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Chromogranin A demonstrates higher expression in preeclamptic placentas than in normal pregnancy
BACKGROUND: Although preeclampsia has long been recognized as a condition affecting late pregnancy, little is known of its pathogenesis or treatment. The placenta releases a number of hormones and molecules that influence the course of pregnancy, one of which is chromogranin A, a soluble protein sec...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496087/ https://www.ncbi.nlm.nih.gov/pubmed/34620125 http://dx.doi.org/10.1186/s12884-021-04139-z |
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author | Bralewska, Michalina Biesiada, Lidia Grzesiak, Mariusz Rybak-Krzyszkowska, Magda Huras, Hubert Gach, Agnieszka Pietrucha, Tadeusz Sakowicz, Agata |
author_facet | Bralewska, Michalina Biesiada, Lidia Grzesiak, Mariusz Rybak-Krzyszkowska, Magda Huras, Hubert Gach, Agnieszka Pietrucha, Tadeusz Sakowicz, Agata |
author_sort | Bralewska, Michalina |
collection | PubMed |
description | BACKGROUND: Although preeclampsia has long been recognized as a condition affecting late pregnancy, little is known of its pathogenesis or treatment. The placenta releases a number of hormones and molecules that influence the course of pregnancy, one of which is chromogranin A, a soluble protein secreted mainly from the chromaffin cells of the adrenal medulla. Its role in pregnancy and pregnancy-related disorders remains unclear. Therefore, the main aim of the proposed study is to determine whether chromogranin A is related with the occurrence of preeclampsia. METHODS: Placental samples were collected from 102 preeclamptic patients and 103 healthy controls, and Chromogranin A gene (CHGA) expression was measured using real-time RT-PCR, The RT-PCR results were verified on the protein level using ELISA. The normal distribution of the data was tested using the Shapiro-Wilk test. The clinical and personal characteristics of the groups were compared using the Student’s t-test for normally-distributed data, and the χ(2) test for categorical variables. The Mann-Whitney U test was used for non-normally distributed data. As the log- transformation was not suitable for the given outcomes, the Box- Cox Transformation was used to normalize data from ELISA tests and CHGA expression. Values of P < .05 were considered statistically significant. RESULTS: Chromogranin A gene expression was found to be significantly higher in the study group than in controls. Protein analyses showed that although the CgA concentration in placental samples did not differ significantly, the catestatin (CST) level was significantly lower in samples obtained from women with preeclampsia, according to the controls. CONCLUSIONS FOR PRACTICE: This study for the first time reveals that chromogranin A gene expression level is associated with preeclampsia. Moreover, the depletion in catestatin level, which plays a protective role in hypertension development, might be a marker of developing preeclampsia. Further studies may unravel role of Chromogranin A in the discussed disease. |
format | Online Article Text |
id | pubmed-8496087 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-84960872021-10-07 Chromogranin A demonstrates higher expression in preeclamptic placentas than in normal pregnancy Bralewska, Michalina Biesiada, Lidia Grzesiak, Mariusz Rybak-Krzyszkowska, Magda Huras, Hubert Gach, Agnieszka Pietrucha, Tadeusz Sakowicz, Agata BMC Pregnancy Childbirth Research BACKGROUND: Although preeclampsia has long been recognized as a condition affecting late pregnancy, little is known of its pathogenesis or treatment. The placenta releases a number of hormones and molecules that influence the course of pregnancy, one of which is chromogranin A, a soluble protein secreted mainly from the chromaffin cells of the adrenal medulla. Its role in pregnancy and pregnancy-related disorders remains unclear. Therefore, the main aim of the proposed study is to determine whether chromogranin A is related with the occurrence of preeclampsia. METHODS: Placental samples were collected from 102 preeclamptic patients and 103 healthy controls, and Chromogranin A gene (CHGA) expression was measured using real-time RT-PCR, The RT-PCR results were verified on the protein level using ELISA. The normal distribution of the data was tested using the Shapiro-Wilk test. The clinical and personal characteristics of the groups were compared using the Student’s t-test for normally-distributed data, and the χ(2) test for categorical variables. The Mann-Whitney U test was used for non-normally distributed data. As the log- transformation was not suitable for the given outcomes, the Box- Cox Transformation was used to normalize data from ELISA tests and CHGA expression. Values of P < .05 were considered statistically significant. RESULTS: Chromogranin A gene expression was found to be significantly higher in the study group than in controls. Protein analyses showed that although the CgA concentration in placental samples did not differ significantly, the catestatin (CST) level was significantly lower in samples obtained from women with preeclampsia, according to the controls. CONCLUSIONS FOR PRACTICE: This study for the first time reveals that chromogranin A gene expression level is associated with preeclampsia. Moreover, the depletion in catestatin level, which plays a protective role in hypertension development, might be a marker of developing preeclampsia. Further studies may unravel role of Chromogranin A in the discussed disease. BioMed Central 2021-10-07 /pmc/articles/PMC8496087/ /pubmed/34620125 http://dx.doi.org/10.1186/s12884-021-04139-z Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Bralewska, Michalina Biesiada, Lidia Grzesiak, Mariusz Rybak-Krzyszkowska, Magda Huras, Hubert Gach, Agnieszka Pietrucha, Tadeusz Sakowicz, Agata Chromogranin A demonstrates higher expression in preeclamptic placentas than in normal pregnancy |
title | Chromogranin A demonstrates higher expression in preeclamptic placentas than in normal pregnancy |
title_full | Chromogranin A demonstrates higher expression in preeclamptic placentas than in normal pregnancy |
title_fullStr | Chromogranin A demonstrates higher expression in preeclamptic placentas than in normal pregnancy |
title_full_unstemmed | Chromogranin A demonstrates higher expression in preeclamptic placentas than in normal pregnancy |
title_short | Chromogranin A demonstrates higher expression in preeclamptic placentas than in normal pregnancy |
title_sort | chromogranin a demonstrates higher expression in preeclamptic placentas than in normal pregnancy |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8496087/ https://www.ncbi.nlm.nih.gov/pubmed/34620125 http://dx.doi.org/10.1186/s12884-021-04139-z |
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