Anti‐seizure medication response and the glymphatic system in patients with focal epilepsy

Author:

Kim Sung‐Tae1,Kim Sung Eun2ORCID,Lee Dong Ah2,Lee Ho‐Joon3,Park Kang Min2ORCID

Affiliation:

1. Department of Neurosugery Inje University Busan Paik Hospital Busan Korea

2. Department of Neurology, Haeundae Paik Hospital Inje University College of Medicine Busan Korea

3. Department of Radiology, Haeundae Paik Hospital Inje University College of Medicine Busan Korea

Abstract

AbstractBackground and purposeWe aimed to evaluate (i) glymphatic system function in patients with focal epilepsy in comparison with healthy controls, and (ii) the association between anti‐seizure medication (ASM) response and glymphatic system function by using diffusion tensor image analysis along the perivascular space (DTI‐ALPS).MethodsWe retrospectively enrolled 100 patients with focal epilepsy who had normal brain magnetic resonance imaging (MRI) findings, and classified them as “poor” or “good” ASM responders according to their seizure control at the time of brain MRI. We also included 79 age‐ and sex‐matched healthy controls. All patients and healthy controls underwent conventional brain MRI and diffusion tensor imaging. The DTI‐ALPS index was calculated using the DSI studio program.ResultsOf the 100 patients with focal epilepsy, 38 and 62 were poor and good ASM responders, respectively. The DTI‐ALPS index differed significantly between patients with focal epilepsy and healthy controls and was significantly lower in patients with focal epilepsy (1.55 vs. 1.70; p < 0.001). The DTI‐ALPS index also differed significantly according to ASM response and was lower in poor ASM responders (1.48 vs. 1.59; p = 0.047). Furthermore, the DTI‐ALPS index was negatively correlated with age (r = −0.234, p = 0.019) and duration of epilepsy (r = −0.240, p = 0.016) in patients with focal epilepsy.ConclusionOur study is the first to identify, in focal epilepsy patients, a greater reduction in glymphatic system function among poor ASM responders compared to good responders. To confirm our results, further prospective multicenter studies with large sample sizes are needed.

Publisher

Wiley

Subject

Neurology (clinical),Neurology

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