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Maternal serum proteomic profiles of pregnant women with type 1 diabetes

Despite improvement in the care of diabetes over the years, pregnancy complicated by type 1 diabetes (T1DM) is still associated with adverse maternal and neonatal outcomes. To date, proteomics studies have been conducted to identify T1DM biomarkers in non-pregnant women, however, no studies included...

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Autores principales: Gutaj, Paweł, Matysiak, Jan, Matuszewska, Eliza, Jaskiewicz, Katarzyna, Kamińska, Dorota, Światły-Błaszkiewicz, Agata, Szczapa, Tomasz, Kalantarova, Anastasia, Gajecka, Marzena, Wender-Ozegowska, Ewa
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130255/
https://www.ncbi.nlm.nih.gov/pubmed/35610262
http://dx.doi.org/10.1038/s41598-022-12221-5
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author Gutaj, Paweł
Matysiak, Jan
Matuszewska, Eliza
Jaskiewicz, Katarzyna
Kamińska, Dorota
Światły-Błaszkiewicz, Agata
Szczapa, Tomasz
Kalantarova, Anastasia
Gajecka, Marzena
Wender-Ozegowska, Ewa
author_facet Gutaj, Paweł
Matysiak, Jan
Matuszewska, Eliza
Jaskiewicz, Katarzyna
Kamińska, Dorota
Światły-Błaszkiewicz, Agata
Szczapa, Tomasz
Kalantarova, Anastasia
Gajecka, Marzena
Wender-Ozegowska, Ewa
author_sort Gutaj, Paweł
collection PubMed
description Despite improvement in the care of diabetes over the years, pregnancy complicated by type 1 diabetes (T1DM) is still associated with adverse maternal and neonatal outcomes. To date, proteomics studies have been conducted to identify T1DM biomarkers in non-pregnant women, however, no studies included T1DM pregnant women. In this study serum proteomic profiling was conducted in pregnant women with T1DM in the late third trimester. Serum samples were collected from 40 women with T1DM and 38 healthy controls within 3 days before delivery at term pregnancy. Significant differences between serum proteomic patterns were revealed, showing discriminative peaks for complement C3 and C4-A, kininogen-1, and fibrinogen alpha chain. Quantification of selected discriminative proteins by ELISA kits was also performed. The serum concentration of kininogen-1 was significantly lower in women with T1DM than in controls. There were no significant differences in serum concentrations of complement C3 and complement C4-A between study groups. These data indicate that pregnant women with T1DM have a distinct proteomic profile involving proteins in the coagulation and inflammatory pathways. However, their utility as biomarkers of pregnancy complications in women with T1DM warrants further investigation.
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spelling pubmed-91302552022-05-26 Maternal serum proteomic profiles of pregnant women with type 1 diabetes Gutaj, Paweł Matysiak, Jan Matuszewska, Eliza Jaskiewicz, Katarzyna Kamińska, Dorota Światły-Błaszkiewicz, Agata Szczapa, Tomasz Kalantarova, Anastasia Gajecka, Marzena Wender-Ozegowska, Ewa Sci Rep Article Despite improvement in the care of diabetes over the years, pregnancy complicated by type 1 diabetes (T1DM) is still associated with adverse maternal and neonatal outcomes. To date, proteomics studies have been conducted to identify T1DM biomarkers in non-pregnant women, however, no studies included T1DM pregnant women. In this study serum proteomic profiling was conducted in pregnant women with T1DM in the late third trimester. Serum samples were collected from 40 women with T1DM and 38 healthy controls within 3 days before delivery at term pregnancy. Significant differences between serum proteomic patterns were revealed, showing discriminative peaks for complement C3 and C4-A, kininogen-1, and fibrinogen alpha chain. Quantification of selected discriminative proteins by ELISA kits was also performed. The serum concentration of kininogen-1 was significantly lower in women with T1DM than in controls. There were no significant differences in serum concentrations of complement C3 and complement C4-A between study groups. These data indicate that pregnant women with T1DM have a distinct proteomic profile involving proteins in the coagulation and inflammatory pathways. However, their utility as biomarkers of pregnancy complications in women with T1DM warrants further investigation. Nature Publishing Group UK 2022-05-24 /pmc/articles/PMC9130255/ /pubmed/35610262 http://dx.doi.org/10.1038/s41598-022-12221-5 Text en © The Author(s) 2022 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/) .
spellingShingle Article
Gutaj, Paweł
Matysiak, Jan
Matuszewska, Eliza
Jaskiewicz, Katarzyna
Kamińska, Dorota
Światły-Błaszkiewicz, Agata
Szczapa, Tomasz
Kalantarova, Anastasia
Gajecka, Marzena
Wender-Ozegowska, Ewa
Maternal serum proteomic profiles of pregnant women with type 1 diabetes
title Maternal serum proteomic profiles of pregnant women with type 1 diabetes
title_full Maternal serum proteomic profiles of pregnant women with type 1 diabetes
title_fullStr Maternal serum proteomic profiles of pregnant women with type 1 diabetes
title_full_unstemmed Maternal serum proteomic profiles of pregnant women with type 1 diabetes
title_short Maternal serum proteomic profiles of pregnant women with type 1 diabetes
title_sort maternal serum proteomic profiles of pregnant women with type 1 diabetes
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9130255/
https://www.ncbi.nlm.nih.gov/pubmed/35610262
http://dx.doi.org/10.1038/s41598-022-12221-5
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