Evidence map›Paper›PMID 24709691›Full record

ArticleThe pharmacogenomics journal2014

PPP3CC gene: a putative modulator of antidepressant response through the B-cell receptor signaling pathway.

C Fabbri, A Marsano, D Albani, A Chierchia, R Calati, A Drago, C Crisafulli, M Calabrò, S Kasper, R Lanzenberger and 6 more

Abstract read
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In one paragraph

Article in The pharmacogenomics journal, 2014. 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
2.0field-weighted citation impact, top 15% 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, 42 citations in OpenAlex.

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  7. Clinical psychopharmacology and neuroscience : the official scientific journal of the Korean College of Neuropsychopharmacology · 2020
    Article
  8. Article
  9. The Genetics of Treatment-Resistant Depression: A Critical Review and Future Perspectives.The international journal of neuropsychopharmacology · 2019
    Review
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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

16 authors at 8 institutions in 5 countries.

C FabbriDepartment of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna, Italy.
A MarsanoDepartment of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna, Italy.
D AlbaniUnit of Genetics of Neurodegenerative Disorders, Neuroscience Department, IRCCS - Istituto di Ricerche Farmacologiche "Mario Negri", Milan, Italy.
A ChierchiaUnit of Genetics of Neurodegenerative Disorders, Neuroscience Department, IRCCS - Istituto di Ricerche Farmacologiche "Mario Negri", Milan, Italy.
R CalatiLaboratoire de Psychologie Medicale, Université Libre de Bruxelles and Psy Pluriel, Centre Europeén de Psychologie Medicale, Brussels, Belgium.
A DragoDepartment of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna, Italy.ORCID 000000015633231X
C CrisafulliDepartment of Biomedical Science and Morphological and Functional Images, University of Messina, Messina, Italy.
M Calabrò1] Department of Biomedical Science and Morphological and Functional Images, University of Messina, Messina, Italy [2] IRCCS Centro Neurolesi "Bonino-Pulejo", Messina, Italy [3] Department of Clinical and Experimental Medicine, University of Messina, Messina, Italy.
S KasperDepartment of Psychiatry and Psychotherapy, Medical University Vienna, Vienna, Austria.
R LanzenbergerDepartment of Psychiatry and Psychotherapy, Medical University Vienna, Vienna, Austria.
J ZoharDepartment of Psychiatry, Sheba Medical Center, Tel Hashomer, and Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
A Juven-WetzlerDepartment of Psychiatry, Sheba Medical Center, Tel Hashomer, and Sackler School of Medicine, Tel Aviv University, Tel Aviv, Israel.
D SoueryLaboratoire de Psychologie Medicale, Universitè Libre de Bruxelles and Psy Pluriel, Centre Européen de Psychologie Medicale, Brussels, Belgium.
S MontgomerySchool of Medicine, Imperial College, London, UK.
J MendlewiczLaboratoire de Psychologie Medicale, Université Libre de Bruxelles and Psy Pluriel, Centre Europeén de Psychologie Medicale, Brussels, Belgium.
A Serretti1] Department of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna, Italy [2] IRCCS Centro S. Giovanni di Dio, Fatebenefratelli, Brescia, Italy.
Université Libre de Bruxelles · BEUniversity of Bologna · ITMario Negri Institute for Pharmacological Research · ITMedical University of Vienna · ATTel Aviv University · ILUniversity of Messina · ITCentro San Giovanni di Dio Fatebenefratelli · ITImperial College London · GB

Funding

TREATMENT RESISTANT DEPRESSIONN01MH90003 · NIMH · UT SOUTHWESTERN MEDICAL CENTER · 2007 to 2008
$9.1M
TREATMENT RESISTANT DEPRESSION-278990003N01MH090003 · NIMH · UNIVERSITY OF TEXAS SW MED CTR/DALLAS · 1999 to 2003
–
NIMH NIH HHS N01MH90003
6 · The paper itself

Abstract

Antidepressant pharmacogenetics represents a stimulating, but often discouraging field. The present study proposes a combination of several methodologies across three independent samples. Genes belonging to monoamine, neuroplasticity, circadian rhythm and transcription factor pathways were investigated in two samples (n=369 and 88) with diagnosis of major depression who were treated with antidepressants. Phenotypes were response, remission and treatment-resistant depression. Logistic regression including appropriate covariates was performed. Genes associated with outcomes were investigated in the STAR*D (Sequenced Treatment Alternatives to Relieve Depression) genome-wide study (n=1861). Top genes were further studied through a pathway analysis. In both original samples, markers associated with outcomes were concentrated in the PPP3CC gene. Other interesting findings were particularly in the HTR2A gene in one original sample and the STAR*D. The B-cell receptor signaling pathway proved to be the putative mediator of PPP3CC's effect on antidepressant response (P=0.03). Among innovative candidates, PPP3CC, involved in the regulation of immune system and synaptic plasticity, seems promising for further investigation.

Indexed as

Antidepressive AgentsCalcineurinDepressionHumansReceptors, Antigen, B-CellSignal TransductionAntidepressive AgentsCalcineurinPPP3CC protein, humanReceptors, Antigen, B-Cell

Identifiers

PMID24709691
OpenAlexW2028370025

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.