# Susceptibility and diffusion MRI biomarkers predict development of Parkinsonism in iRBD

**Authors:** Zsoka Varga, Jiri Nepozitek, Jan Hlavnicka, Jiri Keller, Abhineet Ojha, Patrizia Pantano, Stanislav Marecek, Karel Sonka, Petr Dusek

PMC · DOI: 10.1038/s41531-025-01174-x · NPJ Parkinson's Disease · 2025-11-21

## TL;DR

MRI scans can predict the development of Parkinsonism in patients with REM sleep behavior disorder by detecting brain changes.

## Contribution

This study identifies MRI biomarkers in the cerebral peduncle that predict phenoconversion to synucleinopathy in iRBD patients.

## Key findings

- Increased magnetic susceptibility and fractional anisotropy in the cerebral peduncle correlate with higher phenoconversion risk.
- Combined MRI biomarkers predict phenoconversion with accuracy comparable to dopamine-transporter imaging.
- These MRI changes may reflect compensatory neuroplastic changes in subthalamo-pallidal pathways.

## Abstract

Quantitative MRI techniques, including quantitative susceptibility mapping (QSM) and diffusion tensor imaging (DTI), may detect early neurodegenerative changes in ɑ-synucleinopathies, especially within the midbrain. This study evaluated their potential to predict phenoconversion to overt synucleinopathy in 79 patients with isolated REM sleep behavior disorder (iRBD) followed annually over 5.6 ± 3.0 years. Phenoconversion, defined by emergence of parkinsonism or dementia, occurred in 21 patients. Baseline QSM and DTI data were analyzed to identify regional brain differences, revealing increased magnetic susceptibility and fractional anisotropy (FA) in the bilateral cerebral peduncle of phenoconverters. Increased magnetic susceptibility and FA within this region were associated with higher phenoconversion risk (FA: hazard ratio (HR) = 1.84, susceptibility: HR = 1.67). Their combined score predicted phenoconversion with accuracy similar to dopamine-transporter imaging (HR 2.58 vs 2.85). Findings suggest that increased susceptibility and FA in the cerebral peduncle may serve as biomarkers of early phenoconversion, potentially reflecting compensatory neuroplastic changes in subthalamo-pallidal pathways.

## Linked entities

- **Diseases:** dementia (MONDO:0001627)

## Full-text entities

- **Diseases:** alpha-synucleinopathies (MESH:D000080874), dementia (MESH:D003704), REM sleep behavior disorder (MESH:D020187), Parkinsonism (MESH:D010302), neurodegenerative (MESH:D019636)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

3 references — full list in the complete paper: https://tomesphere.com/paper/PMC12639090/full.md

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Source: https://tomesphere.com/paper/PMC12639090