Plasma Factor XIII Activity in Patients with Disseminated Intravascular Coagulation.
10.3349/ymj.2006.47.2.196
- Author:
Jae Woo SONG
1
;
Jong Rak CHOI
;
Kyung Soon SONG
;
Ji Hyuk RHEE
Author Information
1. Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea. kssong@yumc.yonsei.ac.kr
- Publication Type:Original Article ; Research Support, Non-U.S. Gov't
- Keywords:
Disseminated intravascular coagulation;
factor XIII;
hemostasis
- MeSH:
Prothrombin Time;
Platelet Count;
Partial Thromboplastin Time;
Middle Aged;
Male;
Liver Diseases/pathology;
Liver/pathology;
Kidney Diseases/pathology;
Kidney/pathology;
Inflammation;
Humans;
Hemostasis;
Fibrin Fibrinogen Degradation Products/biosynthesis;
Female;
Factor XIII/*biosynthesis;
Disseminated Intravascular Coagulation/*blood/*diagnosis;
Cross-Linking Reagents/pharmacology/therapeutic use;
Blood Coagulation Tests;
Aged;
Adult
- From:Yonsei Medical Journal
2006;47(2):196-200
- CountryRepublic of Korea
- Language:English
-
Abstract:
The objective of this study was to investigate the correlation between factor XIII (FXIII) activity and disseminated intravascular coagulation (DIC) parameters and also to evaluate the clinical usefulness of DIC diagnosis. Citrated plasma from eighty patients with potential DIC was analyzed for FXIII activity. The primary patient conditions (48 male and 32 female, mean age, 51 years) were malignancy (n = 29), infection (n = 25), inflammation (n = 6), heart disease (n= 3), thrombosis (n = 2), injury (n = 2), and other miscellaneous conditions (n = 13). FXIII testing was performed using the CoaLinkTM FXIII Incorporation Assay Kit (PeopleBio Inc.). Among 80 patients who were suspected to have DIC based on clinical analysis, 46 (57.5%) fulfilled the overt DIC criteria (DIC score > = 5) according to the International Society of Thrombosis and Haemostasis. FXIII levels in the plasma were significantly decreased in overt DIC compared to non-overt DIC patients (mean 75.1% and 199.7% respectively, p < 0.0001). Interestingly, we found a significant inverse correlation between DIC scores and FXIII activity. In addition, FXIII activity significantly correlated with other hemostatic markers that included platelet count, prothrombin time, activated partial thromboplastin time, fibrinogen, and D-dimer. FXIII levels were significantly lower in patients with liver or renal dysfunction. In conclusion, FXIII cross-linking activity measurements may have differential diagnostic value as well as predictive value in patients who are suspected to have DIC.
