Abstract

Background: Modafinil has complex, and as yet unclear, pharmacodynamics mechanisms. The prescribing of modafinil to augment monoamine oxidase inhibitor (MAOI) therapy was investigated for 3 patients with major depressive disorder determined to be treatment-resistant depression. Methods: As a retrospective report from a private psychiatry practice, 2 men and 1 woman with major depressive disorder, aged from 55 to 60 years, were evaluated and treated. All patients met criteria for treatment-resistant depression, with failure of 3 or more trials of medication with augmentation; one patient failed electroconvulsive therapy and vagal nerve stimulation. All patients had reported feeling some improvement before the addition of modafinil to existing MAOI therapy. However, immobilizing exhaustion in the 2 male patients and fatigue in the female patient impaired daily function. All patients suffered multiple serious medical comorbidities. Mitigating the influence of cycling or placebo, a 2-year period of response approximated treatment outcome. Results: With the addition of modafinil to MAOI therapy, modafinil all 3 patients improved in mood and alertness modafinil without adverse events (e.g., blood pressure, cardiac rate, extrapyramidal symptoms). Limitations: Although treatment was effective, the sample size was 3 patients. Conclusion: The mechanism by which modafinil improved the function of the 3 patients is unclear. Although many medications are contraindicated with MAOIs, most contraindications are unsubstantiated. In the present series of patients, there were no adverse events with either higher-than-recommended doses of MAOI or the combination of modafinil or tianeptine modafinil with MAOI.

Highlights

  • Unipolar depression, a probably heterogeneous disease, presents obstacles to research and treatment in part due to no reproducible biomarkers with selectivity and specificity for subtypes of depression

  • The serendipitous discovery that the monoamine oxidase inhibitor (MAOI), iproniazid, prescribed to treat tuberculosis patients, helped alleviate the suffering of many mentally ill patients lead to further research about the intracellular role of the enzyme monoamine oxidase (MAO) in mood modulation

  • Schildkraut questioned the relevance of studies of mood disorder that are based on drug responses, noting, “pathophysiologic hypothesis, derived from studies of the mechanism of action of drugs which induce mood disorders or drugs effective in their treatment are primarily of heuristic value in suggesting directions for further research

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Summary

Introduction

A probably heterogeneous disease, presents obstacles to research and treatment in part due to no reproducible biomarkers with selectivity and specificity for subtypes of depression. Current evaluation and treatment of mood disorder mirrors the challenges that Hippocrates faced evaluating and treating epilepsy without an established biological marker and with frequent placebo response [1]. The serendipitous discovery that the monoamine oxidase inhibitor (MAOI), iproniazid, prescribed to treat tuberculosis patients, helped alleviate the suffering of many mentally ill patients lead to further research about the intracellular role of the enzyme monoamine oxidase (MAO) in mood modulation. Debilitating consequences of depression include anergy, anhedonia, and destabilization of autonomic regulation, as well as impairment in executive function, processing speed, and episodic memory [2,3]. Debilitating phenomenological consequences result from pathological changes in cellular and tissue structure, impairing neuroplasticity [47]. The prescribing of modafinil to augment monoamine oxidase inhibitor (MAOI) therapy was investigated for 3 patients with major depressive disorder determined to be treatment-resistant depression

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