The Effect of Acute Stroke Treatment on S100B, IMA, and Thiol-Disulfide Balance

Neurol India. 2024 Nov 1;72(6):1231-1236. doi: 10.4103/ni.ni_511_22. Epub 2024 Dec 17.

Abstract

Background: A variety of processes, ranging from blood-brain barrier disruption to circulating biomarkers, contributes to reperfusion injury in acute stroke treatment.

Objective: We aimed to investigate the effects of thrombolytic therapy and endovascular thrombectomy therapy on serum S100 calcium-binding protein B, ischemia-modified albumin and thiol-disulfide balance in patients who arrived within the first 6 h of acute ischemic stroke.

Material and methods: The study considered 66 patients with the diagnosis of acute ischemic stroke who underwent thrombolytic therapy or EVT in the first 6 h, as well as 32 healthy volunteers. Venous blood samples were collected before tPA and EVT and 24 h after treatment. S100B, native thiol, disulfide, total thiol, and Ischemia-modified albumin (IMA) levels were measured.

Results: The S100B, total thiol, and native thiol values of the patients in the tPA group before and after the treatment showed statistical significance (P < 0.001). S100B, total thiol, and native thiol values were shown to be lower. The disulfide and IMA values of the patients in the tPA group did not differ significantly (respectively, P = 0.302, P = 0.054). However, disulfide and IMA levels were found to increase after treatment compared to pretreatment. The patients in the EVT group showed a significant difference in terms of S100B values (P < 0.001) and IMA values (P = 0.024).

Conclusions: Determining how to protect the brain from free radical damage is important. More research should be carried out on treatments that prevent free radical damage in ischemia-reperfusion injury, as well as treatments for acute ischemic stroke.

MeSH terms

  • Adult
  • Aged
  • Biomarkers / blood
  • Disulfides* / blood
  • Female
  • Humans
  • Ischemic Stroke / blood
  • Ischemic Stroke / therapy
  • Male
  • Middle Aged
  • S100 Calcium Binding Protein beta Subunit* / blood
  • Serum Albumin, Human / metabolism
  • Stroke / blood
  • Stroke / therapy
  • Sulfhydryl Compounds* / blood
  • Thrombectomy / methods
  • Thrombolytic Therapy / methods

Substances

  • S100 Calcium Binding Protein beta Subunit
  • Sulfhydryl Compounds
  • Disulfides
  • S100B protein, human
  • ischemia-modified albumin
  • Biomarkers
  • Serum Albumin, Human