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Enhancing Outcomes from Major Depression: Using Antidepressant Combination Therapies with Multifunctional Pharmacologic Mechanisms from the Initiation of Treatment

Published online by Cambridge University Press:  07 November 2014

Extract

Traditional guidelines call for treatment of major depression with a sequence of single antidepressants. Augmentation with a second agent generally only occurs when the first agent is well tolerated and when it also provides at least some symptomatic improvement on its own. Since this standard approach leads to low rates of attaining and sustaining remission by the first agent, with diminishing returns for each subsequent agent, there is growing dissatisfaction with this approach to the treatment of major depression. One new trend is to attempt to enhance the rates of sustained remission from a major depressive episode by combining two therapeutic agents from the very initiation of treatment of a major depressive episode.

Traditional treatment of major depression begins with a single “first line” antidepressant, and if it does not work or is not tolerated, trying another and then another. Unfortunately, this strategy results in disappointing remission rates for the first antidepressant (Figure 1), and disappointing rates of maintaining any improvement that is attained by this first agent because of high relapse rates over the next year despite continuing treatment with the first antidepressant (Figure 2A). And that is the good news. The bad news is that with each subsequent antidepressant treatment administered remission rates are progressively reduced (Figure 1). For those patients who do improve, they are progressively less likely to sustain their therapeutic gains despite continuing to take the drug that led to their initial improvement (Figure 2).

Type
Trends in Psychophamacology
Copyright
Copyright © Cambridge University Press 2010

