Second-generation antidepressant: Difference between revisions
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By blocking the ''reuptake'' by the ''releasing'' neuron of [[norepinephrine]], [[serotonin]] or both, second-generation antidepressants may overcome the mono-amine deficiency.<ref name="isbn0-07-145153-6">{{cite book |author=Katzung, Bertram G. |authorlink= |editor= |others= |title=Basic and Clinical Pharmacology |edition=10th |chapter=Antidepressant Agents |chapterurl= |language= |publisher=McGraw-Hill Medical Publishing Division |location=New York |year=2006 |origyear= |pages= |quote= |isbn=0-07-145153-6 |oclc= |doi= |url=http://www.accessmedicine.com/resourceTOC.aspx?resourceID=16 |accessdate=}}</ref> Some members of this class, perhaps in a dose-dependent manner, also block [[dopamine]] release. | By blocking the ''reuptake'' by the ''releasing'' neuron of [[norepinephrine]], [[serotonin]] or both, second-generation antidepressants may overcome the mono-amine deficiency.<ref name="isbn0-07-145153-6">{{cite book |author=Katzung, Bertram G. |authorlink= |editor= |others= |title=Basic and Clinical Pharmacology |edition=10th |chapter=Antidepressant Agents |chapterurl= |language= |publisher=McGraw-Hill Medical Publishing Division |location=New York |year=2006 |origyear= |pages= |quote= |isbn=0-07-145153-6 |oclc= |doi= |url=http://www.accessmedicine.com/resourceTOC.aspx?resourceID=16 |accessdate=}}</ref> Some members of this class, perhaps in a dose-dependent manner, also block [[dopamine]] release. | ||
In contrast, first-generation antidepressants raise norepinephrine and serotonin, in the synaptic gap between the releasing and receiving neurons, by blocking one of two enzymes in the receiving cell which metabolize the | In contrast, first-generation antidepressants raise levels of dopamine, norepinephrine and serotonin, in the synaptic gap between the releasing and receiving neurons, by blocking one of two enzymes in the receiving cell which metabolize the three bioamines. [[Tricyclic antidepressant]]s suppress catechol-O-methyl transferase, while the other class as named for the enzyme they suppress, [[monoamine oxidase]] inhibitors. | ||
Revision as of 14:22, 18 January 2010
Second-generation antidepressants are used to treat depression and are a "structurally and mechanistically diverse group of drugs that are not tricyclics or monoamine oxidase inhibitors. The most clinically important appear to act selectively on serotonergic systems, especially by inhibiting serotonin reuptake."[1]
Classification
Second-generation antidepressants are classified by the biogenic amine receptor that they affect.
Selective serotonin reuptake inhibitors(SSRI)
- Citalopram (generic). Can be combined with bupropion.
- Fluoxetine (generic). Inhibits cytochrome P-450 CYP2D6.
- Paroxetine (generic). Inhibits cytochrome P-450 CYP2D6.
- Sertraline (generic)
Serotonin 5-HT2A–receptor antagonist
Serotonin norepinephrine reuptake inhibitors (SNRI)
- Duloxetine
- Milnacipran
- Venlafaxine (generic)
Norepinephrine uptake inhibitor
Dopamine reuptake inhibitor
Mechanism of action
Depression may be due to the monoamine-deficiency hypothesis, which is a "deficiency in serotonin or norepinephrine neurotransmission in the brain."[2]
By blocking the reuptake by the releasing neuron of norepinephrine, serotonin or both, second-generation antidepressants may overcome the mono-amine deficiency.[3] Some members of this class, perhaps in a dose-dependent manner, also block dopamine release.
In contrast, first-generation antidepressants raise levels of dopamine, norepinephrine and serotonin, in the synaptic gap between the releasing and receiving neurons, by blocking one of two enzymes in the receiving cell which metabolize the three bioamines. Tricyclic antidepressants suppress catechol-O-methyl transferase, while the other class as named for the enzyme they suppress, monoamine oxidase inhibitors.
