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Machine learning approaches for imaging-based prognostication of the outcome of surgery for mesial temporal lobe epilepsy.
Sinclair, Benjamin; Cahill, Varduhi; Seah, Jarrel; Kitchen, Andy; Vivash, Lucy E; Chen, Zhibin; Malpas, Charles B; O'Shea, Marie F; Desmond, Patricia M; Hicks, Rodney J; Morokoff, Andrew P; King, James A; Fabinyi, Gavin C; Kaye, Andrew H; Kwan, Patrick; Berkovic, Samuel F; Law, Meng; O'Brien, Terence J.
Afiliación
  • Sinclair B; Department of Neuroscience, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
  • Cahill V; Department Neurology, Alfred Health, Melbourne, Victoria, Australia.
  • Seah J; Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
  • Kitchen A; Academic Neurology Unit, Royal Hallamshire Hospital, University of Sheffield, Sheffield, UK.
  • Vivash LE; Division of Neuroscience and Experimental Psychology, School of Biological Sciences, University of Manchester, Manchester, UK.
  • Chen Z; Department of Neurology, Melbourne Brain Centre, Royal Melbourne Hospital, Melbourne, Victoria, Australia.
  • Malpas CB; Department of Radiology, Alfred Health, Melbourne, Victoria, Australia.
  • O'Shea MF; Department of Neuroscience, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
  • Desmond PM; Department of Neuroscience, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
  • Hicks RJ; Department Neurology, Alfred Health, Melbourne, Victoria, Australia.
  • Morokoff AP; Department of Neuroscience, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
  • King JA; Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
  • Fabinyi GC; Department of Neuroscience, Central Clinical School, Monash University, Melbourne, Victoria, Australia.
  • Kaye AH; Department Neurology, Alfred Health, Melbourne, Victoria, Australia.
  • Kwan P; Department of Medicine, University of Melbourne, Melbourne, Victoria, Australia.
  • Berkovic SF; Department of Neurology, Melbourne Brain Centre, Royal Melbourne Hospital, Melbourne, Victoria, Australia.
  • Law M; Melbourne School of Psychological Sciences, University of Melbourne, Melbourne, Victoria, Australia.
  • O'Brien TJ; Melbourne School of Psychological Sciences, University of Melbourne, Melbourne, Victoria, Australia.
Epilepsia ; 63(5): 1081-1092, 2022 05.
Article en En | MEDLINE | ID: mdl-35266138
ABSTRACT

OBJECTIVES:

Around 30% of patients undergoing surgical resection for drug-resistant mesial temporal lobe epilepsy (MTLE) do not obtain seizure freedom. Success of anterior temporal lobe resection (ATLR) critically depends on the careful selection of surgical candidates, aiming at optimizing seizure freedom while minimizing postoperative morbidity. Structural MRI and FDG-PET neuroimaging are routinely used in presurgical assessment and guide the decision to proceed to surgery. In this study, we evaluate the potential of machine learning techniques applied to standard presurgical MRI and PET imaging features to provide enhanced prognostic value relative to current practice.

METHODS:

Eighty two patients with drug resistant MTLE were scanned with FDG-PET pre-surgery and T1-weighted MRI pre- and postsurgery. From these images the following features of interest were derived volume of temporal lobe (TL) hypometabolism, % of extratemporal hypometabolism, presence of contralateral TL hypometabolism, presence of hippocampal sclerosis, laterality of seizure onset volume of tissue resected and % of temporal lobe hypometabolism resected. These measures were used as predictor variables in logistic regression, support vector machines, random forests and artificial neural networks.

RESULTS:

In the study cohort, 24 of 82 (28.3%) who underwent an ATLR for drug-resistant MTLE did not achieve Engel Class I (i.e., free of disabling seizures) outcome at a minimum of 2 years of postoperative follow-up. We found that machine learning approaches were able to predict up to 73% of the 24 ATLR surgical patients who did not achieve a Class I outcome, at the expense of incorrect prediction for up to 31% of patients who did achieve a Class I outcome. Overall accuracies ranged from 70% to 80%, with an area under the receiver operating characteristic curve (AUC) of .75-.81. We additionally found that information regarding overall extent of both total and significantly hypometabolic tissue resected was crucial to predictive performance, with AUC dropping to .59-.62 using presurgical information alone. Incorporating the laterality of seizure onset and the choice of machine learning algorithm did not significantly change predictive performance.

SIGNIFICANCE:

Collectively, these results indicate that "acceptable" to "good" patient-specific prognostication for drug-resistant MTLE surgery is feasible with machine learning approaches utilizing commonly collected imaging modalities, but that information on the surgical resection region is critical for optimal prognostication.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Epilepsia del Lóbulo Temporal / Epilepsia Refractaria Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Epilepsia Año: 2022 Tipo del documento: Article País de afiliación: Australia

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Epilepsia del Lóbulo Temporal / Epilepsia Refractaria Tipo de estudio: Prognostic_studies Límite: Humans Idioma: En Revista: Epilepsia Año: 2022 Tipo del documento: Article País de afiliación: Australia