ArticleBrain communications2025
Prematurity is associated with white matter T2 MRI visible perivascular spaces in very preterm-born neonates.
Article in Brain communications, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
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Who cites it
4 citing papers in PubMed.
- Imaging Biomarkers of the Glymphatic System in the Developing Brain.Korean journal of radiology · 2026Review
- Diagnostic Models of Neonatal Respiratory Distress Syndrome and Congenital Pneumonia: A Retrospective Cohort Study.Medical sciences (Basel, Switzerland) · 2026Article
- Brain-specific immune hub activation in paediatric focal lesional epilepsy: a case-control study.Brain communications · 2026Article
- The Glymphatic-Venous Axis in Brain Clearance Failure: Aquaporin-4 Dysfunction, Biomarker Imaging, and Precision Therapeutic Frontiers.International journal of molecular sciences · 2025Review
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Authors and funding
8 authors.
Funding
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Abstract
Perivascular spaces (PVSs), as biomarkers of the brain's neurofluid clearance system, remain largely unexplored in the brains of very preterm and term-born infants. In this retrospective cross-sectional study, we investigate PVSs in very preterm and term-born neonates and explore potential associations with preterm birth, maturation, brain injury and developmental outcome. T2-weighted fast spin echo MRI data of 86 very preterm (<32 gestational weeks) and 43 term-born neonates were acquired at term-equivalent age (mean postmenstrual age = 41.63 ± 2.09 weeks) with a 3T GE HD.xt scanner, using an 8-channel head coil, with echo time/repetition time = 109/5700 ms, field of view = 25.6 cm, acquisition matrix = 256 × 256, reconstruction matrix = 512 × 512 and slice thickness = 2 mm. PVS counts were estimated visually in the basal ganglia and centrum semiovale (CSO) using a validated scoring system. Developmental outcome was evaluated using the Bayley Scales of Infant Development II or III. White and grey matter injuries were evaluated using Woodward's score. Groupwise differences in PVS counts between term-born and very preterm-born neonates and associations with postmenstrual age, preterm birth, brain injury and developmental outcomes were evaluated with Mann-Whitney tests and multiple regression. PVS counts in the basal ganglia did not differ between groups, whereas PVS counts in the CSO were significantly higher in very preterm-born neonates (median = 1, interquartile range: 0-2), compared with term-born neonates (median = 0, interquartile range: 0-0;
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