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    Structural network alterations in focal and generalized epilepsy assessed in a worldwide ENIGMA study follow axes of epilepsy risk gene expression
    Lariviere, S ; Royer, J ; Rodriguez-Cruces, R ; Paquola, C ; Caligiuri, ME ; Gambardella, A ; Concha, L ; Keller, SS ; Cendes, F ; Yasuda, CL ; Bonilha, L ; Gleichgerrcht, E ; Focke, NK ; Domin, M ; von Podewills, F ; Langner, S ; Rummel, C ; Wiest, R ; Martin, P ; Kotikalapudi, R ; O'Brien, TJ ; Sinclair, B ; Vivash, L ; Desmond, PM ; Lui, E ; Vaudano, AE ; Meletti, S ; Tondelli, M ; Alhusaini, S ; Doherty, CP ; Cavalleri, GL ; Delanty, N ; Kalviainen, R ; Jackson, GD ; Kowalczyk, M ; Mascalchi, M ; Semmelroch, M ; Thomas, RH ; Soltanian-Zadeh, H ; Davoodi-Bojd, E ; Zhang, J ; Winston, GP ; Griffin, A ; Singh, A ; Tiwari, VK ; Kreilkamp, BAK ; Lenge, M ; Guerrini, R ; Hamandi, K ; Foley, S ; Ruber, T ; Weber, B ; Depondt, C ; Absil, J ; Carr, SJA ; Abela, E ; Richardson, MP ; Devinsky, O ; Severino, M ; Striano, P ; Tortora, D ; Kaestner, E ; Hatton, SN ; Vos, SB ; Caciagli, L ; Duncan, JS ; Whelan, CD ; Thompson, PM ; Sisodiya, SM ; Bernasconi, A ; Labate, A ; McDonald, CR ; Bernasconi, N ; Bernhardt, BC (NATURE PORTFOLIO, 2022-07-27)
    Epilepsy is associated with genetic risk factors and cortico-subcortical network alterations, but associations between neurobiological mechanisms and macroscale connectomics remain unclear. This multisite ENIGMA-Epilepsy study examined whole-brain structural covariance networks in patients with epilepsy and related findings to postmortem epilepsy risk gene expression patterns. Brain network analysis included 578 adults with temporal lobe epilepsy (TLE), 288 adults with idiopathic generalized epilepsy (IGE), and 1328 healthy controls from 18 centres worldwide. Graph theoretical analysis of structural covariance networks revealed increased clustering and path length in orbitofrontal and temporal regions in TLE, suggesting a shift towards network regularization. Conversely, people with IGE showed decreased clustering and path length in fronto-temporo-parietal cortices, indicating a random network configuration. Syndrome-specific topological alterations reflected expression patterns of risk genes for hippocampal sclerosis in TLE and for generalized epilepsy in IGE. These imaging-transcriptomic signatures could potentially guide diagnosis or tailor therapeutic approaches to specific epilepsy syndromes.
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    Network-based atrophy modeling in the common epilepsies: A worldwide ENIGMA study
    Lariviere, S ; Rodriguez-Cruces, R ; Royer, J ; Caligiuri, ME ; Gambardella, A ; Concha, L ; Keller, SS ; Cendes, F ; Yasuda, C ; Bonilha, L ; Gleichgerrcht, E ; Focke, NK ; Domin, M ; von Podewills, F ; Langner, S ; Rummel, C ; Wiest, R ; Martin, P ; Kotikalapudi, R ; O'Brien, TJ ; Sinclair, B ; Vivash, L ; Desmond, PM ; Alhusaini, S ; Doherty, CP ; Cavalleri, GL ; Delanty, N ; Kalviainen, R ; Jackson, GD ; Kowalczyk, M ; Mascalchi, M ; Semmelroch, M ; Thomas, RH ; Soltanian-Zadeh, H ; Davoodi-Bojd, E ; Zhang, J ; Lenge, M ; Guerrini, R ; Bartolini, E ; Hamandi, K ; Foley, S ; Weber, B ; Depondt, C ; Absil, J ; Carr, SJA ; Abela, E ; Richardson, MP ; Devinsky, O ; Severino, M ; Striano, P ; Tortora, D ; Hatton, SN ; Vos, SB ; Duncan, JS ; Whelan, CD ; Thompson, PM ; Sisodiya, SM ; Bernasconi, A ; Labate, A ; McDonald, CR ; Bernasconi, N ; Bernhardt, BC (AMER ASSOC ADVANCEMENT SCIENCE, 2020-11)
