Literature DB >> 27461515

Whole-genome expression analysis reveals genes associated with treatment response to escitalopram in major depression.

Kristi Pettai1, Lili Milani1, Anu Tammiste1, Urmo Võsa1, Raivo Kolde2, Triin Eller3, David Nutt4, Andres Metspalu5, Eduard Maron6.   

Abstract

The reasons for variability in treatment response in major depressive disorder (MDD) are not fully understood, but there is accumulating evidence suggesting that therapeutic outcomes of antidepressants can be influenced by genetic factors. In the present study we applied the microarray Illumina platform for whole genome expression profiling in depressive patients treated with escitalopram medication in order to identify genes underlying response to antidepressant treatment. The initial study sample consisted of 135 outpatients with major depressive disorder (mean age 31.1±11.6 years, 68% females) treated with escitalopram 10-20mg/day for 12 weeks, from which 87 patients (55 females) were included in gene expression analyzing. The gene expression profiles were measured on peripheral blood cells at baseline, at week 4 and at the end of treatment (week 12) using BeadChips Illumina. The fold change was used to demonstrate rate of changes in average gene expressions between studied groups. Statistical analyses were performed using the false discovery rate (FDR). The most interesting gene, which showed the predictive effect on treatment outcome by delineating low dose responders and treatment-resistant patients at the beginning of medication, was NLGN2, belonging to a family of neuronal cell surface proteins and involving in synapse formation. In addition, the several gene clusters, related to immune response, signal transduction and neurotrophin pathway, have distinguished responders from non-responders at the week 4 of treatment. After 4 weeks of escitalopram treatment (10mg/day), the YWHAZ gene has showed the highest transcriptional change in responders as compared with non-responders. Finally, at the end of the treatment we noticed that at least three genes (NR2C2, ZNF641, FKBP1A) have been strongly associated with resistance to escitalopram. Thus the results of this study support that exploration of peripheral gene expression is a useful tool in the further identification of novel genetic biomarkers for antidepressant treatment response.
Copyright © 2016 Elsevier B.V. and ECNP. All rights reserved.

Entities:  

Keywords:  Escitalopram; Gene expression; Major depression; SSRI; Treatment prediction

Mesh:

Substances:

Year:  2016        PMID: 27461515     DOI: 10.1016/j.euroneuro.2016.06.007

Source DB:  PubMed          Journal:  Eur Neuropsychopharmacol        ISSN: 0924-977X            Impact factor:   4.600


  6 in total

1.  Transcriptomic signatures of treatment response to the combination of escitalopram and memantine or placebo in late-life depression.

Authors:  Adrienne Grzenda; Prabha Siddarth; Kelsey T Laird; Jillian Yeargin; Helen Lavretsky
Journal:  Mol Psychiatry       Date:  2020-05-07       Impact factor: 15.992

2.  A large-scale genome-wide gene expression analysis in peripheral blood identifies very few differentially expressed genes related to antidepressant treatment and response in patients with major depressive disorder.

Authors:  Morana Vitezic; Anders Albrechtsen; Anne Krogh Nøhr; Morten Lindow; Annika Forsingdal; Samuel Demharter; Troels Nielsen; Raimund Buller; Ida Moltke
Journal:  Neuropsychopharmacology       Date:  2021-04-08       Impact factor: 8.294

3.  Differential Peripheral Proteomic Biosignature of Fluoxetine Response in a Mouse Model of Anxiety/Depression.

Authors:  Indira Mendez-David; Céline Boursier; Valérie Domergue; Romain Colle; Bruno Falissard; Emmanuelle Corruble; Alain M Gardier; Jean-Philippe Guilloux; Denis J David
Journal:  Front Cell Neurosci       Date:  2017-08-16       Impact factor: 5.505

4.  Use of DAVID algorithms for clustering custom annotated gene lists in a non-model organism, rainbow trout.

Authors:  Hao Ma; Guangtu Gao; Gregory M Weber
Journal:  BMC Res Notes       Date:  2018-01-23

Review 5.  Recent advances in predicting responses to antidepressant treatment.

Authors:  Thomas Frodl
Journal:  F1000Res       Date:  2017-05-03

6.  Time Course of Changes in Peripheral Blood Gene Expression During Medication Treatment for Major Depressive Disorder.

Authors:  Ian A Cook; Eliza Congdon; David E Krantz; Aimee M Hunter; Giovanni Coppola; Steven P Hamilton; Andrew F Leuchter
Journal:  Front Genet       Date:  2019-09-18       Impact factor: 4.599

  6 in total

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