Literature DB >> 8923126

Milnacipran and selective serotonin reuptake inhibitors in major depression.

J Lopez-Ibor1, J D Guelfi, Y Pletan, A Tournoux, J F Prost.   

Abstract

In drug development the move from tricyclic antidepressants (TCAs) to selective serotonin reuptake inhibitors (SSRIs) involved not only the loss of the direct receptor interactions responsible for the adverse side effects of TCAs, but also the ability to inhibit the reuptake of noradrenaline. Selectivity for the single neurotransmitter, serotonin, may explain why SSRIs tend to be less efficacious than the TCAs, especially in more serious forms of depression. The advent of selective serotonin and noradrenaline reuptake inhibitors (SNRIs) has tended to confirm the idea that an action on both monoamine systems is important for maximal antidepressant efficacy. This paper reviews clinical trials comparing the new SNRI milnacipran with the SSRIs fluoxetine and fluvoxamine. A meta-analysis of the principal trials shows greater response rates (the proportion of patients with a decrease in symptom scores of 50% or more) with milnacipran (50 mg twice a day) than with fluoxetine (20 mg once a day), or fluvoxamine (100 mg twice a day) (milnacipran: 64%; SSRIs: 50%). Remission rates (the proportion of patients with Hamilton Depression Rating Scores of 7 or below) were also higher with milnacipran than with SSRIs (39 versus 28%). In one study, in which 100 mg milnacipran was given once a day in the evening, the higher response rate obtained with fluoxetine appears to be largely attributable to an inappropriate milnacipran dosage regimen. Data from a pharmacovigilance database including all patients participating in clinical trials with milnacipran (n = 5732) showed that, compared with the SSRIs, milnacipran produced fewer gastrointestinal side effects, such as nausea, and less anxiety. Milnacipran was, however, associated with a higher incidence of headache, dry mouth and dysuria. The results of these studies suggest that milnacipran is superior in efficacy to SSRIs and is equally well tolerated. Milnacipran, therefore, appears to offer a therapeutic advantage over the SSRIs.

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Year:  1996        PMID: 8923126     DOI: 10.1097/00004850-199609004-00006

Source DB:  PubMed          Journal:  Int Clin Psychopharmacol        ISSN: 0268-1315            Impact factor:   1.659


  16 in total

1.  Cardiotoxicity and serotonin syndrome complicating a milnacipran overdose.

Authors:  Michael Levine; Carrie A Truitt; Ayrn D O'Connor
Journal:  J Med Toxicol       Date:  2011-12

Review 2.  Fluvoxamine versus other anti-depressive agents for depression.

Authors:  Ichiro M Omori; Norio Watanabe; Atsuo Nakagawa; Andrea Cipriani; Corrado Barbui; Hugh McGuire; Rachel Churchill; Toshi A Furukawa
Journal:  Cochrane Database Syst Rev       Date:  2010-03-17

3.  Piloerection induced by replacing fluvoxamine with milnacipran.

Authors:  Satoko Hori; Nobuko Matsuo; Akiko Yamamoto; Tomomi Hazui; Hiromi Yagi; Marumi Nakano; Yuka Suzuki; Akiko Miki; Hisakazu Ohtani; Yasufumi Sawada
Journal:  Br J Clin Pharmacol       Date:  2007-02-23       Impact factor: 4.335

4.  Remission rates with milnacipran 100 mg/day and 150 mg/day in the long-term treatment of major depression.

Authors:  Kazuo Okumura; Toshiaki A Furukawa
Journal:  Clin Drug Investig       Date:  2006       Impact factor: 2.859

5.  Effects of milnacipran on neurocognition, pain, and fatigue in fibromyalgia: a 13-week, randomized, placebo-controlled, crossover trial.

Authors:  Jeong Lan Kim; Shilpa Rele; David M Marks; Prakash S Masand; Pallavi Yerramsetty; Robert A Millet; Richard S Keefe; Ashwin A Patkar
Journal:  Prim Care Companion CNS Disord       Date:  2014-12-26

Review 6.  Milnacipran. A review of its use in depression.

Authors:  C M Spencer; M I Wilde
Journal:  Drugs       Date:  1998-09       Impact factor: 9.546

Review 7.  Efficacy and tolerability of milnacipran in the treatment of major depression in comparison with other antidepressants : a systematic review and meta-analysis.

Authors:  Atsuo Nakagawa; Norio Watanabe; Ichiro M Omori; Corrado Barbui; Andrea Cipriani; Hugh McGuire; Rachel Churchill; Toshi A Furukawa
Journal:  CNS Drugs       Date:  2008       Impact factor: 5.749

Review 8.  Milnacipran versus other antidepressive agents for depression.

Authors:  Atsuo Nakagawa; Norio Watanabe; Ichiro M Omori; Corrado Barbui; Andrea Cipriani; Hugh McGuire; Rachel Churchill; Toshi A Furukawa
Journal:  Cochrane Database Syst Rev       Date:  2009-07-08

9.  A prospective, open-label study of milnacipran in the prevention of headache in patients with episodic or chronic migraine.

Authors:  Emily Rubenstein Engel; David Kudrow; Alan M Rapoport
Journal:  Neurol Sci       Date:  2013-09-13       Impact factor: 3.307

10.  Double-blind, comparative study of milnacipran and paroxetine in Japanese patients with major depression.

Authors:  Kunitoshi Kamijima; Shinji Hashimoto; Eiichi Nagayoshi; Tsukasa Koyama
Journal:  Neuropsychiatr Dis Treat       Date:  2013-04-26       Impact factor: 2.570

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