Identification of Prodromal Neurodegeneration in Serotonergic-Induced REM Sleep Behavior Disorder

University of Minnesota (UMN)

Status: Enrolling

Conditions: REM Sleep Behavior Disorder; Parkinson Disease; Dementia With Lewy Bodies

Treatments: Diagnostic Test: Skin biopsy; Diagnostic Test: Speech testing; Diagnostic Test: Ultra high field 7T MRI

Study type: Interventional

Funder types: Other

Identifiers

NCT06467461

NEUR-2023-32484

Details and patient eligibility

About

This project will test the hypotheses that people with 5-HT RBD have systemic alpha- synuclein pathology, prodromal DLB signs, and brainstem lesions in regions that control REM sleep. AIM 1 will seek to detect abnormally phosphorylated alpha- synuclein aggregates on targeted skin biopsy in a cohort of people with 5-HT RBD and matched controls (taking SSRIs but without RBD). Aim 2 will use ultra-high field MRI at 7T to examine the pontine region of the coeruleus/subcoeruleus complex for evidence of neurodegeneration as well as segment and parcellate REM sleep related neuronal structures. Aim 3 will test for speech deficits. While these aims are independent we suspect that the severity of autonomic, speech and cognitive deficits will correlate with loss of neuromelanin signal on MRI and pathology on skin biopsy.

The investigation is a longitudinal designed study to examine histopathology, neuroimaging changes and speech function from baseline (Time 1) to a follow-up after 30 months (Time 2). A total of 60 individuals, 30 with 5-HT RBD and 30 controls, will be recruited at Time 1, brought back at Time 2, and tested across all Aims at both study visits.

Enrollment: 60 estimated patients

Sex: All

Ages: 18 to 75 years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

Serotonergic REM sleep behavior (5-HT RBD) participants

Inclusion Criteria:

• Diagnosis of polysomnogram-confirmed RBD with history of dream enactment or clear dream enactment visualized on video from polysomnogram.
• History of dream enactment began shortly after (less than 2 months) starting a serotonergic antidepressant medication. Control Participants

Inclusion Criteria:

• Age (±3 years) and sex matched to participants with 5-HT RBD
• On serotonergic medication for at least 6 months without history of dream enactment.

The following serotonergic medications will be included:

Citalopram, Escitalopram, Fluoxetine, Fluvoxamine, Paroxetine, and Sertraline

Exclusion criteria

Serotonergic REM sleep behavior (5-HT RBD) participants

Exclusion Criteria:

• Younger than 18
• Older than 75
• Meet criteria for Parkinson's disease, dementia with Lewy bodies, Multiple System Atrophy, Pure Autonomic Failure, Alzheimer's disease, other diagnosed neurodegenerative disorder, or other known cause of RBD (e.g. narcolepsy)
• Untreated obstructive sleep apnea, obesity hypoventilation, central sleep apnea or other sleep disordered breathing
• History of dysarthria, aphasia or other condition which could interfere with speech assessment
• Reduced capacity to consent
• MRI exclusion criteria for 7T scans: presence of any metallic clip(s) or implantable medical devices (e.g., heart valve, aneurysm clip, coils or surgery, renal or aortic clips, shunts, stents or stent grafts, metal mesh/coil implants, neurostimulator, insulin pump, IVC filter, etc.).
• History of allergic response to xylocaine or other local anesthesia
• Pregnant women will be excluded due to unknown risk of MRI on developing fetus Control Participants

Exclusion Criteria: same exclusion criteria as 5-HT RBD group, plus the following:

• History of dream enactment that may suggest RBD
• Increased REM motor tone (REM atonia index > 0.10) on PSG suggestive of RBD

Trial design

Primary purpose: Basic Science

Allocation: N/A

Interventional model: Single Group Assignment

Masking: None (Open label)

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60 participants in 1 patient group

Research participants

Other group

Description:

Adults under the age of 75; who do not meet criteria for Parkinson's disease, dementia with Lewy bodies, Alzheimer's disease, other diagnosed neurodegenerative disorder, or other known cause of RBD; and have a history of or currently use the SSRIs of interest.

Treatment:

Diagnostic Test: Ultra high field 7T MRI

Diagnostic Test: Speech testing

Diagnostic Test: Skin biopsy