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

Plain Language Summary

Simplified for easier understanding

This study is investigating whether antidepressants that affect serotonin (such as SSRIs) can cause a condition called REM sleep behavior disorder — where people physically act out their dreams — which may in turn indicate early signs of Parkinson's disease or related conditions. **You may be eligible if...** - You have been diagnosed with REM sleep behavior disorder (confirmed by a sleep study) that started shortly after beginning a serotonergic antidepressant — OR — you are on a serotonergic medication for at least 6 months without any dream-enactment symptoms (as a control) - You are age and sex matched to participants in the study **You may NOT be eligible if...** - You have REM sleep behavior disorder unrelated to antidepressant use - You do not meet the specific timing and medication criteria Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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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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