Circulating levels of DNA-histone complex and dsDNA are independent prognostic factors of disseminated intravascular coagulation. Issue 6 (June 2015)

• Record Type: Journal Article
• Authors: Kim, Ji-Eun; Lee, Nuri; Gu, Ja-Yoon; Yoo, Hyun Ju; Kim, Hyun Kyung
• Is Part Of: Thrombosis research. Volume 135:Issue 6(2015)
• Page Start: 1064
• Page End: 1069
• Publication Date: 2015-06
• Subjects: NET neutrophil extracellular trap -- DIC disseminated intravascular coagulation -- dsDNA double-stranded DNA -- ISTH International Society of Thrombosis and Haemostasis -- PT prothrombin time -- aPTT activated partial thromboplastin time -- ROC receiver operating characteristic -- DNase deoxyribonuclease; Neutrophil extracellular trap (NET) -- D-dimer -- DIC score -- Coagulation -- Cancer; Thrombosis -- Periodicals; 616.135
• DOI: 10.1016/j.thromres.2015.03.014
• Languages: English
• ISSNs: 0049-3848

Abstract

Abstract: Introduction: Neutrophils can be induced to release DNA combined with histones. The resulting neutrophil extracellular trap (NET) provides a scaffold for growing hemostatic plug. Therefore, the NET formation may be inevitable in clinical conditions that are characterized by formation of vascular thrombi. Thus far, there have been no reports on the clinical significance of NET in disseminated intravascular coagulation (DIC). Therefore, we investigated circulating levels of NET in DIC and analyzed their potential values to assess coagulation severity and predict clinical outcome. Methods: The plasma levels of DNA-histone complexes and double-stranded DNA (dsDNA), considered to be in vivo markers of NET, were measured in 199 patients suspected of having DIC and 20 healthy controls. Result: The circulating levels of DNA-histone complexes and dsDNA were significantly elevated in overt-DIC. The increased levels of these two markers correlated with the severity of coagulopathy including DIC score and D-dimer. Multivariable Cox regression analysis, adjusted for the conventional DIC markers, revealed that elevated DNA-histone complexes and dsDNA are poor independent prognostic markers. Conclusion: The circulating levels of NET release reflect the coagulation activation and adverse clinical outcomes in patients with DIC, thereby providing potential clinical relevance for mortality prediction in DIC. Highlights: The circulating levels of DNA-histones complexes and dsDNA were significantly elevated in over-DIC. The circulating DNA-histone complexes and dsDNA correlated well with DIC severity. The high levels of circulating DNA-histone complexes and dsDNA showed significantly independent prognostic values in DIC, providing potential clinical relevance for mortality prediction in DIC.