Infect Chemother.  2009 Apr;41(2):78-81. 10.3947/ic.2009.41.2.78.

Clinical Significance of von Willebrand Factor-Cleaving Protease (ADAMTS13) Deficiency in Patients with Sepsis-Induced Disseminated Intravascular Coagulation

Affiliations
  • 1Department of Internal Medicine, Yonsei University Wonju College of Medicine, Wonju, Korea.
  • 2Department of Laboratory, Medicine, Hanaro Medical Foundation, Seoul, Korea. lee423619@hanmail.net
  • 3Department of Laboratory Medicine, Yonsei University College of Medicine, Seoul, Korea.
  • 4Department of Anesthesiology and Pain Medicine, Konyang University College of Medicine, Daejeon, Korea.

Abstract

BACKGROUND
Deficiency of von Willebrand factor-cleaving protease, a disintegrin-like and metalloprotease with thrombospondin type 1 motif 13 (ADAMTS13), is thought to be responsible for platelet aggregation and microthrombi formation, which in turn cause typical thrombotic microangiopathies. This deficiency is found in patients with thrombocytopenia-associated multiple organ failure such as thrombocytopenic purpura and disseminated intravascular coagulation (DIC). We evaluated the clinical significance of ADAMTS13 deficiency in patients with sepsis-induced DIC. MATERIALS AND METHODS: Nineteen patients with sepsis-induced DIC were enrolled. ADAMTS13 antigen levels were determined by Enzyme-Linked Immunosorbent Assay (ELISA) and activity levels were measured by fluorescence resonance energy transfer assay. Patients were categorized into two groups according to ADAMTS13 antigen level: less than 350 ng/mL or above. Clinical characteristics and survival were compared between the two groups. RESULTS: ADAMTS13 antigen level was less than 350 ng/mL in 7 patients and was above 350 ng/mL in 12 patients. There were no significant differences between the groups for age, sex, severity of illness, and other clinical characteristics. In patients with ADAMTS13 antigen level less than 350 ng/mL, in-hospital mortality was much higher (100% versus 25%, P=0.003) and 7-day survival was much shorter (P=0.023). CONCLUSION: Deficiency of ADAMTS13 could be thought to be associated with unfavorable outcome in patients with sepsis-induced DIC.

Keyword

ADAMTS13; Disseminated intravascular coagulation; Sepsis; Prognosis

MeSH Terms

Dacarbazine
Disseminated Intravascular Coagulation
Enzyme-Linked Immunosorbent Assay
Fluorescence Resonance Energy Transfer
Hospital Mortality
Humans
Multiple Organ Failure
Platelet Aggregation
Prognosis
Purpura, Thrombocytopenic
Sepsis
Thrombospondins
Thrombotic Microangiopathies
Dacarbazine
Thrombospondins

Figure

  • Figure 1 Cumulative survival in patients with sepsis-induced DIC according to the level of ADAMTS13


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