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The usefulness of CYFRA 21–1 to diagnose and predict preeclampsia: a nested case-control study
BACKGROUND: The ability to identify patients at risk for developing preeclampsia is important for preventing morbidity and mortality in both the mother and child. Although CYFRA 21–1 (a fragment of Cytokeratin 19) is considered a promising biomarker for diagnosing preeclampsia, little is known regar...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096295/ https://www.ncbi.nlm.nih.gov/pubmed/27809797 http://dx.doi.org/10.1186/s12884-016-1132-4 |
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author | Kuessel, Lorenz Zeisler, Harald Ristl, Robin Binder, Julia Pateisky, Petra Schmid, Maximilian Marschalek, Julian Perkmann, Thomas Haslacher, Helmuth Husslein, Heinrich |
author_facet | Kuessel, Lorenz Zeisler, Harald Ristl, Robin Binder, Julia Pateisky, Petra Schmid, Maximilian Marschalek, Julian Perkmann, Thomas Haslacher, Helmuth Husslein, Heinrich |
author_sort | Kuessel, Lorenz |
collection | PubMed |
description | BACKGROUND: The ability to identify patients at risk for developing preeclampsia is important for preventing morbidity and mortality in both the mother and child. Although CYFRA 21–1 (a fragment of Cytokeratin 19) is considered a promising biomarker for diagnosing preeclampsia, little is known regarding the levels of CYFRA 21–1 during pregnancy. Here, we measured serum CYFRA 21–1 levels in women with an uneventful pregnancy and in women whose pregnancy was complicated by preeclampsia. Furthermore we evaluated whether maternal CYFRA 21–1 levels can be used to predict and/or diagnose preeclampsia. METHODS: Longitudinal, sequential blood samples were collected prospectively at seven predetermined visits during pregnancy. Maternal CYFRA 21–1 levels were measured in 50 women with an uneventful pregnancy (control group) and in 10 asymptomatic women whose pregnancy was later complicated by preeclampsia (PE_long group). In addition, CYFRA 21–1 levels were measured from a single sample collected from a separate group of 50 pregnant women with symptomatic preeclampsia (PE_state group). RESULTS: The CYFRA 21–1 levels were significantly higher in the PE_state group compared to the control group (p < 0.001). In the PE_long group, CYFRA 21–1 levels were lower from gestational week 11 through 17, but were higher than the control group from gestational weeks 18 through 36. Out of the ROC curves that were calculated to investigate the predictive and diagnostic properties of CYFRA 21–1 levels for preeclampsia, the ROC curve for diagnosing preeclampsia in gestational week 28–32 showed the largest AUC of 0.92, at a cut-off point of 3.1 ng/ml, leading to sensitivity of 92 % and specificity of 80 %. CONCLUSIONS: The elevated serum levels of CYFRA 21–1 observed in both groups of women with preeclampsia may reflect endothelial damage and/or dysfunction. Our results suggest that maternal serum CYFRA 21–1 is a promising biomarker for diagnosing preeclampsia. Although its value for predicting the long-term occurrence of subsequent preeclampsia may be limited, our findings indicate a trend towards elevated maternal CYFRA 21–1 levels preceding the short-term occurrence of preeclampsia in asymptomatic women. Additional prospective longitudinal studies are needed in order to determine the value of measuring maternal serum CYFRA 21–1 in predicting preeclampsia. |
format | Online Article Text |
id | pubmed-5096295 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-50962952016-11-07 The usefulness of CYFRA 21–1 to diagnose and predict preeclampsia: a nested case-control study Kuessel, Lorenz Zeisler, Harald Ristl, Robin Binder, Julia Pateisky, Petra Schmid, Maximilian Marschalek, Julian Perkmann, Thomas Haslacher, Helmuth Husslein, Heinrich BMC Pregnancy Childbirth Research Article BACKGROUND: The ability to identify patients at risk for developing preeclampsia is important for preventing morbidity and mortality in both the mother and child. Although CYFRA 21–1 (a fragment of Cytokeratin 19) is considered a promising biomarker for diagnosing preeclampsia, little is known regarding the levels of CYFRA 21–1 during pregnancy. Here, we measured serum CYFRA 21–1 levels in women with an uneventful pregnancy and in women whose pregnancy was complicated by preeclampsia. Furthermore we evaluated whether maternal CYFRA 21–1 levels can be used to predict and/or diagnose preeclampsia. METHODS: Longitudinal, sequential blood samples were collected prospectively at seven predetermined visits during pregnancy. Maternal CYFRA 21–1 levels were measured in 50 women with an uneventful pregnancy (control group) and in 10 asymptomatic women whose pregnancy was later complicated by preeclampsia (PE_long group). In addition, CYFRA 21–1 levels were measured from a single sample collected from a separate group of 50 pregnant women with symptomatic preeclampsia (PE_state group). RESULTS: The CYFRA 21–1 levels were significantly higher in the PE_state group compared to the control group (p < 0.001). In the PE_long group, CYFRA 21–1 levels were lower from gestational week 11 through 17, but were higher than the control group from gestational weeks 18 through 36. Out of the ROC curves that were calculated to investigate the predictive and diagnostic properties of CYFRA 21–1 levels for preeclampsia, the ROC curve for diagnosing preeclampsia in gestational week 28–32 showed the largest AUC of 0.92, at a cut-off point of 3.1 ng/ml, leading to sensitivity of 92 % and specificity of 80 %. CONCLUSIONS: The elevated serum levels of CYFRA 21–1 observed in both groups of women with preeclampsia may reflect endothelial damage and/or dysfunction. Our results suggest that maternal serum CYFRA 21–1 is a promising biomarker for diagnosing preeclampsia. Although its value for predicting the long-term occurrence of subsequent preeclampsia may be limited, our findings indicate a trend towards elevated maternal CYFRA 21–1 levels preceding the short-term occurrence of preeclampsia in asymptomatic women. Additional prospective longitudinal studies are needed in order to determine the value of measuring maternal serum CYFRA 21–1 in predicting preeclampsia. BioMed Central 2016-11-03 /pmc/articles/PMC5096295/ /pubmed/27809797 http://dx.doi.org/10.1186/s12884-016-1132-4 Text en © The Author(s). 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Kuessel, Lorenz Zeisler, Harald Ristl, Robin Binder, Julia Pateisky, Petra Schmid, Maximilian Marschalek, Julian Perkmann, Thomas Haslacher, Helmuth Husslein, Heinrich The usefulness of CYFRA 21–1 to diagnose and predict preeclampsia: a nested case-control study |
title | The usefulness of CYFRA 21–1 to diagnose and predict preeclampsia: a nested case-control study |
title_full | The usefulness of CYFRA 21–1 to diagnose and predict preeclampsia: a nested case-control study |
title_fullStr | The usefulness of CYFRA 21–1 to diagnose and predict preeclampsia: a nested case-control study |
title_full_unstemmed | The usefulness of CYFRA 21–1 to diagnose and predict preeclampsia: a nested case-control study |
title_short | The usefulness of CYFRA 21–1 to diagnose and predict preeclampsia: a nested case-control study |
title_sort | usefulness of cyfra 21–1 to diagnose and predict preeclampsia: a nested case-control study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5096295/ https://www.ncbi.nlm.nih.gov/pubmed/27809797 http://dx.doi.org/10.1186/s12884-016-1132-4 |
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