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      Changes in the TMS-evoked potential N100 in the dorsolateral prefrontal cortex as a function of depression severity in adolescents

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          Abstract

          Studies using transcranial magnetic stimulation with simultaneous electroencephalography (TMS-EEG) revealed an imbalance between cortical excitation and inhibition (E/I) in the dorsolateral prefrontal cortex (DLPFC) in depression. As adolescence is a developmental period with an increase in depression prevalence and profound neural changes, it is crucial to study the relationship between depression and cortical excitability in adolescence. We aimed to investigate the cortical excitability of the DLPFC in adolescents with depression and a dependency of the TMS-evoked potential N100 on the depression severity. 36 clinical patients (12–18 years of age; 21 females) with a major depressive episode were assessed twice in a longitudinal design: shortly after admission (T0) and after six weeks of intervention (T1). GABA-B-mediated cortical inhibition in the left and right DLPFC, as assessed by the N100, was recorded with EEG. Significantly higher depression scores were reported at T0 compared to T1 ( p < 0.001). N100 amplitudes were significantly increased (i.e., more negative) at T0 compared to T1 ( p = 0.03). No significant hemispheric difference was found in the N100 component. The correlation between the difference in depression severity and the difference in N100 amplitudes (T0–T1) obtained during stimulation of the left DLPFC did not remain significant after correction for testing in both hemispheres. Higher N100 amplitudes during a state of greater depression severity are suggestive of an E/I imbalance in the DLPFC in adolescents with an acute depressive episode. The N100 reduction potentially reflects a normalization of DLPFC over inhibition in association with decreased depressive symptomatology, indicating severity dependency.

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          Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime Version (K-SADS-PL): initial reliability and validity data.

          To describe the psychometric properties of the Schedule for Affective Disorders and Schizophrenia for School-Age Children-Present and Lifetime version (K-SADS-PL) interview, which surveys additional disorders not assessed in prior K-SADS, contains improved probes and anchor points, includes diagnosis-specific impairment ratings, generates DSM-III-R and DSM-IV diagnoses, and divides symptoms surveyed into a screening interview and five diagnostic supplements. Subjects were 55 psychiatric outpatients and 11 normal controls (aged 7 through 17 years). Both parents and children were used as informants. Concurrent validity of the screen criteria and the K-SADS-PL diagnoses was assessed against standard self-report scales. Interrater (n = 15) and test-retest (n = 20) reliability data were also collected (mean retest interval: 18 days; range: 2 to 36 days). Rating scale data support the concurrent validity of screens and K-SADS-PL diagnoses. Interrater agreement in scoring screens and diagnoses was high (range: 93% to 100%). Test-retest reliability kappa coefficients were in the excellent range for present and/or lifetime diagnoses of major depression, any bipolar, generalized anxiety, conduct, and oppositional defiant disorder (.77 to 1.00) and in the good range for present diagnoses of posttraumatic stress disorder and attention-deficit hyperactivity disorder (.63 to .67). Results suggest the K-SADS-PL generates reliable and valid child psychiatric diagnoses.
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            Non-invasive electrical and magnetic stimulation of the brain, spinal cord, roots and peripheral nerves: Basic principles and procedures for routine clinical and research application. An updated report from an I.F.C.N. Committee

            These guidelines provide an up-date of previous IFCN report on “Non-invasive electrical and magnetic stimulation of the brain, spinal cord and roots: basic principles and procedures for routine clinical application” (Rossini et al., 1994). A new Committee, composed of international experts, some of whom were in the panel of the 1994 “Report”, was selected to produce a current state-of-the-art review of non-invasive stimulation both for clinical application and research in neuroscience. Since 1994, the international scientific community has seen a rapid increase in non-invasive brain stimulation in studying cognition, brain–behavior relationship and pathophysiology of various neurologic and psychiatric disorders. New paradigms of stimulation and new techniques have been developed. Furthermore, a large number of studies and clinical trials have demonstrated potential therapeutic applications of non-invasive brain stimulation, especially for TMS. Recent guidelines can be found in the literature covering specific aspects of non-invasive brain stimulation, such as safety (Rossi et al., 2009), methodology (Groppa et al., 2012) and therapeutic applications (Lefaucheur et al., 2014). This up-dated review covers theoretical, physiological and practical aspects of non-invasive stimulation of brain, spinal cord, nerve roots and peripheral nerves in the light of more updated knowledge, and include some recent extensions and developments.
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              Dynamic mapping of human cortical development during childhood through early adulthood.

