Evaluation of malondialdehyde, superoxide dismutase and catalase activity and their diagnostic value in drug naive, first episode, non-smoker major depression patients and healthy controls

被引:56
作者
Camkurt, Mehmet Akif [1 ]
Findikli, Ebru [2 ]
Izci, Filiz [3 ]
Kurutas, Ergul Belge [4 ]
Tuman, Taha Can [5 ]
机构
[1] Afsin State Hosp, Dept Psychiat, Afsin, Kahramanmaras, Turkey
[2] Kahramanmaras Sutcu Imam Univ, Dept Psychiat, Kahramanmaras, Turkey
[3] Istanbul Bilim Univ, Dept Psychiat, Istanbul, Turkey
[4] Kahramanmaras Sutcu Imam Univ, Dept Biochem, Kahramanmaras, Turkey
[5] Izzet Baysal Training & Res Hosp Psychiat, Bolu, Turkey
关键词
TERM ANTIDEPRESSANT TREATMENT; OXIDATIVE STRESS; LIPID-PEROXIDATION; BIPOLAR DISORDER; GENERALIZED ANXIETY; DAMAGE; SCHIZOPHRENIA; METAANALYSIS; PERFORMANCE; BIOMARKERS;
D O I
10.1016/j.psychres.2016.01.075
中图分类号
R749 [精神病学];
学科分类号
100205 ;
摘要
Major depression is a most frequent disorder, its diagnosis depends on pkient interview, and yet we do not have a reliable biomarker for depression. Oxidative stress is defined as increase in oxidation or decrease is antioxidant defense mechanisms. Here, we aimed to investigate malondialdehyde (MDA), superoxide dismutase (SOD) and catalase (CAT) activity and their diagnostic performance in depressed patients and healthy controls. We collected blood samples from 50 patients and 50 controls. We found MDA levels were significantly higher in the patients than controls, with medians at 4.04nmol/mg and 1.64nmol/mg, respectively, p < 0.001. SOD activity was significantly decreased in depressed patients than healthy controls, with means at 143.50U/mg and 298.12U/mg, respectively, p < 0.001. CAT activity was similar in both groups, p=0.517. ROC analysis showed good diagnostic value for MDA and SOD, with the area under the curve at 1.0 for both. We found high correlation between SOD and Ham-D scores (r=0.747, p < 0.0001) and between MDA and Ham-D scores (r=0.785, p < 0.0001). Overall, these results demonstrate that oxidative stress is increased in depressed patients. MDA increase seem to be a common finding for major depression. We believe MDA could be a good biomarker candidate for major depression, but not SOD. Future studies should focus on the diagnostic value of MDA in larger samples. (C) 2016 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:81 / 85
页数:5
相关论文
共 36 条
  • [1] DNA damage in bipolar disorder
    Andreazza, Ana Cristina
    Frey, Benicio Noronha
    Erdtmann, Bernardo
    Salvador, Mirian
    Rombaldi, Fernanda
    Santin, Aida
    Goncalves, Carlos Alberto
    Kapczinski, Flavio
    [J]. PSYCHIATRY RESEARCH, 2007, 153 (01) : 27 - 32
  • [2] Biomarkers and surrogate endpoints: Preferred definitions and conceptual framework
    Atkinson, AJ
    Colburn, WA
    DeGruttola, VG
    DeMets, DL
    Downing, GJ
    Hoth, DF
    Oates, JA
    Peck, CC
    Schooley, RT
    Spilker, BA
    Woodcock, J
    Zeger, SL
    [J]. CLINICAL PHARMACOLOGY & THERAPEUTICS, 2001, 69 (03) : 89 - 95
  • [3] Oxidative Stress and Major Depression
    Bajpai, Ashutosh
    Verma, Akhilesh Kumar
    Srivastava, Mona
    Srivastava, Ragini
    [J]. JOURNAL OF CLINICAL AND DIAGNOSTIC RESEARCH, 2014, 8 (12) : CC4 - CC7
  • [4] BEERS RF, 1952, J BIOL CHEM, V195, P133
  • [5] Beutler E., 1984, RED CELL METABOLISM, P160
  • [6] ASSAYING FOR SUPEROXIDE-DISMUTASE ACTIVITY - SOME LARGE CONSEQUENCES OF MINOR CHANGES IN CONDITIONS
    BEYER, WF
    FRIDOVICH, I
    [J]. ANALYTICAL BIOCHEMISTRY, 1987, 161 (02) : 559 - 566
  • [7] Antioxidative enzyme activities and lipid peroxidation in major depression:: alterations by antidepressant treatments
    Bilici, M
    Efe, H
    Köroglu, MA
    Uydu, HA
    Bekaroglu, M
    Deger, O
    [J]. JOURNAL OF AFFECTIVE DISORDERS, 2001, 64 (01) : 43 - 51
  • [8] Is depression associated with increased oxidative stress? A systematic review and meta-analysis
    Black, Catherine N.
    Bot, Mariska
    Scheffer, Peter G.
    Cuijpers, Pim
    Penninx, Brenda W. J. H.
    [J]. PSYCHONEUROENDOCRINOLOGY, 2015, 51 : 164 - 175
  • [10] Bulut M, 2007, J PSYCHIATR NEUROSCI, V32, P435