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Associate Director
Interventional Psychiatry
DENT Neurologic Institute
Amherst, New York
Michael Asbach, DMSc, PA-C, Psych-CAQ: consultant/advisor/speaker: AbbVie, Avanir, Biogen, Intracellular, Janssen, Neurocrine, Otsuka.
Key Takeaways
Current State of Bipolar Depression
Bipolar depression presents with significant clinical challenges. Over several decades, a nosological evolution has transpired, with bipolar depression now viewed as a “spectrum” illness ranging from depressive dominant to a more traditional manic-depressive modulating illness. These clinical ambiguities have contributed to uncertainty in diagnosis for many healthcare professionals—as well as therapeutic confusion. Timely diagnosis, therapeutic consensus, and diagnostic agreement are all important areas where the current understanding of bipolar depression falls short.
A diagnosis of bipolar depression often lags 6-8 years after the initial onset of symptoms; in some cases, the lag is up to 13 years. One leading reason for the delay in diagnosis is that unipolar depression and bipolar depressive episodes will clinically present indistinguishably. Furthermore, the depressive phase of bipolar disorder represents the majority of time ill, with patients experiencing depression ranging from 70% to 81% of time ill. This predominance of presentation has led to many initial misdiagnoses: As many as 40% of people initially diagnosed with unipolar depression are later diagnosed with bipolar disorder.
Bipolar depression is associated with high rates of functional impairment and disability, as well as morbidity. Suicide risk is 10-30 times higher for patients with bipolar disorder compared with the general population, with depressive and mixed-mood states carrying the highest risk of suicidal behavior. Delays in accurate diagnosis consequently lead to delays in appropriate treatment, thereby playing a large role in these high rates of functional impairment and morbidity.
Shortcomings in the Current Treatment of Bipolar Depression
Bipolar depression is widely thought to require a different pharmacologic approach than major depressive disorder (MDD), despite its clinical similarities. The majority of bipolar disorder is represented by the depressive phase of illness, but there is concern that the use of antidepressants risks switching the patient into a manic or agitated mood state. Although the absolute risk of antidepressant-induced mood activation is not definitive, the STEP-BD trial found that antidepressant performance was similar to placebo as treatment of bipolar depression.
Alternative treatment options include mood stabilizers such as lithium and second-generation antipsychotics. For more than 50 years, lithium has been one of the most effective treatments for bipolar disorder, often recommended as first-line therapy by many treatment guidelines. Yet, it remains underused given the wealth of empirical evidence supporting its efficacy and safety. In the past decade, second-generation antipsychotics have become a mainstay of bipolar depression treatment, with several agents receiving an FDA indication for bipolar depression in the past few years. Most of these approved agents are associated with a modest treatment effect in bipolar depression. However, they also are associated with adverse events at therapeutic dosing including restlessness, sedation, metabolic disorders, and drug-induced movement disorders.
Looking Ahead: Innovations in Bipolar Depression Therapies
The need to innovate and identify novel therapeutic approaches is felt across the mental health spectrum, and bipolar depression is no exception. Several novel therapies have shown promise in the treatment of bipolar depression. Ketamine is a glutamatergic modulator that has emerged as a rapid and effective intervention of acute MDD. There is growing evidence that ketamine may have clinical utility in bipolar depression, but the studies remain small with varying quality. Some case reports of ketamine-inducing affective switching exist, but more research is needed to assess risk of mood destabilization. Esketamine, an enantiomer of ketamine, is indicated for MDD. There are no placebo-controlled trials involving esketamine for bipolar depression, but a recent case study of intranasal esketamine in a patient with bipolar depression—in addition to promising evidence of the efficacy of racemic ketamine—suggests that further investigation is needed.
Other approaches include neurosteroids and psychedelics. Neurosteroids have been a promising realm of clinical research for MDD, postpartum depression, and insomnia. These GABAA-modulating agents should be investigated further, specifically within bipolar depressive illness. Classic psychedelics such as LSD, psilocybin, mescaline, and ayahuasca stimulate the serotonin 2A receptor and have shown promise in the treatment of unipolar depression, posttraumatic stress disorder, and obsessive-compulsive disorder. Unfortunately, patients with bipolar depression have been excluded from psychedelic research due to case reports of manic and psychotic inducement in vulnerable patients.
Neuromodulation also carries promise as an innovative treatment approach for bipolar depression. Repetitive transcranial magnetic stimulation (rTMS) was cleared by the FDA as a treatment of MDD in 2008. Recently, many small-scale studies have demonstrated both efficacy and safety profiles using rTMS for the treatment of bipolar depression.
Conclusion
Treatment of bipolar depression remains an unmet clinical need. Although more treatments are available, the illness remains debilitating and a leading cause of morbidity among mental health disorders. Several second-generation antipsychotics now are approved for use in bipolar depression, and they have been shown to have moderate effect. Although treatment of bipolar depression is far less investigated than MDD, promising innovations are in the development pipeline.
Your Thoughts?
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Bibliography
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