Circulating tissue factor procoagulant activity is elevated in stable moderate to severe chronic obstructive pulmonary disease
Chronic obstructive pulmonary disease (COPD) patients have increased risk for cardiovascular mortality and venous thromboembolism. Tissue factor (TF) is the physiological initiating mechanism for blood coagulation and is pro-inflammatory. We have studied circulating blood-borne TF-procoagulant activ...
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Published in | Thrombosis research Vol. 124; no. 3; pp. 259 - 261 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
United States
Elsevier Ltd
01.07.2009
|
Subjects | |
Online Access | Get full text |
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Summary: | Chronic obstructive pulmonary disease (COPD) patients have increased risk for cardiovascular mortality and venous thromboembolism. Tissue factor (TF) is the physiological initiating mechanism for blood coagulation and is pro-inflammatory.
We have studied circulating blood-borne TF-procoagulant activity (TF-PCA), plasma coagulation factors (F) VIIa and FVIII, and thrombin-antithrombin (TAT) complexes in 11 stable, moderate-severe COPD patients, 10 free of exacerbation for >
3 weeks.
TF-PCA was increased in COPD patients (52.3
±
5.6 U/ml, (SE)) compared to control subjects (20.7
±
1.5, n
=
45, p
<
0.0001). TAT levels were increased (COPD patients: 2.99
±
0.65 ug/l; control subjects: 1.31
±
0.13, n
=
53, p
<
0.0001), indicating enhanced thrombin generation. Plasma FVIIa (the activated form of FVII) was higher in COPD (83
±
11 mU/ml; controls, 64
±
5 mU/ml, n
=
20) but did not reach statistical significance. Plasma FVIIc and FVIII were not increased. TF-PCA levels were inversely related to plasma FVIIa (r
=
-
0.80, p
=
0.003) and FVIIc (r
=
-
0.76, p
=
0.007).
Blood-borne TF-PCA is elevated and constitutes a prothrombotic and proinflammatory state in stable but moderate-severe COPD, and may contribute to the increased risk for vascular events. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0049-3848 1879-2472 1879-2472 |
DOI: | 10.1016/j.thromres.2008.12.030 |