Evidence map›Paper›PMID 41554857›Full record

ArticleScientific reports2026

Manual and automated assessments of general movements in neonates are associated with early autism risk at 18 months.

Annik Beaulieu, Catherine Saint-Georges, Isabelle Hagbarth, Maeva Da Cunha, Pessia Grywac, Muriel Chauvet, Marie-Christine Laznik, Orna Lev-Enacab, Hugues Pellerin, Salvatore Maria Anzalone and 10 more

Abstract read
In one paragraph

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

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–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

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

20 authors.

Annik BeaulieuDepartment of Child and Adolescent Psychiatry, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, 83 boulevard de l'Hôpital, Paris, 75013, France.
Catherine Saint-GeorgesDepartment of Child and Adolescent Psychiatry, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, 83 boulevard de l'Hôpital, Paris, 75013, France.
Isabelle HagbarthDepartment of Child and Adolescent Psychiatry, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, 83 boulevard de l'Hôpital, Paris, 75013, France.
Maeva Da CunhaDoctoral School 450 Psychopathology and psychanalytic research studies, Paris Cité University, Paris, France.
Pessia GrywacInstituto de Psicologia da Universidade de São Paulo, São Paulo, Brazil.
Muriel ChauvetDepartment of Child and Adolescent Psychiatry, Association Santé Mentale du 13ème, Paris, France.
Marie-Christine LaznikDepartment of Child and Adolescent Psychiatry, Association Santé Mentale du 13ème, Paris, France.
Orna Lev-EnacabInterdisciplinary MA and PhD Programs in Child Development, School of Psychology Sciences, University of Haifa, Haifa, Israel.
Hugues PellerinDepartment of Child and Adolescent Psychiatry, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, 83 boulevard de l'Hôpital, Paris, 75013, France.
Salvatore Maria AnzaloneLaboratoire CHArt-THIM, Paris 8 University, Saint-Denis, Paris , EA4004, France.
Giulio BertaminiDepartment of Child and Adolescent Psychiatry, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, 83 boulevard de l'Hôpital, Paris, 75013, France.
David CohenDepartment of Child and Adolescent Psychiatry, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, 83 boulevard de l'Hôpital, Paris, 75013, France.
Midori YamamotoDepartment of Sustainable Health Science, Center for Preventive Medical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Chiba , Japan.
Koji ShimataniFaculty of Health and Welfare, Prefectural University of Hiroshima, 1-1, Gakuen-machi, Mihara, Hiroshima 734-8558, Hiroshima, Japan.
Kenichi SakuraiDepartment of Nutrition and Metabolic Medicine, Center for Preventive Medical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Chiba , Japan.
Chisato MoriDepartment of Sustainable Health Science, Center for Preventive Medical Sciences, Chiba University, 1-33 Yayoi-cho, Inage-ku, Chiba 263-8522, Chiba , Japan.
Akira FuruiGraduate School of Advanced Science and Engineering, Hiroshima University, 1-4-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8527, Hiroshima, Japan.
Toshio TsujiGraduate School of Advanced Science and Engineering, Hiroshima University, 1-4-1 Kagamiyama, Higashi-Hiroshima, Hiroshima 739-8527, Hiroshima, Japan.
Xavier Benarous *Department of Child and Adolescent Psychiatry, Hôpital Pitié-Salpêtrière, AP-HP.Sorbonne Université, 83 boulevard de l'Hôpital, Paris, 75013, France. xavier.benarous@aphp.fr.
Hirokazu Doi *Graduate School of Biomedical Sciences, Nagasaki University, 1-12-4 Sakamoto, Nagasaki, Nagasaki, 852-8523, Japan.

Funding

Japan Society for the Promotion of Science 16H01781, 15H01584Mustela Fondation bourse recherche Action 2022, EF-2022-29883
6 · The paper itself

Abstract

General movements (GMs) refer to infants’ spontaneous motor activities before the emergence of voluntary motor activity. Abnormal GMs in neonates have been regarded as a marker of poor neurodevelopmental outcomes, with preliminary findings in autism. To examine the relation between abnormal GMs in neonates and autism risk, videos of neonates (n = 76) extracted from a Japanese birth cohort were retrospectively exploited. A manual assessment of GMs was completed using the General Movement Assessment Optimality Score (GMOS-R) rated by professionals blinded from all clinical information. An automated assessment of several features of neonates’ motor activity was also conducted using videos of neonates. Outcome measures were the M-CHAT score at 18 months to document autistic risk status and the Strengths and Difficulties Questionnaire (SDQ) at four years to measure non-autistic general psychopathology. The GMOS-R total score and subscores significantly predicted the autistic risk status according to M-CHAT, but not any SDQ scales or the Total Difficulties score. In the manual assessment of GM, “Global poorness of motion” was the most informative feature in predicting ASD risk. The classification performance systematically increased with the addition of automatically extracted features, as indicated by the Loglikelihood tests. In contrast, the DeLong tests for comparison of AUC failed to reach statistical significance. Such improvement came mainly from incorporating information about the imbalance in motion strength between the upper and lower limbs, and was more marked for awake babies. This finding confirms the relevance of considering abnormal motor patterns in neonates as an early marker of autistic risk.

Indexed as

Autistic DisorderMotor ActivityFemaleHumansInfantInfant, NewbornMaleMovementRetrospective StudiesRisk FactorsASDEarly detectionGeneral movement assessmentInfantsMotor developmentNeurodevelopment

Identifiers

PMID41554857
PMCPMC12865176

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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.