A comparative review of escitalopram, paroxetine, and sertraline: are they all alike?

被引:228
作者
Sanchez, Connie [1 ]
Reines, Elin H. [2 ]
Montgomery, Stuart A. [3 ]
机构
[1] Lundbeck Res USA Inc, External Sourcing, Paramus, NJ 07652 USA
[2] H Lundbeck & Co AS, Int Clin Res, Copenhagen, Denmark
[3] Univ London, Imperial Coll Sch Med, London, England
关键词
allosteric; escitalopram (S-citalopram); major depressive disorder; paroxetine; selective serotonin reuptake inhibitor; serotonin; serotonin transporter; sertraline; MAJOR DEPRESSIVE DISORDER; SEROTONIN REUPTAKE INHIBITORS; TRANSPORTER BINDING PROFILE; R-CITALOPRAM; IN-VIVO; CLINICAL PHARMACOKINETICS; ALLOSTERIC MODULATOR; DRUG-INTERACTIONS; ANIMAL-MODELS; ANTIDEPRESSANTS;
D O I
10.1097/YIC.0000000000000023
中图分类号
R9 [药学];
学科分类号
100702 [药剂学];
摘要
It is known that newer antidepressants, such as the selective serotonin reuptake inhibitors (SSRIs), provide advantages in tolerability over antidepressants such as the tricyclics. However, even within the SSRI class, differences in efficacy or tolerability exist between the individual drugs. Among the three most widely prescribed SSRIs are paroxetine, sertraline, and escitalopram. Escitalopram is commonly referred to as an SSRI, but also has well-documented allosteric properties, and thus can be further classed as an allosteric serotonin reuptake inhibitor. All three antidepressants are efficacious compared with placebo, but there is evidence that escitalopram is more effective than a range of other antidepressants. There are no direct data to regard either paroxetine or sertraline as a superior antidepressant. Escitalopram is superior compared with paroxetine, which has a less favorable tolerability profile. Paroxetine is associated with cholinergic muscarinic antagonism and potent inhibition of CYP2D6, and sertraline has moderate drug interaction issues in comparison with escitalopram. Overall, as an allosteric serotonin reuptake inhibitor that is somewhat different from classical SSRIs, escitalopram is the first choice judged by combined efficacy and tolerability, and nonclinical data have offered possible mechanisms through which escitalopram could be more efficacious, based on its interaction with orthosteric and allosteric binding sites at the serotonin transporter. (C) 2014 Wolters Kluwer Health vertical bar Lippincott Williams & Wilkins.
引用
收藏
页码:185 / 196
页数:12
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