Article Data

  • Views 2856
  • Dowloads 146

Original Research

Open Access

Diagnostic role of serum testican and ubiquitin levels in patients with head trauma

  • Ramiz Yazıcı1,*,
  • Ayse Fethiye Basa Kalafat1
  • Hüseyin Mutlu2
  • Eyüp Sarı3
  • Utku Murat Kalafat1
  • Dilek Atik4
  • Başar Cander5

1Department of Emergency Medicine, Istanbul Kanuni Sultan Suleyman Education and Research Hospital, Health Science University, 34303 Istanbul, Turkey

2Department of Emergency Medicine, Aksaray Education and Research Hospital, Aksaray University, 68200 Aksaray, Turkey

3Department of Pediatrics, Gulhane Faculty of Medicine, Health Science University, 06018 Ankara, Turkey

4Department of Emergency Medicine, Karamanoğlu Mehmetbey University, 70100 Karaman, Turkey

5Department of Emergency Medicine, Bezmialem Vakıf University, 34093 Istanbul, Turkey

DOI: 10.22514/sv.2024.131 Vol.20,Issue 10,October 2024 pp.106-112

Submitted: 20 March 2024 Accepted: 13 June 2024

Published: 08 October 2024

*Corresponding Author(s): Ramiz Yazıcı E-mail: ramiz.yazici@sbu.edu.tr

Abstract

We aimed to determine if testican-1 and ubiquitin can serve as early indicators for diagnosing worsening clinical course (presence of intraparenchymal pathology) and mortality in patients with moderate traumatic brain injury (TBI).In this study, we conducted an observational and prospective study in the Emergency Department (ED) of a tertiary care hospital. The department admitted an average of 25,000 patients per month between October 2020 and March 2021. We focused on patients over 18 years old with moderate traumatic brain injury (Glasgow coma score (GCS): 9–13). We compared the prognostic values of blood testican and ubiquitin levels with Receiver Operating Characteristic (ROC) analysis for intracranial pathologies resulting from head trauma. Additionally, we used logistic regression analysis to compare the effectiveness of these markers in diagnosing intraparenchymal injury. The study included a total of 89 patients, with 45 in the case group (moderate TBI) and 44 in the healthy control group. It was found that levels of ubiquitin and testican levels were significantly higher in patients with intraparenchymal pathology (p = 0.048, p = 0.046, respectively). The cut-off point for detecting intraparenchymal pathology was 161.3 pg/mL for testican (Area under curve (AUC): 0.810; min: 0.654; max: 0.965, p = 0.002) and 44.42 ng/mL for Ubiquitin (AUC: 0.863; min: 0.727; max: 1.000, p < 0.001). High testican-1 and ubiquitin levels were independent markers for intraparenchymal pathology in moderate head trauma.


Keywords

Biomarkers; Diagnostics; Moderate traumatic brain injury; Testican; Ubiquitin


Cite and Share

Ramiz Yazıcı,Ayse Fethiye Basa Kalafat,Hüseyin Mutlu,Eyüp Sarı,Utku Murat Kalafat,Dilek Atik,Başar Cander. Diagnostic role of serum testican and ubiquitin levels in patients with head trauma. Signa Vitae. 2024. 20(10);106-112.

References

[1] Maas AIR, Menon DK, Manley GT, Abrams M, Åkerlund C, Andelic N, et al. Traumatic brain injury: progress and challenges in prevention, clinical care, and research. The Lancet Neurology. 2022; 21: 1004–1060.

[2] Hossain I, Rostami E, Marklund N. The management of severe traumatic brain injury in the initial postinjury hours—current evidence and controversies. Current Opinion in Critical Care. 2023; 29: 650–658.

[3] Shultz SR, Shah AD, Huang C, Dill LK, Schittenhelm RB, Morganti-Kossmann MC, et al. Temporal proteomics of human cerebrospinal fluid after severe traumatic brain injury. Journal of Neuroinflammation. 2022; 19: 291.

[4] Hossain I, Marklund N, Czeiter E, Hutchinson P, Buki A. Blood biomarkers for traumatic brain injury: a narrative review of current evidence. Brain and Spine. 2023; 4: 102735.

[5] Silvestro S, Raffaele I, Quartarone A, Mazzon E. Innovative insights into traumatic brain injuries: biomarkers and new pharmacological targets. International Journal of Molecular Sciences. 2024; 25: 2372.

[6] Kim DS, Kim GW. Biofluid-based biomarkers in traumatic brain injury: a narrative review. Brain & Neurorehabilitation. 2024; 17: e8.

[7] Iseki K, Hagino S, Zhang Y, Mori T, Sato N, Yokoya S, et al. Altered expression pattern of testican-1 mRNA after brain injury. Biomedical Research. 2011; 32: 373–378.

[8] Yakovlev AG, Faden AI. Mechanisms of neural cell death: implications for development of neuroprotective treatment strategies. NeuroRx. 2004; 1: 5–16.

[9] Tongaonkar P, Chen L, Lambertson D, Ko B, Madura K. Evidence for an interaction between ubiquitin-conjugating enzymes and the 26S proteasome. Molecular and Cellular Biology. 2000; 20: 4691–4698.

[10] Azar S, Hasan A, Younes R, Najdi F, Baki L, Ghazale H, et al. Biofluid proteomics and biomarkers in traumatic brain injury. Methods in Molecular Biology. 2017; 1598: 45–63.

[11] Liu MC, Akinyi L, Scharf D, Mo J, Larner SF, Muller U, et al. Ubiquitin C-terminal hydrolase-L1 as a biomarker for ischemic and traumatic brain injury in rats. European Journal of Neuroscience. 2010; 31: 722–732.

[12] Welch RD, Ayaz SI, Lewis LM, Unden J, Chen JY, Mika VH, et al. Ability of serum glial fibrillary acidic protein, ubiquitin C-terminal hydrolase-L1, and S100B to differentiate normal and abnormal head computed tomography findings in patients with suspected mild or moderate traumatic brain injury. Journal of Neurotrauma. 2016; 33: 203–214.

[13] Papa L, Lewis LM, Silvestri S, Falk JL, Giordano P, Brophy GM, et al. Serum levels of ubiquitin C-terminal hydrolase distinguish mild traumatic brain injury from trauma controls and are elevated in mild and moderate traumatic brain injury patients with intracranial lesions and neurosurgical intervention. Journal of Trauma and Acute Care Surgery. 2012; 72: 1335–1344.

[14] Mondello S, Kobeissy F, Vestri A, Hayes RL, Kochanek PM, Berger RP. Serum concentrations of ubiquitin C-terminal hydrolase-L1 and glial fibrillary acidic protein after pediatric traumatic brain injury. Scientific Reports. 2016; 6: 28203.


Submission Turnaround Time

Top