RecruitingNot ApplicableNCT06467461

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


Sponsor

University of Minnesota

Enrollment

60 participants

Start Date

Feb 8, 2024

Study Type

INTERVENTIONAL

Conditions

Summary

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.


Eligibility

Min Age: 18 YearsMax Age: 75 Years

Inclusion Criteria7

  • Serotonergic REM sleep behavior (5-HT RBD) participants
  • 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
  • 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 Criteria11

  • Serotonergic REM sleep behavior (5-HT RBD) participants
  • 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
  • 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
  • History of dream enactment that may suggest RBD
  • Increased REM motor tone (REM atonia index \> 0.10) on PSG suggestive of RBD

Interventions

DIAGNOSTIC_TESTSkin biopsy

Skin biopsy to detect systemic alpha-synuclein pathology in 5-HT RBD

DIAGNOSTIC_TESTSpeech testing

Speech Testing to quantify evolving signs of 5-HT RBD

DIAGNOSTIC_TESTUltra high field 7T MRI

7T MRI to examine 5-HT RBD for evidence of brainstem neurodegeneration


Locations(1)

University of Minnesota

Minneapolis, Minnesota, United States

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NCT06467461


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