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References

REFERENCES

1.American Psychiatric Association, Practice Guidelines for Major depressive disorder, second edition, 2005, DOI: 10.1176/appi books.9780890423363.48690Google Scholar
2.Stahl, SM. Stahls Essential Psychopharmacocology 3rd edition. New York, NY: Cambridge University Press; 2008.Google Scholar
3.Rush, AJ, Trivedi, MH, Wisniewski, SR, et al.Acute and longer term outcomes in depressed outpatients requiring one or several treatment steps: A Star*D report. Am J Psychiatry. 2006;163:19051917.CrossRefGoogle ScholarPubMed
4.Warden, D, Rush, AJ, Trivedi, MH, Fava, M, Wisneiwski, SR. The STAR*D project results: a comprehensive review of findings. Curr Psychiatry Rep. 2007;9:449459.CrossRefGoogle ScholarPubMed
5.Cipriani, A, Furukawa, TA, Salanti, G, et al.Comparative efficacy and acceptability of 12 new-generation antidepressants: a multiple-treatments meta analysis. Lancet. 2009;373:746758.Google Scholar
6.Stahl, SM. Multifunctional Drugs: A Novel Concept for Psychopharmacology. CNS Spectr. 2008;14:7173.CrossRefGoogle Scholar
7.Millan, M.Dual and triple acting agents for treating core and comorbid symptoms of major depression: novel concepts, new drugs. Neurotherapeutics 2009;6:5377.Google Scholar
8.Stahl, SM. Combining antidepressant therapies from the initiation of treatment: a paradigm shift for major depression. J Clin Psychiatry. 2009;70:14931494.CrossRefGoogle ScholarPubMed
9.Brunton, LL. Goodman and Gilman's The Pharmacological Basis of Therapeutics, 11th edition. New York, NY: McGraw Hill; 2006.Google Scholar
10.Stahl, SM. Stahls Essential Psychopharmacology Preserver's Guide. New York, NY: Cambridge University Press;2009.Google Scholar
11.Fava, M, Rush, AJ. Current Status of Augmentation and Combination Treatments for Major Depressive Disorder: A literature review and a proposal for a novel approach to improve practice. Psychother Psychosom. 2006;75:139153.Google Scholar
12.Freeman, M, Fava, M, Mischoulon, D, Papakostas, G, Shelton, R. The use of complimentary and alternative medicines to achieve remission in major depressive disorder. J Clin Psychiatry. 2009;70 (suppl 5): 127.Google Scholar
13.Stahl, SM. Novel therapeutics for depression: L-methylfolate (6(S)-5-methyltetrahy-drofolate or MTHF) as a trimonoamine modulator and antidepressant augmenting agent. CNS Spectr. 2007;12:423428.Google Scholar
14.Pan, C-C, McQuoid, DR, Taylor, WD, Payne, ME, Ashley-Koch, A, Staffens, DC. Association analysis of the COMT/MTHFR genes and geriatric depression: an MRI study of the putamen. Int J Geriatr Psychiatry. 2009;24:847855.CrossRefGoogle ScholarPubMed
15.Lewis, SJ, Lawlor, DA, Davey Smith, G, et al.The thermolabile variant of MTHFR is associated with depression in the British Women's heart and health study and a meta analysis. Mol Psychiatry. 2006;11:352360.CrossRefGoogle ScholarPubMed
16.Kelly, CB, McDonnell, AP, Johnston, TG, et al.The MTHFR C677T polymorphism is associated with depressive episodes in patients from Northern Ireland. J Psychopharmacol. 2004;18: 567571.Google Scholar
17.Ariami, T, Yamada, N, Yamakawa-Kobayashi, K. Methylenetetrahydrofolate reductase variant and schizophrenia/depression. Am J Med Genet. 1997;74:526528.Google Scholar
18.Gilbody, S, Lewis, S, Lightfoot, T. Methylenetetrahydrofolate reductase genetic polymorphisms and psychiatric disorders: A Huge review. Am J Epidemiol. 2007;165:113.Google Scholar
19.Stahl, SM. L-methylfolate: a vitamin for your monoamines. J Clin Psychiatry. 2008;69:13521353.Google Scholar
20.Delgado, PL, Miller, HL, Salomon, RM. Tryptophan-depletion in depressed patients treated with desipramine or fluoxetine: implications for the role of serotonin in the mechanism of antidepressant action. Biol Psychiatr. 199:46:212220Google Scholar
21.Godfrey, PS, Toone, BK, Garney, MWB, et al.Enhancement of recovery from psychiatric illness by methylfolate. Lancet. 1990;336:392395.Google Scholar
22.Coppen, A, Bailey, J. Enhancement of the antidepressant action of fluoxetine by folic acid: a randomized, placebo controlled trial. J Affective Dis. 2000;60:121130.Google Scholar
23.Resler, G, Lavie, R, Campos, J, et al.Effect of folic acid combined with fluxetine in patients with major depression on plasma homocysteine and vitamin B12, and serotonin levels in lymphocytes. Neuroimmunomodulation. 2008;15:145152.CrossRefGoogle Scholar
24.Bottiglieri, T. Homocysteine and folate metabolism in depression. Prog Neuropsychopharmacol Biol Psychiatry. 2005;29:11031112.Google Scholar
25.Stahl, SM. Personalized Medicine, Pharmacogenomics, and the Practice of Psychiatry: On the Threshold of Predictive Therapeutics in Psychopharmacology? CNS Spectr 2008;13:115118.Google Scholar
26.Stahl, SM. Epigenetics and methylomics in psychiatry. J Clin Psychiatry. 2009;70:12041205.CrossRefGoogle ScholarPubMed
27.Massat, I, Sourey, D, Del-Favero, J, et al.Association between COMT (Val 148 Met) functional polymorphism and early onset in patients with major depressive disorder in a European multicenter genetic association study. Mol Psychiatry. 2005;10:598605.CrossRefGoogle Scholar
28.Baune, BT, Hohoff, Ch, Berger, K, et al.Association of the COMT val 58 met variant with antidepressant treatment response in major depression. Neuropsychopharmacol. 2008;33:924932.Google Scholar
29.Yoshida, K, Higuchi, H, Takahashi, H, et al.Influence of the tyrosine hydroxylase val81met polymorphism and catechol-0-methyltransferase val 155 met polymorphism on the antidepressant effect of milnacipran. Human Psychopharmacol. 2008;23:121128.Google Scholar
