2002
DOI: 10.1016/s0002-9343(02)01345-1
|View full text |Cite
|
Sign up to set email alerts
|

Coagulation factors, inflammation markers, and venous thromboembolism: the longitudinal investigation of thromboembolism etiology (LITE)

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
1
1

Citation Types

23
328
5
3

Year Published

2003
2003
2016
2016

Publication Types

Select...
6
3

Relationship

4
5

Authors

Journals

citations
Cited by 341 publications
(361 citation statements)
references
References 28 publications
23
328
5
3
Order By: Relevance
“…They concluded that this may be due to cumulative age-related risk factors. In the LITE study consisting only of those above age 45, elevated fibrinogen, even at extreme levels, was not a VT risk factor in our previous report [18] and in updated data here.…”
Section: Discussionsupporting
confidence: 60%
See 1 more Smart Citation
“…They concluded that this may be due to cumulative age-related risk factors. In the LITE study consisting only of those above age 45, elevated fibrinogen, even at extreme levels, was not a VT risk factor in our previous report [18] and in updated data here.…”
Section: Discussionsupporting
confidence: 60%
“…Elevated fibrinogen levels may increase the risk of VT, though this has not been observed consistently [13,18,19]. The fibrinogen -455 G/A polymorphism is located on the β chain in the promoter region and has been associated with higher fibrinogen levels [14,20,21].…”
mentioning
confidence: 99%
“…7 However, none of these factors were associated with the risk of venous thrombosis in the LITE population, and none were confounders of the D-dimer association with venous thromboembolism. 28 Third, because fibrinolytic factors, such as plasminogen activator inhibitor-1 and tissue plasminogen activator, are not generally considered risk factors for venous thrombosis, 29,30 it is likely that higher D-dimer reflects increased fibrin formation rather than fibrinolytic reactivity. Our findings and those of others [5][6][7][8][9][11][12][13] would support further study of phenotypic and genotypic determinants of fibrin formation.…”
Section: Discussionmentioning
confidence: 99%
“…24 Considering levels of factors VIII, IX, XI, fibrinogen, homocysteine, anticoagulant factor deficiencies (proteins C, S and antithrombin), factor V Leiden and prothrombin 20210A, only elevated fibrinogen (> 4.1 g/L) and anticoagulant deficiencies were associated with an elevated recurrence risk (relative risks 1.7 and 1.8, respectively). It is debatable whether elevated fibrinogen is a risk factor for first VT. 25 In a recent 5.6 year study of families with thrombosis attributed to factor V Leiden or deficiencies of anticoagulant proteins, antithrombin deficiency was associated with the highest incidence of recurrent VT (10.5% yearly), and factor V Leiden the lowest incidence (3.5% yearly). 26 In general it is likely that patients with thrombophilic defects who belong to families with a thrombosis history are more likely to have recurrence than unselected patients with thrombophilic defects.…”
Section: Benefits Of Thrombophilia Testingmentioning
confidence: 99%