Review Article
Intracerebral Hemorrhage, Oxidative Stress, and Antioxidant Therapy
Table 1
Human biomarkers and oxidative stress after ICH.
| Biomarkers | Sample | Methods | Value | References |
|
8-iso-Prostaglandin F2α | Urinary | Liquid chromatography, tandem mass spectrometry | Independent biomarker of prediction of the risk for incident stroke | [140] |
|
8-iso-Prostaglandin F2α | Plasma | Enzyme-linked immunosorbent assay | Disease severity and clinical outcome after acute ICH associated with concentration | [101] |
| 8-OHdG | Plasma | HPLC-electrochemical detector | Level associated with 30-day outcome after ICH | [106] |
| Bilirubin | Plasma | Reflectance spectrophotometry | Serum bilirubin levels were significantly elevated in the early phases in hemorrhagic stroke | [141] |
| Vitamin C, uric acid (UA), vitamin E, ubiquinol-10 | Plasma | HPLC-electrochemical detector | Lower plasma levels of UA and higher plasma levels of others correlated with the severity of the neurological impairment after ICH | [142] |
| ROOH | Plasma | HPLC-electrochemical detector | Predictor of poor clinical outcome in sICH survivors | [102] |
| TAC, TOS | Plasma | Spectrophotometrically | TOS levels increased and TAC levels decreased in acute hemorrhagic stroke | [127] |
|
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MDA, myeloperoxidase; erythrocyte glutathione peroxidase; 8-OHdG, leukocyte 8-hydroxy-2′-deoxyguanosine; HPLC, high-performance liquid chromatography; TAC, total antioxidant capacity; TOS, total oxidant status.
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