Substantia nigra and locus coeruleus microstructural abnormalities in isolated rapid eye movement sleep behaviour disorder and Parkinson’s disease

Substantia nigra (SN) and locus coeruleus (LC) are two catecholaminergic, neuromelanin-rich nuclei that are affected in Parkinson's disease (PD) and may show neuroimaging abnormalities before the onset of motor manifestations. The simultaneous, multimodal investigation of their microstructural abnormalities may provide useful insights on the spatial diffusion and tissue characteristics of neurodegeneration, and this may in turn help develop markers for disease-modifying clinical trials. Therefore, through neuromelanin-sensitive and diffusion MRI, we aimed to investigate microstructural abnormalities in those nuclei in isolated REM sleep behaviour disorder (iRBD) and PD. Fourteen participants with polysomnography-confirmed iRBD, 18 with PD and 18 healthy controls were scanned with structural, neuromelanin-sensitive and neurite orientation dispersion and density imaging (NODDI) MRI. iRBD participants also underwent dopamine transporter imaging. SN neuromelanin and NODDI diffusion parameters and LC neuromelanin signals were extracted. Motor and global cognitive assessments were also collected. iRBD and PD participants showed significantly reduced neuromelanin contrast in the LC middle section compared with healthy controls. PD also showed significantly reduced caudal LC and posterior SN neuromelanin signal. No differences in SN NODDI parameters were detected between iRBD and healthy controls. Five iRBD participants showed reduced striatal dopamine transporter. In the combined disease groups (iRBD and PD), significant associations were shown between SN neuromelanin signal and neurite density index (<i>r</i> = -0.610, corr-<i>p</i> = 0.001) and between SN neurite density index and free water fraction (<i>r</i> = 0.417, corr-<i>p</i> = 0.042). In the same group, motor scores were negatively associated with nigral neuromelanin signal (<i>r</i> = -0.404, corr-<i>p</i> = 0.044) and free water fraction (<i>r</i> = 0.486, corr-<i>p</i> = 0.018). In conclusion, iRBD participants showed significant neuromelanin loss in the LC, with a minority showing initial nigrostriatal dopaminergic abnormalities. Across the entire iRBD-PD spectrum, the association between SN neuromelanin signal loss, diffusion parameters and motor scores has the potential to capture different yet related aspects of SN degeneration.

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Publication Details

Journal
Brain Communications
Published
2024-12-24
DOI
https://doi.org/10.1093/braincomms/fcaf023
Citations
3
Primary Topic
Parkinson's Disease Mechanisms and Treatments
Type
article
Field-Weighted Citation Impact
1.11

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article

Substantia nigra and locus coeruleus microstructural abnormalities in isolated rapid eye movement sleep behaviour disorder and Parkinson’s disease

Rory Durcan, Nicola Pavese, Michael John Firbank, Vincenzo Silani et al.
3 citations
Brain Communications
Parkinson's Disease Mechanisms and Treatments
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article

Substantia nigra and locus coeruleus microstructural abnormalities in isolated rapid eye movement sleep behaviour disorder and Parkinson’s disease

Rory Durcan, Nicola Pavese, Michael John Firbank, Vincenzo Silani, Laura Best, Charlotte B. Stewart, George Petrides, Gemma Roberts, David J. Brooks, Jacopo Pasquini, Victoria Foster, Kirstie N. Anderson, Roberto Ceravolo
article en
3 citations

Abstract

Substantia nigra (SN) and locus coeruleus (LC) are two catecholaminergic, neuromelanin-rich nuclei that are affected in Parkinson's disease (PD) and may show neuroimaging abnormalities before the onset of motor manifestations. The simultaneous, multimodal investigation of their microstructural abnormalities may provide useful insights on the spatial diffusion and tissue characteristics of neurodegeneration, and this may in turn help develop markers for disease-modifying clinical trials. Therefore, through neuromelanin-sensitive and diffusion MRI, we aimed to investigate microstructural abnormalities in those nuclei in isolated REM sleep behaviour disorder (iRBD) and PD. Fourteen participants with polysomnography-confirmed iRBD, 18 with PD and 18 healthy controls were scanned with structural, neuromelanin-sensitive and neurite orientation dispersion and density imaging (NODDI) MRI. iRBD participants also underwent dopamine transporter imaging. SN neuromelanin and NODDI diffusion parameters and LC neuromelanin signals were extracted. Motor and global cognitive assessments were also collected. iRBD and PD participants showed significantly reduced neuromelanin contrast in the LC middle section compared with healthy controls. PD also showed significantly reduced caudal LC and posterior SN neuromelanin signal. No differences in SN NODDI parameters were detected between iRBD and healthy controls. Five iRBD participants showed reduced striatal dopamine transporter. In the combined disease groups (iRBD and PD), significant associations were shown between SN neuromelanin signal and neurite density index (<i>r</i> = -0.610, corr-<i>p</i> = 0.001) and between SN neurite density index and free water fraction (<i>r</i> = 0.417, corr-<i>p</i> = 0.042). In the same group, motor scores were negatively associated with nigral neuromelanin signal (<i>r</i> = -0.404, corr-<i>p</i> = 0.044) and free water fraction (<i>r</i> = 0.486, corr-<i>p</i> = 0.018). In conclusion, iRBD participants showed significant neuromelanin loss in the LC, with a minority showing initial nigrostriatal dopaminergic abnormalities. Across the entire iRBD-PD spectrum, the association between SN neuromelanin signal loss, diffusion parameters and motor scores has the potential to capture different yet related aspects of SN degeneration.

Brain CommunicationsVol. 7(1)
University of Pisa (IT), University of Ulster (GB), University of Milan (IT), Aarhus University (DK), Newcastle upon Tyne Hospitals NHS Foundation Trust (GB), Beaumont Hospital (IE), Royal Victoria Hospital (GB), IRCCS Istituto Auxologico Italiano (IT), Newcastle Hospitals - Campus for Ageing and Vitality (GB), Istituti di Ricovero e Cura a Carattere Scientifico (IT), Ferrari (Italy) (IT), Royal Victoria Hospital (GB), Azienda Ospedaliera Universitaria Pisana (IT), Newcastle University (GB)
Multiple System Atrophy Trust, Parkinson's UK, European Academy of Neurology
Openalex Percentile: Top 19%
Parkinson's Disease Mechanisms and Treatments
1.11
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