Figures
Abstract
Free radicals and an oxidant/antioxidant imbalance have been involved in the schizophrenia pathophysiology. The total antioxidant capacity (TAC) is a measure of the antioxidant capacity of a system. Day/night changes are a biological characteristic of hormones such as melatonin or cortisol. There is little information about TAC day/night changes in schizophrenia patients. The aim of this research is to study if there are day/night changes in serum TAC levels of schizophrenia patients. Thirty-two DSM-IV schizophrenia paranoid patients were studied. Blood was sampled at 12:00 and 00:00 h at admission, discharge and three months after hospital discharge (TMAHD). TAC results are expressed as mmol of Trolox/L. Patients did not have day/night TAC differences at admission (12:00: 0.67±0.12 vs. 00:00: 0.61±0.14, p>0.14) or discharge (12:00: 0.65±0.15 vs. 00:00: 0.65±0.12, p>0.99). At TMHD, patients had significantly higher TAC levels at midday than midnight (12:00: 0.83±0.10 vs. 00:00: 0.74±0.12, p<0.006) as it has been reported in healthy subjects. There were no significant TAC differences at 12.00 and 00:00 between admission and discharge. At TMAHD, patients had significantly higher TAC levels than at admission and discharge, both at 12:00 and 00:00 h. In conclusion, the absence of day/night serum TAC changes when clinically relapsed and the normalization of day/night serum TAC changes at TMHD can be considered as a biological marker of schizophrenia evolution.
Citation: Morera-Fumero AL, Díaz-Mesa E, Abreu-Gonzalez P, Fernandez-Lopez L, Guillen-Pino F (2017) A three-month longitudinal study of changes in day/night serum total antioxidant capacity in paranoid schizophrenia. PLoS ONE 12(12): e0189348. https://doi.org/10.1371/journal.pone.0189348
Editor: Weihua YUE, Peking University, Institute of Mental Health, CHINA
Received: September 5, 2017; Accepted: November 24, 2017; Published: December 8, 2017
Copyright: © 2017 Morera-Fumero et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: All relevant data are within the paper.
Funding: This work was partly supported by a research grant (PI: 08/115) of the Fundacion Canaria de Investigacion y Salud (FUNCIS), which is part of the local government of the Canary Islands. The Consultoria Psiquiatrica SC provided support in the form of salary for authors (ALMF) but did not play a role in the study design, data collection and analysis, decision to publish, or preparation of the manuscript. There was no additional external funding received for this study.
Competing interests: The authors have declared that no competing interests exist. The Consultoria Psiquiatrica SC affiliation with one author (ALMF) does not alter our adherence to PLOS ONE policies on sharing data and materials.
Introduction
Schizophrenia is a chronic mental disorder characterized by delusions, hallucinations, disorganized speech and behaviour, and other symptoms that cause social or occupational dysfunction [1]. This disease affects 0.5–1% of the worldwide population. Its biological aetiology is multifactorial and is still under investigation [2].
Free radicals (FRs) are compounds with unpaired electrons or an open shell configuration that may have positive, negative, or zero charge. Depending on the atom placed at its core, the radical can be described as oxygen, carbon, nitrogen or metal centred radical [3]. The unpaired electrons cause radicals to be highly reactive chemical molecules.
FRs have been involved in the pathophysiology of schizophrenia [4]. An excess of FR generation and/or an impairment of the antioxidant defence system (AODS) have been reported in schizophrenia [5]. FRs are partly responsible for negative symptoms [6], tardive dyskinesia [7], neurological soft signs [8] and cognitive impairment [9].
Increased, decreased or unchanged activity of antioxidant enzymes has been reported in patients with schizophrenia [10]. Blood concentrations of specific antioxidants can be measured individually, but those measurements are time consuming and expensive compared to the measure of the total antioxidant capacity (TAC) that reflects the antioxidant capacity of water-soluble molecules of plasma/serum. Synonymous of TAC are TAA (Total Antioxidant Activity), TAOP (Total Antioxidant Power), TAS (Total Antioxidant Status) and TAR (Total Antioxidant Response) [11].
Decreased [12–14] and unchanged [15] TAC concentrations have been reported in schizophrenic patients compared to healthy controls.
Several biological variables of the oxidant-antioxidant status such as, melatonin and malondialdehyde (MDA) present circadian and seasonal rhythms [16,17]. However, there is scanty information about TAC circadian rhythms in humans. A circadian rhythm of serum TAC levels, with higher levels at night (01:00 h) compared to daytime levels (13:00 h) [18] as well as higher midnight than midday levels [19] have also been reported in healthy subjects. In a recent study [13], it was published that acute relapsed paranoid schizophrenia patients present higher nocturnal than diurnal TAC levels when admitted to hospitalization, but three weeks later, at discharge, this difference was not present. There is no information about day/night differences in TAC levels of patients with schizophrenia in long-term studies.
