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Chapter 1 - Current depression landscape

a state of the field today

Published online by Cambridge University Press:  19 October 2021

Chad E. Beyer
Affiliation:
University of Colorado School of Medicine
Stephen M. Stahl
Affiliation:
University of California, San Diego
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Summary

More than two dozen pharmacological treatments are currently available for depression, working by more than a half dozen mechanisms, yet there remain many unmet therapeutic needs. Available antidepressants act directly on monoamine mechanisms, influencing receptors and transporters for serotonin, norepinephrine, and/or dopamine. Truly novel therapeutic targets beyond the monoamines have not emerged in the past few decades. Advances have been mostly in improved tolerability, and as a result, limitations in efficacy persist for all agents in the antidepressant class. Specifically, far too few patients, perhaps only a third, attain a full remission of symptoms, and those who have had many episodes of depression are not likely to sustain any remission for more than a few months. Thus, there is the urgent need for antidepressants with improved efficacy. Although the “holy grail” of antidepressant treatment has long been rapid onset of action, the reality is that more robust and sustained efficacy, even if delayed, is the unmet need of today. This is unlikely to be met by targeting the same monoamine transporters and receptors where current antidepressants act, so novel therapeutic targets must be identified if there is to be novel therapeutic efficacy of more robust and sustained antidepressant action.

Other issues in the treatment of depression include the increasing confusion between unipolar and bipolar depression, particularly at onset of first depressive episodes, as well as the confusion between treatment-resistant unipolar depression versus difficult-to-treat rapid cycling, mixed episodes of bipolar depression. Treatments for bipolar depression such as anticonvulsants and atypical antipsychotics are increasingly being used for bipolar and treatment-resistant cases. Future therapeutics may usefully exploit these mechanisms, and treatment of difficult cases in the future will likely involve use of multiple simultaneous mechanisms, either with multiple drugs or with multifunctional drugs.

There is also concern that depression may be a progressive illness, with unipolar depression progressing to treatment-resistant depression or even to bipolar spectrum disorder, and bipolar disorder progressing to rapid cycling and mixed treatment-resistant bipolar episodes. Future treatments of depression may not only have the potential to treat current symptoms and prevent their relapse, but also to halt progression and thus be disease-modifying, altering the course of untreated or inadequately treated illness.

Type
Chapter
Information
Next Generation Antidepressants
Moving Beyond Monoamines to Discover Novel Treatment Strategies for Mood Disorders
, pp. 1 - 11
Publisher: Cambridge University Press
Print publication year: 2010

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References

Rubinow, D. R. 2006. N. Engl. J. Med., 354, 1305.Google Scholar
Selikoff, I. J., and Robitzek, E. H. 1952. Dis. Chest, 21(4), 385.Google Scholar
Healy, D. 1996. The Psychopharmacologists: Interviews, London, Chapman & Hall.Google Scholar
Healy, D. 1999. J. Nerv. Ment. Dis., 187(3), 174.Google Scholar
Stahl, S. M. 2008. Stahl’s Essential Psychopharmacology, third edition, New York, Cambridge University Press.Google Scholar
Duman, R. S., Nakagawa, S., and Malberg, J. 2001. Neuropsychopharmacology, 25, 836.Google Scholar
Warden, D., Rush, A. J., Trivedi, M. H., Fava, M., and Wisniewski, S. R. 2007. Curr. Psychiatry. Rep., 9, 449.Google Scholar
Fava, M., and Rush, A. J. 2006. Psychother. Psychosom., 75, 139.CrossRefGoogle Scholar
Fava, G. A. 2003. J. Clin. Psychiatry, 64, 123.CrossRefGoogle Scholar
Fava, G. A., and Kellner, R. 1993. Acta Psychiatr. Scand., 87, 223.CrossRefGoogle Scholar
McGorry, P. D., Hichie, I. B., Yang, A. R., Pantelis, C., and Jackson, H. J. 2006. Aust. N. Z. J. Psychiatry, 40, 616.Google Scholar
Fava, G. A., and Tossani, E. 2007. Early Interv. Psychiatry, 1, 9.CrossRefGoogle Scholar
Fava, G. A., Tomba, E., and Grandi, S. 2007. Psychother. Psychosom., 76, 260.Google Scholar
Stahl, S. M. 2009. Essential Psychopharmacology: The Prescriber’s Guide, third edition, New York, Cambridge University Press.Google Scholar
Wise, D. D., Felker, A., and Stahl, S. M. 2008. CNS Spectr., 13, 647.Google Scholar
Papakostas, G. I., Shelton, R. C., Smith, J., and Fava, M. 2007. J. Clin. Psychiatry, 68, 826.Google Scholar
Grady, M. M., and Stahl, S. M. 2010. Encyclopedia of Psychopharmacology, Heidelberg, Springer-Verlag.Google Scholar
Fava, M. 2007. J. Clin. Psychiatry, 68(suppl 10), 4.Google Scholar
Benazzi, F. 2007. Psychother. Psychosom., 76, 70.Google Scholar

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