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Increased frontal [123I]FP-CIT binding in Parkinson’s disease patients with self-reported REM sleep behavior disorder

Jaakkola, Elina; Ijas, Jani; Joutsa, Juho; Vahlberg, Tero; Myller, Elina; Eklund, Mikael; Nuuttila, Simo; Murtomäki, Kirsi; Mertsalmi, Tuomas; Levo, Reeta; Noponen, Tommi; Ihalainen, Toni; Scheperjans, Filip; Kaasinen, Valtteri

Increased frontal [123I]FP-CIT binding in Parkinson’s disease patients with self-reported REM sleep behavior disorder

Jaakkola, Elina
Ijas, Jani
Joutsa, Juho
Vahlberg, Tero
Myller, Elina
Eklund, Mikael
Nuuttila, Simo
Murtomäki, Kirsi
Mertsalmi, Tuomas
Levo, Reeta
Noponen, Tommi
Ihalainen, Toni
Scheperjans, Filip
Kaasinen, Valtteri
Katso/Avaa
s41531-025-01116-7.pdf (541.4Kb)
Lataukset: 

Springer Science and Business Media LLC
doi:10.1038/s41531-025-01116-7
URI
https://doi.org/10.1038/s41531-025-01116-7
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe202601215608
Tiivistelmä
Rapid eye movement (REM) sleep behavior disorder (RBD) is a frequent non-motor symptom of Parkinson's disease (PD) and a potential early marker of synucleinopathy-related neurodegeneration. While striatal dopaminergic dysfunction in PD-RBD has been extensively studied, the role of extrastriatal monoaminergic alterations -particularly those involving serotonin - remains poorly understood. In this study, 155 PD patients underwent [I-123]FP-CIT SPECT imaging to assess striatal and extrastriatal tracer binding, reflecting dopaminergic and broader monoaminergic function, respectively. Probable RBD was identified using a validated single-question screening tool with high sensitivity and specificity. Patients with probable RBD (RBD + , n = 44) were compared to those without (RBD - , n = 111) using voxel-wise and region-of-interest analyses, controlling for age, sex, disease duration, motor and non-motor symptom severity, and cognitive function. No significant differences were observed in striatal dopamine transporter binding. However, RBD+ patients showed significantly higher extrastriatal binding in the prefrontal cortex (pFWE < 0.05), suggesting a potential role for altered extrastriatal monoaminergic neurotransmission, possibly involving serotonergic pathways, in PD-RBD pathophysiology. These findings should be interpreted with caution due to the non-selective binding profile of the radiotracer.
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