4.7 Article

The impact of neutrophil extracellular traps on deep venous thrombosis in patients with traumatic fractures

Journal

CLINICA CHIMICA ACTA
Volume 519, Issue -, Pages 231-238

Publisher

ELSEVIER
DOI: 10.1016/j.cca.2021.04.021

Keywords

Deep venous thrombosis; Neutrophil extracellular traps; Traumatic fractures; Citrullinated Histone H3; Cell-free DNA

Funding

  1. Beijing Health System 215 talented investigators fund [2015-3-034]
  2. Ministry of Education research fund for study abroad [2013-693]
  3. Science and Technology activities for overseas students of the Ministry of Human Resources and Social Security [[2015]192]

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This study investigated the role of NETs in thrombosis in patients with traumatic fractures and found that H3Cit and cfDNA can assist in the diagnosis of DVT in these patients. The study suggests that NET biomarkers may be used to predict the risk of thrombosis in such patients.
Background: Deep venous thrombosis (DVT) is the most common complication in patients with traumatic fractures. The neutrophil extracellular traps (NETs) can promote thrombus formation. In this prospective study, we investigated the role of NETs in thrombosis in patients with traumatic fractures to evaluate whether the biomarkers of NETs can be used to help predict the risk of thrombosis. Methods: Traumatic fracture patients were enrolled in this prospective observational cohort study. Healthy controls (Control); patients with lower extremity fractures who neither present with nor develop DVT (Trauma non-DVT); patients with lower extremity fractures who do not present with DVT but do develop DVT (Trauma DVT); and patients with lower extremity fractures who present with DVT (DVT) were included. NETs biomarker levels of Citrullinated Histone H3 (H3Cit), cell-free DNA (cfDNA) and nucleosomes in the plasma were determined. The D-dimer and fibrin(-ogen) degradation products (FDP) level in plasma was measured. Statistical analysis of the test results was performed to assess changes in NETs biomarker levels during thrombosis in patients with traumatic fractures. Results: The H3Cit levels in the DVT group were significantly greater than in the Trauma non-DVT group and Trauma DVT group (1.88(1.11, 3.35) ng/ml Vs 0.38(0.10, 1.17) ng/ml, P <= 0.05). The level of cfDNA was significantly greater in patients with traumatic fractures and was higher after thrombosis than before. The levels of D-dimer in the DVT, Trauma DVT, and Trauma non-DVT groups were significantly greater than in the Control group (5.11(3.97, 8.11) mg/l; 6.12(2.59, 18.49) mg/l; 2.99(0.99, 9.02) mg/l Vs 0.18(0.08,0.24) mg/l, P < 0.05). The distribution of FDP levels in each group was similar to that of D-dimer. Data are presented as medians (25th percentile, 75th percentile). Conclusions: NETs released by neutrophils are involved in the formation of DVTs in patients with traumatic fractures. H3Cit and cfDNA can assist the diagnosis of DVT in patients with traumatic fractures.

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