Literature DB >> 12383038

Spotlight on sertraline in the management of major depressive disorder in elderly patients.

Richard B R Muijsers1, Greg L Plosker, Stuart Noble.   

Abstract

UNLABELLED: Sertraline is a selective serotonin reuptake inhibitor (SSRI) with well established antidepressant and anxiolytic activity. Results from several well designed trials show that sertraline (50-200 mg/day) is effective in the treatment of major depressive disorder in elderly patients (> or =60 years of age). Primary endpoints in most studies included the Hamilton Depression Rating Scale (HDRS), Clinical Global Impression score and the Montgomery-Asberg Depression Rating Scale. Sertraline was significantly more effective than placebo and was as effective as fluoxetine, nortriptyline and imipramine in elderly patients. During one trial, amitriptyline was significantly more effective than sertraline (mean reduction from baseline on one of six primary outcomes [HDRS]), although no quantitative data were provided. Subgroup analysis of data from a randomised, double-blind trial in elderly patients with major depressive disorder suggests that vascular morbidity, diabetes mellitus or arthritis does not affect the antidepressant effect of sertraline. Secondary endpoints from these clinical trials suggest that sertraline has significant benefits over nortriptyline in terms of quality of life. In addition, significant differences favouring sertraline in comparison with nortriptyline and fluoxetine have been recorded for a number of cognitive functioning parameters. Sertraline is generally well tolerated in elderly patients with major depressive disorder and lacks the marked anticholinergic effects that characterise the adverse event profiles of tricyclic antidepressants (TCAs). The most frequently reported adverse events in patients aged > or =60 years with major depressive disorder receiving sertraline 50-150 mg/day were dry mouth, headache, diarrhoea, nausea, insomnia, somnolence, constipation, dizziness, sweating and taste abnormalities. The tolerability profile of sertraline is generally similar in younger and elderly patients. Sertraline has a low potential for drug interactions at the level of the cytochrome P450 enzyme system. In addition, no dosage adjustments are warranted for elderly patients solely based on age.
CONCLUSION: Sertraline is an effective and well tolerated antidepressant for the treatment of major depressive disorder in patients aged > or =60 years. Since elderly patients are particularly prone to the anticholinergic effects of TCAs as a class, SSRIs such as sertraline are likely to be a better choice for the treatment of major depressive disorder in this age group. In addition, sertraline may have advantages over the SSRIs paroxetine, fluoxetine and fluvoxamine in elderly patients because of the drug's comparatively low potential for drug interactions, which is of importance in patient groups such as the elderly who are likely to receive more than one drug regimen.

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Year:  2002        PMID: 12383038     DOI: 10.2165/00023210-200216110-00011

Source DB:  PubMed          Journal:  CNS Drugs        ISSN: 1172-7047            Impact factor:   5.749


  28 in total

1.  Evidence for involvement of polymorphic CYP2C19 and 2C9 in the N-demethylation of sertraline in human liver microsomes.

Authors:  Z H Xu; W Wang; X J Zhao; S L Huang; B Zhu; N He; Y Shu; Z Q Liu; H H Zhou
Journal:  Br J Clin Pharmacol       Date:  1999-09       Impact factor: 4.335

Review 2.  Hyponatraemia and selective serotonin re-uptake inhibitors in elderly patients.

Authors:  D Kirby; D Ames
Journal:  Int J Geriatr Psychiatry       Date:  2001-05       Impact factor: 3.485

3.  Antidepressant efficacy and safety of low-dose sertraline and standard-dose imipramine for the treatment of depression in older adults: results from a double-blind, randomized, controlled clinical trial.

Authors:  O V Forlenza; O P Almeida; A Stoppe; E S Hirata
Journal:  Int Psychogeriatr       Date:  2001-03       Impact factor: 3.878

4.  Acute effects of sertraline, amitriptyline, and placebo on the psychomotor performance of healthy subjects over 50 years of age.

Authors:  M J Mattila; U Saarialho-Kere; M Mattila
Journal:  J Clin Psychiatry       Date:  1988-08       Impact factor: 4.384

5.  Sertraline. Chronopharmacokinetics and the effect of coadministration with food.

Authors:  R A Ronfeld; K D Wilner; B A Baris
Journal:  Clin Pharmacokinet       Date:  1997       Impact factor: 6.447

Review 6.  Clinically relevant pharmacology of selective serotonin reuptake inhibitors. An overview with emphasis on pharmacokinetics and effects on oxidative drug metabolism.

Authors:  S H Preskorn
Journal:  Clin Pharmacokinet       Date:  1997       Impact factor: 6.447

7.  Double-blind, multicenter comparison of sertraline and amitriptyline in elderly depressed patients.

Authors:  C K Cohn; R Shrivastava; J Mendels; J B Cohn; L F Fabre; J L Claghorn; E C Dessain; T M Itil; A Lautin
Journal:  J Clin Psychiatry       Date:  1990-12       Impact factor: 4.384

8.  A double-blind comparison of sertraline and fluoxetine in depressed elderly outpatients.

Authors:  P A Newhouse; K R Krishnan; P M Doraiswamy; E M Richter; E D Batzar; C M Clary
Journal:  J Clin Psychiatry       Date:  2000-08       Impact factor: 4.384

Review 9.  Pharmacological differences of serotonin reuptake inhibitors and possible clinical relevance.

Authors:  B E Leonard
Journal:  Drugs       Date:  1992       Impact factor: 9.546

Review 10.  SSRI safety in overdose.

Authors:  J T Barbey; S P Roose
Journal:  J Clin Psychiatry       Date:  1998       Impact factor: 4.384

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  3 in total

Review 1.  Revisiting the Serotonin Hypothesis: Implications for Major Depressive Disorders.

Authors:  Marc Fakhoury
Journal:  Mol Neurobiol       Date:  2015-04-01       Impact factor: 5.590

2.  Controlled withdrawal of selective serotonin reuptake inhibitor drugs in elderly patients in nursing homes with no indication of depression.

Authors:  Johanna Ulfvarson; Johanna Adami; Regina Wredling; Bengt Kjellman; Marie Reilly; Christer von Bahr
Journal:  Eur J Clin Pharmacol       Date:  2003-11-01       Impact factor: 2.953

3.  Possible etiology of improvements in both quality of life and overlapping gastroesophageal reflux disease by proton pump inhibitor treatment in a prospective randomized controlled trial.

Authors:  Hubert Mönnikes; Thomas Schwan; Christo van Rensburg; Andrzej Straszak; Carmen Theek; Reinhold Lühmann; Peter Sander; Anne Tholen
Journal:  BMC Gastroenterol       Date:  2013-10-01       Impact factor: 3.067

  3 in total

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