White blood cell count measured prior to cancer development is associated with future risk of venous thromboembolism--the Tromsø study.

BACKGROUND: Elevated white blood cell (WBC) count is associated with risk of venous thromboembolism (VTE) in cancer patients initiating chemotherapy. It is not known whether the risk of VTE by WBC count in cancer patients is causal or merely a consequence of the malignant disease. To address this qu...

Full description

Bibliographic Details
Main Authors: Kristine Blix, Hilde Jensvoll, Sigrid K Brækkan, John-Bjarne Hansen
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2013-01-01
Series:PLoS ONE
Online Access:http://europepmc.org/articles/PMC3762748?pdf=render
id doaj-1204cd99c86641a18f7dc3496cafd969
record_format Article
spelling doaj-1204cd99c86641a18f7dc3496cafd9692020-11-25T00:47:04ZengPublic Library of Science (PLoS)PLoS ONE1932-62032013-01-0189e7344710.1371/journal.pone.0073447White blood cell count measured prior to cancer development is associated with future risk of venous thromboembolism--the Tromsø study.Kristine BlixHilde JensvollSigrid K BrækkanJohn-Bjarne HansenBACKGROUND: Elevated white blood cell (WBC) count is associated with risk of venous thromboembolism (VTE) in cancer patients initiating chemotherapy. It is not known whether the risk of VTE by WBC count in cancer patients is causal or merely a consequence of the malignant disease. To address this question, we studied the association between WBC count, measured prior to cancer development, and risk of VTE in subjects who did and did not develop cancer during follow-up in a prospective population-based study. METHODS: Baseline characteristics, including WBC and neutrophil counts, were measured in 24304 initially cancer-free subjects who participated in the Tromsø Study in 1994-1995. Incident cancer diagnosis and VTE events were registered up to September 1, 2007. In the cancer cohort, WBC and neutrophil counts were measured in average 7.1 years before cancer development. Cox-regression models were used to calculate hazard ratios (HRs) for VTE by WBC and neutrophil counts as categorized variables (<40(th), 40-80(th), and >80(th) percentile) with 95% confidence intervals (CIs). RESULTS: During follow-up, 1720 subjects developed cancer and there were 388 VTE events, of which 116 occurred in the cancer-group (6.9 per 1000 person-years) and 272 in the cancer-free group (1.1 per 1000 person-years). In those who developed cancer, WBC count above the 80(th) percentile (≥ 8.6 x 10(9) cells/L) was associated with a 2.4-fold higher risk (HR 2.36, 95% CI: 1.44-3.87) of VTE compared to WBC count below the 40(th) percentile (<6.4 x 10(9) cells/L). No association was found between WBC count and VTE in those who stayed cancer-free (HR 0.94, 95% CI 0.65-1.36). Similar findings were observed for neutrophils. COMMENT: Pre-cancer WBC count was associated with risk of VTE in cancer patients, but not in cancer-free subjects. Our findings suggest that leukocytes may play a causal role in cancer-related VTE rather than only reflecting the low-grade inflammation associated with cancer.http://europepmc.org/articles/PMC3762748?pdf=render
collection DOAJ
language English
format Article
sources DOAJ
author Kristine Blix
Hilde Jensvoll
Sigrid K Brækkan
John-Bjarne Hansen
spellingShingle Kristine Blix
Hilde Jensvoll
Sigrid K Brækkan
John-Bjarne Hansen
White blood cell count measured prior to cancer development is associated with future risk of venous thromboembolism--the Tromsø study.
PLoS ONE
author_facet Kristine Blix
Hilde Jensvoll
Sigrid K Brækkan
John-Bjarne Hansen
author_sort Kristine Blix
title White blood cell count measured prior to cancer development is associated with future risk of venous thromboembolism--the Tromsø study.
title_short White blood cell count measured prior to cancer development is associated with future risk of venous thromboembolism--the Tromsø study.
title_full White blood cell count measured prior to cancer development is associated with future risk of venous thromboembolism--the Tromsø study.
title_fullStr White blood cell count measured prior to cancer development is associated with future risk of venous thromboembolism--the Tromsø study.
title_full_unstemmed White blood cell count measured prior to cancer development is associated with future risk of venous thromboembolism--the Tromsø study.
title_sort white blood cell count measured prior to cancer development is associated with future risk of venous thromboembolism--the tromsø study.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2013-01-01
description BACKGROUND: Elevated white blood cell (WBC) count is associated with risk of venous thromboembolism (VTE) in cancer patients initiating chemotherapy. It is not known whether the risk of VTE by WBC count in cancer patients is causal or merely a consequence of the malignant disease. To address this question, we studied the association between WBC count, measured prior to cancer development, and risk of VTE in subjects who did and did not develop cancer during follow-up in a prospective population-based study. METHODS: Baseline characteristics, including WBC and neutrophil counts, were measured in 24304 initially cancer-free subjects who participated in the Tromsø Study in 1994-1995. Incident cancer diagnosis and VTE events were registered up to September 1, 2007. In the cancer cohort, WBC and neutrophil counts were measured in average 7.1 years before cancer development. Cox-regression models were used to calculate hazard ratios (HRs) for VTE by WBC and neutrophil counts as categorized variables (<40(th), 40-80(th), and >80(th) percentile) with 95% confidence intervals (CIs). RESULTS: During follow-up, 1720 subjects developed cancer and there were 388 VTE events, of which 116 occurred in the cancer-group (6.9 per 1000 person-years) and 272 in the cancer-free group (1.1 per 1000 person-years). In those who developed cancer, WBC count above the 80(th) percentile (≥ 8.6 x 10(9) cells/L) was associated with a 2.4-fold higher risk (HR 2.36, 95% CI: 1.44-3.87) of VTE compared to WBC count below the 40(th) percentile (<6.4 x 10(9) cells/L). No association was found between WBC count and VTE in those who stayed cancer-free (HR 0.94, 95% CI 0.65-1.36). Similar findings were observed for neutrophils. COMMENT: Pre-cancer WBC count was associated with risk of VTE in cancer patients, but not in cancer-free subjects. Our findings suggest that leukocytes may play a causal role in cancer-related VTE rather than only reflecting the low-grade inflammation associated with cancer.
url http://europepmc.org/articles/PMC3762748?pdf=render
work_keys_str_mv AT kristineblix whitebloodcellcountmeasuredpriortocancerdevelopmentisassociatedwithfutureriskofvenousthromboembolismthetromsøstudy
AT hildejensvoll whitebloodcellcountmeasuredpriortocancerdevelopmentisassociatedwithfutureriskofvenousthromboembolismthetromsøstudy
AT sigridkbrækkan whitebloodcellcountmeasuredpriortocancerdevelopmentisassociatedwithfutureriskofvenousthromboembolismthetromsøstudy
AT johnbjarnehansen whitebloodcellcountmeasuredpriortocancerdevelopmentisassociatedwithfutureriskofvenousthromboembolismthetromsøstudy
_version_ 1725262125289439232