# White Matter Integrity Differences in 2‐Year‐Old Children Treated With ECMO: A Diffusion‐Weighted Imaging Study

**Authors:** Michaela Ruttorf, Julia Filip, Thomas Schaible, Meike Weis, Frank G. Zöllner

PMC · DOI: 10.1111/ejn.70026 · 2025-02-17

## TL;DR

This study finds that 2-year-old children who received ECMO treatment show early white matter changes in the brain that may predict later neurodevelopmental delays.

## Contribution

The study introduces early diffusion-weighted imaging as a non-invasive method to detect white matter alterations in ECMO-treated children.

## Key findings

- ECMO-treated children show significant differences in white matter metrics like FA, F1, RD, and MD compared to non-ECMO children.
- Key brain regions with altered diffusion measures include the corpus callosum and internal capsule, linked to later cognitive delays.
- DWI can detect structural brain changes in early childhood without requiring child cooperation, unlike traditional testing.

## Abstract

School‐aged and adolescent survivors of neonatal extracorporeal membrane oxygenation (ECMO) treatment still suffer from neurodevelopmental delays such as verbal, visuo‐spatial and working memory problems, motor dysfunction and sensorineural hearing loss, respectively, later in life, which is well‐documented by neuropsychological testing within follow‐up programs. In this study, we demonstrate that diffusion‐weighted imaging (DWI) in 2‐year‐old survivors of neonatal ECMO treatment reveals white matter (WM) alterations in brain regions related to neurodevelopmental outcome seen later in life. From the DWI data of 56 children, fractional anisotropy (FA), first fibre partial volume fraction estimate (F1), radial diffusivity (RD) and mean diffusivity (MD) are calculated and compared using tract‐based spatial statistics adapted to a paediatric brain atlas. Significant differences in FA, F1, RD and MD between the no‐ECMO and ECMO groups are seen in major WM tracts. Additionally, we examine individual diffusion measures by looking at 50 regions supplied with the paediatric brain atlas. We find the following regions to have significantly different means in the no‐ECMO compared with the ECMO group matching reports of neuropsychological delays found in behavioural tests: left anterior corona radiata, left anterior limb of internal capsule, left anterior commissure, left and right corpus callosum (genu, body and splenium), left and right crus of fornix and left tapetum. Analysing diffusion measures at an early stage of life serves as a good tool to detect structural WM changes in survivors of neonatal ECMO treatment. Compared with neuropsychological testing, DWI does not depend on the child's active participation.

Statistically significant differences in the contrast no‐ECMO > ECMO are shown for fractional anisotropy (FA—red) and first fibre partial volume fraction estimate (F1—yellow) and in the contrast ECMO > no‐ECMO for radial diffusivity (RD—blue), respectively. The mean FA skeleton (green) is overlaid on the FA image.

## Full-text entities

- **Diseases:** memory problems (MESH:D008569), motor dysfunction (MESH:D000068079), neurodevelopmental delays (MESH:D006968), sensorineural hearing loss (MESH:D006319)

## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11833286/full.md

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Source: https://tomesphere.com/paper/PMC11833286