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Variability of serum IgG sialylation and galactosylation degree in women with advanced endometriosis
Endometriosis is an inflammatory disease which diagnostics is difficult and often invasive, therefore non-invasive diagnostics methods and parameters are needed for endometriosis detection. The aim of our study was to analyse the glycosylation of native serum IgG and IgG isolated from sera of women...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970930/ https://www.ncbi.nlm.nih.gov/pubmed/33692455 http://dx.doi.org/10.1038/s41598-021-85200-x |
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author | Sołkiewicz, Katarzyna Krotkiewski, Hubert Jędryka, Marcin Kratz, Ewa M. |
author_facet | Sołkiewicz, Katarzyna Krotkiewski, Hubert Jędryka, Marcin Kratz, Ewa M. |
author_sort | Sołkiewicz, Katarzyna |
collection | PubMed |
description | Endometriosis is an inflammatory disease which diagnostics is difficult and often invasive, therefore non-invasive diagnostics methods and parameters are needed for endometriosis detection. The aim of our study was to analyse the glycosylation of native serum IgG and IgG isolated from sera of women classified as: with endometriosis, without endometriosis but with some benign ginecological disease, and control group of healthy women, in context of its utility for differentiation of advanced endometriosis from the group of healthy women. IgG sialylation and galactosylation/agalactosylation degree was determined using specific lectins: MAA and SNA detecting sialic acid α2,3- and α2,6-linked, respectively, RCA-I and GSL-II specific to terminal Gal and terminal GlcNAc, respectively. The results of ROC and cluster analysis showed that the serum IgG MAA-reactivity, sialylation and agalactosylation factor may be used as supplementary parameters for endometriosis diagnostics and could be taken into account as a useful clinical tool to elucidate women with high risk of endometriosis development. Additionally, we have shown that the analysis of native serum IgG glycosylation, without the prior time-consuming and expensive isolation of the protein, is sufficient to differentiation endometriosis from a group of healthy women. |
format | Online Article Text |
id | pubmed-7970930 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-79709302021-03-19 Variability of serum IgG sialylation and galactosylation degree in women with advanced endometriosis Sołkiewicz, Katarzyna Krotkiewski, Hubert Jędryka, Marcin Kratz, Ewa M. Sci Rep Article Endometriosis is an inflammatory disease which diagnostics is difficult and often invasive, therefore non-invasive diagnostics methods and parameters are needed for endometriosis detection. The aim of our study was to analyse the glycosylation of native serum IgG and IgG isolated from sera of women classified as: with endometriosis, without endometriosis but with some benign ginecological disease, and control group of healthy women, in context of its utility for differentiation of advanced endometriosis from the group of healthy women. IgG sialylation and galactosylation/agalactosylation degree was determined using specific lectins: MAA and SNA detecting sialic acid α2,3- and α2,6-linked, respectively, RCA-I and GSL-II specific to terminal Gal and terminal GlcNAc, respectively. The results of ROC and cluster analysis showed that the serum IgG MAA-reactivity, sialylation and agalactosylation factor may be used as supplementary parameters for endometriosis diagnostics and could be taken into account as a useful clinical tool to elucidate women with high risk of endometriosis development. Additionally, we have shown that the analysis of native serum IgG glycosylation, without the prior time-consuming and expensive isolation of the protein, is sufficient to differentiation endometriosis from a group of healthy women. Nature Publishing Group UK 2021-03-10 /pmc/articles/PMC7970930/ /pubmed/33692455 http://dx.doi.org/10.1038/s41598-021-85200-x Text en © The Author(s) 2021 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/. |
spellingShingle | Article Sołkiewicz, Katarzyna Krotkiewski, Hubert Jędryka, Marcin Kratz, Ewa M. Variability of serum IgG sialylation and galactosylation degree in women with advanced endometriosis |
title | Variability of serum IgG sialylation and galactosylation degree in women with advanced endometriosis |
title_full | Variability of serum IgG sialylation and galactosylation degree in women with advanced endometriosis |
title_fullStr | Variability of serum IgG sialylation and galactosylation degree in women with advanced endometriosis |
title_full_unstemmed | Variability of serum IgG sialylation and galactosylation degree in women with advanced endometriosis |
title_short | Variability of serum IgG sialylation and galactosylation degree in women with advanced endometriosis |
title_sort | variability of serum igg sialylation and galactosylation degree in women with advanced endometriosis |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7970930/ https://www.ncbi.nlm.nih.gov/pubmed/33692455 http://dx.doi.org/10.1038/s41598-021-85200-x |
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