# Hippocampal abnormality and response to vagus nerve stimulation in epilepsy

## TL;DR

This study finds that people with epilepsy who don't respond to vagus nerve stimulation have more hippocampal structural abnormalities than those who do respond.

## Contribution

The study introduces a multivariate approach to detect hippocampal abnormalities linked to VNS response in epilepsy.

## Key findings

- Non-responders to VNS showed significantly greater hippocampal abnormality using multivariate analysis (p=.005).
- Univariate measures did not show significant differences between responders and non-responders (p>.05).
- Multivariate analysis revealed hippocampal abnormalities vary across individuals.

## Abstract

Vagus nerve stimulation (VNS) reduces seizure frequency and severity in some, but not all, individuals with epilepsy. The hippocampus has been implicated in VNS response, but is yet to be studied structurally using T1‐weighted (T1w) magnetic resonance imaging (MRI). In this study we hypothesized greater hippocampal abnormality in VNS non‐responders. Using hippocampal morphometrics, we extracted the volumes of four hippocampal regions from T1w MRI across three groups; VNS responders (n=42), non‐responders (n=50), and healthy controls (n=100). We first calculated the multivariate Mahalanobis distance using z‐scores from all four hippocampal regions to measure abnormality relative to controls. We then compared traditional univariate measures to the Mahalanobis distance. Response to VNS was defined as having a ≥50% seizure reduction 2 years post‐implantation. Hippocampal morphometrics were significantly more abnormal in non‐responders than responders (p=.005,biserialr=.32) using the multivariate Mahalanobis distance. Univariate approaches did not differ significantly between responders and non‐responders (p>.05). At the group level, non‐responders to VNS had greater structural hippocampal abnormality when using the multivariate approach. Conversely, this effect was lost with the univariate analysis. This suggests that abnormality is likely present in different parts of the hippocampus in different individuals. Future studies should incorporate multivariate, and potentially multi‐modal, information to better characterize the mechanisms of VNS response.