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White matter abnormalities across different epilepsy syndromes in adults: an ENIGMA-Epilepsy study.
Hatton, Sean N; Huynh, Khoa H; Bonilha, Leonardo; Abela, Eugenio; Alhusaini, Saud; Altmann, Andre; Alvim, Marina K M; Balachandra, Akshara R; Bartolini, Emanuele; Bender, Benjamin; Bernasconi, Neda; Bernasconi, Andrea; Bernhardt, Boris; Bargallo, Núria; Caldairou, Benoit; Caligiuri, Maria E; Carr, Sarah J A; Cavalleri, Gianpiero L; Cendes, Fernando; Concha, Luis; Davoodi-Bojd, Esmaeil; Desmond, Patricia M; Devinsky, Orrin; Doherty, Colin P; Domin, Martin; Duncan, John S; Focke, Niels K; Foley, Sonya F; Gambardella, Antonio; Gleichgerrcht, Ezequiel; Guerrini, Renzo; Hamandi, Khalid; Ishikawa, Akari; Keller, Simon S; Kochunov, Peter V; Kotikalapudi, Raviteja; Kreilkamp, Barbara A K; Kwan, Patrick; Labate, Angelo; Langner, Soenke; Lenge, Matteo; Liu, Min; Lui, Elaine; Martin, Pascal; Mascalchi, Mario; Moreira, José C V; Morita-Sherman, Marcia E; O'Brien, Terence J; Pardoe, Heath R; Pariente, José C.
Afiliação
  • Hatton SN; Department of Neurosciences, Center for Multimodal Imaging and Genetics, University of California San Diego, La Jolla 92093 CA, USA.
  • Huynh KH; Center for Multimodal Imaging and Genetics, University of California San Diego, La Jolla 92093 CA, USA.
  • Bonilha L; Department of Neurology, Medical University of South Carolina, Charleston 29425 SC, USA.
  • Abela E; Maurice Wohl Clinical Neuroscience Institute, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London SE5 9NU UK.
  • Alhusaini S; Neurology Department, Yale School of Medicine, New Haven 6510 CT, USA.
  • Altmann A; Molecular and Cellular Therapeutics, The Royal College of Surgeons in Ireland, Dublin, Ireland.
  • Alvim MKM; Centre of Medical Image Computing, Department of Medical Physics and Biomedical Engineering, University College London, London WC1V 6LJ, UK.
  • Balachandra AR; Department of Neurology, University of Campinas - UNICAMP, Campinas 13083-888 São Paulo, Brazil.
  • Bartolini E; Center for Multimodal Imaging and Genetics, UCSD School of Medicine, La Jolla 92037 CA, USA.
  • Bender B; Boston University School of Medicine, Boston 2118 MA, USA.
  • Bernasconi N; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Children's Hospital A. Meyer-University of Florence, Florence, Italy.
  • Bernasconi A; USL Centro Toscana, Neurology Unit, Nuovo Ospedale Santo Stefano, Prato, Italy.
  • Bernhardt B; Department of Diagnostic and Interventional Neuroradiology, University Hospital Tübingen, Tübingen 72076, Germany.
  • Bargallo N; Neuroimaging of Epilepsy Laboratory, Montreal Neurological Institute, McGill University, Montreal H3A 2B4 QC, Canada.
  • Caldairou B; Neuroimaging of Epilepsy Laboratory, Montreal Neurological Institute, McGill University, Montreal H3A 2B4 QC, Canada.
  • Caligiuri ME; Montreal Neurological Institute, McGill University, Montreal H3A2B4 QC, Canada.
  • Carr SJA; Magnetic Resonance Image Core Facility, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), Barcelona 8036 Barcelona, Spain.
  • Cavalleri GL; Neuroimaging of Epilepsy Laboratory, Montreal Neurological Institute, McGill University, Montreal H3A 2B4 QC, Canada.
  • Cendes F; Neuroscience Research Center, University Magna Graecia, viale Europa, Germaneto, 88100, Catanzaro, Italy.
  • Concha L; Neuroscience, Institute of Psychiatry, Psychology and Neuroscience, De Crespigny Park, London SE5 8AF, UK.
  • Davoodi-Bojd E; Royal College of Surgeons in Ireland, School of Pharmacy and Biomolecular Sciences, Dublin D02 YN77 Ireland.
  • Desmond PM; FutureNeuro Research Centre, Science Foundation Ireland, Dublin D02 YN77, Ireland.
  • Devinsky O; Department of Neurology, University of Campinas - UNICAMP, Campinas 13083-888 São Paulo, Brazil.
  • Doherty CP; Institute of Neurobiology, Universidad Nacional Autonoma de Mexico, Queretaro 76230, Mexico.
  • Domin M; Radiology and Research Administration, Henry Ford Hospital, 1 Detroit 48202 MI, USA.
  • Duncan JS; Department of Radiology, Royal Melbourne Hospital, University of Melbourne, Melbourne 3050 Victoria, Australia.
  • Focke NK; Director, NYU Epilepsy Center, New York 10016 NY, USA.
  • Foley SF; Division of Neurology, Trinity College Dublin, TBSI, Pearce Street, Dublin D02 R590, Ireland.
  • Gambardella A; FutureNeuro SFI Centre for Neurological Disease, RCSI, St Stephen's Green, Dublin D02 H903, Ireland.
  • Gleichgerrcht E; Functional Imaging Unit, University Medicine Greifswald, Greifswald 17475 M/V, Germany.
