Evidence map›Paper›PMID 27272046›Full record

ArticleThe pharmacogenomics journal2016

Pharmacogenetic study of antipsychotic induced acute extrapyramidal symptoms in a first episode psychosis cohort: role of dopamine, serotonin and glutamate candidate genes.

S Mas, P Gassó, A Lafuente, M Bioque, A Lobo, A Gonzàlez-Pinto, M S Olmeda, I Corripio, A Llerena, B Cabrera and 3 more

Open access · greenAbstract readMulticenter Study
PubMed Publisher
In one paragraph

Article in The pharmacogenomics journal, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
4.0field-weighted citation impact, top 6% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

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  9. International journal of molecular sciences · 2020
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  16. Risperidone-Induced Adverse Drug Reactions and Role ofJournal of pharmacology & pharmacotherapeutics
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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

13 authors at 6 institutions in 1 country.

S MasDepartment of Pathological Anatomy, Pharmacology and Microbiology, University of Barcelona, Barcelona, Spain.
P GassóDepartment of Pathological Anatomy, Pharmacology and Microbiology, University of Barcelona, Barcelona, Spain.
A LafuenteDepartment of Pathological Anatomy, Pharmacology and Microbiology, University of Barcelona, Barcelona, Spain.
M BioqueInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
A LoboCentro de Investigación Biomédica en Red de Salud Mental (CIBERSAM),Madrid, Spain.
A Gonzàlez-PintoCentro de Investigación Biomédica en Red de Salud Mental (CIBERSAM),Madrid, Spain.
M S OlmedaDepartment of Psychiatry, Hospital General Universitario Gregorio Marañón, Madrid, Spain.
I CorripioCentro de Investigación Biomédica en Red de Salud Mental (CIBERSAM),Madrid, Spain.
A LlerenaCICAB Clinical Research Centre, Extremadura University Hospital and Medical School Servicio Extremeño de Salud, Badajoz, Spain.
B CabreraInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
J Saiz-RuizCentro de Investigación Biomédica en Red de Salud Mental (CIBERSAM),Madrid, Spain.
M BernardoInstitut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona, Spain.
PEPs GROUP
Centro de Investigación Biomédica en Red de Salud Mental · ESHospital de Sant Pau · ESHospital General Universitario Gregorio Marañón · ESUniversidad de Alcalá · ESUniversidad de Zaragoza · ESUniversity of the Basque Country · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

This study investigated whether the risk of presenting antipsychotic (AP)-induced extrapyramidal symptoms (EPS) could be related to single-nucleotide polymorphisms (SNPs) in a naturalistic cohort of first episode psychosis (FEP) patients. Two hundred and two SNPs in 31 candidate genes (involved in dopamine, serotonin and glutamate pathways) were analyzed in the present study. One hundred and thirteen FEP patients (43 presenting EPS and 70 non-presenting EPS) treated with high-potency AP (amisulpride, paliperidone, risperidone and ziprasidone) were included in the analysis. The statistical analysis was adjusted by age, gender, AP dosage, AP combinations and concomitant treatments as covariates. Four SNPs in different genes (DRD2, SLC18A2, HTR2A and GRIK3) contributed significantly to the risk of EPS after correction for multiple testing (P<1 × 10(-4)). These findings support the involvement of dopamine, serotonin and glutamate pathways in AP-induced EPS.

Indexed as

Pharmacogenomic VariantsPolymorphism, Single NucleotideAdolescentAdultAntipsychotic AgentsBasal Ganglia DiseasesCase-Control StudiesChildDopamineFemaleFollow-Up StudiesGenetic Association StudiesGenetic Predisposition to DiseaseGluK3 Kainate ReceptorGlutamic AcidHaplotypesAntipsychotic AgentsDopamineDRD2 protein, humanGluK3 Kainate ReceptorGlutamic AcidKainic Acid ReceptorsReceptors, Dopamine D2Receptor, Serotonin, 5-HT2ASerotoninSLC18A2 protein, humanVesicular Monoamine Transport Proteins

Identifiers

PMID27272046
OpenAlexW2415617743

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.