Evidence map›Paper›PMID 31631822›Full record

SynthesisCurrent neuropharmacology2020

Human Dermal Fibroblast: A Promising Cellular Model to Study Biological Mechanisms of Major Depression and Antidepressant Drug Response.

Pierre Mesdom, Romain Colle, Elise Lebigot, Séverine Trabado, Eric Deflesselle, Bruno Fève, Laurent Becquemont, Emmanuelle Corruble, Céline Verstuyft

Abstract readSystematic Review
In one paragraph

Synthesis in Current neuropharmacology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed
0.4field-weighted citation impact, top 45% 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

15 citing papers in PubMed, 20 citations in OpenAlex.

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  15. Fibroblasts as an experimental model system for the study of comparative physiology.Comparative biochemistry and physiology. Part B, Biochemistry & molecular biology
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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

9 authors at 4 institutions in 1 country.

Pierre MesdomUniversite Paris-Saclay, UVSQ, Inserm, CESP, Team MOODS, 94270, Le Kremlin-Bicetre, France.
Romain ColleUniversite Paris-Saclay, UVSQ, Inserm, CESP, Team MOODS, 94270, Le Kremlin-Bicetre, France.
Elise LebigotService de Biochimie Pharmaco-Toxicologie, APHP, Hopitaux Universitaires Paris-Sud, Hopital de Bicetre, Le Kremlin Bicêtre, F-94275, France.
Séverine TrabadoUniversite Paris Saclay, Faculte de Medecine Paris Saclay, Le Kremlin Bicetre, F-94276, France.
Eric DeflesselleUniversite Paris-Saclay, UVSQ, Inserm, CESP, Team MOODS, 94270, Le Kremlin-Bicetre, France.
Bruno FèveSorbonne University-Saint-Antoine Research Center, UMR-S938, Hospitalo-Universitary Institute of Cardiometabolism ICAN, Department of Endocrinology, Sant-Antoine Hospital, APHP, F-75012, Paris, France.
Laurent BecquemontUniversite Paris-Saclay, UVSQ, Inserm, CESP, Team MOODS, 94270, Le Kremlin-Bicetre, France.
Emmanuelle CorrubleUniversite Paris-Saclay, UVSQ, Inserm, CESP, Team MOODS, 94270, Le Kremlin-Bicetre, France.
Céline VerstuyftUniversite Paris-Saclay, UVSQ, Inserm, CESP, Team MOODS, 94270, Le Kremlin-Bicetre, France.
Inserm · FRAssistance Publique – Hôpitaux de Paris · FRSorbonne Université · FRUniversité Paris-Saclay · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman dermal fibroblasts (HDF) can be used as a cellular model relatively easily and without genetic engineering. Therefore, HDF represent an interesting tool to study several human diseases including psychiatric disorders. Despite major depressive disorder (MDD) being the second cause of disability in the world, the efficacy of antidepressant drug (AD) treatment is not sufficient and the underlying mechanisms of MDD and the mechanisms of action of AD are poorly understood.

objectiveThe aim of this review is to highlight the potential of HDF in the study of cellular mechanisms involved in MDD pathophysiology and in the action of AD response.

methodsThe first part is a systematic review following PRISMA guidelines on the use of HDF in MDD research. The second part reports the mechanisms and molecules both present in HDF and relevant regarding MDD pathophysiology and AD mechanisms of action.

resultsHDFs from MDD patients have been investigated in a relatively small number of works and most of them focused on the adrenergic pathway and metabolism-related gene expression as compared to HDF from healthy controls. The second part listed an important number of papers demonstrating the presence of many molecular processes in HDF, involved in MDD and AD mechanisms of action.

conclusionThe imbalance in the number of papers between the two parts highlights the great and still underused potential of HDF, which stands out as a very promising tool in our understanding of MDD and AD mechanisms of action.

Indexed as

Antidepressive AgentsBrainFibroblastsHumansMajor Depressive DisorderMesenchymal Stem CellsModels, BiologicalSkinSkin Physiological PhenomenaAntidepressive Agentsantidepressant drugcellular modelHuman dermal fibroblastshuman skin fibroblastsmajor depressionmajor depressive episode.

Identifiers

PMID31631822
PMCPMC7327943
OpenAlexW2981480576

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.