Oxidative stress biomarkers in treatment-responsive and treatment-resistant schizophrenia patients

被引:25
作者
Buosi, Patrick [1 ,2 ]
Borghi, Fabio Aparecido [1 ,2 ]
Lopes, Angelica Marta [2 ]
Facincani, Isabela da Silva [2 ]
Fernandes-Ferreira, Rafael [3 ,4 ]
Oliveira-Brancati, Camila Ive Ferreira [2 ]
do Carmo, Tayanne Silva [2 ]
Silva, Doroteia Rossi [2 ]
da Silva, Danilo Grunig Humberto [5 ]
de Almeida, Eduardo Alves [6 ]
de Araujo Filho, Gerardo Maria [1 ,2 ]
机构
[1] Fac Med Sao Jose do Rio Preto FAMERP, Hosp Base, Sao Jose Do Rio Preto, SP, Brazil
[2] FAMERP, Sao Jose Do Rio Preto, SP, Brazil
[3] Univ Estadual Campinas UNICAMP, Campinas, SP, Brazil
[4] Univ Paulista UNIP, Sao Jose Do Rio Preto, SP, Brazil
[5] Univ Estadual Paulista, Inst Biociencias Letras & Ciencias Exatas Campus, Sao Jose Do Rio Preto Campus UNESP, Sao Jose Do Rio Preto, SP, Brazil
[6] Univ Reg Blumenau FURB, Dept Ciencias Nat, Blumenau, SC, Brazil
基金
巴西圣保罗研究基金会;
关键词
Psychotic disorders; oxidative stress; antioxidants; free radicals; treatment resistance; GLUTATHIONE REDOX STATE; LIPID-PEROXIDATION; ANTIOXIDANT ENZYMES; MALONDIALDEHYDE LEVELS; SUPEROXIDE-DISMUTASE; ASSOCIATION; PSYCHOSIS; DRUG;
D O I
10.47626/2237-6089-2020-0078
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Introduction: Schizophrenia is a complex psychiatric disorder that affects approximately twenty million people worldwide. Various factors have been associated with the physiopathology of this disease such as oxidative stress, which is an imbalance between pro-oxidant and antioxidant molecules. Objective: This study evaluated the association between biomarkers of oxidative stress and response to pharmacological treatment among patients with schizophrenia in the context of their clinical information, demographic data, and lifestyle. Methods: A total of 89 subjects were included, 26 of whom were treatment-responsive schizophrenia patients (Group 1), 27 treatment-resistant schizophrenia patients (Group 2), and 36 healthy controls (Group 3). All of the subjects completed a questionnaire to provide clinical and demographic data, and all provided peripheral blood samples. The oxidative stress markers analyzed using spectrophotometry were catalase (CAT), superoxide dismutase (SOD), glutathione peroxidase (GPx), total glutathione (GSH-t), malondialdehyde (MDA), and Trolox-equivalent antioxidant capacity (TEAC; p < 0.05). Results: When all schizophrenia patients (G1 + G2) were compared to the control group, SOD levels were found to be lower among schizophrenia patients (p < 0.0001), while MDA and CAT levels were higher (p < 0.0001 and p = 0.0191, respectively). GPx, GSH-t, and TEAC levels were similar in all three groups (p > 0.05). Conclusion: Lower SOD levels and higher MDA and CAT levels indicate oxidative damage in schizophrenia patients, regardless of their response to pharmacological treatment. Smoking is associated with oxidative stress, in addition, a family history of the disease was also found to be correlated with cases of schizophrenia, which reflects the relevance of genetics in disease development.
引用
收藏
页码:278 / 285
页数:8
相关论文
共 51 条
[1]  
Akerboom T P, 1981, Methods Enzymol, V77, P373
[2]  
American Psychiatric Association, 2000, DIAGN STAT MAN MENT, DOI DOI 10.1176/DSM10.1176/APPI.BOOKS.9780890420249.DSM-IV-TR
[3]   A Diet and Fitness Program Similarly Affects Weight Reduction in Schizophrenia Patients Treated with Typical or Atypical Medications [J].
Amiaz, R. ;
Rubinstein, K. ;
Czerniak, E. ;
Karni, Y. ;
Weiser, M. .
PHARMACOPSYCHIATRY, 2016, 49 (03) :112-116
[4]  
[Anonymous], 2017, REV INT INVESTIG ADI, DOI DOI 10.28931/RIIAD.2017.1.04
[5]  
Bai Xiang, 2013, J Biochem Pharmacol Res, V1, P228
[6]   No evidence of exogenous origin for the abnormal glutathione redox state in schizophrenia [J].
Ballesteros, Alejandro ;
Jiang, Pan ;
Summerfelt, Ann ;
Du, Xiaoming ;
Chiappelli, Joshua ;
O'Donnell, Patricio ;
Kochunov, Peter ;
Hong, L. Elliot .
SCHIZOPHRENIA RESEARCH, 2013, 146 (1-3) :184-189
[7]  
Beutler E., 1975, Red Cell Metabolism. A manual of biochemical methods, V2nd
[8]  
Bhagat J, 2016, ISJ-INVERT SURVIV J, V13, P336
[9]   The mediating role of depression in pathways linking positive and negative symptoms in schizophrenia. A longitudinal analysis using latent variable structural equation modelling [J].
Carra, Giuseppe ;
Crocamo, Cristina ;
Bartoli, Francesco ;
Angermeyer, Matthias ;
Brugha, Traolach ;
Toumi, Mondher ;
Bebbington, Paul .
PSYCHOLOGICAL MEDICINE, 2020, 50 (04) :566-574
[10]   Reduced superoxide dismutase-1 (SOD1) in cerebrospinal fluid of patients with early psychosis in association with clinical features [J].
Coughlin, Jennifer M. ;
Hayes, Lindsay N. ;
Tanaka, Teppei ;
Xiao, Meifang ;
Yolken, Robert H. ;
Worley, Paul ;
Leweke, F. Markus ;
Sawa, Akira .
SCHIZOPHRENIA RESEARCH, 2017, 183 :64-69