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Pilot study of novel lab methodology and testing of platelet function in adolescent women with heavy menstrual bleeding
INTRODUCTION: Approximately 40% of adolescent women experience heavy menstrual bleeding (HMB), and 10–62% of them have an underlying bleeding disorder (BD). Diagnosing BD remains challenging due to limitations of available clinical platelet function assays. AIM: To characterize platelet function in...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902421/ https://www.ncbi.nlm.nih.gov/pubmed/29166373 http://dx.doi.org/10.1038/pr.2017.298 |
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author | Rocheleau, Anne D. Khader, Ayesha Ngo, Anh T.P. Boehnlein, Colin McDavitt, Cara Lattimore, Susan Recht, Michael McCarty, Owen J.T. Haley, Kristina M. |
author_facet | Rocheleau, Anne D. Khader, Ayesha Ngo, Anh T.P. Boehnlein, Colin McDavitt, Cara Lattimore, Susan Recht, Michael McCarty, Owen J.T. Haley, Kristina M. |
author_sort | Rocheleau, Anne D. |
collection | PubMed |
description | INTRODUCTION: Approximately 40% of adolescent women experience heavy menstrual bleeding (HMB), and 10–62% of them have an underlying bleeding disorder (BD). Diagnosing BD remains challenging due to limitations of available clinical platelet function assays. AIM: To characterize platelet function in a population of adolescent women with HMB using small-volume whole blood assays. METHODS: Anticoagulated whole blood was used to assess platelet GPIIbIIIa activation, α-granule secretion, and aggregation in response to multiple agonists. Platelet adhesion on collagen or von Willebrand Factor (VWF) under static and shear flow was also assessed. RESULTS: Fifteen participants with HMB were included in the study, of which eight were diagnosed with a clinically-identifiable BD. Platelet activation was blunted in response to calcium ionophore in participants without a BD diagnosis compared to all other participants. Impaired GPIIbIIIa activation was observed in response to all GPCR agonists, except ADP, in participants with qualitative platelet disorders. Our assays detected platelet aggregation in the majority of participants with a BD in response to ADP, CRP, TRAP-6, or U46619. Platelet adhesion and aggregation on collagen and VWF was decreased for participants with VWD. CONCLUSION: Participants with and without BD exhibited aberrant platelet function in several assays in response to select agonists. |
format | Online Article Text |
id | pubmed-5902421 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
record_format | MEDLINE/PubMed |
spelling | pubmed-59024212018-07-03 Pilot study of novel lab methodology and testing of platelet function in adolescent women with heavy menstrual bleeding Rocheleau, Anne D. Khader, Ayesha Ngo, Anh T.P. Boehnlein, Colin McDavitt, Cara Lattimore, Susan Recht, Michael McCarty, Owen J.T. Haley, Kristina M. Pediatr Res Article INTRODUCTION: Approximately 40% of adolescent women experience heavy menstrual bleeding (HMB), and 10–62% of them have an underlying bleeding disorder (BD). Diagnosing BD remains challenging due to limitations of available clinical platelet function assays. AIM: To characterize platelet function in a population of adolescent women with HMB using small-volume whole blood assays. METHODS: Anticoagulated whole blood was used to assess platelet GPIIbIIIa activation, α-granule secretion, and aggregation in response to multiple agonists. Platelet adhesion on collagen or von Willebrand Factor (VWF) under static and shear flow was also assessed. RESULTS: Fifteen participants with HMB were included in the study, of which eight were diagnosed with a clinically-identifiable BD. Platelet activation was blunted in response to calcium ionophore in participants without a BD diagnosis compared to all other participants. Impaired GPIIbIIIa activation was observed in response to all GPCR agonists, except ADP, in participants with qualitative platelet disorders. Our assays detected platelet aggregation in the majority of participants with a BD in response to ADP, CRP, TRAP-6, or U46619. Platelet adhesion and aggregation on collagen and VWF was decreased for participants with VWD. CONCLUSION: Participants with and without BD exhibited aberrant platelet function in several assays in response to select agonists. 2018-01-03 2018-03 /pmc/articles/PMC5902421/ /pubmed/29166373 http://dx.doi.org/10.1038/pr.2017.298 Text en http://www.nature.com/authors/editorial_policies/license.html#terms Users may view, print, copy, and download text and data-mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use:http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Rocheleau, Anne D. Khader, Ayesha Ngo, Anh T.P. Boehnlein, Colin McDavitt, Cara Lattimore, Susan Recht, Michael McCarty, Owen J.T. Haley, Kristina M. Pilot study of novel lab methodology and testing of platelet function in adolescent women with heavy menstrual bleeding |
title | Pilot study of novel lab methodology and testing of platelet function in adolescent women with heavy menstrual bleeding |
title_full | Pilot study of novel lab methodology and testing of platelet function in adolescent women with heavy menstrual bleeding |
title_fullStr | Pilot study of novel lab methodology and testing of platelet function in adolescent women with heavy menstrual bleeding |
title_full_unstemmed | Pilot study of novel lab methodology and testing of platelet function in adolescent women with heavy menstrual bleeding |
title_short | Pilot study of novel lab methodology and testing of platelet function in adolescent women with heavy menstrual bleeding |
title_sort | pilot study of novel lab methodology and testing of platelet function in adolescent women with heavy menstrual bleeding |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5902421/ https://www.ncbi.nlm.nih.gov/pubmed/29166373 http://dx.doi.org/10.1038/pr.2017.298 |
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