  • Guerrini R; Department of Clinical and Experimental Epilepsy, UCL Queen Square Institute of Neurology, Queen Square, London WC1N 3BG, UK.
  • Hamandi K; MRI Unit, Chalfont Centre for Epilepsy, Chalfont-St-Peter, Buckinghamshire SL9 0RJ, UK.
  • Ishikawa A; Clinical Neurophysiology, University Medicine Göttingen, 37099 Göttingen, Germany.
  • Keller SS; Department of Epileptology, University of Tübingen, 72076 Tübingen, Germany.
  • Kochunov PV; CUBRIC, Cardiff University, Cardiff CF24 4HQ, Wales.
  • Kotikalapudi R; Royal College of Surgeons in Ireland, School of Pharmacy and Biomolecular Sciences, Dublin D02 YN77 Ireland.
  • Kreilkamp BAK; Institute of Neurology, University Magna Graecia, 88100, Catanzaro, Italy.
  • Kwan P; Department of Neurology, Medical University of South Carolina, Charleston 29425 SC, USA.
  • Labate A; Pediatric Neurology, Neurogenetics and Neurobiology Unit and Laboratories, Children's Hospital A. Meyer-University of Florence, Florence, Italy.
  • Langner S; The Wales Epilepsy Unit, Cardiff and Vale University Health Board, Cardiff CF144XW, UK.
  • Lenge M; Brain Research Imaging Centre, Cardiff University, Cardiff CF24 4HQ, UK.
  • Liu M; Department of Neurology, University of Campinas - UNICAMP, Campinas 13083-888 São Paulo, Brazil.
  • Lui E; Institute of Translational Medicine, University of Liverpool, Liverpool L69 3BX, UK.
  • Martin P; Walton Centre NHS Foundation Trust, Liverpool L9 7LJ, UK.
  • Mascalchi M; Maryland Psychiatric Research Center, 55 Wade Ave, Baltimore 21228, MD, USA.
  • Moreira JCV; Department of Neurology and Epileptology, University Hospital Tübingen, Tübingen 72076 BW, Germany.
  • Morita-Sherman ME; Department of Diagnostic and Interventional Neuroradiology, University Hospital Tübingen, Tübingen 72076 BW, Germany.
  • O'Brien TJ; Institute of Translational Medicine, University of Liverpool, Liverpool L69 3BX, UK.
  • Pardoe HR; Walton Centre NHS Foundation Trust, Liverpool L9 7LJ, UK.
  • Pariente JC; Department of Neuroscience, Central Clinical School, Monash University, Melbourne 3004 Victoria, Australia.
Brain ; 143(8): 2454-2473, 2020 08 01.
Article em En | MEDLINE | ID: mdl-32814957
ABSTRACT
The epilepsies are commonly accompanied by widespread abnormalities in cerebral white matter. ENIGMA-Epilepsy is a large quantitative brain imaging consortium, aggregating data to investigate patterns of neuroimaging abnormalities in common epilepsy syndromes, including temporal lobe epilepsy, extratemporal epilepsy, and genetic generalized epilepsy. Our goal was to rank the most robust white matter microstructural differences across and within syndromes in a multicentre sample of adult epilepsy patients. Diffusion-weighted MRI data were analysed from 1069 healthy controls and 1249 patients temporal lobe epilepsy with hippocampal sclerosis (n = 599), temporal lobe epilepsy with normal MRI (n = 275), genetic generalized epilepsy (n = 182) and non-lesional extratemporal epilepsy (n = 193). A harmonized protocol using tract-based spatial statistics was used to derive skeletonized maps of fractional anisotropy and mean diffusivity for each participant, and fibre tracts were segmented using a diffusion MRI atlas. Data were harmonized to correct for scanner-specific variations in diffusion measures using a batch-effect correction tool (ComBat). Analyses of covariance, adjusting for age and sex, examined differences between each epilepsy syndrome and controls for each white matter tract (Bonferroni corrected at P < 0.001). Across 'all epilepsies' lower fractional anisotropy was observed in most fibre tracts with small to medium effect sizes, especially in the corpus callosum, cingulum and external capsule. There were also less robust increases in mean diffusivity. Syndrome-specific fractional anisotropy and mean diffusivity differences were most pronounced in patients with hippocampal sclerosis in the ipsilateral parahippocampal cingulum and external capsule, with smaller effects across most other tracts. Individuals with temporal lobe epilepsy and normal MRI showed a similar pattern of greater ipsilateral than contralateral abnormalities, but less marked than those in patients with hippocampal sclerosis. Patients with generalized and extratemporal epilepsies had pronounced reductions in fractional anisotropy in the corpus callosum, corona radiata and external capsule, and increased mean diffusivity of the anterior corona radiata. Earlier age of seizure onset and longer disease duration were associated with a greater extent of diffusion abnormalities in patients with hippocampal sclerosis. We demonstrate microstructural abnormalities across major association, commissural, and projection fibres in a large multicentre study of epilepsy. Overall, patients with epilepsy showed white matter abnormalities in the corpus callosum, cingulum and external capsule, with differing severity across epilepsy syndromes. These data further define the spectrum of white matter abnormalities in common epilepsy syndromes, yielding more detailed insights into pathological substrates that may explain cognitive and psychiatric co-morbidities and be used to guide biomarker studies of treatment outcomes and/or genetic research.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Substância Branca / Síndromes Epilépticas Tipo de estudo: Guideline Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Encéfalo / Substância Branca / Síndromes Epilépticas Tipo de estudo: Guideline Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Estados Unidos