Interaction of interictal epileptiform activity with sleep spindles is associated with cognitive deficits and adverse surgical outcome in pediatric focal epilepsy

Author:

Yu Han1,Kim Woojoong2,Park David K.3ORCID,Phi Ji Hoon4,Lim Byung Chan2,Chae Jong‐Hee2,Kim Seung‐Ki4,Kim Ki Joong2,Provenzano Frank A.5,Khodagholy Dion1,Gelinas Jennifer N.56ORCID

Affiliation:

1. Department of Electrical Engineering Columbia University New York New York USA

2. Division of Pediatric Neurology, Department of Pediatrics Pediatric Clinical Neuroscience Center, Seoul National University Children's Hospital Seoul South Korea

3. Department of Biomedical Engineering Columbia University New York New York USA

4. Division of Pediatric Neurosurgery, Department of Neurosurgery Pediatric Clinical Neuroscience Center, Seoul National University Children's Hospital Seoul South Korea

5. Department of Neurology Columbia University New York New York USA

6. Institute for Genomic Medicine, Columbia University Medical Center New York New York USA

Abstract

AbstractObjectiveTemporal coordination between oscillations enables intercortical communication and is implicated in cognition. Focal epileptic activity can affect distributed neural networks and interfere with these interactions. Refractory pediatric epilepsies are often accompanied by substantial cognitive comorbidity, but mechanisms and predictors remain mostly unknown. Here, we investigate oscillatory coupling across large‐scale networks in the developing brain.MethodsWe analyzed large‐scale intracranial electroencephalographic recordings in children with medically refractory epilepsy undergoing presurgical workup (n = 25, aged 3–21 years). Interictal epileptiform discharges (IEDs), pathologic high‐frequency oscillations (HFOs), and sleep spindles were detected. Spatiotemporal metrics of oscillatory coupling were determined and correlated with age, cognitive function, and postsurgical outcome.ResultsChildren with epilepsy demonstrated significant temporal coupling of both IEDs and HFOs to sleep spindles in discrete brain regions. HFOs were associated with stronger coupling patterns than IEDs. These interactions involved tissue beyond the clinically identified epileptogenic zone and were ubiquitous across cortical regions. Increased spatial extent of coupling was most prominent in older children. Poor neurocognitive function was significantly correlated with high IED–spindle coupling strength and spatial extent; children with strong pathologic interactions additionally had decreased likelihood of postoperative seizure freedom.SignificanceOur findings identify pathologic large‐scale oscillatory coupling patterns in the immature brain. These results suggest that such intercortical interactions could predict risk for adverse neurocognitive and surgical outcomes, with the potential to serve as novel therapeutic targets to restore physiologic development.

Funder

National Institutes of Health

National Science Foundation

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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