    Epilepsy is increasingly conceptualized as a network disorder. In this cross-sectional mega-analysis, we integrated neuroimaging and connectome analysis to identify network associations with atrophy patterns in 1021 adults with epilepsy compared to 1564 healthy controls from 19 international sites. In temporal lobe epilepsy, areas of atrophy colocalized with highly interconnected cortical hub regions, whereas idiopathic generalized epilepsy showed preferential subcortical hub involvement. These morphological abnormalities were anchored to the connectivity profiles of distinct disease epicenters, pointing to temporo-limbic cortices in temporal lobe epilepsy and fronto-central cortices in idiopathic generalized epilepsy. Negative effects of age on atrophy further revealed a strong influence of connectome architecture in temporal lobe, but not idiopathic generalized, epilepsy. Our findings were reproduced across individual sites and single patients and were robust across different analytical methods. Through worldwide collaboration in ENIGMA-Epilepsy, we provided deeper insights into the macroscale features that shape the pathophysiology of common epilepsies.
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    The ENIGMA-Epilepsy working group: Mapping disease from large data sets
    Sisodiya, SM ; Whelan, CD ; Hatton, SN ; Huynh, K ; Altmann, A ; Ryten, M ; Vezzani, A ; Caligiuri, ME ; Labate, A ; Gambardella, A ; Ives-Deliperi, V ; Meletti, S ; Munsell, BC ; Bonilha, L ; Tondelli, M ; Rebsamen, M ; Rummel, C ; Vaudano, AE ; Wiest, R ; Balachandra, AR ; Bargallo, N ; Bartolini, E ; Bernasconi, A ; Bernasconi, N ; Bernhardt, B ; Caldairou, B ; Carr, SJA ; Cavalleri, GL ; Cendes, F ; Concha, L ; Desmond, PM ; Domin, M ; Duncan, JS ; Focke, NK ; Guerrini, R ; Hamandi, K ; Jackson, GD ; Jahanshad, N ; Kalviainen, R ; Keller, SS ; Kochunov, P ; Kowalczyk, MA ; Kreilkamp, BAK ; Kwan, P ; Lariviere, S ; Lenge, M ; Lopez, SM ; Martin, P ; Mascalchi, M ; Moreira, JCV ; Morita-Sherman, ME ; Pardoe, HR ; Pariente, JC ; Raviteja, K ; Rocha, CS ; Rodriguez-Cruces, R ; Seeck, M ; Semmelroch, MKHG ; Sinclair, B ; Soltanian-Zadeh, H ; Stein, DJ ; Striano, P ; Taylor, PN ; Thomas, RH ; Thomopoulos, SI ; Velakoulis, D ; Vivash, L ; Weber, B ; Yasuda, CL ; Zhang, J ; Thompson, PM ; McDonald, CR (WILEY, 2022-01)
    Epilepsy is a common and serious neurological disorder, with many different constituent conditions characterized by their electro clinical, imaging, and genetic features. MRI has been fundamental in advancing our understanding of brain processes in the epilepsies. Smaller-scale studies have identified many interesting imaging phenomena, with implications both for understanding pathophysiology and improving clinical care. Through the infrastructure and concepts now well-established by the ENIGMA Consortium, ENIGMA-Epilepsy was established to strengthen epilepsy neuroscience by greatly increasing sample sizes, leveraging ideas and methods established in other ENIGMA projects, and generating a body of collaborating scientists and clinicians to drive forward robust research. Here we review published, current, and future projects, that include structural MRI, diffusion tensor imaging (DTI), and resting state functional MRI (rsfMRI), and that employ advanced methods including structural covariance, and event-based modeling analysis. We explore age of onset- and duration-related features, as well as phenomena-specific work focusing on particular epilepsy syndromes or phenotypes, multimodal analyses focused on understanding the biology of disease progression, and deep learning approaches. We encourage groups who may be interested in participating to make contact to further grow and develop ENIGMA-Epilepsy.