Changes in Gray Matter Morphology and White Matter Microstructure Across the Adult Lifespan in People With Temporal Lobe Epilepsy.
Publisher DOI
PubMed ID
40845263
Abstract
Background And Objectives
Temporal lobe epilepsy (TLE) is commonly associated with mesiotemporal pathology and widespread alterations of gray and white matter structures. Evidence supports a progressive condition, although the temporal evolution of TLE is poorly defined. In this ENIGMA-Epilepsy study, we aim to investigate structural alterations in gray and white matter across the adult lifespan in patients with TLE by charting both gray and white matter changes and explore the covariance of age-related alterations in both compartments.Methods
Mega-analysis of parcellated T1-weighted and diffusion MRI data across 18 international sites for patients with TLE was compared against healthy controls. We combined median-age split groupwise comparisons with cross-sectional sliding age-window analyses to explore gray (cortical thickness, subcortical volume) and white matter microstructure (fractional anisotropy, mean diffusivity) age-related changes. Five-year range age windows were constructed from mean z scores of all patients. Covariance analyses examined the coupled correlations of gray and white matter lifespan curves for each region.Results
We studied 769 patients with TLE and 885 healthy controls across an age range of 17-73 years. Robust (pFDR < 0.05) gray matter thickness/volume decline (d < -0.20) was seen across a broad cortico-subcortical territory, extending beyond the mesiotemporal lobe throughout the adult lifespan in patients with TLE. White matter changes were also widespread across multiple fiber tracts with peak effects in temporolimbic fibers in fractional anisotropy (d < -0.3, pFDR < 0.05) and mean diffusivity measures (d > 0.3, pFDR < 0.05). Changes spanned the adult time window and effects exceeded typical aging-related processes in patients at the level of cortical thickness, subcortical volume, and diffusion measures, particularly in patients older than 55 years. Covariance analyses revealed strong associations across multiple white matter tracts, subcortical structures, and cortical regions within and beyond the temporolimbic system.Discussion
This study highlights that patients with TLE exhibit more pronounced and widespread gray and white matter atrophy across the lifespan. The cross-sectional nature of our study limits definitive conclusions on whether the atrophy shown is progressive but emphasizes the importance of prompt diagnosis and intervention in patients. Collectively, our results motivate future longitudinal studies to clarify consequences of drug-resistant epilepsy.
Temporal lobe epilepsy (TLE) is commonly associated with mesiotemporal pathology and widespread alterations of gray and white matter structures. Evidence supports a progressive condition, although the temporal evolution of TLE is poorly defined. In this ENIGMA-Epilepsy study, we aim to investigate structural alterations in gray and white matter across the adult lifespan in patients with TLE by charting both gray and white matter changes and explore the covariance of age-related alterations in both compartments.Methods
Mega-analysis of parcellated T1-weighted and diffusion MRI data across 18 international sites for patients with TLE was compared against healthy controls. We combined median-age split groupwise comparisons with cross-sectional sliding age-window analyses to explore gray (cortical thickness, subcortical volume) and white matter microstructure (fractional anisotropy, mean diffusivity) age-related changes. Five-year range age windows were constructed from mean z scores of all patients. Covariance analyses examined the coupled correlations of gray and white matter lifespan curves for each region.Results
We studied 769 patients with TLE and 885 healthy controls across an age range of 17-73 years. Robust (pFDR < 0.05) gray matter thickness/volume decline (d < -0.20) was seen across a broad cortico-subcortical territory, extending beyond the mesiotemporal lobe throughout the adult lifespan in patients with TLE. White matter changes were also widespread across multiple fiber tracts with peak effects in temporolimbic fibers in fractional anisotropy (d < -0.3, pFDR < 0.05) and mean diffusivity measures (d > 0.3, pFDR < 0.05). Changes spanned the adult time window and effects exceeded typical aging-related processes in patients at the level of cortical thickness, subcortical volume, and diffusion measures, particularly in patients older than 55 years. Covariance analyses revealed strong associations across multiple white matter tracts, subcortical structures, and cortical regions within and beyond the temporolimbic system.Discussion
This study highlights that patients with TLE exhibit more pronounced and widespread gray and white matter atrophy across the lifespan. The cross-sectional nature of our study limits definitive conclusions on whether the atrophy shown is progressive but emphasizes the importance of prompt diagnosis and intervention in patients. Collectively, our results motivate future longitudinal studies to clarify consequences of drug-resistant epilepsy.
Date Issued
2025-09-23
Publication Type
Article
Subject(s)
Language(s)
en
Author(s)
Chen, Judy | |
Ngo, Alexander | |
Rodriguez-Cruces, Raul | |
Royer, Jessica | |
Caligiuri, Maria Eugenia | |
Gambardella, Antonio | |
Concha, Luis | |
Keller, Simon Sean | |
Cendes, Fernando | |
Yasuda, Clarissa Lin | |
Alvim, Marina Koutsodontis Machado | |
Bonilha, Leonardo | |
Gleichgerrcht, Ezequiel | |
Focke, Niels K | |
Kreilkamp, Barbara A K | |
Domin, Martin | |
Von Podewils, Felix | |
Langner, Soenke | |
Bender, Benjamin | |
O'Brien, Terence J | |
Sinclair, Benjamin | |
Vivash, Lucy | |
Kwan, Patrick | |
Desmond, Patricia | |
Lui, Elaine | |
Duma, Gian Marco | |
Bonanni, Paolo | |
Ballerini, Alice | |
Vaudano, Anna Elisabetta | |
Meletti, Stefano | |
Tondelli, Manuela | |
Alhusaini, Saud | |
Doherty, Colin P | |
Cavalleri, Gianpiero | |
Delanty, Norman | |
Kalviainen, Reetta | |
Jackson, Graeme D | |
Kowalczyk, Magdalena | |
Mascalchi, Mario | |
Semmelroch, Mira K H G | |
Thomas, Rhys H | |
Soltanian-Zadeh, Hamid | |
Davoodi-Bojd, Esmaeil | |
Zhang, Junsong | |
Lenge, Matteo | |
Guerrini, Renzo | |
Bartolini, Emanuele | |
Hamandi, Khalid | |
Foley, Sonya | |
Rüber, Theodor | |
Bauer, Tobias | |
Weber, Bernd | |
Caldairou, Benoit | |
Depondt, Chantal | |
Absil, Julie | |
Carr, Sarah J A | |
Richardson, Mark P | |
Devinsky, Orrin | |
Pardoe, Heath R | |
Severino, Mariasavina | |
Striano, Pasquale | |
Tortora, Domenico | |
Kaestner, Erik | |
Hatton, Sean N | |
Arienzo, Donatello | |
Vos, Sjoerd B | |
Ryten, Mina | |
Taylor, Peter N | |
Duncan, John S | |
Whelan, Christopher D | |
Galovic, Marian | |
Winston, Gavin P | |
Thomopoulos, Sophia I | |
Thompson, Paul M | |
Sisodiya, Sanjay M | |
Labate, Angelo | |
Mcdonald, Carrie | |
Bernasconi, Neda | |
Bernasconi, Andrea | |
Lariviere, Sara | |
Schrader, Dewi Victoria | |
Bernhardt, Boris C |
Additional Credits
Journal
Neurology
ISSN
1526-632X
Access(Rights)
restricted