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      The anterior nucleus of the thalamus plays a role in the epileptic network

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          Abstract

          Objectives

          We investigated both the metabolic differences and interictal/ictal discharges of the anterior nucleus of the thalamus (ANT) in patients with epilepsy to clarify the relationship between the ANT and the epileptic network.

          Methods

          Nineteen patients with drug‐resistant epilepsy who underwent stereoelectroencephalography were studied. Metabolic differences in ANT were analyzed using [18F] fluorodeoxyglucose–positron emission tomography with three‐dimensional (3D) visual and quantitative analyses. Interictal and ictal discharges in the ANT were analyzed using visual and time‐frequency analyses. The relationship between interictal discharge and metabolic differences was analyzed.

          Results

          We found that patients with temporal lobe epilepsy (TLE) showed significant metabolic differences in bilateral ANT compared with extratemporal lobe epilepsy in 3D visual and quantitative analyses. Four types of interictal activities were recorded from the ANT: spike, high‐frequency oscillation (HFO), slow‐wave, and α‐rhythmic activity. Spike and HFO waveforms were recorded mainly in patients with TLE. Two spike patterns were recorded: synchronous and independent. In 83.3% of patients, ANT was involved during seizures. Three seizure onset types of ANT were recorded: low‐voltage fast activity, rhythmic spikes, and theta band discharge. The time interval of seizure onset between the seizure onset zone and ANT showed two patterns: immediate and delayed.

          Interpretation

          ANT can receive either interictal discharges or ictal discharges which propagate from the epileptogenic zones. Independent epileptic discharges can also be recorded from the ANT in some patients. Metabolic anomalies and epileptic discharges in the ANT indicate that the ANT plays a role in the epileptic network in most patients with epilepsy, especially TLE.

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          Most cited references49

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          Operational classification of seizure types by the International League Against Epilepsy: Position Paper of the ILAE Commission for Classification and Terminology

          The International League Against Epilepsy (ILAE) presents a revised operational classification of seizure types. The purpose of such a revision is to recognize that some seizure types can have either a focal or generalized onset, to allow classification when the onset is unobserved, to include some missing seizure types, and to adopt more transparent names. Because current knowledge is insufficient to form a scientifically based classification, the 2017 Classification is operational (practical) and based on the 1981 Classification, extended in 2010. Changes include the following: (1) "partial" becomes "focal"; (2) awareness is used as a classifier of focal seizures; (3) the terms dyscognitive, simple partial, complex partial, psychic, and secondarily generalized are eliminated; (4) new focal seizure types include automatisms, behavior arrest, hyperkinetic, autonomic, cognitive, and emotional; (5) atonic, clonic, epileptic spasms, myoclonic, and tonic seizures can be of either focal or generalized onset; (6) focal to bilateral tonic-clonic seizure replaces secondarily generalized seizure; (7) new generalized seizure types are absence with eyelid myoclonia, myoclonic absence, myoclonic-atonic, myoclonic-tonic-clonic; and (8) seizures of unknown onset may have features that can still be classified. The new classification does not represent a fundamental change, but allows greater flexibility and transparency in naming seizure types.
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            Electrical stimulation of the anterior nucleus of thalamus for treatment of refractory epilepsy.

            We report a multicenter, double-blind, randomized trial of bilateral stimulation of the anterior nuclei of the thalamus for localization-related epilepsy. Participants were adults with medically refractory partial seizures, including secondarily generalized seizures. Half received stimulation and half no stimulation during a 3-month blinded phase; then all received unblinded stimulation. One hundred ten participants were randomized. Baseline monthly median seizure frequency was 19.5. In the last month of the blinded phase the stimulated group had a 29% greater reduction in seizures compared with the control group, as estimated by a generalized estimating equations (GEE) model (p = 0.002). Unadjusted median declines at the end of the blinded phase were 14.5% in the control group and 40.4% in the stimulated group. Complex partial and "most severe" seizures were significantly reduced by stimulation. By 2 years, there was a 56% median percent reduction in seizure frequency; 54% of patients had a seizure reduction of at least 50%, and 14 patients were seizure-free for at least 6 months. Five deaths occurred and none were from implantation or stimulation. No participant had symptomatic hemorrhage or brain infection. Two participants had acute, transient stimulation-associated seizures. Cognition and mood showed no group differences, but participants in the stimulated group were more likely to report depression or memory problems as adverse events. Bilateral stimulation of the anterior nuclei of the thalamus reduces seizures. Benefit persisted for 2 years of study. Complication rates were modest. Deep brain stimulation of the anterior thalamus is useful for some people with medically refractory partial and secondarily generalized seizures.
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              A PROPOSED MECHANISM OF EMOTION

