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Progressive DNA and RNA damage from oxidation after aneurysmal subarachnoid haemorrhage in humans

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  1. Urinary markers of nucleic acid oxidation in Danish overweight/obese children and youths

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  2. Assays for urinary biomarkers of oxidatively damaged nucleic acids

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  4. Body iron is a contributor to oxidative damage of DNA

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  3. A visual rating scale for cingulate island sign on 18F-FDG-PET to differentiate dementia with Lewy bodies and Alzheimer's disease

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  4. Brain Changes Induced by Electroconvulsive Therapy Are Broadly Distributed

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Free radical toxicity is considered as a key mechanism in the neuronal damage occurring after aneurysmal subarachnoid haemorrhage (SAH). We measured markers of DNA and RNA damage from oxidation (8-oxodG and 8-oxoGuo, respectively) in cerebrospinal fluid from 45 patients with SAH on day 1-14 after ictus and 45 age-matched healthy control subjects. At baseline, both markers were significantly increased in patients compared to controls (p values < .001), and exhibited a progressive further increase (to >20-fold above control levels) from day 5-14. None of the markers predicted the occurrence of vasospasms or mortality, although there was a trend that the 8-oxoGuo marker was more strongly associated with mortality than the 8-oxodG marker. We conclude that SAH leads to a massive increase in damage to nucleic acids from oxidative stress, which is likely to play a role in neuronal dysfunction and death. As only patients in need of a ventriculostomy catheter were included in the study, the findings cannot necessarily be extrapolated to all patients with SAH.

Original languageEnglish
JournalFree Radical Research
Volume52
Issue number1
Pages (from-to)51-56
Number of pages6
ISSN1071-5762
DOIs
Publication statusPublished - 2018

    Research areas

  • Journal Article

ID: 52167630