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Using Low-Frequency Oscillations to Detect Temporal Lobe Epilepsy with Machine Learning.
Hwang, Gyujoon; Nair, Veena A; Mathis, Jed; Cook, Cole J; Mohanty, Rosaleena; Zhao, Gengyan; Tellapragada, Neelima; Ustine, Candida; Nwoke, Onyekachi O; Rivera-Bonet, Charlene; Rozman, Megan; Allen, Linda; Forseth, Courtney; Almane, Dace N; Kraegel, Peter; Nencka, Andrew; Felton, Elizabeth; Struck, Aaron F; Birn, Rasmus; Maganti, Rama; Conant, Lisa L; Humphries, Colin J; Hermann, Bruce; Raghavan, Manoj; DeYoe, Edgar A; Binder, Jeffrey R; Meyerand, Elizabeth; Prabhakaran, Vivek.
Afiliação
  • Hwang G; 1 Department of Medical Physics, University of Wisconsin-Madison, Madison, Wisconsin.
  • Nair VA; 2 Department of Radiology, University of Wisconsin-Madison, Madison, Wisconsin.
  • Mathis J; 3 Department of Radiology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Cook CJ; 1 Department of Medical Physics, University of Wisconsin-Madison, Madison, Wisconsin.
  • Mohanty R; 4 Department of Electrical Engineering, University of Wisconsin-Madison, Madison, Wisconsin.
  • Zhao G; 1 Department of Medical Physics, University of Wisconsin-Madison, Madison, Wisconsin.
  • Tellapragada N; 2 Department of Radiology, University of Wisconsin-Madison, Madison, Wisconsin.
  • Ustine C; 5 Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Nwoke OO; 6 School of Pharmacy, University of Wisconsin-Madison, Madison, Wisconsin.
  • Rivera-Bonet C; 7 Neuroscience Training Program, University of Wisconsin-Madison, Madison, Wisconsin.
  • Rozman M; 5 Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Allen L; 5 Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Forseth C; 8 Department of Neurology, University of Wisconsin-Madison, Madison, Wisconsin.
  • Almane DN; 8 Department of Neurology, University of Wisconsin-Madison, Madison, Wisconsin.
  • Kraegel P; 5 Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Nencka A; 3 Department of Radiology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Felton E; 8 Department of Neurology, University of Wisconsin-Madison, Madison, Wisconsin.
  • Struck AF; 8 Department of Neurology, University of Wisconsin-Madison, Madison, Wisconsin.
  • Birn R; 1 Department of Medical Physics, University of Wisconsin-Madison, Madison, Wisconsin.
  • Maganti R; 9 Department of Psychiatry, University of Wisconsin-Madison, Madison, Wisconsin.
  • Conant LL; 8 Department of Neurology, University of Wisconsin-Madison, Madison, Wisconsin.
  • Humphries CJ; 5 Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Hermann B; 5 Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Raghavan M; 8 Department of Neurology, University of Wisconsin-Madison, Madison, Wisconsin.
  • DeYoe EA; 5 Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Binder JR; 3 Department of Radiology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Meyerand E; 5 Department of Neurology, Medical College of Wisconsin, Milwaukee, Wisconsin.
  • Prabhakaran V; 1 Department of Medical Physics, University of Wisconsin-Madison, Madison, Wisconsin.
Brain Connect ; 9(2): 184-193, 2019 03.
Article em En | MEDLINE | ID: mdl-30803273
ABSTRACT
The National Institutes of Health-sponsored Epilepsy Connectome Project aims to characterize connectivity changes in temporal lobe epilepsy (TLE) patients. The magnetic resonance imaging protocol follows that used in the Human Connectome Project, and includes 20 min of resting-state functional magnetic resonance imaging acquired at 3T using 8-band multiband imaging. Glasser parcellation atlas was combined with the FreeSurfer subcortical regions to generate resting-state functional connectivity (RSFC), amplitude of low-frequency fluctuations (ALFFs), and fractional ALFF measures. Seven different frequency ranges such as Slow-5 (0.01-0.027 Hz) and Slow-4 (0.027-0.073 Hz) were selected to compute these measures. The goal was to train machine learning classification models to discriminate TLE patients from healthy controls, and to determine which combination of the resting state measure and frequency range produced the best classification model. The samples included age- and gender-matched groups of 60 TLE patients and 59 healthy controls. Three traditional machine learning models were trained support vector machine, linear discriminant analysis, and naive Bayes classifier. The highest classification accuracy was obtained using RSFC measures in the Slow-4 + 5 band (0.01-0.073 Hz) as features. Leave-one-out cross-validation accuracies were ∼83%, with receiver operating characteristic area-under-the-curve reaching close to 90%. Increased connectivity from right area posterior 9-46v in TLE patients contributed to the high accuracies. With increased sample sizes in the near future, better machine learning models will be trained not only to aid the diagnosis of TLE, but also as a tool to understand this brain disorder.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia do Lobo Temporal / Conectoma Tipo de estudo: Guideline / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Connect Ano de publicação: 2019 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Epilepsia do Lobo Temporal / Conectoma Tipo de estudo: Guideline / Prognostic_studies Limite: Adult / Female / Humans / Male / Middle aged Idioma: En Revista: Brain Connect Ano de publicação: 2019 Tipo de documento: Article