From: Clinical significance of neutrophil extracellular traps biomarkers in thrombosis
First author/year | Study design | Included patients | Groups (No. patients) | Samples processing | NETs biomarkers | Analytical methods for NETs biomarkers | Detailed values |
---|---|---|---|---|---|---|---|
Thålin et al (2016) [88] | Case–control | Patients with IS | Cancers (n = 8) vs. No cancers (n = 23) | Plasma, 2000 × g, 20 min | H3Cit | ELISA | 0.22 vs. 0.07 OD |
MPO | ELISA | 74.1 vs. 37.8Â ng/mL | |||||
DNA | PicoGreen fluorimetry | 504.0 vs. 407.9Â ng/mL | |||||
Mauracher et al (2018) [94] | Cohort | Adult patients with newly diagnosed malignancy or progression of disease after remission | VTE (n = 89) vs. No VTE (n = 857) | Plasma, 3000 × g, 10 min | H3Cit | ELISA | 52.4 vs. 24.1 ng/mL |
Nucleosomes | ELISA | 1.3 vs. 1.2 MoM | |||||
DNA | PicoGreen fluorimetry | 384.5 vs. 355.8Â ng/mL | |||||
Bang et al (2019) [95] | Case–control | Patients with active cancer | Cancer-stroke (n = 38) vs. Stroke-control (n = 40) vs. Cancer-control (n = 27) vs. HC (n = 33) | Plasma, 2000 × g, 15 min | Nucleosomes | ELISA | 0.379 vs. 0.189 vs. 0.251 vs. 0.194 OD |
DNA | PicoGreen fluorimetry | 40.35 vs. 34.38 vs. 34.52 vs. 30.48Â mg/mL | |||||
Grilz et al (2019) [96] | Cohort | Adult patients with newly diagnosed malignancy or a progression of disease after complete or partial remission | ATE (n = 22) vs. No ATE (n = 935) | Plasma, 3000 × g, 10 min | H3Cit | ELISA | NA |
Nucleosomes | ELISA | NA | |||||
DNA | PicoGreen fluorimetry | NA | |||||
Guy et al (2019) [98] | Case–control | Patients with MPN | Thrombosis (n = 16) vs. No thrombosis (n = 15) | Plasma, 2400 × g, 15 min | DNA | PicoGreen fluorimetry | NA |
MPO-DNA | ELISA | NA | |||||
Seo et al (2019) [97] | Case–control | Patients with HCC | PVT (n = 77) vs. No PVT (n = 100) | Plasma, 1550 × g, 15 min | DNA-histone | ELISA | 159 vs. 83 AU |
NE | ELISA | NA | |||||
DNA | PicoGreen fluorimetry | 142.1 vs. 127.0Â ng/mL |