2011
DOI: 10.4103/0976-500x.77091
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Effects of fluoxetine and escitalopram on C-reactive protein in patients of depression

Abstract: Objective:To study the anti-inflammatory activity of fluoxetine and escitalopram in newly diagnosed patients of depression and also to evaluate the association between depression and inflammation.Materials and Methods:Ninety-eight newly diagnosed patients of depression were recruited as cases. From these, 48 had started treatment with fluoxetine (20 mg/day) and 50 had started treatment with escitalopram (20 mg/day). After 2 months of treatment of these patients, Hamilton rating scale for depression (HRSD scale… Show more

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Cited by 34 publications
(15 citation statements)
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“…Besides its antioxidant effect, escitalopram attenuated HFFD/ STZ-induced cardiac inflammation and fibrosis where it significantly reduced NF-κB p65, TNF-α and TGF-β1 contents in cardiac tissues of HFFD/STZ diabetic rats. The present results confirm the anti-inflammatory and anti-fibrotic actions of escitalopram that have been documented in both experimental and clinical studies (Bah et al, 2011;Chavda et al, 2011;van Noort et al, 2014;Ibrahim et al, 2019). The aforementioned antioxidant activity of escitalopram, observed herein, might contribute to the inhibition of NF-κB p65 with the subsequent reduction of TNF-α and TGF-β1 contents.…”
Section: Discussionsupporting
confidence: 91%
“…Besides its antioxidant effect, escitalopram attenuated HFFD/ STZ-induced cardiac inflammation and fibrosis where it significantly reduced NF-κB p65, TNF-α and TGF-β1 contents in cardiac tissues of HFFD/STZ diabetic rats. The present results confirm the anti-inflammatory and anti-fibrotic actions of escitalopram that have been documented in both experimental and clinical studies (Bah et al, 2011;Chavda et al, 2011;van Noort et al, 2014;Ibrahim et al, 2019). The aforementioned antioxidant activity of escitalopram, observed herein, might contribute to the inhibition of NF-κB p65 with the subsequent reduction of TNF-α and TGF-β1 contents.…”
Section: Discussionsupporting
confidence: 91%
“… 2010 ; Chavda et al. 2011 ), probably due to Cyclooxygenase-2 (COX-2) inhibition (Taler et al. 2007 ; Knights et al.…”
Section: Introductionmentioning
confidence: 99%
“…The anti-inflammatory properties of SSRIs have been documented [6, 9, 10], although the extent to which these correlate with the effects of these drugs on depressive symptoms remains uncertain. Response to antidepressant treatment using mirtazapine, however, has been shown to correlate with significant effects on inflammatory cytokines in a double-blind placebo controlled study of patients with depression postmyocardial infarction [7].…”
Section: Discussionmentioning
confidence: 99%
“…There is growing evidence that not only tricyclic antidepressants (TCAs) and selective serotonin reuptake inhibitors (SSRIs) but also newer noradrenergic and specific serotonergic antidepressants (NaSSAs) such as mirtazapine may modulate the inflammatory response as part of their mode of action [5]. Reduction in the levels of inflammatory markers such as CRP, the Erythrocyte Sedimentation Rate (ESR), and White Cell Count (WCC) has been observed in direct response to SSRI treatment, although it remains unclear how this relates to the therapeutic effect of antidepressants [6]. …”
Section: Introductionmentioning
confidence: 99%