» Articles » PMID: 31598840

High Serum DNA and RNA Oxidative Damage in Non-surviving Patients with Spontaneous Intracerebral Hemorrhage

Overview
Journal Neurocrit Care
Specialty Critical Care
Date 2019 Oct 11
PMID 31598840
Citations 6
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: One study found higher leukocytes 8-hydroxy-2'-deoxyguanosine (8-OHdG) levels in patients with spontaneous intracerebral hemorrhage (ICH) than in healthy subjects due to the oxidation of guanosine from deoxyribonucleic acid (DNA). The objective of this study was to determine whether there is an association between oxidative damage of serum DNA and ribonucleic acid (RNA) and mortality in patients with ICH.

Methods: In this observational and prospective study, patients with severe supratentorial ICH (defined as Glasgow Coma Scale < 9) were included from six Intensive Care Units of Spanish hospitals. At the time of severe ICH diagnosis, concentrations in serum of malondialdehyde (as lipid peroxidation biomarker) and of the three oxidized guanine species (OGS) (8-hydroxyguanosine from RNA, 8-hydroxyguanine from DNA or RNA, and 8-OHdG from DNA) were determined. Thirty-day mortality was considered the end-point study.

Results: Serum levels of OGS (p < 0.001) and malondialdehyde (p = 0.002) were higher in non-surviving (n = 46) than in surviving patients (n = 54). There was an association of serum OGS levels with serum malondialdehyde levels (rho = 0.36; p = 0.001) and 30-day mortality (OR = 1.568; 95% CI 1.183-2.078; p = 0.002).

Conclusions: The novel and most important finding of our study was that serum OGS levels in ICH patients are associated with mortality.

Citing Articles

The role of potential oxidative biomarkers in the prognosis of intracerebral hemorrhage and the exploration antioxidants as possible preventive and treatment options.

Yao J, Dai X, Yv X, Zheng L, Zheng J, Kuang B Front Mol Biosci. 2025; 12:1541230.

PMID: 39967652 PMC: 11832355. DOI: 10.3389/fmolb.2025.1541230.


Integrated Network Pharmacology and in vivo Experimental Validation Approach to Explore the Potential Antioxidant Effects of Annao Pingchong Decoction in Intracerebral Hemorrhage Rats.

Zhou X, Wang X, Li J, Zhang M, Yang Y, Lei S Drug Des Devel Ther. 2024; 18:699-717.

PMID: 38465266 PMC: 10922012. DOI: 10.2147/DDDT.S439873.


Secondary Brain Injury by Oxidative Stress After Cerebral Hemorrhage: Recent Advances.

Shao L, Chen S, Ma L Front Cell Neurosci. 2022; 16:853589.

PMID: 35813506 PMC: 9262401. DOI: 10.3389/fncel.2022.853589.


Inflammatory and oxidative stress markers in intracerebral hemorrhage: Relevance as prognostic markers for quantification of the edema volume.

Rendevski V, Aleksovski B, Rendevska A, Hadzi-Petrushev N, Manusheva N, Shuntov B Brain Pathol. 2022; 33(2):e13106.

PMID: 35762501 PMC: 10041164. DOI: 10.1111/bpa.13106.


Mechanisms of Oxidative Stress and Therapeutic Targets following Intracerebral Hemorrhage.

Yao Z, Bai Q, Wang G Oxid Med Cell Longev. 2021; 2021:8815441.

PMID: 33688394 PMC: 7920740. DOI: 10.1155/2021/8815441.


References
1.
Hu X, Tao C, Gan Q, Zheng J, Li H, You C . Oxidative Stress in Intracerebral Hemorrhage: Sources, Mechanisms, and Therapeutic Targets. Oxid Med Cell Longev. 2016; 2016:3215391. PMC: 4710930. DOI: 10.1155/2016/3215391. View

2.
Kumagai S, Jikimoto T, Saegusa J . [Pathological roles of oxidative stress in autoimmune diseases]. Rinsho Byori. 2003; 51(2):126-32. View

3.
Malins D, Haimanot R . Major alterations in the nucleotide structure of DNA in cancer of the female breast. Cancer Res. 1991; 51(19):5430-2. View

4.
Teasdale G, Jennett B . Assessment of coma and impaired consciousness. A practical scale. Lancet. 1974; 2(7872):81-4. DOI: 10.1016/s0140-6736(74)91639-0. View