              We report the dynamic anatomical sequence of human cortical gray matter development between the age of 4-21 years using quantitative four-dimensional maps and time-lapse sequences. Thirteen healthy children for whom anatomic brain MRI scans were obtained every 2 years, for 8-10 years, were studied. By using models of the cortical surface and sulcal landmarks and a statistical model for gray matter density, human cortical development could be visualized across the age range in a spatiotemporally detailed time-lapse sequence. The resulting time-lapse "movies" reveal that (i) higher-order association cortices mature only after lower-order somatosensory and visual cortices, the functions of which they integrate, are developed, and (ii) phylogenetically older brain areas mature earlier than newer ones. Direct comparison with normal cortical development may help understanding of some neurodevelopmental disorders such as childhood-onset schizophrenia or autism.
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                Author and article information

                Contributors
                lea.biermann@uk-koeln.de
                heidrun.wunram@uk-koeln.de
                lena.pokorny@uk-koeln.de
                eva.breitinger@uk-koeln.de
                n.grossheinrich@katho-nrw.de
                jarczok.tomasz@josefinum.de
                stephan.bender@uk-koeln.de
                Journal
                J Neural Transm (Vienna)
                J Neural Transm (Vienna)
                Journal of Neural Transmission
                Springer Vienna (Vienna )
                0300-9564
                1435-1463
                27 August 2022
                27 August 2022
                2022
                : 129
                : 11
                : 1339-1352
                Affiliations
                [1 ]GRID grid.6190.e, ISNI 0000 0000 8580 3777, Department of Child and Adolescent Psychiatry, Psychosomatics, and Psychotherapy, , University of Cologne, Faculty of Medicine and University Hospital Cologne, ; Cologne, Germany
                [2 ]GRID grid.466086.a, ISNI 0000 0001 1010 8830, Catholic University of Applied Sciences North-Rhine-Westphalia/Cologne, ; Cologne, Germany
                [3 ]GRID grid.411088.4, ISNI 0000 0004 0578 8220, Department of Child and Adolescent Psychiatry, Psychosomatics and Psychotherapy, , University Hospital Frankfurt, ; Frankfurt, Germany
                [4 ]Department of Child and Adolescent Psychiatry and Psychotherapy, KJF Klinik Josefinum, Augsburg, Germany
                Author information
                http://orcid.org/0000-0001-7834-9366
                http://orcid.org/0000-0002-9140-6000
                http://orcid.org/0000-0001-5638-0813
                http://orcid.org/0000-0003-3462-7242
                http://orcid.org/0000-0001-6445-3672
                http://orcid.org/0000-0002-6939-666X
                http://orcid.org/0000-0001-8199-3785
                Article
                2539
                10.1007/s00702-022-02539-9
                9550695
                36029418
                b275d153-450a-42d7-b248-880cc1af5b98
                © The Author(s) 2022

                Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 24 May 2022
                : 12 August 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100011566, Marga und Walter Boll-Stiftung;
                Award ID: 210-04.00-16
                Award ID: 210-04.00-16
                Award ID: 210-04.00-16
                Award Recipient :
                Funded by: Universitätsklinikum Köln (8977)
                Categories
                Psychiatry and Preclinical Psychiatric Studies - Original Article
                Custom metadata
                © Springer-Verlag GmbH Austria, part of Springer Nature 2022

                tms-eeg,n100,depression,adolescents,teps
                tms-eeg, n100, depression, adolescents, teps

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