Improvements in neurocognitive function and mood following adjunctive treatment with mifepristone (RU-486) in bipolar disorder
- PMID: 15127079
- DOI: 10.1038/sj.npp.1300471
Improvements in neurocognitive function and mood following adjunctive treatment with mifepristone (RU-486) in bipolar disorder
Abstract
High cortisol levels are found in severe mood disorders, particularly bipolar disorder. Hypercortisolaemia may cause or exacerbate both neurocognitive impairment and depressive symptoms. We hypothesized that antiglucocorticoid treatments, particularly corticosteroid receptor antagonists, would improve neurocognitive functioning and attenuate depressive symptoms in this disorder. To test this hypothesis, 20 bipolar patients were treated with 600 mg/day of the corticosteroid receptor antagonist mifepristone (RU-486) or placebo for 1 week in a double-blind crossover design. Over the total 6 weeks of the study, neurocognitive and neuroendocrine function were evaluated at baseline, days 21 and 42. Mood symptoms were evaluated weekly. Nineteen subjects completed the protocol; there were no drop-outs due to adverse events. Following treatment with mifepristone, selective improvement in neurocognitive functioning was observed. Spatial working memory performance was significantly improved compared to placebo (19.8% improvement over placebo). Measures of verbal fluency and spatial recognition memory were also improved after mifepristone. Beneficial effects on mood were found; Hamilton Depression Rating Scale scores were significantly reduced compared to baseline (mean reduction of 5.1 points) as were Montgomery-Asberg Depression Rating Scale scores (mean reduction of 6.05 points). No significant change occurred after placebo. These data require replication but provide preliminary evidence that glucocorticoid receptor antagonists may have useful cognitive-enhancing and possibly antidepressant properties in bipolar disorder.
Similar articles
-
Effects of adjunctive mifepristone (RU-486) administration on neurocognitive function and symptoms in schizophrenia.Biol Psychiatry. 2005 Jan 15;57(2):155-61. doi: 10.1016/j.biopsych.2004.10.017. Biol Psychiatry. 2005. PMID: 15652874 Clinical Trial.
-
Changes in brain-derived neurotrophic factor following treatment with mifepristone in bipolar disorder and schizophrenia.Aust N Z J Psychiatry. 2007 Apr;41(4):321-6. doi: 10.1080/00048670701213211. Aust N Z J Psychiatry. 2007. PMID: 17464718 Clinical Trial.
-
Persistent effects of mifepristone (RU-486) on cortisol levels in bipolar disorder and schizophrenia.J Psychiatr Res. 2008 Oct;42(12):1037-41. doi: 10.1016/j.jpsychires.2007.12.005. Epub 2008 Feb 5. J Psychiatr Res. 2008. PMID: 18255098 Clinical Trial.
-
Cognitive and psychomotor effects of risperidone in schizophrenia and schizoaffective disorder.Clin Ther. 2008 Sep;30(9):1565-89. doi: 10.1016/j.clinthera.2008.09.014. Clin Ther. 2008. PMID: 18840365 Review.
-
Baseline cortisol and the efficacy of antiglucocorticoid treatment in mood disorders: A meta-analysis.Psychoneuroendocrinology. 2019 Dec;110:104420. doi: 10.1016/j.psyneuen.2019.104420. Epub 2019 Aug 23. Psychoneuroendocrinology. 2019. PMID: 31499391
Cited by
-
Effects of chronic stress on cognitive function - From neurobiology to intervention.Neurobiol Stress. 2024 Sep 2;33:100670. doi: 10.1016/j.ynstr.2024.100670. eCollection 2024 Nov. Neurobiol Stress. 2024. PMID: 39295772 Free PMC article. Review.
-
Neuronal nitric oxide synthase and affective disorders.IBRO Rep. 2018 Nov 17;5:116-132. doi: 10.1016/j.ibror.2018.11.004. eCollection 2018 Dec. IBRO Rep. 2018. PMID: 30591953 Free PMC article. Review.
-
New drugs for bipolar disorder.Curr Psychiatry Rep. 2011 Dec;13(6):513-21. doi: 10.1007/s11920-011-0231-1. Curr Psychiatry Rep. 2011. PMID: 21877160 Review.
-
Double-blind, placebo-controlled trial of mifepristone on cognition and depression in alcohol dependence.Trials. 2020 Sep 16;21(1):796. doi: 10.1186/s13063-020-04726-z. Trials. 2020. PMID: 32938477 Free PMC article. Clinical Trial.
-
A single-day treatment with mifepristone is sufficient to normalize chronic glucocorticoid induced suppression of hippocampal cell proliferation.PLoS One. 2012;7(9):e46224. doi: 10.1371/journal.pone.0046224. Epub 2012 Sep 25. PLoS One. 2012. PMID: 23049985 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical