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Menstrual Phase Affects Coagulation and Hematological Parameters during Central Hypovolemia

Background: It has been reported that women have a higher number of heart attacks in the “follicular phase” of the menstrual cycle. We, therefore, tested the hypothesis that women in the follicular phase exhibit higher coagulability. As lower body negative pressure (LBNP) has been used previously to...

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Autores principales: Goswami, Nandu, Brix, Bianca, Roessler, Andreas, Koestenberger, Martin, Reibnegger, Gilbert, Cvirn, Gerhard
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600806/
https://www.ncbi.nlm.nih.gov/pubmed/32992471
http://dx.doi.org/10.3390/jcm9103118
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author Goswami, Nandu
Brix, Bianca
Roessler, Andreas
Koestenberger, Martin
Reibnegger, Gilbert
Cvirn, Gerhard
author_facet Goswami, Nandu
Brix, Bianca
Roessler, Andreas
Koestenberger, Martin
Reibnegger, Gilbert
Cvirn, Gerhard
author_sort Goswami, Nandu
collection PubMed
description Background: It has been reported that women have a higher number of heart attacks in the “follicular phase” of the menstrual cycle. We, therefore, tested the hypothesis that women in the follicular phase exhibit higher coagulability. As lower body negative pressure (LBNP) has been used previously to assess coagulation changes in whole blood (WB) samples in men and women, effects of menstrual phase on coagulation was assessed during LBNP. Methods: Seven women, all healthy young participants, with no histories of thrombotic disorders and not on medications, were tested in two phases of the menstrual cycle (early follicular (EF) and mid-luteal (ML)). LBNP was commenced at −10 mmHg and increased by −10 mmHg every 5 min until a maximum of −40 mmHg. Recovery up to 10 min was also monitored. Blood samples were collected at baseline, at end of LBNP, and at end of recovery. Hemostatic profiling included comparing the effects of LBNP on coagulation values in both phases of the menstrual cycle using standard coagulation tests, calibrated automated thrombogram, thrombelastometry, impedance aggregometry, and markers of thrombin formation. Results: LBNP led to coagulation activation determined in both plasma and WB samples. During both phases, coagulation was affected during LBNP, as reflected in their decreased partial thromboplastin time (PTT) and elevated coagulation factor VIII FVIII, F1 + 2, and thrombin-antithrombin (TAT) levels. Additionally, during the ML phase, greater PT [%] and shorter time to peak (ttPeak) values (implying faster maximum thrombin formation) suggest that women in the ML phase are relatively hypercoagulable compared to the early follicular phase. Conclusions: These results suggest that thrombosis occurs more during the midluteal phase, a finding with substantial medical implications.
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spelling pubmed-76008062020-11-01 Menstrual Phase Affects Coagulation and Hematological Parameters during Central Hypovolemia Goswami, Nandu Brix, Bianca Roessler, Andreas Koestenberger, Martin Reibnegger, Gilbert Cvirn, Gerhard J Clin Med Article Background: It has been reported that women have a higher number of heart attacks in the “follicular phase” of the menstrual cycle. We, therefore, tested the hypothesis that women in the follicular phase exhibit higher coagulability. As lower body negative pressure (LBNP) has been used previously to assess coagulation changes in whole blood (WB) samples in men and women, effects of menstrual phase on coagulation was assessed during LBNP. Methods: Seven women, all healthy young participants, with no histories of thrombotic disorders and not on medications, were tested in two phases of the menstrual cycle (early follicular (EF) and mid-luteal (ML)). LBNP was commenced at −10 mmHg and increased by −10 mmHg every 5 min until a maximum of −40 mmHg. Recovery up to 10 min was also monitored. Blood samples were collected at baseline, at end of LBNP, and at end of recovery. Hemostatic profiling included comparing the effects of LBNP on coagulation values in both phases of the menstrual cycle using standard coagulation tests, calibrated automated thrombogram, thrombelastometry, impedance aggregometry, and markers of thrombin formation. Results: LBNP led to coagulation activation determined in both plasma and WB samples. During both phases, coagulation was affected during LBNP, as reflected in their decreased partial thromboplastin time (PTT) and elevated coagulation factor VIII FVIII, F1 + 2, and thrombin-antithrombin (TAT) levels. Additionally, during the ML phase, greater PT [%] and shorter time to peak (ttPeak) values (implying faster maximum thrombin formation) suggest that women in the ML phase are relatively hypercoagulable compared to the early follicular phase. Conclusions: These results suggest that thrombosis occurs more during the midluteal phase, a finding with substantial medical implications. MDPI 2020-09-27 /pmc/articles/PMC7600806/ /pubmed/32992471 http://dx.doi.org/10.3390/jcm9103118 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Goswami, Nandu
Brix, Bianca
Roessler, Andreas
Koestenberger, Martin
Reibnegger, Gilbert
Cvirn, Gerhard
Menstrual Phase Affects Coagulation and Hematological Parameters during Central Hypovolemia
title Menstrual Phase Affects Coagulation and Hematological Parameters during Central Hypovolemia
title_full Menstrual Phase Affects Coagulation and Hematological Parameters during Central Hypovolemia
title_fullStr Menstrual Phase Affects Coagulation and Hematological Parameters during Central Hypovolemia
title_full_unstemmed Menstrual Phase Affects Coagulation and Hematological Parameters during Central Hypovolemia
title_short Menstrual Phase Affects Coagulation and Hematological Parameters during Central Hypovolemia
title_sort menstrual phase affects coagulation and hematological parameters during central hypovolemia
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7600806/
https://www.ncbi.nlm.nih.gov/pubmed/32992471
http://dx.doi.org/10.3390/jcm9103118
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