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Abstract Details

What Happens to Glucose During Multidien Interictal or Ictal Cycles?
Epilepsy/Clinical Neurophysiology (EEG)
P16 - Poster Session 16 (5:30 PM-6:30 PM)
12-006
To study tissue glucose during multi-day active and quiet interictal and ictal epochs from a patient with type I diabetes and refractory bitemporal epilepsy.
Evidence from RNS-Neuropace patients suggests multiday interictal epileptiform activities (IEA) and ictal cycles occur. Mechanisms driving multidien IEA and seizures are unclear, glucose influences may be important. This patient has continuous glucose monitoring (CGM) and responsive neurostimulator (RNS) devices. We previously reported differences in glucose levels and lateralized RNS evident seizures as well as 24-hour circadian patterns of IEA, seizure and glucose.

RNS-defined long events (LE), locations and hourly IEA were matched with hourly CGM of tissue glucose over a continuous 3-year period without any RNS detection setting changes. “Active” and "Quiet" IEA periods were defined by Z-scoring daily IEA and retaining consecutive 4-day intervals with Z>1 and Z<-1 respectively. A second analysis studied LE and confirmed ictal/seizure activities. If multiple events occurred within 4 days, they were designated “active.” Average glucose levels during active and quiet periods were compared using two-tailed t-tests. 4-day minimum intervals defined epochs as they were the most common duration between seizures.

Average glucose during active (n=121) and quiet (n=110) IEA was 165 mg/dl and 150 mg/dl respectively (p=0.01). Average glucose during active (n=61) and quiet (n=43) Ictal periods was 161 mg/dl and 151 mg/dl respectively (p>0.3). LE that were not clearly seizures (n=123) showed an average glucose of 180 mg/dl while LE that were clearly seizures (n=104) showed an average glucose of 157 mg/dl (p=0.02).

Glucose elevations are evident during epochs of volatile IEA and RNS evident “long events” that are NOT clearly seizures. However, for clearly evident seizure, glucose does not differ between active and inactive multidien clusters.  

Authors/Disclosures

PRESENTER
No disclosure on file
No disclosure on file
Nicole M. Warner, ARNP (Swedish Neuroscience Institute) No disclosure on file
No disclosure on file
No disclosure on file
Maxime Baud, MD, PhD (University of California, SF (UCSF)) No disclosure on file
Michael J. Doherty, MD, FÂé¶¹´«Ã½Ó³»­ (Swedish Epilepsy Center) No disclosure on file