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Abstract Details

Correlates of Obstructive Sleep Apnea in Late-onset Unexplained Epilepsy
Epilepsy/Clinical Neurophysiology (EEG)
P4 - Poster Session 4 (8:00 AM-9:00 AM)
11-004

This study aimed to evaluate the clinical and neuroimaging correlates of obstructive sleep apnea (OSA) in adults with late-onset unexplained epilepsy (LOUE).

The recurrent apnea/hypopnea cycles in OSA drive inflammation and endothelial dysfunction which may contribute to seizure exacerbation in LOUE. Thus, identifying and treating OSA may improve outcomes for adults with LOUE. 

We prospectively recruited adults with LOUE (unexplained seizure after age 55) who underwent polysomnography or home sleep testing as part of their clinical care. Participants were dichotomized into no/mild OSA (apnea-hypopnea index [AHI]<15) and moderate/severe OSA (AHI≥15) groups. We evaluated their plasma phospho-tau-217 (ptau-217) levels and extracted seizure semiology variables, SSRI/SNRI use, and number of anti-seizure medications (ASMs). Participants also underwent magnetic resonance imaging (MRI), and we quantified their hippocampal and amygdala volumes using FreeSurfer.

Of the 85 enrolled participants, 31 underwent sleep testing, and 2 were excluded due to a prior diagnosis and treatment of OSA. The final cohort (n=29) had a mean age of 69.89±6.66 years and was 45% female. 15 participants (51.7%) had no/mild OSA and 14 (48.3%) had moderate/severe OSA. The mean time between sleep study and MRI was 1.5 years. After controlling for age and sex, participants with moderate/severe OSA were more likely to be on an SSRI/SNRI (OR=65.93, p=0.020), less likely to present with a nocturnal generalized tonic-clonic seizure (GTCS, OR=0.082, p=0.038), and had lower total amygdala volumes (β=-0.00027, p=0.049) relative to those with no/mild OSA. There were no significant differences in ptau-217 levels (p=0.89) or ASM number (p=0.45) between the two groups.

Moderate/severe OSA is common in LOUE and is associated with greater SSRI/SNRI use and amygdala atrophy, which could reflect underlying dysfunction in the limbic system. Older adults with LOUE and moderate/severe OSA are also less likely to present with a nocturnal GTCS. 
Authors/Disclosures
Michael Sadek
PRESENTER
Mr. Sadek has nothing to disclose.
Alexis M. Hankerson, MPH Miss Hankerson has nothing to disclose.
Janet Orozco, BS Ms. Orozco has nothing to disclose.
Milena Pavlova, MD (Brigham and Womens Hospital Dept of Neurology) Dr. Pavlova has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Pear Therapeutics. Dr. Pavlova has received personal compensation in the range of $500-$4,999 for serving on a Speakers Bureau for Oakstone. The institution of Dr. Pavlova has received research support from Jazz. The institution of Dr. Pavlova has received research support from Vanda. The institution of Dr. Pavlova has received research support from Biomobie. Dr. Pavlova has received personal compensation in the range of $500-$4,999 for serving as a Didactic article with Neurodiem.
Gad Marshall, MD (Brigham and Women's Hospital) Dr. Marshall has received personal compensation in the range of $500-$4,999 for serving as a Consultant for Ono Pharma USA Inc. Dr. Marshall has received personal compensation in the range of $500-$4,999 for serving on a Scientific Advisory or Data Safety Monitoring board for Beth Israel Deaconness Medical Center. Dr. Marshall has received personal compensation in the range of $500-$4,999 for serving as an Editor, Associate Editor, or Editorial Advisory Board Member for Harvard Health Publications.
Rani A. Sarkis, MD, MSc (Brigham and Women'S) The institution of Dr. Sarkis has received research support from NINDS.