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Glycosylated fibronectin as a first trimester marker for gestational diabetes
PURPOSE: To evaluate the performance of first trimester maternal serum glycosylated (Sambucus nigra lectin-reactive) fibronectin in prediction of gestational diabetes mellitus (GDM). METHODS: In this case–control study, first trimester maternal serum glycosylated fibronectin and fibronectin were mea...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471182/ https://www.ncbi.nlm.nih.gov/pubmed/32653948 http://dx.doi.org/10.1007/s00404-020-05670-8 |
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author | Alanen, Julia Appelblom, Heidi Korpimaki, Teemu Kouru, Heikki Sairanen, Mikko Gissler, Mika Ryynanen, Markku Nevalainen, Jaana |
author_facet | Alanen, Julia Appelblom, Heidi Korpimaki, Teemu Kouru, Heikki Sairanen, Mikko Gissler, Mika Ryynanen, Markku Nevalainen, Jaana |
author_sort | Alanen, Julia |
collection | PubMed |
description | PURPOSE: To evaluate the performance of first trimester maternal serum glycosylated (Sambucus nigra lectin-reactive) fibronectin in prediction of gestational diabetes mellitus (GDM). METHODS: In this case–control study, first trimester maternal serum glycosylated fibronectin and fibronectin were measured in 19 women who consequently developed GDM and in 59 control women with normal pregnancy outcomes. Adiponectin was used as a reference protein to evaluate relation of glycoprotein to SNA-lectin-reactive assay format. Samples were taken during gestational weeks 9(+6)–11(+6). Data concerning GDM was obtained from the National Institute for Health and Welfare, which records the pregnancy outcomes of all women in Finland. RESULTS: There was no difference in maternal serum glycosylated fibronectin concentrations between women with consequent GDM [447.5 μg/mL, interquartile range (IQR) 254.4–540.9 μg/mL] and control women (437.6 μg/mL, IQR 357.1–569.1 μg/mL). Maternal serum fibronectin levels were significantly lower in GDM group (224.2 μg/mL, IQR 156.8–270.6 μg/mL), compared to the control group (264.8 μg/mL, IQR 224.6–330.6 μg/mL, p < 0.01). There was no difference in assay formats for adiponectin. CONCLUSION: There was no association between first trimester maternal serum glycosylated (SNA-reactive) fibronectin and GDM. |
format | Online Article Text |
id | pubmed-7471182 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-74711822020-09-16 Glycosylated fibronectin as a first trimester marker for gestational diabetes Alanen, Julia Appelblom, Heidi Korpimaki, Teemu Kouru, Heikki Sairanen, Mikko Gissler, Mika Ryynanen, Markku Nevalainen, Jaana Arch Gynecol Obstet Maternal-Fetal Medicine PURPOSE: To evaluate the performance of first trimester maternal serum glycosylated (Sambucus nigra lectin-reactive) fibronectin in prediction of gestational diabetes mellitus (GDM). METHODS: In this case–control study, first trimester maternal serum glycosylated fibronectin and fibronectin were measured in 19 women who consequently developed GDM and in 59 control women with normal pregnancy outcomes. Adiponectin was used as a reference protein to evaluate relation of glycoprotein to SNA-lectin-reactive assay format. Samples were taken during gestational weeks 9(+6)–11(+6). Data concerning GDM was obtained from the National Institute for Health and Welfare, which records the pregnancy outcomes of all women in Finland. RESULTS: There was no difference in maternal serum glycosylated fibronectin concentrations between women with consequent GDM [447.5 μg/mL, interquartile range (IQR) 254.4–540.9 μg/mL] and control women (437.6 μg/mL, IQR 357.1–569.1 μg/mL). Maternal serum fibronectin levels were significantly lower in GDM group (224.2 μg/mL, IQR 156.8–270.6 μg/mL), compared to the control group (264.8 μg/mL, IQR 224.6–330.6 μg/mL, p < 0.01). There was no difference in assay formats for adiponectin. CONCLUSION: There was no association between first trimester maternal serum glycosylated (SNA-reactive) fibronectin and GDM. Springer Berlin Heidelberg 2020-07-11 2020 /pmc/articles/PMC7471182/ /pubmed/32653948 http://dx.doi.org/10.1007/s00404-020-05670-8 Text en © The Author(s) 2020 Open AccessThis 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/. |
spellingShingle | Maternal-Fetal Medicine Alanen, Julia Appelblom, Heidi Korpimaki, Teemu Kouru, Heikki Sairanen, Mikko Gissler, Mika Ryynanen, Markku Nevalainen, Jaana Glycosylated fibronectin as a first trimester marker for gestational diabetes |
title | Glycosylated fibronectin as a first trimester marker for gestational diabetes |
title_full | Glycosylated fibronectin as a first trimester marker for gestational diabetes |
title_fullStr | Glycosylated fibronectin as a first trimester marker for gestational diabetes |
title_full_unstemmed | Glycosylated fibronectin as a first trimester marker for gestational diabetes |
title_short | Glycosylated fibronectin as a first trimester marker for gestational diabetes |
title_sort | glycosylated fibronectin as a first trimester marker for gestational diabetes |
topic | Maternal-Fetal Medicine |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7471182/ https://www.ncbi.nlm.nih.gov/pubmed/32653948 http://dx.doi.org/10.1007/s00404-020-05670-8 |
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