Topographic divergence of atypical cortical asymmetry and atrophy patterns in temporal lobe epilepsy.
СтатьяПоддержка исследования: вне правительства СШАПоддержка NIH: внешняя программаНазвание и аннотация: Перевод пока не подготовлен
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Park Bo-Yong, Larivière Sara, Rodríguez-Cruces Raul, Royer Jessica, Tavakol Shahin, Wang Yezhou, Caciagli Lorenzo, Caligiuri Maria Eugenia, Gambardella Antonio, Concha Luis, Keller Simon S, Cendes Fernando, Alvim Marina K M, Yasuda Clarissa, Bonilha Leonardo, Gleichgerrcht Ezequiel, Focke Niels K, Kreilkamp Barbara A K, Domin Martin, von Podewils Felix, Langner Soenke, Rummel Christian, Rebsamen Michael, Wiest Roland, Martin Pascal, Kotikalapudi Raviteja, Bender Benjamin, O'Brien Terence J, Law Meng, Sinclair Benjamin, Vivash Lucy, Kwan Patrick, Desmond Patricia M, Malpas Charles B, Lui Elaine, Alhusaini Saud, Doherty Colin P, Cavalleri Gianpiero L, Delanty Norman, Kälviäinen Reetta, Jackson Graeme D, Kowalczyk Magdalena, Mascalchi Mario, Semmelroch Mira, Thomas Rhys H, Soltanian-Zadeh Hamid, Davoodi-Bojd Esmaeil, Zhang Junsong, Lenge Matteo, Guerrini Renzo, Bartolini Emanuele, Hamandi Khalid, Foley Sonya, Weber Bernd, Depondt Chantal, Absil Julie, Carr Sarah J A, Abela Eugenio, Richardson Mark P, Devinsky Orrin, Severino Mariasavina, Striano Pasquale, Parodi Costanza, Tortora Domenico, Hatton Sean N, Vos Sjoerd B, Duncan John S, Galovic Marian, Whelan Christopher D, Bargalló Núria, Pariente Jose, Conde-Blanco Estefania, Vaudano Anna Elisabetta, Tondelli Manuela, Meletti Stefano, Kong Xiang-Zhen, Francks Clyde, Fisher Simon E, Caldairou Benoit, Ryten Mina, Labate Angelo, Sisodiya Sanjay M, Thompson Paul M, McDonald Carrie R, Bernasconi Andrea, Bernasconi Neda, Bernhardt Boris C
Аннотация
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.