ArticleCommunications biology2025
Dynamic structure-function coupling in macroscale neonatal brain networks.
Article in Communications biology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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.
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.
Who cites it
1 citing paper in PubMed.
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
The neonatal period is critical for brain development, yet the mechanisms linking structural differentiation to functional reorganization remain poorly understood. Using multi-modal MRI data from 399 neonates (348 term-born, 51 preterm-born), here we characterize the dynamic structure-function coupling (SFC) across macroscale brain networks and examine its associations with cortical microstructure (indexed by the T1w/T2w ratio) and network flexibility. We show that the dynamic SFC varies markedly across the neocortex and increases with postmenstrual age, particularly within the default mode network (DMN). Notably, the dynamic SFC in the posterior DMN mediates the relationship between the T1w/T2w ratio and network flexibility. Preterm infants exhibit a significantly reduced dynamic SFC relative to term-born peers, along with an altered developmental trajectory of DMN linked to premature extra-uterine exposure. These findings establish dynamic SFC, especially within the DMN, as a potential biomarker for neonatal brain maturation, offering insight into the early emergence of internally directed cognition and its vulnerability to early-life adversity.
Indexed as
Identifiers
What Socratic holds
Registered trials
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.