Evidence map›Paper›PMID 32509197›Full record

ArticleAmerican journal of translational research2020

Response to fluoxetine in children and adolescents: a weighted gene co-expression network analysis of peripheral blood.

Teresa Torres, Daniel Boloc, Natalia Rodríguez, Ana Blázquez, Maria Teresa Plana, Eva Varela, Patricia Gassó, Albert Martinez-Pinteño, Luisa Lázaro, Joan Albert Arnaiz and 1 more

Open access · greenAbstract read
In one paragraph

Article in American journal of translational research, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.1field-weighted citation impact, top 70% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 3 citations in OpenAlex.

  1. Pooled it
  2. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors at 1 institution in 1 country.

Teresa TorresDepartment of Clinical Foundations, Pharmacology Unit, University of Barcelona Barcelona, Spain.
Daniel BolocDepartment of Medicine, University of Barcelona Barcelona, Spain.
Natalia RodríguezFundació Clinic per la Recerca Biomédica (FCRB) Barcelona, Spain.
Ana BlázquezDepartment of Child and Adolescent Psychiatry and Psychology, Institute of Neurosciences, Hospital Clinic de Barcelona Barcelona, Spain.
Maria Teresa PlanaDepartment of Child and Adolescent Psychiatry and Psychology, Institute of Neurosciences, Hospital Clinic de Barcelona Barcelona, Spain.
Eva VarelaDepartment of Child and Adolescent Psychiatry and Psychology, Institute of Neurosciences, Hospital Clinic de Barcelona Barcelona, Spain.
Patricia GassóDepartment of Clinical Foundations, Pharmacology Unit, University of Barcelona Barcelona, Spain.
Albert Martinez-PinteñoDepartment of Clinical Foundations, Pharmacology Unit, University of Barcelona Barcelona, Spain.
Luisa LázaroDepartment of Medicine, University of Barcelona Barcelona, Spain.
Joan Albert ArnaizDepartment of Clinical Foundations, Pharmacology Unit, University of Barcelona Barcelona, Spain.
Sergi MasDepartment of Clinical Foundations, Pharmacology Unit, University of Barcelona Barcelona, Spain.
Universitat de Barcelona · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The inconclusive and non-replicated results of pharmacogenetic studies of antidepressant response could be related to the lack of acknowledgement of its mechanism of action. In this scenario, gene expression studies provide and interesting framework to reveal new candidate genes for pharmacogenetic studies or peripheral biomarkers of fluoxetine response. We propose a system biology approach to analyse changes in gene expression induced by eight weeks of treatment with fluoxetine in peripheral blood. 21 naïve child and adolescents participated in the present study. Our analysis include the identification of gene co-expression modules, using Weighted Gene Co-expression Network Analysis (WGCNA), followed by protein-protein interaction (PPi) network construction coupled with functional annotation. Our results revealed two modules of co-expression genes related to fluoxetine treatment. The constructed networks from these modules were enriched for biological processes related to cellular and metabolic processes, cell communication, immune system processes, cell death, response to stimulus and neurogenesis. Some of these processes, such as immune system, replicated previous findings in the literature, whereas, neurogenesis, a mechanism proposed to be involved in fluoxetine response, had been identified for first time using peripheral tissues. In conclusion, our study identifies several biological processes in relation to fluoxetine treatment in peripheral blood, offer new candidate genes for pharmacogenetic studies and valuable markers for peripheral moderator biomarkers discovery.

Indexed as

childrenconvergent functional genomicsgene expressionneurogenesispharmacogenomicsSelective serotonin reuptake inhibitors

Identifiers

PMID32509197
PMCPMC7269974
OpenAlexW3033319854

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.