62 underwent normal term pregnancy and 13 were diagnosed with GDM. Targeted metabolomics was used to select serum biomarkers with predictive power to identify women who will later be diagnosed with GDM. RESULTS: Candidate metabolites were selected to generate an early identification model employing a criterion used when performing Random Forest decision tree analysis. A model composed of two short-chain acylcarnitines was generated: isovalerylcarnitine (C5) and tiglylcarnitine (C5:1). An analysis by ROC curves was performed to determine the classification performance of the acylcarnitines identified in the study, obtaining an area under the curve (AUC) of 0.934 (0.873–0.995, 95% CI). The model correctly classified all cases with GDM, while it misclassified ten controls as in the GDM group. An analysis was also carried out to establish the concentrations of the acylcarnitines for the identification of the GDM group, obtaining concentrations of C5 in a range of 0.015–0.25 μmol/L and of C5:1 with a range of 0.015–0.19 μmol/L. CONCLUSION: Early pregnancy maternal metabolites can be used to screen and identify pregnant women who will later develop GDM. Regardless of their gestational body mass index, lipid metabolism is impaired even in the early stages of pregnancy in women who develop GDM. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-023-01098-7.
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spelling pubmed-102340272023-06-02 An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers Razo-Azamar, Melissa Nambo-Venegas, Rafael Meraz-Cruz, Noemí Guevara-Cruz, Martha Ibarra-González, Isabel Vela-Amieva, Marcela Delgadillo-Velázquez, Jaime Santiago, Xanic Caraza Escobar, Rafael Figueroa Vadillo-Ortega, Felipe Palacios-González, Berenice Diabetol Metab Syndr Research BACKGROUND: Gestational diabetes mellitus (GDM) represents the main metabolic alteration during pregnancy. The available methods for diagnosing GDM identify women when the disease is established, and pancreatic beta-cell insufficiency has occurred.The present study aimed to generate an early prediction model (under 18 weeks of gestation) to identify those women who will later be diagnosed with GDM. METHODS: A cohort of 75 pregnant women was followed during gestation, of which 62 underwent normal term pregnancy and 13 were diagnosed with GDM. Targeted metabolomics was used to select serum biomarkers with predictive power to identify women who will later be diagnosed with GDM. RESULTS: Candidate metabolites were selected to generate an early identification model employing a criterion used when performing Random Forest decision tree analysis. A model composed of two short-chain acylcarnitines was generated: isovalerylcarnitine (C5) and tiglylcarnitine (C5:1). An analysis by ROC curves was performed to determine the classification performance of the acylcarnitines identified in the study, obtaining an area under the curve (AUC) of 0.934 (0.873–0.995, 95% CI). The model correctly classified all cases with GDM, while it misclassified ten controls as in the GDM group. An analysis was also carried out to establish the concentrations of the acylcarnitines for the identification of the GDM group, obtaining concentrations of C5 in a range of 0.015–0.25 μmol/L and of C5:1 with a range of 0.015–0.19 μmol/L. CONCLUSION: Early pregnancy maternal metabolites can be used to screen and identify pregnant women who will later develop GDM. Regardless of their gestational body mass index, lipid metabolism is impaired even in the early stages of pregnancy in women who develop GDM. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13098-023-01098-7. BioMed Central 2023-06-01 /pmc/articles/PMC10234027/ /pubmed/37264408 http://dx.doi.org/10.1186/s13098-023-01098-7 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Research
Razo-Azamar, Melissa
Nambo-Venegas, Rafael
Meraz-Cruz, Noemí
Guevara-Cruz, Martha
Ibarra-González, Isabel
Vela-Amieva, Marcela
Delgadillo-Velázquez, Jaime
Santiago, Xanic Caraza
Escobar, Rafael Figueroa
Vadillo-Ortega, Felipe
Palacios-González, Berenice
An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers
title An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers
title_full An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers
title_fullStr An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers
title_full_unstemmed An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers
title_short An early prediction model for gestational diabetes mellitus based on metabolomic biomarkers
title_sort early prediction model for gestational diabetes mellitus based on metabolomic biomarkers
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10234027/
https://www.ncbi.nlm.nih.gov/pubmed/37264408
http://dx.doi.org/10.1186/s13098-023-01098-7
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