Related Experiment Video
Updated: Jun 14, 2026

Diffusion Tensor Magnetic Resonance Imaging in the Analysis of Neurodegenerative Diseases
Published on: July 28, 2013
Relationship between environmental factors and gray matter atrophy in refractory MTLE
C L Yasuda1, M E Morita, A Alessio
1Department of Neurology, University of Campinas, Cidade Universitaria, Campinas, SP, Brazil 13083-970.
Objective:
To investigate clinical, neuropsychological, and MRI abnormalities (gray matter atrophy [GMA] and white matter atrophy [WMA]) in surgical mesial temporal lobe epilepsy (MTLE) patients with and without familial antecedent for epilepsy.
Methods:
A cohort study including 69 operated patients with unilateral MTLE, divided into a group of 29 patients (mean age 35.8 +/- 10.4 years) with a negative family history (FH) of epilepsy and a group of 40 patients (32.8 +/- 10 years) with a positive FH. We performed voxel-based morphometry (VBM) on preoperative MRIs and investigated possible clinical and neuropsychological differences between the 2 groups. We also performed VBM and t tests to compare the patients' groups with normal controls.
Results:
The negative-FH group had lower IQ scores (p = 0.004), performed poorer on the Boston Naming Test (p = 0.02) and on delayed recall (p = 0.03), and presented a more prominent asymmetry index of hippocampal volume (p = 0.04) and more frequent initial precipitating injuries (p = 0.023). VBM showed a more restricted pattern of GMA in the positive-FH group and a more bilateral and widespread pattern of GMA in the negative-FH group, involving thalami, temporal, frontal, parietal, and occipital lobes. WMA was widespread and bilateral in both groups.
Conclusions:
The more widespread structural voxel-based morphometry abnormalities and worse IQ performance identified in the negative-family history (FH) group may result from a stronger environmental influence, including initial precipitating injuries. This is further support for the hypothesis that hippocampal sclerosis in mesial temporal lobe epilepsy with positive FH is determined by a stronger genetic predisposition with less influence of environmental factors compared with patients in the negative-FH group.
Insights
Patients with mesial temporal lobe epilepsy (MTLE) and no family history of epilepsy showed more widespread brain atrophy and lower IQ. This suggests a greater environmental influence in these cases compared to those with a positive family history.
Area of Science:
- Neurology
- Neuroimaging
- Epilepsy Research
Background:
- Mesial temporal lobe epilepsy (MTLE) is a common form of epilepsy.
- Understanding the interplay of genetic and environmental factors in MTLE is crucial for treatment.
- Familial history (FH) may indicate differing underlying etiologies in MTLE.
Purpose of the Study:
- To compare clinical, neuropsychological, and MRI (gray matter atrophy [GMA] and white matter atrophy [WMA]) findings in surgical MTLE patients with and without a familial history of epilepsy.
- To investigate the influence of genetic versus environmental factors in MTLE pathogenesis.
Main Methods:
- A cohort study of 69 operated unilateral MTLE patients (29 negative FH, 40 positive FH).
- Voxel-based morphometry (VBM) analysis of preoperative MRIs to assess GMA and WMA.
- Clinical and neuropsychological assessments, including IQ and Boston Naming Test, were performed.
Main Results:
- The negative-FH group exhibited lower IQ scores, poorer performance on naming and delayed recall tasks, and a more asymmetric hippocampal volume.
- VBM revealed a more restricted GMA pattern in the positive-FH group.
- The negative-FH group showed a more bilateral and widespread GMA pattern across multiple brain lobes, alongside frequent initial precipitating injuries.
Conclusions:
- Widespread structural abnormalities and poorer cognitive performance in the negative-FH group suggest a stronger environmental influence, including initial injuries.
- Positive-FH MTLE may be driven by stronger genetic predisposition with less environmental impact.
- Findings support distinct pathogenic pathways in MTLE based on familial history.
Related Concept Videos
Alzheimer Disease ll: Pathophysiology
Alzheimer Disease l: Introduction

