Oxidative stress markers in bipolar disorder: a meta-analysis

J Affect Disord. 2008 Dec;111(2-3):135-44. doi: 10.1016/j.jad.2008.04.013. Epub 2008 Jun 9.

Abstract

Background: Oxidative stress is thought to mediate neuropathological processes of a number of neuropsychiatric disorders and recent data suggest that oxidative stress may be involved in the pathophysiology of bipolar disorder (BD). In the present investigation, we conducted a meta-analysis of studies that evaluated markers of oxidative stress in individuals with BD, as compared to healthy controls.

Methods: A Medline search was conducted to identify studies that measured peripheral markers of oxidative stress in bipolar disorder. Data were subjected to meta-analysis using a random effects model to examine the effect sizes of the pooled results. Bias assessment (Egger's test) and assessment of heterogeneity (I(2)) were also carried out.

Results: Thiobarbituric acidic reactive substances (TBARS) (p = 0.001) as well as NO activity (p = 0.02) were significantly increased in BD with a large effect size for TBARS and a moderate effect size for increase in NO. No significant effect sizes were observed for the antioxidant enzymes superoxide dismutase, catalase and glutathione peroxidase (all p>0.05).

Limitations: Some caution is warranted in interpreting these results: (1) Egger's test was positive for SOD, suggesting that SOD results may have been influenced by a publication bias. (2) We analyzed the absolute values of each antioxidant enzyme separately and the literature suggests that an imbalance between the antioxidant enzymes is a better indication of the presence of oxidative stress.

Conclusions: The present meta-analysis suggests that oxidative stress markers are increased in BD and that oxidative stress may play a role in the pathophysiology of BD.

Publication types

  • Comparative Study
  • Meta-Analysis
  • Research Support, Non-U.S. Gov't
  • Review

MeSH terms

  • Antioxidants / metabolism
  • Antioxidants / physiology
  • Biomarkers / metabolism
  • Bipolar Disorder / enzymology
  • Bipolar Disorder / metabolism
  • Bipolar Disorder / physiopathology*
  • Control Groups
  • Erythrocytes / metabolism
  • Glutathione Peroxidase / metabolism
  • Humans
  • Lipid Peroxidation / physiology
  • Nitric Oxide / metabolism
  • Oxidative Stress / physiology*
  • Protein Carbonylation / physiology
  • Superoxide Dismutase / metabolism
  • Thiobarbituric Acid Reactive Substances / metabolism

Substances

  • Antioxidants
  • Biomarkers
  • Thiobarbituric Acid Reactive Substances
  • Nitric Oxide
  • Glutathione Peroxidase
  • Superoxide Dismutase