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Hematocrit and incidence of venous thromboembolism

BACKGROUND: Patients with polycythemia vera with high hematocrit have increased risk of venous thromboembolism (VTE). OBJECTIVE: To determine whether high hematocrit in the general population is also associated with elevated VTE risk. METHODS: The prospective Atherosclerosis Risk in Communities Stud...

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Autores principales: Folsom, Aaron R., Wang, Wendy, Parikh, Romil, Lutsey, Pamela L., Beckman, Joan D., Cushman, Mary
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086464/
https://www.ncbi.nlm.nih.gov/pubmed/32211576
http://dx.doi.org/10.1002/rth2.12325
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author Folsom, Aaron R.
Wang, Wendy
Parikh, Romil
Lutsey, Pamela L.
Beckman, Joan D.
Cushman, Mary
author_facet Folsom, Aaron R.
Wang, Wendy
Parikh, Romil
Lutsey, Pamela L.
Beckman, Joan D.
Cushman, Mary
author_sort Folsom, Aaron R.
collection PubMed
description BACKGROUND: Patients with polycythemia vera with high hematocrit have increased risk of venous thromboembolism (VTE). OBJECTIVE: To determine whether high hematocrit in the general population is also associated with elevated VTE risk. METHODS: The prospective Atherosclerosis Risk in Communities Study performed a complete blood count in 13 891 adults aged 45 to 64 in 1987 to 1989. We identified incident hospitalized VTEs through 2015 and performed proportional hazards regression analyses using race‐sex–specific categorization of hematocrit percentiles (ie, <5th, 5th to <25th, 25th to <75th, 75th to <95th, and 95th‐100th percentiles, with the 25th to <75th percentile serving as the reference). RESULTS: Over a median follow‐up of 26 years, 800 participants had an incident venous thrombosis of the leg and/or a pulmonary embolism. There was a nonlinear association of hematocrit with VTE incidence, with risk elevated 72% for participants above the 95th percentile of hematocrit compared with the reference. Specifically, hazard ratios (95% confidence intervals) of incident VTE were 1.27 (0.91‐1.76), 1.06 (0.87‐1.28), 1 (reference), 1.17 (0.98‐1.40) and 1.72 (1.30‐2.27) across the 5 hematocrit percentiles, adjusted for age, race, sex, body mass index, smoking status and pack‐years, and other confounding variables. The association of high hematocrit with VTE was limited to provoked VTE, with little evidence for unprovoked VTE. Hemoglobin above the 95th percentile also was associated with an increased risk of VTE. In contrast, there were no significant associations of platelet, leukocyte, neutrophil, or lymphocyte counts with VTE incidence. CONCLUSION: High hematocrit and hemoglobin in a general middle‐aged population sample were associated with increased long‐term risk of VTE, particularly provoked VTE.
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spelling pubmed-70864642020-03-24 Hematocrit and incidence of venous thromboembolism Folsom, Aaron R. Wang, Wendy Parikh, Romil Lutsey, Pamela L. Beckman, Joan D. Cushman, Mary Res Pract Thromb Haemost Original Articles: Thrombosis BACKGROUND: Patients with polycythemia vera with high hematocrit have increased risk of venous thromboembolism (VTE). OBJECTIVE: To determine whether high hematocrit in the general population is also associated with elevated VTE risk. METHODS: The prospective Atherosclerosis Risk in Communities Study performed a complete blood count in 13 891 adults aged 45 to 64 in 1987 to 1989. We identified incident hospitalized VTEs through 2015 and performed proportional hazards regression analyses using race‐sex–specific categorization of hematocrit percentiles (ie, <5th, 5th to <25th, 25th to <75th, 75th to <95th, and 95th‐100th percentiles, with the 25th to <75th percentile serving as the reference). RESULTS: Over a median follow‐up of 26 years, 800 participants had an incident venous thrombosis of the leg and/or a pulmonary embolism. There was a nonlinear association of hematocrit with VTE incidence, with risk elevated 72% for participants above the 95th percentile of hematocrit compared with the reference. Specifically, hazard ratios (95% confidence intervals) of incident VTE were 1.27 (0.91‐1.76), 1.06 (0.87‐1.28), 1 (reference), 1.17 (0.98‐1.40) and 1.72 (1.30‐2.27) across the 5 hematocrit percentiles, adjusted for age, race, sex, body mass index, smoking status and pack‐years, and other confounding variables. The association of high hematocrit with VTE was limited to provoked VTE, with little evidence for unprovoked VTE. Hemoglobin above the 95th percentile also was associated with an increased risk of VTE. In contrast, there were no significant associations of platelet, leukocyte, neutrophil, or lymphocyte counts with VTE incidence. CONCLUSION: High hematocrit and hemoglobin in a general middle‐aged population sample were associated with increased long‐term risk of VTE, particularly provoked VTE. John Wiley and Sons Inc. 2020-03-11 /pmc/articles/PMC7086464/ /pubmed/32211576 http://dx.doi.org/10.1002/rth2.12325 Text en © 2020 The Authors. Research and Practice in Thrombosis and Haemostasis published by Wiley Periodicals, Inc on behalf of International Society on Thrombosis and Haemostasis. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Articles: Thrombosis
Folsom, Aaron R.
Wang, Wendy
Parikh, Romil
Lutsey, Pamela L.
Beckman, Joan D.
Cushman, Mary
Hematocrit and incidence of venous thromboembolism
title Hematocrit and incidence of venous thromboembolism
title_full Hematocrit and incidence of venous thromboembolism
title_fullStr Hematocrit and incidence of venous thromboembolism
title_full_unstemmed Hematocrit and incidence of venous thromboembolism
title_short Hematocrit and incidence of venous thromboembolism
title_sort hematocrit and incidence of venous thromboembolism
topic Original Articles: Thrombosis
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7086464/
https://www.ncbi.nlm.nih.gov/pubmed/32211576
http://dx.doi.org/10.1002/rth2.12325
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