# Listening to mom in the neonatal intensive care unit: a randomized trial of increased maternal speech exposure on white matter connectivity in infants born preterm

**Authors:** Katherine E. Travis, Melissa Scala, Virginia A. Marchman, Hua Wu, Cory K. Dodson, Lisa Bruckert, Molly F. Lazarus, Rocío Velasco Poblaciones, Kristen W. Yeom, Heidi M. Feldman

PMC · DOI: 10.3389/fnhum.2025.1673471 · 2025-10-14

## TL;DR

This study shows that preterm infants exposed to more maternal speech in the NICU have more mature brain structures linked to language processing.

## Contribution

The study provides causal evidence that maternal speech exposure in the NICU affects white matter development in preterm infants.

## Key findings

- Increased maternal speech exposure was linked to lower mean diffusivity in the left arcuate fasciculus of preterm infants.
- The T-group showed higher fractional anisotropy and R1 values in the left arcuate, indicating more mature brain microstructure.
- These effects were specific to the left hemisphere, not the right arcuate fasciculus.

## Abstract

Early speech experiences are presumed to contribute to the development of brain structures involved in processing speech. Previous research has been limited to correlational studies. Here, we conducted a randomized trial with neonates born preterm to determine whether increased exposure to maternal speech during NICU hospitalization is causally linked to structural white matter maturation.

We enrolled 46 neonates born preterm (24–31 weeks gestational age). Participants were randomly assigned to receive increased (T: n = 21) or routine (C: n = 25) exposure to mother’s speech. The T-group heard 10-min audio recordings of their mothers reading a children’s story two times/hour between 10pm and 6am, increasing speech exposure by 2.67 h/day. The C-group did not hear recorded speech. At near-term-equivalent age, we obtained two high-angular resolution diffusion MRI (scan 1: b = 700, scan 2: b = 1500) and T1 relaxometry scans. We assessed mean diffusivity (MD), pre-registered primary outcome (NCT02847689), of the left and right arcuate fasciculus, tracts implicated in language processing. Secondary outcomes included fractional anisotropy (FA) and R1 (1/T1). We hypothesized that neonates randomized to the T-group would show evidence for increased maturation within the arcuate, indexed as decreased MD and increased FA and R1, compared to neonates in the C-group.

Groups were equivalent on medical and demographic variables. Linear mixed models demonstrated that compared to the C-group, the T-group demonstrated significantly lower MD in the left (scan 1: β = −0.11, Marginal R2 = 0.27; scan 2: β = −0.12, Marginal R2 = 0.33) but not right arcuate (scan 1: β = −0.06, Marginal R2 = 0.09; scan 2: β = −0.03, Marginal R2 = 0.01). The T-group also demonstrated significantly higher FA (scan 1 β = 0.02, Marginal R2 = 0.20; scan 2: β = 0.03, Marginal R2 = 0.31) and R1 (β = 0.02, Marginal R2 = 0.39) in the left but not right arcuate.

Preterm neonates with increased maternal speech exposure showed more mature left arcuate microstructure, supporting a causal role of exposure to speech in brain development. Enhancing speech exposure in the NICU may benefit preterm children’s language outcomes.

## Full-text entities

- **Diseases:** oxygen desaturation (MESH:D000860), bradycardia (MESH:D001919), hydrocephalus (MESH:D006849), hearing loss (MESH:D034381), central nervous system infections (MESH:D002494), malformation syndromes (MESH:C564254), periventricular leukomalacia (MESH:D007969), prematurity (MESH:C536271), -based learning disabilities (MESH:D007859), necrotizing enterocolitis (MESH:D020345), intraventricular hemorrhage (MESH:D000074042), matter (MESH:D056784), weight gain (MESH:D015430), delays in language development (MESH:D007805), sleep disruption (MESH:D019958), infection (MESH:D007239), preterm birth (MESH:D047928), CD (MESH:D003424), apnea (MESH:D001049), intra-uterine growth restriction (MESH:D005317), birth (MESH:D000014), seizure disorders (MESH:D004827), congenital anomalies (MESH:D000013), arcuate fasciculus (MESH:D012607), inflammatory (MESH:D007249), neurological conditions (MESH:D019636)
- **Chemicals:** T (MESH:D014316)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12558918/full.md

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Source: https://tomesphere.com/paper/PMC12558918