Evidence map›Paper›PMID 42755989›Full record

ArticleFrontiers in neuroscience2026

Amino acid profiles and clinical phenotypes in young children with autism spectrum disorder.

Ilaria Serati, Luca Lalli, Andrea Riccardo Dallapiccola, Pietro Baso, Martina Tosi, Francesca Brustia, Maria Paola Canevini, Michele Mussap, Livia Pisciotta, Emilia Ricci and 14 more

Abstract read
In one paragraph

Article in Frontiers in neuroscience, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

24 authors.

Ilaria SeratiChild and Adolescent Neuropsychiatry Unit, ASST Fatebenefratelli Sacco, Milan, Italy.
Luca LalliUnit of Translational Immunology, IRCCS Foundation National Cancer Institute, Milan, Italy.
Andrea Riccardo DallapiccolaChild Neuropsychiatry Unit, Epilepsy Center, San Paolo Hospital, Milan, Italy.
Pietro BasoDepartment of Child Neurology and Psychiatry, IRCCS Mondino Foundation, Pavia, Italy.
Martina TosiDepartment of Health Sciences, University of Milan, Milan, Italy.
Francesca BrustiaChild Neuropsychiatry Unit, University Hospital Maggiore della Carità, Novara, Italy.
Maria Paola CaneviniChild Neuropsychiatry Unit, Epilepsy Center, San Paolo Hospital, Milan, Italy.
Michele MussapLaboratory Medicine, Hospital Foundation Villa Salus, Venice, Italy.
Livia PisciottaChild and Adolescent Neuropsychiatry Unit, ASST Fatebenefratelli Sacco, Milan, Italy.
Emilia RicciChild Neuropsychiatry Unit, Epilepsy Center, San Paolo Hospital, Milan, Italy.
Maura RossiChild and Adolescent Neuropsychiatry Unit, ASST Fatebenefratelli Sacco, Milan, Italy.
Marco Di DarioLaboratory of Clinical Pathology, Department of Diagnostic Services, ASST Santi Paolo e Carlo, Milan, Italy.
Maria Cristina StrafaceLaboratory of Clinical Pathology, Department of Diagnostic Services, ASST Santi Paolo e Carlo, Milan, Italy.
Amanda PapaChild Neuropsychiatry Unit, University Hospital Maggiore della Carità, Novara, Italy.
Sabrina FedeCenter of Functional Genomics and Rare Diseases, Buzzi Children's Hospital, Milan, Italy.
Salvatore FazzoneCenter of Functional Genomics and Rare Diseases, Buzzi Children's Hospital, Milan, Italy.
Elena SpadaLaboratorio Della Conoscenza Carlo Corchia, Florence, Italy.
Federica GioiaChild Neuropsychiatry Unit, Epilepsy Center, San Paolo Hospital, Milan, Italy.
Roberto LongoCorporate Information Systems, Buzzi Children's Hospital, Milan, Italy.
Pierangelo VeggiottiDepartment of Biomedical and Clinical Sciences, University of Milan, Milan, Italy.
Gianvincenzo ZuccottiDepartment of Pediatrics, Buzzi Children's Hospital, Milan, Italy.
Cristina CeredaCenter of Functional Genomics and Rare Diseases, Buzzi Children's Hospital, Milan, Italy.
Bruno Mario Cesana *Laboratory of Medical Statistics, Biometry and Epidemiology "G.A. Maccacaro", Department of Clinical Sciences and Community Health, University of Milan, Milan, Italy.
Simona Ferraro *Department of Pediatrics, Buzzi Children's Hospital, Milan, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: In 394 children with autism spectrum disorder (ASD), we investigated the association between plasma amino acid (AA) concentrations and clinical phenotypes. Methods: Multivariable logistic regression models were used to evaluate the associations between 22 AAs and clinical features, reporting odds ratios. Results: The median age at diagnosis was 3.5 years (interquartile range: 2.8-4.6 years) for boys and 3.1 years (interquartile range: 2.3-3.8 years) for girls; 81.5% of the participants were boys. A 25-unit increase in cystine concentration was associated with stereotypies (OR = 2.07), hyperactivity (OR = 1.79), and aggressive behavior (OR = 2.13), suggesting a potential role of oxidative stress in these phenotypes. Similarly, a 25-unit increase in taurine levels was associated with hyperactivity (OR = 1.24) and intellectual disability (OR = 1.38), consistent with oxidative imbalance. Higher arginine levels appeared to have a protective effect against hyperactivity (OR = 0.70), indicating a potential role in ammonia detoxification. Increased glutamine and tyrosine levels were associated with ORs < 1 for stereotypies, supporting potential neuroprotective roles. Discussion: These findings suggest oxidative stress, urea cycle dysfunction, and altered neurotransmission may contribute to the pathophysiology of ASD and related clinical phenotypes in young children, warranting further investigation to inform the development of personalized clinical and nutritional interventions.

Indexed as

amino acidautism spectral disorderchildrenclinical phenotypesnutrition

Identifiers

PMID42755989
PMCPMC13582212

What Socratic holds

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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 Socratic graph.