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The high platelet counts as predictor for early foetal demise
OBJECTIVES: Early fetal demise (absence of cardiac activity in a visible fetus) is a very common event, but there are no reliable biomarkers to predict it. The purpose of the study was to assess the association of platelet parameters with early fetal demise. METHODS: In this case-control study, we i...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Taylor & Francis
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405072/ https://www.ncbi.nlm.nih.gov/pubmed/34431412 http://dx.doi.org/10.1080/07853890.2021.1968027 |
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author | Shao, Xiaowen Wang, Dandan Xu, Yue Guo, Ling Yang, Hui Zhou, Jieru Liang, Jiayi Qian, Jie Cheng, Jiajing Sun, Lihua Xiang, Yaozu |
author_facet | Shao, Xiaowen Wang, Dandan Xu, Yue Guo, Ling Yang, Hui Zhou, Jieru Liang, Jiayi Qian, Jie Cheng, Jiajing Sun, Lihua Xiang, Yaozu |
author_sort | Shao, Xiaowen |
collection | PubMed |
description | OBJECTIVES: Early fetal demise (absence of cardiac activity in a visible fetus) is a very common event, but there are no reliable biomarkers to predict it. The purpose of the study was to assess the association of platelet parameters with early fetal demise. METHODS: In this case-control study, we included women with normal deliveries or those ultrasound diagnosed as early fetal demise. For those who were identified with early fetal demise, the platelet parameters were analyzed before the ultrasound diagnosis, which is based on the absence of either an embryo within a gestational sac or cardiac activity in a visible embryo in the 5-10 weeks of gestation. The association between the risk of early fetal demise with the women's mean platelet volume (MPV) and platelet counts was calculated by logistic regression. Duplicate measurements of platelet aggregation were performed with VerifyNow. RESULTS: In total, 99 women identified with early fetal demise and 170 women who had an uncomplicated pregnancy with normal delivery from January 2017 and August 2020 were included in the study. We found that platelet counts in the early fetal demise group were significantly higher than healthy pregnancies. In addition, platelet reactivity is higher in the normal delivery group than those in early fetal demise group (p < .05). High levels of platelet counts resulted in an adjusted odds ratio (OR) of 2.075 (95% confidence interval [95% CI], 1.215–3.544; p = .008) for early fetal demise. CONCLUSIONS: Increased platelet counts in the first trimester may be a predictor for the risk of early fetal demise. |
format | Online Article Text |
id | pubmed-8405072 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Taylor & Francis |
record_format | MEDLINE/PubMed |
spelling | pubmed-84050722021-08-31 The high platelet counts as predictor for early foetal demise Shao, Xiaowen Wang, Dandan Xu, Yue Guo, Ling Yang, Hui Zhou, Jieru Liang, Jiayi Qian, Jie Cheng, Jiajing Sun, Lihua Xiang, Yaozu Ann Med Pregnancy, Childbirth & Women's Health OBJECTIVES: Early fetal demise (absence of cardiac activity in a visible fetus) is a very common event, but there are no reliable biomarkers to predict it. The purpose of the study was to assess the association of platelet parameters with early fetal demise. METHODS: In this case-control study, we included women with normal deliveries or those ultrasound diagnosed as early fetal demise. For those who were identified with early fetal demise, the platelet parameters were analyzed before the ultrasound diagnosis, which is based on the absence of either an embryo within a gestational sac or cardiac activity in a visible embryo in the 5-10 weeks of gestation. The association between the risk of early fetal demise with the women's mean platelet volume (MPV) and platelet counts was calculated by logistic regression. Duplicate measurements of platelet aggregation were performed with VerifyNow. RESULTS: In total, 99 women identified with early fetal demise and 170 women who had an uncomplicated pregnancy with normal delivery from January 2017 and August 2020 were included in the study. We found that platelet counts in the early fetal demise group were significantly higher than healthy pregnancies. In addition, platelet reactivity is higher in the normal delivery group than those in early fetal demise group (p < .05). High levels of platelet counts resulted in an adjusted odds ratio (OR) of 2.075 (95% confidence interval [95% CI], 1.215–3.544; p = .008) for early fetal demise. CONCLUSIONS: Increased platelet counts in the first trimester may be a predictor for the risk of early fetal demise. Taylor & Francis 2021-08-25 /pmc/articles/PMC8405072/ /pubmed/34431412 http://dx.doi.org/10.1080/07853890.2021.1968027 Text en © 2021 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Pregnancy, Childbirth & Women's Health Shao, Xiaowen Wang, Dandan Xu, Yue Guo, Ling Yang, Hui Zhou, Jieru Liang, Jiayi Qian, Jie Cheng, Jiajing Sun, Lihua Xiang, Yaozu The high platelet counts as predictor for early foetal demise |
title | The high platelet counts as predictor for early foetal demise |
title_full | The high platelet counts as predictor for early foetal demise |
title_fullStr | The high platelet counts as predictor for early foetal demise |
title_full_unstemmed | The high platelet counts as predictor for early foetal demise |
title_short | The high platelet counts as predictor for early foetal demise |
title_sort | high platelet counts as predictor for early foetal demise |
topic | Pregnancy, Childbirth & Women's Health |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8405072/ https://www.ncbi.nlm.nih.gov/pubmed/34431412 http://dx.doi.org/10.1080/07853890.2021.1968027 |
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