30.Benedetti, F, Colombo, C, Pirovano, A, Marino, E, Smeraldi, E. The catechol-0-methyltransferase Val(108/158)Met polymorphism affects antidepressant response to paroxetine in a naturalistic setting. Psychopharmacology (Berl). 2009;203:155160.Google Scholar
31.Tsai, SJ, Gau, YT, Hong, CJ, Liou, YJ, Yu, YW, Chen, TJ. Sexually dimorphic effect of catechol-0-methyltransferase val158met polymorphism on clinical response to fluoxetine in major depressive patients. J Affect Disord. 2009;113:183187.Google Scholar
32.Arias, B, Serretti, A, Lorenzi, C, Gastó, C, Catalán, R, Fañanás L. Analysis of COMT gene (Val 158 Met polymorphism) in the clinical response to SSRIs in depressive patients of European origin. J Affect Disord 2006;90:251256.Google Scholar
33.Funke, B, Malhotra, AK, Finn, CT, et al.COMT genetic variation confers risk for psychotic and affective disorders: a case control study. Behav Brain Funct. 2005;1:19.Google Scholar
34.Szegedi, A, Rujescu, D, Tadic, A, et al.The catechol-0-methyltransferase Val108/158Met polymorphism affects short-term treatment response to mirtazapine, but not to paroxetine in major depression. Pharmacogenomics J. 2005;5:4953.CrossRefGoogle Scholar
35.Potter, GG, Taylor, WD, McQuoid, DR, Steffens, DC, Welsh-Bohmer, KA, Krishnan, KR. The COMT Val158Met polymorphism and cognition in depressed and nondepressed older adults. Int J Geriatr Psychiatry. 2009;24:11271133.Google Scholar
36.Zalsman, G, Huang, YY, Oquendo, MA, et al.No association of COMT Val158Met polymorphism with suicidal behavior or CSF monoamine metabolites in mood disorders. Arch Suicide Res. 2008;12:327335.Google Scholar
37.Baekken, PM, Skorpen, F, Stordal, E, Zwart, JA, Hagen, K. Depression and anxiety in relation to catechol-0-methyltransferase Val158Met genotype in the general population: the Nord-Trendelag Health Study (HUNT). BMC Psychiatry. 2008;8:48.Google Scholar
38.Tunbridge, EM, Harrison, PJ, Warden, DR, Johnston, C, Refsum, H, Smith, AD. Polymorphisms in the catechol-0-methyltransferase (COMT) gene influence plasma total homocysteine levels. Am J Med Genet B Neuropsychiatr Genet. 2008;147B:996999.CrossRefGoogle Scholar
39.Nestler, EJ. Epigenetic mechanisms in psychiatry. Biol Psychiatry. 2009;65:189190.Google Scholar
40.Jiang, Y, Sun, T, Xiong, J, Cao, J, Li, G, Want, S. Hyperhomocysteinemia-mediated DNA hypmethylation and its potential epigenetic role in rats. Acta Biochlmica et Biophysica Sinica. 2007;39:657667.CrossRefGoogle ScholarPubMed
41.Sasaki, M, Kaneuchi, M, Sakuragi, N, Dahiya, R. Multiple promoters of catechol-0-methyltransferase gene are selectively inactivated by CpG hypermethylation in endometrial cancer. Cancer Res. 2003;63:31013106.Google Scholar
42.Abdolmaleky, HM, Cheng, KH, Faraone, SV, et al.Hypomethylation of MB-COMT promoter is a major risk factor for schizophrenia and bipolar disorder. Hum Mol Genet. 2006;15:31323145.CrossRefGoogle Scholar
43.Mill, J, Dempster, E, Caspi, A, Williams, B, Moffitt, T, Craig, I. Evidence for monozygotic twin (MZ) discordance in methylation level at two CpG sites in the promoter region of the catechol-0-methyltransferase (COMT) gene. Am J Med Genet B Neuropsychiatr Genet. 2006;141B:421425.Google Scholar
44.Nierenberg, A, Bronwyn, RK, Leslie, VC, et al.Residual symptoms in depressed patients who respond acutely to fluoxetine. J Clin Psychiatry. 1999;60:221225.CrossRefGoogle ScholarPubMed
45.Stahl, SM. Selective Histamine H1 Antagonism: Novel Hypnotic and Pharmacologic Actions Challenge Classical Notions of Antihistamines. CNS Spectr. 2008;13:10271038.Google Scholar
46.Stahl, SM. Mechanism of action of trazodone, a multifunctional drug. CNS Spectr. 2009;14:536546.Google Scholar
47.Stahl, SM, Fava, M, Trivedi, M, Caputo, A, Shah, A, Post, A. Agomelatine in the Treatment of Major Depressive Disorder: An 8 week, Multicenter, Randomized, Placebo-controlled Trial. Journal of Clinical Psychiatry. In press.Google Scholar
48.Fava, M, Asnis, GM, Shrivastava, R, et al.Zolpidem extended-release improves sleep and next-day symptoms in comorbid insomnia and generalized anxiety disorder. J Clin Psychopharmacol. 2009;29:222230.Google Scholar
49.Pollack, M, Kinrys, G, Krystal, A, et al.Eszopiclone coadministered with escitalopram in patients with insomnia and comorbid generalized anxiety disorder. Arch Gen Psychiatry. 2008;65:551562.Google Scholar
50.Nutt, D, Stahl, SM. Searching for perfect sleep: the continuing evolution of GABAA receptor modulators as hypnotics. Journal of Psychopharmacology. In press.Google Scholar
51.Fava, M, McCall Krystal, A, Wessel, T, et al.Eszopiclone co-administered with fluoxetine in patients with insomnia coexisting with major depressive disorder. Biol Psychiatry. 2006;59:10521060.Google Scholar
52.Nelson, JC, Mazure, CM, Jatlow, PI, Bowers, MB, Price, LH, Combining norepinephrine and serotonin reuptake inhibition mechanism for treatment of depression: a double-blind, randomized study. Biol Psychiatry. 2004;55:296300.Google Scholar
53.Blier, RGobbi, G, Turcotte, JE, et al.Mirtazapine and paroxetine in major depression: a comparison of monotherapy versus their combination from treatment initiation. Eur Neuropsychopharmacol. 2009;19:457465.Google Scholar
54.Blier, RWard, HE, Tremblay, RLaberge, L, Hebert, C, Bergeron, R. Combination of antidepressant medications from treatment initiation for major depressive disorder: a double blind randomized study. Am J Psychiatry. Epub ahead of print.Google Scholar
55.Bares, M, Novak, T, Kopecek, M, Kopecek, M, Stopkova, RSos, P. Is combined treatment more effective than switching to monotherapy in patients with resistant depression? A retrospective study. Neuro Endocrinol Lett. Dec 30, 2009. Epub ahead of print.Google Scholar