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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.
Afiliación
  • Jorgensen A; a Psychiatric Centre Copenhagen , Copenhagen , Denmark.
  • Staalsoe JM; b Department of Biomedicine, Faculty of Health and Medical Sciences , University of Copenhagen , Copenhagen , Denmark.
  • Simonsen AH; c Department of Neurology , University Hospital Bispebjerg , Copenhagen , Denmark.
  • Hasselbalch SG; d Danish Dementia Research Centre, Department of Neurology , University Hospital Rigshospitalet , Copenhagen , Denmark.
  • Høgh P; b Department of Biomedicine, Faculty of Health and Medical Sciences , University of Copenhagen , Copenhagen , Denmark.
  • Weimann A; d Danish Dementia Research Centre, Department of Neurology , University Hospital Rigshospitalet , Copenhagen , Denmark.
  • Poulsen HE; b Department of Biomedicine, Faculty of Health and Medical Sciences , University of Copenhagen , Copenhagen , Denmark.
  • Olsen NV; e Department of Neurology , University Hospital Zealand , Roskilde , Denmark.
Free Radic Res ; 52(1): 51-56, 2018 Jan.
Article en En | MEDLINE | ID: mdl-29157018
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.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Hemorragia Subaracnoidea / Daño del ADN / ARN Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Free Radic Res Asunto de la revista: BIOQUIMICA Año: 2018 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Hemorragia Subaracnoidea / Daño del ADN / ARN Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Idioma: En Revista: Free Radic Res Asunto de la revista: BIOQUIMICA Año: 2018 Tipo del documento: Article