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Changes in Gray Matter Morphology and White Matter Microstructure Across the Adult Lifespan in People With Temporal Lobe Epilepsy

Title: Changes in Gray Matter Morphology and White Matter Microstructure Across the Adult Lifespan in People With Temporal Lobe Epilepsy
Authors: Chen J; Ngo A; Rodriguez-Cruces R; Royer J; Caligiuri ME; Gambardella A; Concha L; Keller SS; Cendes F; Yasuda CL; Alvim MKM; Bonilha L; Gleichgerrcht E; Focke NK; Kreilkamp BAK; Domin M; Von Podewils F; Langner S; Rummel C; Wiest R; Martin P; Kotikalapudi R; Bender B; O'Brien TJ; Sinclair B; Vivash L; Kwan P; Desmond P; Lui E; Duma GM; Bonanni P; Ballerini A; Vaudano AE; Meletti S; Tondelli M; Alhusaini S; Doherty CP; Cavalleri G; Delanty N; Kalviainen R; Jackson GD; Kowalczyk M; Mascalchi M; Semmelroch MKHG; Thomas RH; Soltanian-Zadeh H; Davoodi-Bojd E; Zhang J; Lenge M; Guerrini R; Bartolini E; Hamandi K; Foley S; Ruber T; Bauer T; Weber B; Caldairou B; Depondt C; Absil J; Carr SJA; Abela E; Richardson MP; Devinsky O; Pardoe HR; Severino M; Striano P; Tortora D; Kaestner E; Hatton SN; Arienzo D; Vos SB; Ryten M; Taylor PN; Duncan JS; Whelan CD; Galovic M; Winston GP; Thomopoulos SI; Thompson PM; Sisodiya SM; Labate A; McDonald C; Caciagli L; Bernasconi N; Bernasconi A; Lariviere S; Schrader DV; Bernhardt BC
Source: Neurology, 23 September 2025
Publisher Information: Lippincott Williams and Wilkins
Publication Year: 2025
Collection: Newcastle University Library ePrints Service
Description: Copyright © 2025 American Academy of Neurology. 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 ...
Document Type: article in journal/newspaper
Language: unknown
Relation: https://eprints.ncl.ac.uk/307669
Availability: https://eprints.ncl.ac.uk/307669
Accession Number: edsbas.24FA66E9
Database: BASE