Increased systemic oxidatively generated DNA and RNA damage in schizophrenia

Abstract Schizophrenia is associated with a substantially increased somatic morbidity and mortality, which may partly be caused by accelerated cellular aging. Oxidative stress is an established mediator of aging and a suggested aetiological mechanism in both schizophrenia and age-related medical dis...

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Veröffentlicht in:Psychiatry research 2013-10, Vol.209 (3), p.417-423
Hauptverfasser: Jorgensen, Anders, Broedbaek, Kasper, Fink-Jensen, Anders, Knorr, Ulla, Greisen Soendergaard, Mia, Henriksen, Trine, Weimann, Allan, Jepsen, Peter, Lykkesfeldt, Jens, Enghusen Poulsen, Henrik, Balslev Jorgensen, Martin
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Sprache:eng
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Zusammenfassung:Abstract Schizophrenia is associated with a substantially increased somatic morbidity and mortality, which may partly be caused by accelerated cellular aging. Oxidative stress is an established mediator of aging and a suggested aetiological mechanism in both schizophrenia and age-related medical disorders such as cardiovascular disease, type 2 diabetes and dementia. We determined the urinary excretion of markers of systemic Deoxyribonucleic Acid (DNA) and Ribonucleic Acid (RNA) oxidation, 8-oxo-7,8-dihydro-2′-deoxyguanosine and 8-oxo-7,8-dihydroguanosine, respectively, in 40 schizophrenia patients and 40 age- and sex-matched controls, using ultra-performance liquid chromatography with tandem mass spectrometry. Measures of psychopathology, perceived stress and cortisol secretion were collected. Patients were re-examined after four months. We found a 20% increase in the median excretion of both markers in schizophrenia patients vs. healthy controls ( P =0.003 and
ISSN:0165-1781
1872-7123
DOI:10.1016/j.psychres.2013.01.033