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

Research output: Contribution to journalJournal articleResearchpeer-review

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Progressive DNA and RNA damage from oxidation after aneurysmal subarachnoid haemorrhage in humans. / Jorgensen, Anders; Staalsoe, Jonatan M; Simonsen, Anja H; Hasselbalch, Steen G; Høgh, Peter; Weimann, Allan; Poulsen, Henrik E; Olsen, Neils V.

In: Free Radical Research, Vol. 52, No. 1, 01.2018, p. 51-56.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Jorgensen, A, Staalsoe, JM, Simonsen, AH, Hasselbalch, SG, Høgh, P, Weimann, A, Poulsen, HE & Olsen, NV 2018, 'Progressive DNA and RNA damage from oxidation after aneurysmal subarachnoid haemorrhage in humans', Free Radical Research, vol. 52, no. 1, pp. 51-56. https://doi.org/10.1080/10715762.2017.1407413

APA

Jorgensen, A., Staalsoe, J. M., Simonsen, A. H., Hasselbalch, S. G., Høgh, P., Weimann, A., Poulsen, H. E., & Olsen, N. V. (2018). Progressive DNA and RNA damage from oxidation after aneurysmal subarachnoid haemorrhage in humans. Free Radical Research, 52(1), 51-56. https://doi.org/10.1080/10715762.2017.1407413

Vancouver

Jorgensen A, Staalsoe JM, Simonsen AH, Hasselbalch SG, Høgh P, Weimann A et al. Progressive DNA and RNA damage from oxidation after aneurysmal subarachnoid haemorrhage in humans. Free Radical Research. 2018 Jan;52(1):51-56. https://doi.org/10.1080/10715762.2017.1407413

Author

Jorgensen, Anders ; Staalsoe, Jonatan M ; Simonsen, Anja H ; Hasselbalch, Steen G ; Høgh, Peter ; Weimann, Allan ; Poulsen, Henrik E ; Olsen, Neils V. / Progressive DNA and RNA damage from oxidation after aneurysmal subarachnoid haemorrhage in humans. In: Free Radical Research. 2018 ; Vol. 52, No. 1. pp. 51-56.

Bibtex

@article{122a3812e1f649ae9a1eb7b29e439352,
title = "Progressive DNA and RNA damage from oxidation after aneurysmal subarachnoid haemorrhage in humans",
abstract = "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.",
keywords = "Journal Article",
author = "Anders Jorgensen and Staalsoe, {Jonatan M} and Simonsen, {Anja H} and Hasselbalch, {Steen G} and Peter H{\o}gh and Allan Weimann and Poulsen, {Henrik E} and Olsen, {Neils V}",
year = "2018",
month = jan,
doi = "10.1080/10715762.2017.1407413",
language = "English",
volume = "52",
pages = "51--56",
journal = "Free Radical Research",
issn = "1071-5762",
publisher = "Taylor & Francis",
number = "1",

}

RIS

TY - JOUR

T1 - Progressive DNA and RNA damage from oxidation after aneurysmal subarachnoid haemorrhage in humans

AU - Jorgensen, Anders

AU - Staalsoe, Jonatan M

AU - Simonsen, Anja H

AU - Hasselbalch, Steen G

AU - Høgh, Peter

AU - Weimann, Allan

AU - Poulsen, Henrik E

AU - Olsen, Neils V

PY - 2018/1

Y1 - 2018/1

N2 - 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.

AB - 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.

KW - Journal Article

U2 - 10.1080/10715762.2017.1407413

DO - 10.1080/10715762.2017.1407413

M3 - Journal article

C2 - 29157018

VL - 52

SP - 51

EP - 56

JO - Free Radical Research

JF - Free Radical Research

SN - 1071-5762

IS - 1

ER -

ID: 189623632