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Effectiveness
Regarding the use of second-generation antidepressants, clinical practice guidelines by the American College of Physicians recommend:[4] [5]
- "when clinicians choose pharmacologic therapy to treat patients with acute major depression, they select second-generation antidepressants on the basis of adverse effect profiles, cost, and patient preferences"
- "second-generation antidepressants did not significantly differ in efficacy, effectiveness, or quality of life. Mirtazapine had a significantly faster onset of action"
- "when treating symptom clusters in patients with accompanying depression, second-generation antidepressants did not differ in efficacy in treating accompanying anxiety, pain, and somatization. Limited evidence suggests that some agents may be more effective in treating insomnia"
- "most of the second-generation antidepressants had similar adverse effects...paroxetine was associated with an increased risk for sexual dysfunction."
The effectiveness is antidepressants depends on the severity of a patient's depression. This relationship may be due to thedeclining effect of placebo among more severely depressed patients.[6]
| American Psychiatric Association classification of severity[7] | Hamilton Depression Rating Scale (HDRS) | Number needed to treat | Clinical significance (NICE)[8] |
|---|---|---|---|
| Mild to moderate | < 19 | 16 | No |
| Severe | 19 - 22 | 11 | No |
| Very severe | > 22 | 4 | Yes |
Meta-analyses conflict about the relative effectiveness of the second-generation antidepressants with no difference reported[9] and superiority of sertraline and escitalopram reported. [10]
References
- ↑ Anonymous (2024), Second-generation antidepressants (English). Medical Subject Headings. U.S. National Library of Medicine.
- ↑ Belmaker RH, Agam G (2008). "Major depressive disorder". N. Engl. J. Med. 358 (1): 55–68. DOI:10.1056/NEJMra073096. PMID 18172175. Research Blogging.
- ↑ Katzung, Bertram G. (2006). “Antidepressant Agents”, Basic and Clinical Pharmacology, 10th. New York: McGraw-Hill Medical Publishing Division. ISBN 0-07-145153-6.
- ↑ Gartlehner, Gerald; Bradley N. Gaynes, Richard A. Hansen, Patricia Thieda, Angela DeVeaugh-Geiss, Erin E. Krebs, Charity G. Moore, Laura Morgan, Kathleen N. Lohr (2008-11-18). "Comparative Benefits and Harms of Second-Generation Antidepressants: Background Paper for the American College of Physicians". Ann Intern Med 149 (10): 734-750. Retrieved on 2008-11-18.
- ↑ Qaseem, Amir; Vincenza Snow, Thomas D. Denberg, Mary Ann Forciea, Douglas K. Owens, for the Clinical Efficacy Assessment Subcommittee of the American College of Physicians (2008-11-18). "Using Second-Generation Antidepressants to Treat Depressive Disorders: A Clinical Practice Guideline from the American College of Physicians". Ann Intern Med 149 (10): 725-733. Retrieved on 2008-11-18.
- ↑ 6.0 6.1 Lo B (2010). "Commentary: Conflict of interest policies: an opportunity for the medical profession to take the lead.". Acad Med 85 (1): 9-11. DOI:10.1097/ACM.0b013e3181c46e96. PMID 20042812. Research Blogging.
- ↑ First, Michael B. (2007). Handbook of Psychiatric Measures, Second Edition. American Psychiatric Publishing, Inc. ISBN 1-58562-218-4.
- ↑ National Institute for Clinical Excellence. Depression: Management of Depression in Primary and Secondary Care. London, England: National Institute for Clinical Excellence; 2004.
- ↑ Gartlehner, Gerald; Bradley N. Gaynes, Richard A. Hansen, Patricia Thieda, Angela DeVeaugh-Geiss, Erin E. Krebs, Charity G. Moore, Laura Morgan, Kathleen N. Lohr (2008-11-18). "Comparative Benefits and Harms of Second-Generation Antidepressants: Background Paper for the American College of Physicians". Ann Intern Med 149 (10): 734-750. Retrieved on 2008-11-18.
- ↑ Cipriani A. et al (2009). Comparative efficacy and acceptability of 12 new-generation antidepressants: a multiple-treatments meta-analysis. The Lancet DOI:10.1016/s0140-6736(09)60046-5