Rapid Eye Movement Sleep Behavior Disorder with Clinical Dementia with Lewy Bodies Phenotype but Lacking Postmortem
Gerard Mayà1, Alex Iranzo1, Raquel Sánchez-Valle2
1Sleep Disorders Center, Neurology Service, Hospital Clínic de Barcelona, Universitat de Barcelona, Fundació Recerca Clínic Barcelona-IDIBAPS, Barcelona, Spain.
Introduction:
Idiopathic rapid eye movement (REM) sleep behavior disorder (IRBD) has been linked to the synucleinopathies.
Methods And Results:
An 80-year-old man treated with venlafaxine for depression presented with IRBD. Cerebrospinal fluid (CSF) α-synuclein seeding amplification assay (SAA) was negative. During 16 years of follow up he was diagnosed with dementia with Lewy bodies. He died at the age of 96 years. Neuropathology revealed aging-related tau astrogliopathy, limbic-predominant age-related TDP-43 encephalopathy, primary age-related tauopathy, and diffuse small vessel disease. Lewy pathology was nearly absent with isolated neurites confined to the dorsal motor nucleus of the vagus nerve. Brainstem nuclei that modulate REM sleep were spared.
Conclusions:
RBD may arise independently of α-synuclein pathology. In the present case, RBD might be caused by dysregulation of the brainstem REM sleep-related structures due to age-related proteinopathies impairing the limbic system, and venlafaxine overactive monoaminergic transmission. In neuroprotective trials, CSF α-synuclein SAA may be useful to exclude IRBD patients without synuclein pathology. © 2026 International Parkinson and Movement Disorder Society.
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