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Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy.

Bo-Yong Park | Sara Larivière | Raul Rodríguez-Cruces | Jessica Royer | Shahin Tavakol | Yezhou Wang | Lorenzo Caciagli | Maria Eugenia Caligiuri | Antonio Gambardella | Luis Concha | Simon S Keller | Fernando Cendes | Marina K M Alvim | Clarissa Yasuda | Leonardo Bonilha | Ezequiel Gleichgerrcht | Niels K Focke | Barbara A K Kreilkamp | Martin Domin | Felix von Podewils | Soenke Langner | Christian Rummel | Michael Rebsamen | Roland Wiest | Pascal Martin | Raviteja Kotikalapudi | Benjamin Bender | Terence J O'Brien | Meng Law | Benjamin Sinclair | Lucy Vivash | Patrick Kwan | Patricia M Desmond | Charles B Malpas | Elaine Lui | Saud Alhusaini | Colin P Doherty | Gianpiero L Cavalleri | Norman Delanty | Reetta Kälviäinen | Graeme D Jackson | Magdalena Kowalczyk | Mario Mascalchi | Mira Semmelroch | Rhys H Thomas | Hamid Soltanian-Zadeh | Esmaeil Davoodi-Bojd | Junsong Zhang | Matteo Lenge | Renzo Guerrini | Emanuele Bartolini | Khalid Hamandi | Sonya Foley | Bernd Weber | Chantal Depondt | Julie Absil | Sarah J A Carr | Eugenio Abela | Mark P Richardson | Orrin Devinsky | Mariasavina Severino | Pasquale Striano | Costanza Parodi | Domenico Tortora | Sean N Hatton | Sjoerd B Vos | John S Duncan | Marian Galovic | Christopher D Whelan | Núria Bargalló | Jose Pariente | Estefania Conde-Blanco | Anna Elisabetta Vaudano | Manuela Tondelli | Stefano Meletti | Xiang-Zhen Kong | Clyde Francks | Simon E Fisher | Benoit Caldairou | Mina Ryten | Angelo Labate | Sanjay M Sisodiya | Paul M Thompson | Carrie R McDonald | Andrea Bernasconi | Neda Bernasconi | Boris C Bernhardt
Brain : a journal of neurology | 2022

Temporal lobe epilepsy, a common drug-resistant epilepsy in adults, is primarily a limbic network disorder associated with predominant unilateral hippocampal pathology. Structural MRI has provided an in vivo window into whole-brain grey matter structural alterations in temporal lobe epilepsy relative to controls, by either mapping (i) atypical inter-hemispheric asymmetry; or (ii) regional atrophy. However, similarities and differences of both atypical asymmetry and regional atrophy measures have not been systematically investigated. Here, we addressed this gap using the multisite ENIGMA-Epilepsy dataset comprising MRI brain morphological measures in 732 temporal lobe epilepsy patients and 1418 healthy controls. We compared spatial distributions of grey matter asymmetry and atrophy in temporal lobe epilepsy, contextualized their topographies relative to spatial gradients in cortical microstructure and functional connectivity calculated using 207 healthy controls obtained from Human Connectome Project and an independent dataset containing 23 temporal lobe epilepsy patients and 53 healthy controls and examined clinical associations using machine learning. We identified a marked divergence in the spatial distribution of atypical inter-hemispheric asymmetry and regional atrophy mapping. The former revealed a temporo-limbic disease signature while the latter showed diffuse and bilateral patterns. Our findings were robust across individual sites and patients. Cortical atrophy was significantly correlated with disease duration and age at seizure onset, while degrees of asymmetry did not show a significant relationship to these clinical variables. Our findings highlight that the mapping of atypical inter-hemispheric asymmetry and regional atrophy tap into two complementary aspects of temporal lobe epilepsy-related pathology, with the former revealing primary substrates in ipsilateral limbic circuits and the latter capturing bilateral disease effects. These findings refine our notion of the neuropathology of temporal lobe epilepsy and may inform future discovery and validation of complementary MRI biomarkers in temporal lobe epilepsy.

Pubmed ID: 35333312 RIS Download

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Associated grants

  • Agency: NINDS NIH HHS, United States
    Id: R21 NS107739
  • Agency: Medical Research Council, United Kingdom
    Id: MR/K013998/1
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS122827
  • Agency: Medical Research Council, United Kingdom
    Id: MR/N008324/1
  • Agency: NIMH NIH HHS, United States
    Id: U54 MH091657
  • Agency: NINDS NIH HHS, United States
    Id: R01 NS110347

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FreeSurfer (tool)

RRID:SCR_001847

Open source software suite for processing and analyzing human brain MRI images. Used for reconstruction of brain cortical surface from structural MRI data, and overlay of functional MRI data onto reconstructed surface. Contains automatic structural imaging stream for processing cross sectional and longitudinal data. Provides anatomical analysis tools, including: representation of cortical surface between white and gray matter, representation of the pial surface, segmentation of white matter from rest of brain, skull stripping, B1 bias field correction, nonlinear registration of cortical surface of individual with stereotaxic atlas, labeling of regions of cortical surface, statistical analysis of group morphometry differences, and labeling of subcortical brain structures.Operating System: Linux, macOS.

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ENIGMA: Enhancing Neuro Imaging Genetics Through Meta-Analysis (tool)

RRID:SCR_005515

Network that brings together researchers in imaging genomics, to understand brain structure and function, based on MRI, DTI, fMRI and genomewide association scan (GWAS) data. The ENIGMA Network has several goals: * to create a network of like-minded individuals, interested in pushing forward the field of imaging genetics * to ensure promising findings are replicated via member collaborations, in order to satisfy the mandates of most journals * to share ideas, algorithms, data, and information on promising findings or methods * to facilitate training, including workshops and conferences on key methods and emerging directions in imaging genetics. Data sharing with other members of the ENIGMA Network is optional and by no means a requirement of joining the network. Genetics and Imaging Protocols are available.

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ComBat (tool)

RRID:SCR_010974

Adjusting batch effects in microarray expression data using Empirical Bayes methods.

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