The objective of this research is to study if there are day-night changes in serum TAC levels in a group of schizophrenia patients at admission, discharge and three month after hospital discharge (TMAHD).
Materials and methods
Forty-eight subjects meeting DSM-IV diagnostic criteria for schizophrenia psychosis, paranoid type, comprised the initial sample of patients.
From the initial sample of 48 patients, at TMAHD, 35 patients were contacted by telephone; three of them did not attend to the control visit. Therefore, thirty-two subjects comprised the final study sample.
The patient’s clinical status was evaluated with the Clinical Global Impressions (CGI) scale [20]. Both, the severity of psychopathology (CGI-S) and the improvement (CGI-I) of the clinical evolution were evaluated by the same psychiatrist. To make antipsychotic treatments comparable, antipsychotic doses were transformed into chlorpromazine equivalent doses (CED) [21]. Haematological and general biochemical blood tests were carried out in order to exclude physical diseases.
The protocol study was carried out in accordance with the Helsinki declaration and was approved by the Ethic and Investigation Committee of the Canary Islands University Hospital. Written informed consent was obtained from all subjects after full explanation of the study.
TAC was measured to evaluate the antioxidant capacity. After 4 h of fasting, blood samples were collected at 12:00 (light period) and 00:00 (dark period) hours the day after admission, the day before discharge and at TMAHD. After each blood extraction, blood was placed in vacutainer tubes without anticoagulant. Blood was allowed to clot at room temperature during 15 minutes and then was centrifuged at 3000 rpm during 10 minutes. Serum samples were aliquot in Eppendorf tubes and kept frozen at -70° C until analysis.
Serum TAC was measured by the ABTS radical cation technique [22], with commercially available kits (Antioxidant Assay kit, SIGMA, Madrid, Spain). A detailed description of the technique has been published elsewhere. All serum samples were analysed the same day and by the same analyst, who was blind with respect to the characteristics of the samples.
Data were analysed with the 21st version of the Statistical Package for Social Sciences (SPSS, Illinois, Chicago, USA). The comparison of two quantitative variables was carried out by means of paired or independent t-test. The comparison of more than two quantitative variables was carried out with an analysis of variance (ANOVA) for repeated measures. If the result was significant, posterior multiple comparisons were carried out according to Bonferroni test. Chi-square was applied to analyse qualitative variable associations. All statistical tests were two-tailed and their significance level was set at 0.05. Quantitative data are presented as mean ± SD.
Results
Table 1 shows that both samples, TMAHD sample (N = 32) and the only admission-discharge sample (N = 16), are comparable in the demographic and clinical data.
Quantitative data are given as mean ± SD. Qualitative data are given as absolute frequency.
The comparison of serum TAC levels in patients at midday and midnight at the three time-points was highly significant (midday: F = 14.9, p < 0.001; midnight: F = 7.7, p < 0.012). Multiple comparisons using Bonferroni’s correction showed that at admission and discharge patients had significantly lower serum TAC levels at 12:00 and 00:00 h than at TMAHD (p < 0.05). There were no significant differences between midday or midnight TAC levels at admission and discharge. Fig 1 shows the specific data.
Day/night comparisons: a vs b, p: ns; c vs d, p: ns; e vs f, p < 0.006. Serum TAC levels comparisons of at the three time points in patients at midday and midnight: a vs c, p: ns; a vs e, p < 0.05; c vs e, p < 0.05; b vs d, p: ns; b vs f, p < 0.05; d vs f, p < 0.05.
If we consider the data of the control group published in a previous paper [13], the comparisons of serum TAC levels between patients and controls at midday and midnight showed that patients at 12:00 and 00:00 h had significantly lower serum TAC levels at admission and discharge than controls. At TMAHD, there were no significant differences in TAC levels between patients and controls neither at 12:00 nor 00:00 h. Table 2 shows the data.
Discussion
To the best of our knowledge, this is the first time that the absence at admission and discharge and then the existence of a day/night serum TAC concentration difference at TMAHD is reported in paranoid schizophrenia patients. This day/night difference was absent at admission and discharge despite the clinical improvement of the patients. However, at TMAHD, midday TAC concentrations were significantly higher than midnight concentrations. This pattern, higher at midday than midnight, has been reported in healthy subjects [19].
From our point of view, the absence at admission and discharge, and then the presence at TMAHD of a day/night TAC change suggests that patients have undergone a normalization of TAC levels. There are two facts that support this statement. First, the patients have recovered the pattern (higher at midday than at midnight) of TAC difference that is present in healthy subjects [13]. Second, the outpatient’s serum levels at midday and midnight are very similar to the serum levels of a group of healthy subjects [13].
