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Contribution of White Matter Fiber Bundle Damage to Language Change After Surgery for Temporal Lobe Epilepsy
Lawrence Peter Binding1, Debayan Dasgupta2, Peter Neal Taylor2
1From the Department of Computer Science (L.P.B., S.B.V.), Centre for Medical Image Computing, Department of Clinical and Experimental Epilepsy (L.B.P., D.D., P.N.T., P.J.T., J.d.T., A.W.M., A.M., G.P.W., J.S.D.), UCL Queen Square Institute of Neurology, and Neuroradiological Academic Unit (S.B.V.), UCL Queen Square Institute of Neurology, University College London; Victor Horsley Department of Neurosurgery (D.D., A.W.M., A.M.), and Department of Neuropsychology (P.J.T.), National Hospital for Neurology and Neurosurgery, Queen Square, London; CNNP Lab (P.N.T.), Interdisciplinary Computing and Complex BioSystems Group, School of Computing Science, Newcastle University; School of Mathematical Sciences (A.G.O.), University of Nottingham; Epilepsy Society MRI Unit (J.d.T., G.P.W., J.S.D.), Chalfont Centre for Epilepsy, Chalfont St Peter, United Kingdom; Department of Medicine (G.P.W.), Division of Neurology, Queen's University, Kingston, Canada; and Centre for Microscopy (S.B.V), Characterisation, and Analysis, The University of Western Australia, Nedlands, Australia. lawrence.binding.19@ucl.ac.uk.
Background And Objectives:
In medically refractory temporal lobe epilepsy (TLE), 30%-50% of patients experience substantial language decline after resection in the language-dominant hemisphere. In this study, we investigated the contribution of white matter fiber bundle damage to language change at 3 and 12 months after surgery.
Methods:
We studied 127 patients who underwent TLE surgery from 2010 to 2019. Neuropsychological testing included picture naming, semantic fluency, and phonemic verbal fluency, performed preoperatively and 3 and 12 months postoperatively. Outcome was assessed using reliable change index (RCI; clinically significant decline) and change across timepoints (postoperative scores minus preoperative scores). Functional MRI was used to determine language lateralization. The arcuate fasciculus (AF), inferior fronto-occipital fasciculus (IFOF), inferior longitudinal fasciculus, middle longitudinal fasciculus (MLF), and uncinate fasciculus were mapped using diffusion MRI probabilistic tractography. Resection masks, drawn comparing coregistered preoperative and postoperative T1 MRI scans, were used as exclusion regions on preoperative tractography to estimate the percentage of preoperative tracts transected in surgery. Chi-squared assessments evaluated the occurrence of RCI-determined language decline. Independent sample t tests and MM-estimator robust regressions were used to assess the impact of clinical factors and fiber transection on RCI and change outcomes, respectively.
Results:
Language-dominant and language-nondominant resections were treated separately for picture naming because postoperative outcomes were significantly different between these groups. In language-dominant hemisphere resections, greater surgical damage to the AF and IFOF was related to RCI decline at 3 months. Damage to the inferior frontal subfasciculus of the IFOF was related to change at 3 months. In language-nondominant hemisphere resections, increased MLF resection was associated with RCI decline at 3 months, and damage to the anterior subfasciculus was related to change at 3 months. Language-dominant and language-nondominant resections were treated as 1 cohort for semantic and phonemic fluency because there were no significant differences in postoperative decline between these groups. Postoperative seizure freedom was associated with an absence of significant language decline 12 months after surgery for semantic fluency.
Discussion:
We demonstrate a relationship between fiber transection and naming decline after temporal lobe resection. Individualized surgical planning to spare white matter fiber bundles could help to preserve language function after surgery.
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