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                Author and article information

                Contributors
                yutaoly@sina.com
                rlkbrain2000@yahoo.com
                Journal
                Ann Clin Transl Neurol
                Ann Clin Transl Neurol
                10.1002/(ISSN)2328-9503
                ACN3
                Annals of Clinical and Translational Neurology
                John Wiley and Sons Inc. (Hoboken )
                2328-9503
                05 November 2022
                December 2022
                : 9
                : 12 ( doiID: 10.1002/acn3.v9.12 )
                : 2010-2024
                Affiliations
                [ 1 ] Department of Functional Neurosurgery Beijing Institute of Functional Neurosurgery, Xuanwu Hospital, Capital Medical University Beijing China
                [ 2 ] Department of Neurology, Comprehensive Epilepsy Center of Beijing, Beijing Key Laboratory of Neuromodulation Xuanwu Hospital, Capital Medical University Beijing China
                Author notes
                [*] [* ] Correspondence

                Tao Yu, Beijing Institute of Functional Neurosurgery, Department of Functional Neurosurgery, Xuanwu Hospital Capital Medical University, Beijing 100053, China. Tel: +86 10 83198671; Fax: +86 10 83163174; E‐mail: yutaoly@ 123456sina.com

                Liankun Ren, Department of Neurology, Xuanwu Hospital, Capital Medical University, 45 Changchun Street, 100053 Beijing, China. Tel: +86 10 83198273; Fax: +86 10 83157841; E‐mail: rlkbrain2000@ 123456yahoo.com

                [ a ]

                Co‐first authors.

                [ b ]

                Co‐corresponding authors.

                Author information
                https://orcid.org/0000-0001-7765-7404
                https://orcid.org/0000-0003-2463-748X
                https://orcid.org/0000-0001-6885-7105
                https://orcid.org/0000-0001-5147-3068
                Article
                ACN351693 ACN3-2022-08-0401.R1
                10.1002/acn3.51693
                9735375
                36334281
                0f460e5a-9567-4f28-bb4e-a5a3c8482126
                © 2022 The Authors. Annals of Clinical and Translational Neurology published by Wiley Periodicals LLC on behalf of American Neurological Association.

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.

                History
                : 10 October 2022
                : 17 August 2022
                : 24 October 2022
                Page count
                Figures: 6, Tables: 2, Pages: 2024, Words: 8834
                Funding
                Funded by: Beijing Natural Science Foundation Of China ‐ Beijing Municipal Education Commission Joint Fund
                Award ID: KZ202110025036
                Funded by: Natural Science Foundation of Beijing Municipality , doi 10.13039/501100005089;
                Award ID: Z210009
                Funded by: Science and Technology Innovation Project , doi 10.13039/501100013090;
                Award ID: 2021ZD0201605
                This work was funded by Beijing Natural Science Foundation Of China ‐ Beijing Municipal Education Commission Joint Fund grant KZ202110025036; Natural Science Foundation of Beijing Municipality , doi 10.13039/501100005089; grant Z210009; Science and Technology Innovation Project , doi 10.13039/501100013090; grant 2021ZD0201605.
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                December 2022
                Converter:WILEY_ML3GV2_TO_JATSPMC version:6.2.2 mode:remove_FC converted:10.12.2022

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