Evidence map›Paper›PMID 33293633›Full record

ArticleScientific reports2020

Plasma amino acids profile in first-episode psychosis, unaffected siblings and community-based controls.

Camila Marcelino Loureiro, Daiane Leite da Roza, Fabiana Corsi-Zuelli, Rosana Shuhama, Helene Aparecida Fachim, Lívia Maria Cordeiro Simões-Ambrosio, Rafael Deminice, Alceu Afonso Jordão, Paulo Rossi Menezes, Cristina Marta Del-Ben and 1 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.5field-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

4 citing papers in PubMed, 13 citations in OpenAlex.

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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

11 authors at 3 institutions in 2 countries.

Camila Marcelino LoureiroDivision of Clinical Immunology, Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, Avenida Bandeirantes, 3900, Monte Alegre, Ribeirão Preto, CEP: 14049-900, Brazil. camila.loureiro@usp.br.
Daiane Leite da RozaDivision of Psychiatry, Department of Neurosciences and Behaviour, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.
Fabiana Corsi-ZuelliCenter for Research in Inflammatory Diseases, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.
Rosana ShuhamaPopulation Mental Health Research Centre, São Paulo, Brazil.
Helene Aparecida FachimDepartment of Endocrinology and Metabolism, Salford Royal Foundation Trust, Salford, UK.
Lívia Maria Cordeiro Simões-AmbrosioDivision of Clinical Immunology, Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, Avenida Bandeirantes, 3900, Monte Alegre, Ribeirão Preto, CEP: 14049-900, Brazil.
Rafael DeminiceDepartment of Physical Education, State University of Londrina, Londrina, Brazil.
Alceu Afonso JordãoDivision of Nutrition and Metabolism, Department of Health Sciences, Ribeirão Preto Medical School, University of São Paulo, Ribeirão Preto, Brazil.
Paulo Rossi MenezesPopulation Mental Health Research Centre, São Paulo, Brazil.
Cristina Marta Del-BenPopulation Mental Health Research Centre, São Paulo, Brazil.
Paulo Louzada-JuniorDivision of Clinical Immunology, Department of Internal Medicine, Ribeirão Preto Medical School, University of São Paulo, Avenida Bandeirantes, 3900, Monte Alegre, Ribeirão Preto, CEP: 14049-900, Brazil.
Universidade de São Paulo · BRSalford Royal NHS Foundation Trust · GBUniversidade Estadual de Londrina · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Investigations of plasma amino acids in early psychosis and their unaffected siblings are rare. We measured plasma amino acids involved in the co-activation of dopaminergic, GABAergic, glutamatergic, and serotoninergic neurotransmitters in first-episode psychosis (FEP) patients (n = 166), unaffected siblings (n = 76), and community-based controls (n = 166) included in a cross-sectional study. Plasma levels of glutamic acid (GLU), glutamine, glycine, proline (PRO), tryptophan (TRP), tyrosine, serine and GABA were quantified by gas-chromatography-mass spectrometry. We used the generalized linear model adjusted by sex, age, and body mass index for group comparison and paired t-test for FEP-Sibling pairs. FEP had reduced GABA plasma levels compared to siblings and controls (p < 0.05 for both). Siblings had lower GLU, Glx and PRO (p < 0.05 for all) but increased TRP compared to patients and controls (p < 0.05 for both). FEP patients with longer duration of pharmacological treatment and medicated only with antipsychotics had increased GLU compared to FEP with shorter periods, or with those treated with a combination of medications (p < 0.05 for both). Finally, FEP patients treated only with antipsychotics presented higher Glx compared to those with mixed medications (p = 0.026). Our study suggests that FEP have low a GABA plasma profile. Unaffected siblings may be a possible risk group for metabolic abnormalities.

Indexed as

SiblingsAdultAmino AcidsAntipsychotic AgentsBody Mass IndexCase-Control StudiesCross-Sectional StudiesFemalegamma-Aminobutyric AcidGas Chromatography-Mass SpectrometryGlutamic AcidGlutamineGlycineHumansLinear ModelsMaleAmino AcidsAntipsychotic Agentsgamma-Aminobutyric AcidGlutamic AcidGlutamineGlycineProlineTryptophan

Identifiers

PMID33293633
PMCPMC7722891
OpenAlexW3111706478

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.