Citation: | LIU Fang, WANG Xiaobei. Value of plasma neutrophil extracellular traps on illness condition and prognosis in patients with acute cerebral infarction[J]. Journal of Clinical Medicine in Practice, 2023, 27(17): 127-132. DOI: 10.7619/jcmp.20232055 |
To analyze correlations of the main components of neutrophil extracellular traps (NETs)[citrulline histone 3 (CitH3) and double-stranded DNA (dsDNA)] with the ill severity in patients with acute cerebral infarction (ACI)and its predictive value in prognosis.
A total of 120 patients with ACI were collected as study objects, and were divided into mild group[65 cases, the National Institutes of Health Stroke Scale (NIHSS) score of 0 to 4] and severe group (55 cases, the NIHSS score of 4 to 15) according to severity of illness. Before and after treatment, plasma CitH3, dsDNA, N-terminal B-type natriuretic peptide (NT-proBNP), platelet (PLT), prothrombin time (PT), international standardized ratio (INR), neutrophil-to-lymphocyte ratio (NLR), platelet-to-lymphocyte ratio (PLR), monocyte-to-high density lipoprotein cholesterol ratio(MHR) and modified Edinburgh-Scandinavian Stroke Scale (MESSS) score were detected in two groups, and the correlations of above clinical indexes with the NIHSS scores were analyzed. According to the modified Rankin Scale score at the last follow-up, the patients were divided into good prognosis group (98 cases) and poor prognosis group (22 cases). The difference of clinical indicators between the two groups was compared, and the correlations of clinical indicators with poor prognosis of ACI patients were analyzed. Receiver operating characteristic (ROC) curve was drawn to analyze the diagnostic performance of plasma CitH3 combined with dsDNA for the prognosis of ACI patients.
The levels of CitH3, dsDNA, NT-proBNP, MHR and MESSS before and after the treatment in the severe group were all higher than those in the mild group (P<0.05), but the levels of PLT, PT, INR, NLR and PLR showed no significant differences between two groups (P>0.05). The positive correlation of the indexes of CitH3, dsDNA and NT-proBNP with the NIHSS scores were found (r=0.814, 0.775, 0.725; P<0.05). After 1-year follow-up, the levels of plasma CitH3, dsDNA and NT-proBNP in the poor prognosis group were higher than those in the good prognosis group(P<0.05). The increased CitH3 and dsDNA were the risk factors to the short-term poor prognosis in patients with ACI (OR=2.913, P=0.029; OR=2.887, P=0.036). The area under the curve of plasma CitH3 combined with plasma dsDNA in predicting poor prognosis of ACI patients at 1 year follow-up was 0.823, sensitivity was 84.5%, and specificity was 89.5%.
The combined detection of main components of CitH3 and dsDNA of plasma NETs can effectively evaluate the ill severity of patients with ACI, and has good predictive value of the short-term prognosis.
