Do antiphospholipid antibodies interfere with tissue factor pathway inhibitor?

Citation
Em. Jacobsen et al., Do antiphospholipid antibodies interfere with tissue factor pathway inhibitor?, THROMB RES, 94(4), 1999, pp. 213-220
Citations number
31
Categorie Soggetti
Cardiovascular & Hematology Research
Journal title
THROMBOSIS RESEARCH
ISSN journal
00493848 → ACNP
Volume
94
Issue
4
Year of publication
1999
Pages
213 - 220
Database
ISI
SICI code
0049-3848(19990515)94:4<213:DAAIWT>2.0.ZU;2-3
Abstract
This study was conducted to investigate whether antiphospholipid antibodies (APA) can interfere with the phospholipid-dependent inhibition of coagulat ion exerted by tissue factor pathway inhibitor (TFPI). Eleven patients with APA and eleven healthy controls matched for age and gender were enrolled. Blood samples were drawn before and 5 minutes after an intravenous injectio n of unfractionated heparin 5000 IE, which is known to cause TFPI release i n healthy individuals. The preheparin samples showed significantly higher T FPI free antigen levels in the APA positive patients than in the controls ( 21.7 vs. 14.2 ng/ml, p=0.03). TFPI activity as measured in a chromogenic su bstrate assay also was higher in patients, but this difference was not stat istically significant (1.13 vs. 1.01 U/ml, p=0.2). The TFPI levels showed a considerable rise in both patients and controls after heparin injection. I n both assays, the postheparin levels were significantly higher in patients than in controls (TFPI antigen: 179 vs. 153 ng/ml, p=0.05; TFPI activity: 3.26 vs. 2.51 U/ml,p=0.03). A modified diluted prothrombin time assay (dPT) was used to measure TFPI anticoagulant activity. In this assay, samples fr om the patients with the strongest effect of lupus anticoagulants (LAs) on preheparin coagulation times showed little or no increase after heparin inj ection. This result may reflect an inhibition of TFPI anticoagulant activit y by strong LAs. In conclusion, we have found that patients with APA have h igher TFPI amidolytic activity/antigen level both before and after heparin stimulation of TFPI release. These observations do not explain the higher t hrombotic risk in these patients but may reflect an upregulated tissue fact or activity, which has been demonstrated in these patients. TFPI anticoagul ant activity, however, as measured in a dPT assay, may be inhibited by stro ng LAs. (C) 1999 Elsevier Science Ltd. All rights reserved.