TY - JOUR
T1 - Plasma glutathione suggests oxidative stress is equally present in early and late onset bipolar disorder
AU - Singh, Nisha
AU - McMahon, Hannah
AU - Bilderbeck, Amy
AU - Reed, Zoe E.
AU - Tunbridge, Elizabeth
AU - Brett, Daniel
AU - Geddes, John R.
AU - Churchill, Grant C.
AU - Goodwin, Guy M.
PY - 2019/2/26
Y1 - 2019/2/26
N2 - Objectives: We previously demonstrated oxidative stress in bipolar patients and a relationship between the age of illness onset and glutathione, a principal antioxidant. In this study, we sought to replicate these findings in a new cohort of patients.
Methods: We recruited bipolar patients from the OXTEXT cohort, Warneford Hospital, Oxford, UK, of similar age and grouped them according to age of onset of illness. The early onset group comprised patients with onset <23 years, and the late group > 30 years. A third group, comprising age-matched healthy volunteers, was also included. Reduced and oxidised glutathione, cysteine, and cystine were determined in plasma, using high performance liquid chromatography. Mitochondrial DNA copy number, measured in whole blood, was also compared between patients and healthy controls.
Results: Significant increases in oxidative stress were observed in the patient groups, compared with the control group; however, no differences in glutathione-related oxidative stress measures were detected between the early and late onset bipolar patient groups. No differences were observed in the amount of mitochondrial DNA, and there was no correlation with mood state.
Conclusion: Using a more accurate method to quantify oxidative stress than in our previous study, we show that oxidative stress is a consistent feature of bipolar disorder. Although we did not reproduce our finding correlating age of onset of illness to oxidative stress, we have shown, once again, that oxidative stress is a consistent feature of bipolar disorder.
AB - Objectives: We previously demonstrated oxidative stress in bipolar patients and a relationship between the age of illness onset and glutathione, a principal antioxidant. In this study, we sought to replicate these findings in a new cohort of patients.
Methods: We recruited bipolar patients from the OXTEXT cohort, Warneford Hospital, Oxford, UK, of similar age and grouped them according to age of onset of illness. The early onset group comprised patients with onset <23 years, and the late group > 30 years. A third group, comprising age-matched healthy volunteers, was also included. Reduced and oxidised glutathione, cysteine, and cystine were determined in plasma, using high performance liquid chromatography. Mitochondrial DNA copy number, measured in whole blood, was also compared between patients and healthy controls.
Results: Significant increases in oxidative stress were observed in the patient groups, compared with the control group; however, no differences in glutathione-related oxidative stress measures were detected between the early and late onset bipolar patient groups. No differences were observed in the amount of mitochondrial DNA, and there was no correlation with mood state.
Conclusion: Using a more accurate method to quantify oxidative stress than in our previous study, we show that oxidative stress is a consistent feature of bipolar disorder. Although we did not reproduce our finding correlating age of onset of illness to oxidative stress, we have shown, once again, that oxidative stress is a consistent feature of bipolar disorder.
KW - bipolar disorder
KW - glutathione
KW - oxidative stress
KW - plasma redox state
UR - http://www.scopus.com/inward/record.url?scp=85044505083&partnerID=8YFLogxK
U2 - 10.1111/bdi.12640
DO - 10.1111/bdi.12640
M3 - Article (Academic Journal)
C2 - 29600584
AN - SCOPUS:85044505083
SN - 1399-5618
VL - 21
SP - 61
EP - 67
JO - Bipolar Disorders
JF - Bipolar Disorders
IS - 1
ER -