[1] |
MUN K T, HINMAN J D. Inflammation and the link to vascular brain health: timing is brain[J]. Stroke, 2022, 53(2): 427-436. doi: 10.1161/STROKEAHA.121.032613
|
[2] |
KIM S W, DAVAANYAM D, SEOL S I, et al. Adenosine triphosphate accumulated following cerebral ischemia induces neutrophil extracellular trap formation[J]. Int J Mol Sci, 2020, 21(20): 7668. doi: 10.3390/ijms21207668
|
[3] |
BERNIS M E, ZWEYER M, MAES E, et al. Neutrophil extracellular traps release following hypoxic-ischemic brain injury in newborn rats treated with therapeutic hypothermia[J]. Int J Mol Sci, 2023, 24(4): 3598. doi: 10.3390/ijms24043598
|
[4] |
KIM E, CHO S. CNS and peripheral immunity in cerebral ischemia: partition and interaction[J]. Exp Neurol, 2021, 335: 113508. doi: 10.1016/j.expneurol.2020.113508
|
[5] |
WU X Y, ZENG H H, CAI L X, et al. Role of the extracellular traps in central nervous system[J]. Front Immunol, 2021, 12: 783882. doi: 10.3389/fimmu.2021.783882
|
[6] |
中华医学会神经病学分会, 中华医学会神经病学分会脑血管病学组, 彭斌, 等. 中国急性缺血性脑卒中诊治指南2018[J]. 中华神经科杂志, 2018, 51(9): 666-682. doi: 10.3760/cma.j.issn.1006-7876.2018.09.004
|
[7] |
WANG C Y, LIN T T, HU L, et al. Neutrophil extracellular traps as a unique target in the treatment of chemotherapy-induced peripheral neuropathy[J]. EBioMedicine, 2023, 90: 104499. doi: 10.1016/j.ebiom.2023.104499
|
[8] |
XU X B, WU Y T, XU S X, et al. Clinical significance of neutrophil extracellular traps biomarkers in thrombosis[J]. Thromb J, 2022, 20(1): 63. doi: 10.1186/s12959-022-00421-y
|
[9] |
PIR G J, PARRAY A, AYADATHIL R, et al. Platelet-neutrophil association in NETs-rich areas in the retrieved AIS patient thrombi[J]. Int J Mol Sci, 2022, 23(22): 14477. doi: 10.3390/ijms232214477
|
[10] |
PUY L, CORSEAUX D, PERBET R, et al. Neutrophil extracellular traps (NETs) infiltrate haematoma and surrounding brain tissue after intracerebral haemorrhage: a post-mortem study[J]. Neuropathol Appl Neurobiol, 2021, 47(6): 867-877. doi: 10.1111/nan.12733
|
[11] |
WANG R R, ZHU Y B, LIU Z W, et al. Neutrophil extracellular traps promote tPA-induced brain hemorrhage via cGAS in mice with stroke[J]. Blood, 2021, 138(1): 91-103. doi: 10.1182/blood.2020008913
|
[12] |
WILDE M D, DESENDER L, TERSTEEG C, et al. Spatiotemporal profile of neutrophil extracellular trap formation in a mouse model of ischemic stroke[J]. Res Pract Thromb Haemost, 2023, 7(1): 100028. doi: 10.1016/j.rpth.2022.100028
|
[13] |
ZHOU J R, GUO P W, HAO X K, et al. Neutrophil extracellular traps (NETs): a new therapeutic target for neuroinflammation and microthrombosis after subarachnoid hemorrhage[J]. Transl Stroke Res, 2023, 14(4): 443-445. doi: 10.1007/s12975-022-01039-y
|
[14] |
ZHAO Z Y, PAN Z R, ZHANG S, et al. Neutrophil extracellular traps: a novel target for the treatment of stroke[J]. Pharmacol Ther, 2023, 241: 108328. doi: 10.1016/j.pharmthera.2022.108328
|
[15] |
ZHANG S Q, CAO Y Z, DU J W, et al. Neutrophil extracellular traps contribute to tissue plasminogen activator resistance in acute ischemic stroke[J]. FASEB J, 2021, 35(9): e21835. doi: 10.1096/fj.202100471RR
|
[16] |
LARCO J A, ABBASI M, MADHANI S I, et al. Correlation of neutrophil to lymphocyte ratio with expression of neutrophil extracellular traps within stroke emboli[J]. Interv Neuroradiol, 2022, 28(6): 726-730. doi: 10.1177/15910199211065530
|
[17] |
DENORME F, PORTIER I, RUSTAD J L, et al. Neutrophil extracellular traps regulate ischemic stroke brain injury[J]. J Clin Invest, 2022, 132(10): e154225. doi: 10.1172/JCI154225
|
[18] |
HAO X K, ZENG Z W, LIANG L, et al. The role of neutrophil extracellular traps in early microthrombosis and brain injury after subarachnoid hemorrhage in mice[J]. Transl Stroke Res, 2023, 14(5): 752-765. doi: 10.1007/s12975-022-01074-9
|
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