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Characterization of intravascular cellular activation in relationship to subclinical atherosclerosis in postmenopausal women

OBJECTIVE: Mechanisms and interactions among intravascular cells contributing to development of subclinical atherosclerosis are poorly understood. In women, both menopausal status and pregnancy history influence progression of atherosclerosis. This study examined activation and interactions among bl...

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Autores principales: Jayachandran, Muthuvel, Garovic, Vesna D., Mielke, Michelle M., Bailey, Kent R., Lahr, Brian D., Miller, Virginia M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598935/
https://www.ncbi.nlm.nih.gov/pubmed/28910282
http://dx.doi.org/10.1371/journal.pone.0183159
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author Jayachandran, Muthuvel
Garovic, Vesna D.
Mielke, Michelle M.
Bailey, Kent R.
Lahr, Brian D.
Miller, Virginia M.
author_facet Jayachandran, Muthuvel
Garovic, Vesna D.
Mielke, Michelle M.
Bailey, Kent R.
Lahr, Brian D.
Miller, Virginia M.
author_sort Jayachandran, Muthuvel
collection PubMed
description OBJECTIVE: Mechanisms and interactions among intravascular cells contributing to development of subclinical atherosclerosis are poorly understood. In women, both menopausal status and pregnancy history influence progression of atherosclerosis. This study examined activation and interactions among blood elements with subclinical atherosclerosis in menopausal women with known pregnancy histories. METHODS: Carotid intima-media thickness (CIMT), as a marker of subclinical atherosclerosis, was measured using B-mode ultrasound in age- and parity-matched women [40 with and 40 without a history of preeclampsia] 35 years after the index pregnancy. Interactions among intravascular cells (38 parameters) were measured by flow cytometry in venous blood. Data analysis was by principal component which retained 7 independent dimensions accounting for 63% of the variability among 38 parameters. RESULTS: CIMT was significantly greater in women with a history of preeclampsia (P = 0.004). Platelet aggregation and platelet interactions with granulocytes and monocytes positively associated with CIMT in postmenopausal women independent of their pregnancy history (ρ = 0.258, P< 0.05). However, the association of the number of platelets, platelet activation and monocyte-platelet interactions with CIMT differed significantly depending upon pregnancy history (test for interaction, P<0.001). CONCLUSION: Interactions among actived intravascular cells and their association with subclinical atherosclerosis differ in women depending upon their pregnancy histories.
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spelling pubmed-55989352017-09-22 Characterization of intravascular cellular activation in relationship to subclinical atherosclerosis in postmenopausal women Jayachandran, Muthuvel Garovic, Vesna D. Mielke, Michelle M. Bailey, Kent R. Lahr, Brian D. Miller, Virginia M. PLoS One Research Article OBJECTIVE: Mechanisms and interactions among intravascular cells contributing to development of subclinical atherosclerosis are poorly understood. In women, both menopausal status and pregnancy history influence progression of atherosclerosis. This study examined activation and interactions among blood elements with subclinical atherosclerosis in menopausal women with known pregnancy histories. METHODS: Carotid intima-media thickness (CIMT), as a marker of subclinical atherosclerosis, was measured using B-mode ultrasound in age- and parity-matched women [40 with and 40 without a history of preeclampsia] 35 years after the index pregnancy. Interactions among intravascular cells (38 parameters) were measured by flow cytometry in venous blood. Data analysis was by principal component which retained 7 independent dimensions accounting for 63% of the variability among 38 parameters. RESULTS: CIMT was significantly greater in women with a history of preeclampsia (P = 0.004). Platelet aggregation and platelet interactions with granulocytes and monocytes positively associated with CIMT in postmenopausal women independent of their pregnancy history (ρ = 0.258, P< 0.05). However, the association of the number of platelets, platelet activation and monocyte-platelet interactions with CIMT differed significantly depending upon pregnancy history (test for interaction, P<0.001). CONCLUSION: Interactions among actived intravascular cells and their association with subclinical atherosclerosis differ in women depending upon their pregnancy histories. Public Library of Science 2017-09-14 /pmc/articles/PMC5598935/ /pubmed/28910282 http://dx.doi.org/10.1371/journal.pone.0183159 Text en © 2017 Jayachandran et al http://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/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Jayachandran, Muthuvel
Garovic, Vesna D.
Mielke, Michelle M.
Bailey, Kent R.
Lahr, Brian D.
Miller, Virginia M.
Characterization of intravascular cellular activation in relationship to subclinical atherosclerosis in postmenopausal women
title Characterization of intravascular cellular activation in relationship to subclinical atherosclerosis in postmenopausal women
title_full Characterization of intravascular cellular activation in relationship to subclinical atherosclerosis in postmenopausal women
title_fullStr Characterization of intravascular cellular activation in relationship to subclinical atherosclerosis in postmenopausal women
title_full_unstemmed Characterization of intravascular cellular activation in relationship to subclinical atherosclerosis in postmenopausal women
title_short Characterization of intravascular cellular activation in relationship to subclinical atherosclerosis in postmenopausal women
title_sort characterization of intravascular cellular activation in relationship to subclinical atherosclerosis in postmenopausal women
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5598935/
https://www.ncbi.nlm.nih.gov/pubmed/28910282
http://dx.doi.org/10.1371/journal.pone.0183159
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