Evidence map›Paper›PMID 38587680›Full record

ArticleEuropean child & adolescent psychiatry2024

Exploring genetic testing requests, genetic alterations and clinical associations in a cohort of children with autism spectrum disorder.

Nathalia Garrido-Torres, Renata Marqués Rodríguez, María Alemany-Navarro, Javier Sánchez-García, Susana García-Cerro, María Irene Ayuso, Antonio González-Meneses, Amalia Martinez-Mir, Miguel Ruiz-Veguilla, Benedicto Crespo-Facorro

Abstract read
In one paragraph

Article in European child & adolescent psychiatry, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed, 1 pooled it
–field-weighted citation impact
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

5 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
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  3. Review
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  5. Article
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

10 authors.

Nathalia Garrido-TorresInstituto de Biomedicina de Sevilla, Seville, Spain.
Renata Marqués RodríguezDepartment of pediatrics, Hospital La Merced de Osuna, Seville, Spain.
María Alemany-NavarroInstituto de Biomedicina de Sevilla, Seville, Spain.
Javier Sánchez-GarcíaInstituto de Biomedicina de Sevilla, Seville, Spain.
Susana García-CerroInstituto de Biomedicina de Sevilla, Seville, Spain.
María Irene AyusoInstituto de Biomedicina de Sevilla, Seville, Spain.
Antonio González-MenesesUniversity of Seville, Seville, Spain.
Amalia Martinez-MirInstituto de Biomedicina de Sevilla, Seville, Spain.
Miguel Ruiz-VeguillaInstituto de Biomedicina de Sevilla, Seville, Spain.
Benedicto Crespo-FacorroInstituto de Biomedicina de Sevilla, Seville, Spain. benedicto.crespo.sspa@juntadeandalucia.es.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several studies show great heterogeneity in the type of genetic test requested and in the clinicopathological characteristics of patients with ASD. The following study aims, firstly, to explore the factors that might influence professionals' decisions about the appropriateness of requesting genetic testing for their patients with ASD and, secondly, to determine the prevalence of genetic alterations in a representative sample of children with a diagnosis of ASD. Methods: We studied the clinical factors associated with the request for genetic testing in a sample of 440 children with ASD and the clinical factors of present genetic alterations. Even though the main guidelines recommend genetic testing all children with an ASD diagnosis, only 56% of children with an ASD diagnosis were genetically tested. The prevalence of genetic alterations was 17.5%. These alterations were more often associated with intellectual disability and dysmorphic features. There are no objective data to explicitly justify the request for genetic testing, nor are there objective data to justify requesting one genetic study versus multiple studies. Remarkably, only 28% of males were genetically tested with the recommended tests (fragile X and CMA). Children with dysmorphic features and organic comorbidities were more likely to be genetic tested than those without. Previous diagnosis of ASD (family history of ASD) and attendance at specialist services were also associated with Genetically tested Autism Spectrum Disorder GTASD. Our findings emphasize the importance of establishing algorithms to facilitate targeted genetic consultation for individuals with ASD who are likely to benefit, considering clinical phenotypes, efficiency, ethics, and benefits.

Indexed as

Autism Spectrum DisorderGenetic TestingAdolescentChildChild, PreschoolCohort StudiesFemaleHumansIntellectual DisabilityMaleAutism spectrum disorderChild psychiatryDiagnosisGeneticsNeurodevelopmental disorders

Identifiers

PMID38587680
PMCPMC11588872

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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.