We cannot know if this normalization is present in the serum of patients in the period between discharge and the check at TMAHD. Taking into account that the mean duration of the hospitalization period was 21.1 days (sd. 7.5), it is possible that the improvement in TAC figures would take more than one month because the change of serum TAC concentration between admission and discharge was not significant. A recent study [5] proposes that in schizophrenia patients low TAC levels can take until two and a half months to normalize.
As far as we know, this is the first time that TAC levels in schizophrenia patients at three different clinical points (admission, discharge, and at TMAHD) are compared. Serum TAC levels at TMAHD (00:00 and 12:00 h) are significantly higher than TAC levels at admission and discharge (00:00 and 12:00 h). There were no differences in TAC levels between admission and discharge at 00:00 or 12:00 h.
Some of the previous researches were carried out with a transversal design using inpatients [23] or outpatients [24,25] finding that patients had lower TAC levels than healthy subjects. Other studies applied a longitudinal design with outpatient being studied for a shorter period. Al-Chalabi et al. [26] studied the TAC level previous olanzapine treatment and two months later. They found that previous treatment; patients had lower TAC level than control subjects did. At two months of treatment olanzapine increased TAC levels compared to the basal level. Sarandol et al. [27] compared the TAC level of a combination of schizophrenia outpatients and inpatients before treatment and six weeks after treatment, finding that there was no change in TAC level.
In our opinion, the absence of difference between TAC levels at admission and discharge (12:00 and 00:00 h) is due to the relatively short period of time that exist between admission and discharge measurement (21.1 ± 7.5 days of hospitalization). The third TAC measurement was carried at TMAHD (approximately four times the admission-discharge period). The normalization of TAC levels is found at TMAHD, when serum TAC levels are similar between patients and healthy subjects. From the point of view of TAC levels, patients behave as healthy subjects at TMAHD.
There are several limitations in our study. First, the number of patient is limited. One of the disadvantages of studying circadian rhythms in humans, is that requires taking several biological measures [28] and because of the clinical characteristics of the patients (acutely relapsed), this is a difficult task to perform. Second, the effect of individual antipsychotics was not analysed because the number of subjects treated with each individual antipsychotic was small (less than five cases); this is the reason why we converted all antipsychotic treatment into CED. Our research also has some strengths. First, the same group of subjects comprises the sample of patients studied at admission, discharge and at TMAHD. Second, despite the small sample size, the patients improved significantly.
Conclusion
It is very interesting to point the fact that not only the absolute values of TAC levels have normalized at TMAHD but also that the day/night rhythm that was absent at admission and discharge, appears at TMAHD. The present study adds more evidence that reduced TAC levels and the day/night changes may be involved in the pathophysiology of schizophrenia, although the specific role that these changes play in its aetiology remains unclear.
Acknowledgments
We would like to thank to Dr. Aram Morera-Mesa (freelance translator) for his assistance in the translation of this article.
References
- 1.
American Psychiatric Association (APA). Diagnostic and Statistical Manual of Mental Disorders (5th ed.). Washington, DC: American Psychiatric Association, 2013.
- 2. Falkai P, Moller HJ. Neurobiology of schizophrenia: from outcome to pathophysiological insights. Eur Arch Psychiatry Clin Neurosci 2012;262:93–4. pmid:22271345
- 3.
International Union of Pure and Applied Chemistry (IUPAC). Radicals (free radicals). Compendium of chemical terminology. Gold book. 2 ed. Oxford: 1997. p. 1234.
- 4. Wu JQ, Kosten TR, Zhang XY. Free radicals, antioxidant defense systems, and schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry 2013;46:200–6. pmid:23470289
- 5. Flatow J, Buckley P, Miller BJ. Meta-analysis of oxidative stress in schizophrenia. Biol Psychiatry 2013;74:400–9. pmid:23683390
- 6. Nakano Y, Yoshimura R, Nakano H, Ikenouchi-Sugita A, Hori H, Umene-Nakano W, et al. Association between plasma nitric oxide metabolites levels and negative symptoms of schizophrenia: a pilot study. Hum Psychopharmacol 2010;25:139–44. pmid:20196178
- 7. Chen dC, Xiu MH, Liu H, Zhang BS, Wang Y, Kosten TR, et al. Reduced status of plasma total antioxidant capacity in schizophrenia with tardive dyskinesia. J Psychiatr Res 2010;44:1111–2. pmid:20398909
- 8. Raffa M, Fendri C, Ben OL, Slama H, Amri M, Kerkeni A, et al. The reduction of superoxide dismutase activity is associated with the severity of neurological soft signs in patients with schizophrenia. Prog Neuropsychopharmacol Biol Psychiatry 2012;39:52–6. pmid:22658981
- 9. Zhang XY, Chen dC, Xiu MH, Tang W, Zhang F, Liu L, et al. Plasma total antioxidant status and cognitive impairments in schizophrenia. Schizophr Res 2012;139:66–72. pmid:22555016
- 10. Raffa M, Atig F, Mhalla A, Kerkeni A, Mechri A. Decreased glutathione levels and impaired antioxidant enzyme activities in drug-naive first-episode schizophrenic patients. BMC Psychiatry 2011;11:124. pmid:21810251
- 11. Erel O. A novel automated direct measurement method for total antioxidant capacity using a new generation, more stable ABTS radical cation. Clin Biochem 2004;37:277–85. pmid:15003729
- 12. Gunes M, Altindag A, Bulut M, Demir S, Ibiloglu A, Kaya M, et al. Oxidative metabolism may be associated with negative symptoms in schizophrenia. Psychiatry Clin Psychopharmacol 2017;27:54–61.
