Evidence map›Paper›PMID 42544723›Full record

ArticleAutism research : official journal of the International Society for Autism Research2026

Heterogeneity of Response to Early Start Denver Model: Identifying Developmental Trajectories and Predictors of Cognitive Outcomes.

I Ilaridou, N Kojovic, T Chataing, K Latrèche, F Journal, S Akhavan, C Sandini, M Schaer

Abstract read
In one paragraph

Article in Autism research : official journal of the International Society for Autism Research, 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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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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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

I IlaridouDepartment of Psychiatry, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID https://orcid.org/0009-0001-2280-6350
N KojovicDepartment of Psychiatry, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID https://orcid.org/0000-0003-0116-2485
T ChataingDepartment of Psychiatry, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
K LatrècheDepartment of Psychiatry, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID https://orcid.org/0000-0003-0264-4048
F JournalDepartment of Psychiatry, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID https://orcid.org/0009-0001-8269-3765
S AkhavanDepartment of Psychiatry, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID https://orcid.org/0009-0003-7207-229X
C SandiniDepartment of Psychiatry, Faculty of Medicine, University of Geneva, Geneva, Switzerland.
M SchaerDepartment of Psychiatry, Faculty of Medicine, University of Geneva, Geneva, Switzerland.ORCID https://orcid.org/0000-0001-8479-6365

Funding

Fondation Pôle AutismeFondation Privée des Hôpitaux Universitaires de GenèveFoundation NeuronaNational Centre of Competence in Research Evolving Language 51NF40_225146Swiss National Foundation for Scientific Research 163859Swiss National Foundation for Scientific Research 190084Swiss National Foundation for Scientific Research 202235Swiss National Foundation for Scientific Research 212653Swiss National Foundation for Scientific Research PZ00-1_233424/1Swiss National Foundation Synapsy 51NF40-185897
6 · The paper itself

Abstract

Autism is a highly heterogenous neurodevelopmental condition that can significantly compromise the quality of life. For children showing atypical trajectories of development in their early years, early and intensive intervention has shown promise in enhancing the development of language, cognition, and social skills. Yet, marked variability in intervention response remains insufficiently understood. Characterizing this heterogeneity is essential for informing intervention strategies tailored to each child's developmental profile. The aim of the present work was to identify subgroups based on intervention response trajectories and investigate subgroup-specific predictors of intervention outcomes. We analyzed longitudinal data from 125 children (15.2-42.0 months) receiving the Early Start Denver Model (ESDM) intervention over an average follow-up period of 2 years (mean = 1.93 ± 0.25). Children gained an average of 17 points in Developmental Quotient (DQ), showed significant improvement in their adaptive skills and exhibited diminution of autism features. Using K-means clustering, we identified 3 subgroups: Progressive Group A (PrGA; 36%), which had the highest baseline cognitive scores (82.3) and gained 17 DQ points in average throughout the intervention; Progressive Group B (PrGB; 41.6%), which showed significant developmental delay at baseline (mean DQ = 56.3) and gained 30 DQ points; and the Persistent Support Needs Group (PSNG; 22.4%), which also started in the range of delay (mean DQ = 47.7) and remained in this range throughout intervention (mean DQ = 41.1). Subgroup-specific analysis revealed distinct patterns of baseline factors, including stronger adaptive skills and fewer autism features, associated with a higher cognitive outcome for PrGA and PrGB. Comparison of PrGB and PSNG further identified factors distinguishing children with similar levels of cognitive delay at baseline who nevertheless followed markedly different developmental trajectories. Lower levels of repetitive and restricted behaviors, stronger adaptive functioning, and greater cumulative intervention exposure characterized the PrGB group, suggesting that both child-related and intervention-related factors may contribute to variability in developmental outcomes.

Indexed as

Autism Spectrum DisorderAutistic DisorderChild DevelopmentCognitionEarly Intervention, EducationalChild, PreschoolFemaleHumansInfantLongitudinal StudiesMaleTreatment Effect HeterogeneityautismESDMheterogeneityoutcomepredictorstrajectory

Identifiers

PMID42544723
PMCPMC13599680

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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.