Evidence map›Paper›PMID 36393977›Full record

ArticlePharmacogenomics and personalized medicine2022

CES1 and SLC6A2 Genetic Variants As Predictors of Response To Methylphenidate in Autism Spectrum Disorders.

Marta H Hernandez, Valentin Bote, Alexandre Serra-LLovich, Marc Cendros, Juliana Salazar, Conxita Mestres, Silvina Guijarro, Aida Alvarez, Cristina Lamborena, Iria Mendez and 3 more

Open access · goldAbstract read
In one paragraph

Article in Pharmacogenomics and personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.5field-weighted citation impact, top 39% 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, 4 citations in OpenAlex.

  1. Review
  2. Review
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 4 institutions in 1 country.

Marta H Hernandez *Research Laboratory Unit, Fundació Docència i Recerca Mútua Terrassa, Terrassa, Spain.ORCID 0000-0002-6983-413X
Valentin Bote *Department of Child and Adolescent Psychiatry, Hospital Universitari Mútua Terrassa, Terrassa, Spain.
Alexandre Serra-LLovichResearch Laboratory Unit, Fundació Docència i Recerca Mútua Terrassa, Terrassa, Spain.
Marc CendrosResearch Laboratory Unit, Fundació Docència i Recerca Mútua Terrassa, Terrassa, Spain.
Juliana SalazarTranslational Medical Oncology Laboratory, Institut de Recerca Biomèdica Sant Pau (IIB-Sant Pau), Barcelona, Spain.ORCID 0000-0002-3581-4499
Conxita MestresSchool of Health Sciences Blanquerna, University Ramon Llull, Barcelona, Spain.ORCID 0000-0002-0494-3108
Silvina GuijarroDepartment of Child and Adolescent Psychiatry, Hospital Universitari Mútua Terrassa, Terrassa, Spain.
Aida AlvarezDepartment of Child and Adolescent Psychiatry, Hospital Universitari Mútua Terrassa, Terrassa, Spain.
Cristina LamborenaDepartment of Child and Adolescent Psychiatry, Hospital Universitari Mútua Terrassa, Terrassa, Spain.
Iria MendezDepartment of Child and Adolescent Psychiatry, Hospital Universitari Mútua Terrassa, Terrassa, Spain.
Bernardo SanchezDepartment of Child and Adolescent Psychiatry, Hospital Universitari Mútua Terrassa, Terrassa, Spain.
Amaia HervasDepartment of Child and Adolescent Psychiatry, Hospital Universitari Mútua Terrassa, Terrassa, Spain.
Maria J ArranzResearch Laboratory Unit, Fundació Docència i Recerca Mútua Terrassa, Terrassa, Spain.ORCID 0000-0002-6757-9198
Mútua Terrassa · ESUniversity Hospital Mútua de Terrassa · ESHospital de Sant Pau · ESUniversitat Ramon Llull · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Purpose: Autistic spectrum disorders (ASD) children and adolescents usually present comorbidities, with 40-70% of them affected by attention deficit hyperactivity disorders (ADHD). The first option of pharmacological treatment for these patients is methylphenidate (MPH). ASD children present more side effects and poorer responses to MPH than ADHD children. The objective of our study is to identify genetic biomarkers of response to MPH in ASD children and adolescents to improve its efficacy and safety. Patients and Methods: A retrospective study with a total of 140 ASD children and adolescents on MPH treatment was included. Fifteen polymorphisms within genes coding for the MPH target NET1 ( Results: Single marker analyses considering gender, age, and dose as covariates showed association between Conclusion: CES1 genetic variants may influence the clinical outcome of MPH treatment in ASD comorbid with ADHD children and adolescents.

Indexed as

ADHDASDattention deficit hyperactivity disordersautistic spectrum disordersCES1methylphenidateSLC6A2

Identifiers

PMID36393977
PMCPMC9653043
OpenAlexW4308397819

What OpenQuestion 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 OpenQuestion graph.