The Prognostic Value of Deleted in Colorectal Cancer (DCC) Receptor and Serum Netrin-1 in Severe Traumatic Brain Injury.
DCC receptor
Netrin-1
traumatic brain injury
Journal
Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588
Informations de publication
Date de publication:
27 Jun 2022
27 Jun 2022
Historique:
received:
19
05
2022
revised:
06
06
2022
accepted:
21
06
2022
entrez:
9
7
2022
pubmed:
10
7
2022
medline:
10
7
2022
Statut:
epublish
Résumé
Traumatic brain injury (TBI) is a common neurological disease. Netrin-1 and deleted in colorectal cancer (DCC) receptor are potential biomarkers associated with nerve regeneration and immune regulation. We aimed to investigate the ability of the DCC receptor and Netrin-1 to predict a high ICP level after operation in severe traumatic brain injury and their prognostic significance. This study is a prospective observational study. We selected 23 patients with traumatic brain injury who had undergone surgical operations as subjects. Immunohistochemical staining was performed on the contusion tissue that was removed by the operation to determine the expression of DCC receptor. At the same time, enzyme-linked immunosorbent assay (ELISA) kits were used to detect the serum Netrin-1 content. Determination of intracranial pressure (ICP) value was measured by intraventricular catheter. The Glasgow Outcome Scale (GOS) score at six months after trauma was defined as the main study endpoint. The results showed that serum Netrin-1 concentrations of patients in the critical TBI group (GCS 3-5 points) was significantly lower than that in the severe TBI group (GCS 6-8 points). The ICP peak and average mannitol consumption in the high Netrin-1 group were significantly lower than those in the low Netrin-1 group. DCC receptor-positive patients had a significantly lower ICP peak. There was no significant difference in six month-GOS scores between patients in the high and low Netrin-1 groups, while DCC receptor concentrations below 3.82 ng/mL predicted poor prognosis (GOS 1-3 points). In conclusion, the expression level of the DCC receptor can better evaluate the postoperative high ICP level and prognosis than the level of serum Netrin-1 in severe traumatic brain injury.
Identifiants
pubmed: 35806983
pii: jcm11133700
doi: 10.3390/jcm11133700
pmc: PMC9267364
pii:
doi:
Types de publication
Journal Article
Langues
eng
Subventions
Organisme : National Natural Science Foundation of China
ID : 81771316
Références
J Neurol Sci. 2006 Jan 15;240(1-2):85-91
pubmed: 16266720
Nutr Metab Cardiovasc Dis. 2021 Mar 10;31(3):852-859
pubmed: 33546947
Neural Regen Res. 2013 Jan 5;8(1):64-9
pubmed: 25206373
J Neurotrauma. 2008 Sep;25(9):1079-85
pubmed: 18729720
Brain Behav Immun. 2018 Mar;69:190-202
pubmed: 29162556
Neuropharmacology. 2017 Jun;119:123-133
pubmed: 28347836
Oncogene. 1999 Apr 29;18(17):2747-54
pubmed: 10348349
J Neurosci Res. 2017 Sep;95(9):1850-1857
pubmed: 28084632
J Athl Train. 2014 Nov-Dec;49(6):830-50
pubmed: 25299445
Neurosurg Clin N Am. 2016 Oct;27(4):397-407
pubmed: 27637392
Proc Natl Acad Sci U S A. 2005 Oct 11;102(41):14729-34
pubmed: 16203981
Trends Biochem Sci. 2020 Jan;45(1):6-12
pubmed: 31704057
Eur J Neurosci. 2010 Feb;31(4):722-32
pubmed: 20384815
Stem Cell Res Ther. 2017 Oct 10;8(1):223
pubmed: 29017609
Int J Mol Sci. 2021 Dec 27;23(1):
pubmed: 35008701
Int J Mol Sci. 2017 Feb 24;18(3):
pubmed: 28245592
J Biochem Mol Toxicol. 2013 Apr;27(4):231-6
pubmed: 23335440
Lancet Neurol. 2020 Aug;19(8):670-677
pubmed: 32702336
Neuroscience. 2004;129(4):1021-9
pubmed: 15561417
Pediatrics. 2002 Feb;109(2):E31
pubmed: 11826241
Clin Chim Acta. 2021 Jul;518:22-27
pubmed: 33741358
Glia. 2011 Oct;59(10):1503-17
pubmed: 21656855
J Neuropathol Exp Neurol. 1999 Sep;58(9):982-92
pubmed: 10499440
J Neurotrauma. 2004 Oct;21(10):1443-56
pubmed: 15672634
Lancet Neurol. 2019 Mar;18(3):286-295
pubmed: 30784557
Prog Biophys Mol Biol. 2015 Sep;118(3):153-60
pubmed: 25881791
J Int Med Res. 2020 Aug;48(8):300060520941291
pubmed: 32854551
Nat Rev Neurol. 2012 Jun 19;8(7):380-90
pubmed: 22710628