Oxidative Stress Level in Patients with Subarachnoid Hemorrhage

Author:

Abdallah Anas1ORCID,Guler Eray Metin23ORCID,Çınar İrfan1ORCID,Papaker Meliha Gündağ4ORCID,Yapar Selçuk4ORCID,Ozer Omer Faruk5ORCID,Yurtsever Ismail6ORCID,Dündar Tolga Turan4ORCID

Affiliation:

1. Department of Neurosurgery, Aile Hospital, Istanbul, Turkey

2. Department of Medical Biochemistry, Hamidiye School of Medicine, University of Health Sciences, Istanbul, Turkey

3. Department of Medical Biochemistry, Haydarpasa Numune Health Application and Research Center, Hamidiye Faculty of Medicine, University of Health Sciences, Istanbul, Turkey

4. Department of Neurosurgery, Bezmialem Vakif University, Istanbul, Turkey

5. Department of Biochemistry, Bezmialem Vakif University, Istanbul, Turkey

6. Department of Radiology, Bezmialem Vakif University, Istanbul, Turkey

Abstract

Abstract Background One of the antioxidant mechanisms is the dynamic balance between thiol and disulfide, which, in subarachnoid hemorrhage and other chronic diseases, is disrupted in favor of the latter. The two most commonly used oxidative stress (OS) biochemical markers are the oxidative stress index (OSI) value, which indicates the total oxidant status (TOS) and total antioxidant status (TAS) balance, and the thiol–disulfide (TDS) value, which indicates the total thiol (TT) and native thiol (NT) balance. High OS levels require further investigations. We aimed to investigate the OS level in aneurysmal SAH (aSAH) patients. methods In this clinical prospective study, blood samples were collected from 50 consecutively treated patients with aSAH and 50 volunteers. Serum TOS, TAS, TT, and NT levels were measured using Erel's method via a spectrophotometer. The Glasgow Coma Scale (GCS) scores, Fisher grades, length of hospital stay (LOS), and the Glasgow Outcome Scale (GOS) scores were recorded. Consequently, the OSI and TDS values were calculated in all participants. Results A statistically significant difference was observed in the TAS, TOS, OSI, and TDS values between the aSAH patients and the controls. The TT and NT values were significantly lower in aSAH patients than in the controls. A correlation was identified between the OSI values and the GCS scores. Although a correlation was observed between the TDS values and the LOS, no correlation was found between the OSI and the TDS values. Conclusion The OSI and TDS, which are OS indicators, might serve as the additional objective nominal data to evaluate the treatment efficacy and follow-up for SAH patients. Moreover, decreasing the OSI values and increasing the TT values can be used as improvement indicators in the treated aSAH patients. If we can reduce the OS at the early stage of SAH, it could improve the prognosis by reducing both the morbidity and mortality rates. Further randomized investigations are required to prove the findings in this prospective study.

Publisher

Georg Thieme Verlag KG

Subject

Neurology (clinical),Surgery

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