Evidence map›Paper›PMID 41238842›Full record

ArticleMolecular psychiatry2026

Age-varying distinct neuroanatomy in young children with autism spectrum disorder and fragile X syndrome.

Danyong Feng, Dongyun Li, Chunchun Hu, Yuxin Tian, Xiu Xu, Randi Jenssen Hagerman, Qiong Xu, Rihui Li

Abstract read
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Article in Molecular psychiatry, 2026. 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
–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

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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

2 citing papers in PubMed.

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4 · The record

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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

8 authors.

Danyong Feng *Centre for Cognitive and Brain Sciences, Institute of Collaborative Innovation, University of Macau, Taipa, Macau S.A.R, 999078, China.ORCID http://orcid.org/0009-0009-7279-8705
Dongyun Li *Department of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102, China.
Chunchun HuDepartment of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102, China.
Yuxin TianDepartment of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102, China.
Xiu XuDepartment of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102, China.
Randi Jenssen HagermanMedical Investigation of Neurodevelopmental Disorders (MIND) Institute, University of California Davis, Sacramento, California, 95817, US.ORCID http://orcid.org/0000-0001-5029-8448
Qiong XuDepartment of Child Health Care, Children's Hospital of Fudan University, Shanghai, 201102, China. xuqiong@fudan.edu.cn.ORCID http://orcid.org/0000-0001-8065-8766
Rihui LiCentre for Cognitive and Brain Sciences, Institute of Collaborative Innovation, University of Macau, Taipa, Macau S.A.R, 999078, China. rihuili@um.edu.mo.ORCID http://orcid.org/0000-0001-8006-7333

Funding

National Natural Science Foundation of China (National Science Foundation of China) 82301743Natural Science Foundation of Anhui Province (Anhui Provincial Natural Science Foundation) 2308085MH255Universidade de Macau (University of Macau) MYRG-CRG2024-00022-ICIUniversidade de Macau (University of Macau) MYRG-GRG2024-00296-ICIUniversidade de Macau (University of Macau) SRG2023-00015-ICI
6 · The paper itself

Abstract

Autism spectrum disorder (ASD) is a commonly associated behavioral diagnosis in individuals with fragile X syndrome (FXS). The present study aimed to identify the neuroanatomical profiles and the age effects on brain's developing trajectories that might be distinct or shared in FXS and idiopathic ASD. A total of 190 children were consecutively recruited including 46 with FXS (5.39 ± 2.68 years), 90 with idiopathic ASD (3.38 ± 1.36 years), and 54 typically developing children (5.40 ± 2.90 years). T1-weighted structural magnetic resonance imaging scans of the brain were acquired, and behavioral assessments were collected from all participants. Age-varying, voxel-based morphometry (VBM) was conducted to identify neuroanatomical differences between groups. The most pronounced differences in brain morphological patterns were observed in the FXS group. Children with FXS had increased gray matter volume (GMV) in subcortical regions including caudate and Crus I of the cerebellum, but decreased GMV in frontal insular regions and cerebellar vermis lobules VIII/IX compared to the ASD and TD groups. Children with ASD had significantly faster growth rates of GMV. The identified neuroanatomical profiles correlated with behavior assessments and differed between diagnosis groups. Our findings suggest that FXS and ASD have distinct neuroanatomical signatures during early childhood, particularly in subcortical and cerebellar regions, which are associated with divergent developmental trajectories. Together with their distinct brain-behavior associations, we conclude that these two conditions have distinct neurobiological underpinnings at spatial and temporal scales, despite their overlapping clinical symptoms. These findings have important implications for diagnosis and targeted interventions for children with ASD and FXS.

Indexed as

Autism Spectrum DisorderFragile X SyndromeAge FactorsBrainCerebellumChildChild, PreschoolFemaleGray MatterHumansMagnetic Resonance ImagingMaleNeuroanatomy

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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.