- 13. Morera-Fumero AL, Diaz-Mesa E, Abreu-Gonzalez P, Fernandez-Lopez L, Cejas-Mendez MD. Low levels of serum total antioxidant capacity and presence at admission and absence at discharge of a day/night change as a marker of acute paranoid schizophrenia relapse. Psychiatry Res 2017;249:200–5. pmid:28126575
- 14. Yao JK, Reddy R, McElhinny LG, van Kammen DP. Reduced status of plasma total antioxidant capacity in schizophrenia. Schizophr Res 1998;32:1–8. pmid:9690328
- 15. Pazvantoglu O, Selek S, Okay IT, Sengul C, Karabekiroglu K, Dilbaz N, et al. Oxidative mechanisms in schizophrenia and their relationship with illness subtype and symptom profile. Psychiatry Clin Neurosci 2009;63:693–700. pmid:19788631
- 16. Morera AL, Abreu P. Daytime/night-time and summer/winter melatonin and malondialdehyde rhythms: an inverse relationship. J Pineal Res 2007;43:313–4. pmid:17803530
- 17. Morera AL, Intxausti A, Abreu-Gonzalez P. Winter/summer seasonal changes in malondialdehyde formation as a source of variance in oxidative stress schizophrenia research. World J Biol Psychiatry 2009;10:576–80. pmid:18609445
- 18. Benot S, Goberna R, Reiter RJ, Garcia-Maurino S, Osuna C, Guerrero JM. Physiological levels of melatonin contribute to the antioxidant capacity of human serum. J Pineal Res 1999;27:59–64. pmid:10451025
- 19. Morera-Fumero AL, Abreu-Gonzalez P, Henry-Benitez M, Fernandez-Lopez L, Diaz-Mesa E, Cejas-Mendez MDR3, Guillen-Pino F. Day/night and summer/winter changes in serum total antioxidant capacity. Med Chem. 2018;14:1–5.
- 20.
Guy W. ECDEU Assessment Manual for Psychopharmacology. Rockville, MD: US Department of Health, Education, and Welfare Public Health Service Alcohol, Drug Abuse, and Mental Health Administration; 1976.
- 21. Woods SW. Chlorpromazine equivalent doses for the newer atypical antipsychotics. J Clin Psychiatry 2003;64:663–7. pmid:12823080
- 22. Miller NJ, Rice-Evans C, Davies MJ, Gopinathan V, Milner A. A novel method for measuring antioxidant capacity and its application to monitoring the antioxidant status in premature neonates. Clin Sci (Lond) 1993;84:407–12.
- 23. Dietrich-Muszalska A, Kontek B. Lipid peroxidation in patients with schizophrenia. Psychiatry Clin Neurosci 2010;64:469–75. pmid:20923426
- 24. M Ustundag B, Atmaca M, Kirtas O, Selek S, Metin K, Tezcan E. Total antioxidant response in patients with schizophrenia. Psychiatry Clin Neurosci 2006;60:458–64. pmid:16884448
- 25. Virit O, Altindag A, Yumru M, Dalkilic A, Savas HA, Selek S, et al. A defect in the antioxidant defense system in schizophrenia. Neuropsychobiology 2009;60:87–93. pmid:19776652
- 26. Al-Chalabi BM, Thanoon A, Ahmed FA. Potential effect of olanzapine on total antioxidant status and lipid peroxidation in schizophrenic patients. Neuropsychobiology 2009;59:8–11. pmid:19221442
- 27. Sarandol A, Kirli S, Akkaya C, Altin A, Demirci M, Sarandol E. Oxidative-antioxidative systems and their relation with serum S100 B levels in patients with schizophrenia: effects of short term antipsychotic treatment. Prog Neuropsychopharmacol Biol Psychiatry 2007;31:1164–9. pmid:17459548
- 28. Morera-Fumero AL, Abreu-Gonzalez P. Role of melatonin in schizophrenia. Int J Mol Sci 2013;14:9037–50. pmid:23698762