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Early Gestational Blood Markers to Predict Preeclampsia Complicating Gestational Diabetes Mellitus
OBJECTIVE: Gestational diabetes mellitus (GDM) and preeclampsia (PE) are common pregnancy complications that share some common risk factors. GDM patients are also at high risk for PE. There are no sensitive markers for prediction, especially for the occurrence of PE in GDM patients. This study inves...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Dove
2023
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216866/ https://www.ncbi.nlm.nih.gov/pubmed/37252009 http://dx.doi.org/10.2147/DMSO.S410912 |
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author | Xie, Yan Zhou, Wenni Tao, Xiang Lv, Hui Cheng, Zhongping |
author_facet | Xie, Yan Zhou, Wenni Tao, Xiang Lv, Hui Cheng, Zhongping |
author_sort | Xie, Yan |
collection | PubMed |
description | OBJECTIVE: Gestational diabetes mellitus (GDM) and preeclampsia (PE) are common pregnancy complications that share some common risk factors. GDM patients are also at high risk for PE. There are no sensitive markers for prediction, especially for the occurrence of PE in GDM patients. This study investigated plasma proteins for the prediction of PE in GDM patients. METHODS: A total of 10 PE, 10 GDM, and 5 PE complicated with GDM cases, as well as 10 pregnant controls without obvious complications, were included in the nested cohort. The proteomics in the plasma collected at 12–20 weeks of gestational age (GA) were analyzed by liquid chromatography‒mass spectrometry/mass spectrometry. Some potential markers, such as soluble transferrin receptor (sTfR), ceruloplasmin (CP), apolipoprotein E (ApoE) and inositol 1,4,5-trisphosphate receptor 1 (ITPR1), were validated using enzyme-linked immunosorbent assays. RESULTS: Functional analysis of the plasma showed that proteasome activation, pancreatic secretion, and fatty acid degradation were activated in the GDM group, and renin secretion-, lysosome-, and proteasome pathways involving iron transport and lipid metabolism were enriched in the PE group, distinguishing PE complicating GDM. CONCLUSION: Through proteomics analysis of plasma in early pregnancy, PE complicating GDM may have a unique mechanism from that of PE alone. Plasma sTfR, CP and ApoE levels have potential clinical applications in early screening. |
format | Online Article Text |
id | pubmed-10216866 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Dove |
record_format | MEDLINE/PubMed |
spelling | pubmed-102168662023-05-27 Early Gestational Blood Markers to Predict Preeclampsia Complicating Gestational Diabetes Mellitus Xie, Yan Zhou, Wenni Tao, Xiang Lv, Hui Cheng, Zhongping Diabetes Metab Syndr Obes Original Research OBJECTIVE: Gestational diabetes mellitus (GDM) and preeclampsia (PE) are common pregnancy complications that share some common risk factors. GDM patients are also at high risk for PE. There are no sensitive markers for prediction, especially for the occurrence of PE in GDM patients. This study investigated plasma proteins for the prediction of PE in GDM patients. METHODS: A total of 10 PE, 10 GDM, and 5 PE complicated with GDM cases, as well as 10 pregnant controls without obvious complications, were included in the nested cohort. The proteomics in the plasma collected at 12–20 weeks of gestational age (GA) were analyzed by liquid chromatography‒mass spectrometry/mass spectrometry. Some potential markers, such as soluble transferrin receptor (sTfR), ceruloplasmin (CP), apolipoprotein E (ApoE) and inositol 1,4,5-trisphosphate receptor 1 (ITPR1), were validated using enzyme-linked immunosorbent assays. RESULTS: Functional analysis of the plasma showed that proteasome activation, pancreatic secretion, and fatty acid degradation were activated in the GDM group, and renin secretion-, lysosome-, and proteasome pathways involving iron transport and lipid metabolism were enriched in the PE group, distinguishing PE complicating GDM. CONCLUSION: Through proteomics analysis of plasma in early pregnancy, PE complicating GDM may have a unique mechanism from that of PE alone. Plasma sTfR, CP and ApoE levels have potential clinical applications in early screening. Dove 2023-05-22 /pmc/articles/PMC10216866/ /pubmed/37252009 http://dx.doi.org/10.2147/DMSO.S410912 Text en © 2023 Xie et al. https://creativecommons.org/licenses/by-nc/3.0/This work is published and licensed by Dove Medical Press Limited. The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/ (https://creativecommons.org/licenses/by-nc/3.0/) ). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed. For permission for commercial use of this work, please see paragraphs 4.2 and 5 of our Terms (https://www.dovepress.com/terms.php). |
spellingShingle | Original Research Xie, Yan Zhou, Wenni Tao, Xiang Lv, Hui Cheng, Zhongping Early Gestational Blood Markers to Predict Preeclampsia Complicating Gestational Diabetes Mellitus |
title | Early Gestational Blood Markers to Predict Preeclampsia Complicating Gestational Diabetes Mellitus |
title_full | Early Gestational Blood Markers to Predict Preeclampsia Complicating Gestational Diabetes Mellitus |
title_fullStr | Early Gestational Blood Markers to Predict Preeclampsia Complicating Gestational Diabetes Mellitus |
title_full_unstemmed | Early Gestational Blood Markers to Predict Preeclampsia Complicating Gestational Diabetes Mellitus |
title_short | Early Gestational Blood Markers to Predict Preeclampsia Complicating Gestational Diabetes Mellitus |
title_sort | early gestational blood markers to predict preeclampsia complicating gestational diabetes mellitus |
topic | Original Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10216866/ https://www.ncbi.nlm.nih.gov/pubmed/37252009 http://dx.doi.org/10.2147/DMSO.S410912 |
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