Evidence map›Paper›PMID 42173856›Full record

ArticleTranslational psychiatry2026

White matter structure-function coupling in neonatal brain and its association with Autism-related traits in early childhood.

Zhe Zhang, Chi Zhang, Xinlin Zhang, Junrui Zhang, Yongxuan Xu, Wenjie Dou, Mingyang Li, Weihao Zheng, Baoming Li

Abstract read
In one paragraph

Article in Translational psychiatry, 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

9 authors.

Zhe ZhangInstitute of Brain Science and Department of Physiology, School of Basic Medical Sciences, Hangzhou Normal University, Hangzhou, China.ORCID http://orcid.org/0000-0002-2725-4014
Chi ZhangInstitute of Brain Science and Department of Physiology, School of Basic Medical Sciences, Hangzhou Normal University, Hangzhou, China.
Xinlin ZhangInstitute of Brain Science and Department of Physiology, School of Basic Medical Sciences, Hangzhou Normal University, Hangzhou, China.
Junrui ZhangInstitute of Brain Science and Department of Physiology, School of Basic Medical Sciences, Hangzhou Normal University, Hangzhou, China.
Yongxuan XuInstitute of Brain Science and Department of Physiology, School of Basic Medical Sciences, Hangzhou Normal University, Hangzhou, China.
Wenjie DouInstitute of Brain Science and Department of Physiology, School of Basic Medical Sciences, Hangzhou Normal University, Hangzhou, China.
Mingyang LiKey Laboratory for Biomedical Engineering of Ministry of Education, Department of Biomedical Engineering, College of Biomedical Engineering & Instrument Science, Zhejiang University, Hangzhou, China.ORCID http://orcid.org/0000-0002-1639-9891
Weihao ZhengGansu Provincial Key Laboratory of Wearable Computing, School of Information Science and Engineering, Lanzhou University, Lanzhou, China.
Baoming LiInstitute of Brain Science and Department of Physiology, School of Basic Medical Sciences, Hangzhou Normal University, Hangzhou, China. bmli@hznu.edu.cn.ORCID http://orcid.org/0009-0006-1554-9700

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The neonatal brain undergoes a rapid maturation of white matter pathways, yet how structural refinement within these tracts drives concurrent functional reorganization remains poorly understood. Using multimodal MRI data from 399 infants (348 term-born and 51 preterm-born) from the Developing Human Connectome Project, here we characterize the developmental trajectories of white matter structure-function coupling (SFC) and examine its associations with myelination (indexed by the T1w/T2w ratio), prematurity, and later autism-related traits. We find that SFC strength and its temporal variance develop heterogeneously across major fiber tracts, in which the inferior longitudinal and inferior fronto-occipital fasciculi exhibit a marked left-lateralized tendency, supporting the formation of nascent language and social cognition. The association between SFC and myelination is also dynamic, weakening over time in most tracts but strengthening selectively in the inferior longitudinal fasciculus. Preterm infants exhibit significantly reduced SFC across most tracts compared to term-born peers. Notably, reduced SFC in the right corticospinal tract partially mediates the association between prematurity and higher autism-related traits at 18 months. Furthermore, neonatal SFC predicts these traits only in preterm infants. These findings delineate a dynamic, tract-specific interplay between structure and function in early-life brain and establish neonatal SFC as a key link between prematurity and subsequent neurodevelopmental risk.

Indexed as

Autistic DisorderBrainWhite MatterConnectomeFemaleHumansInfantInfant, NewbornInfant, PrematureMagnetic Resonance ImagingMale

Identifiers

PMID42173856
PMCPMC13369871

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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.