TY - JOUR A1 - Koenig, Julian A1 - Abler, Birgit A1 - Agartz, Ingrid A1 - akerstedt, Torbjorn A1 - Andreassen, Ole A. A1 - Anthony, Mia A1 - Baer, Karl-Juergen A1 - Bertsch, Katja A1 - Brown, Rebecca C. A1 - Brunner, Romuald A1 - Carnevali, Luca A1 - Critchley, Hugo D. A1 - Cullen, Kathryn R. A1 - de Geus, Eco J. C. A1 - de la Cruz, Feliberto A1 - Dziobek, Isabel A1 - Ferger, Marc D. A1 - Fischer, Hakan A1 - Flor, Herta A1 - Gaebler, Michael A1 - Gianaros, Peter J. A1 - Giummarra, Melita J. A1 - Greening, Steven G. A1 - Guendelman, Simon A1 - Heathers, James A. J. A1 - Herpertz, Sabine C. A1 - Hu, Mandy X. A1 - Jentschke, Sebastian A1 - Kaess, Michael A1 - Kaufmann, Tobias A1 - Klimes-Dougan, Bonnie A1 - Koelsch, Stefan A1 - Krauch, Marlene A1 - Kumral, Deniz A1 - Lamers, Femke A1 - Lee, Tae-Ho A1 - Lekander, Mats A1 - Lin, Feng A1 - Lotze, Martin A1 - Makovac, Elena A1 - Mancini, Matteo A1 - Mancke, Falk A1 - Mansson, Kristoffer N. T. A1 - Manuck, Stephen B. A1 - Mather, Mara A1 - Meeten, Frances A1 - Min, Jungwon A1 - Mueller, Bryon A1 - Muench, Vera A1 - Nees, Frauke A1 - Nga, Lin A1 - Nilsonne, Gustav A1 - Ordonez Acuna, Daniela A1 - Osnes, Berge A1 - Ottaviani, Cristina A1 - Penninx, Brenda W. J. H. A1 - Ponzio, Allison A1 - Poudel, Govinda R. A1 - Reinelt, Janis A1 - Ren, Ping A1 - Sakaki, Michiko A1 - Schumann, Andy A1 - Sorensen, Lin A1 - Specht, Karsten A1 - Straub, Joana A1 - Tamm, Sandra A1 - Thai, Michelle A1 - Thayer, Julian F. A1 - Ubani, Benjamin A1 - van Der Mee, Denise J. A1 - van Velzen, Laura S. A1 - Ventura-Bort, Carlos A1 - Villringer, Arno A1 - Watson, David R. A1 - Wei, Luqing A1 - Wendt, Julia A1 - Schreiner, Melinda Westlund A1 - Westlye, Lars T. A1 - Weymar, Mathias A1 - Winkelmann, Tobias A1 - Wu, Guo-Rong A1 - Yoo, Hyun Joo A1 - Quintana, Daniel S. T1 - Cortical thickness and resting-state cardiac function across the lifespan BT - a cross-sectional pooled mega-analysis JF - Psychophysiology : journal of the Society for Psychophysiological Research N2 - Understanding the association between autonomic nervous system [ANS] function and brain morphology across the lifespan provides important insights into neurovisceral mechanisms underlying health and disease. Resting-state ANS activity, indexed by measures of heart rate [HR] and its variability [HRV] has been associated with brain morphology, particularly cortical thickness [CT]. While findings have been mixed regarding the anatomical distribution and direction of the associations, these inconsistencies may be due to sex and age differences in HR/HRV and CT. Previous studies have been limited by small sample sizes, which impede the assessment of sex differences and aging effects on the association between ANS function and CT. To overcome these limitations, 20 groups worldwide contributed data collected under similar protocols of CT assessment and HR/HRV recording to be pooled in a mega-analysis (N = 1,218 (50.5% female), mean age 36.7 years (range: 12-87)). Findings suggest a decline in HRV as well as CT with increasing age. CT, particularly in the orbitofrontal cortex, explained additional variance in HRV, beyond the effects of aging. This pattern of results may suggest that the decline in HRV with increasing age is related to a decline in orbitofrontal CT. These effects were independent of sex and specific to HRV; with no significant association between CT and HR. Greater CT across the adult lifespan may be vital for the maintenance of healthy cardiac regulation via the ANS-or greater cardiac vagal activity as indirectly reflected in HRV may slow brain atrophy. Findings reveal an important association between CT and cardiac parasympathetic activity with implications for healthy aging and longevity that should be studied further in longitudinal research. KW - aging KW - autonomic nervous system KW - cortical thickness KW - heart rate KW - heart KW - rate variability KW - sex Y1 - 2020 U6 - https://doi.org/10.1111/psyp.13688 SN - 0048-5772 SN - 1469-8986 VL - 58 IS - 7 PB - Wiley CY - Hoboken ER - TY - GEN A1 - Kaminski, Jakob A1 - Schlagenhauf, Florian A1 - Rapp, Michael Armin A1 - Awasthi, Swapnil A1 - Ruggeri, Barbara A1 - Deserno, Lorenz A1 - Laura, Daedelow A1 - Banaschewski, Tobias A1 - Bokde, Arun A1 - Quinlan, Erin Burke A1 - Buechel, Christian A1 - Bromberg, Uli A1 - Desrivieres, Sylvane A1 - Flor, Herta A1 - Frouin, Vincent A1 - Garavan, Hugh A1 - Gowland, Penny A1 - Ittermann, Bernd A1 - Martinot, Jean-Luc A1 - Martinot, Marie-Laure Paillere A1 - Nees, Frauke A1 - Orfanos, Dimitri Papadopoulos A1 - Paus, Tomas A1 - Poustka, Luise A1 - Smolka, Michael A1 - Froehner, Juliane A1 - Walter, Henrik A1 - Whelan, Robert A1 - Ripke, Stephan A1 - Schumann, Gunter A1 - Heinz, Andreas T1 - Variance in Dopaminergic Markers BT - a possible marker of individual differences in IQ? T2 - Biological psychiatry : a journal of psychiatric neuroscience and therapeutics ; a publication of the Society of Biological Psychiatry KW - Intelligence KW - Dopamine KW - Epigenetic Biomarkers KW - Reward Anticipation KW - Polygenic Risk Score Y1 - 2018 U6 - https://doi.org/10.1016/j.biopsych.2018.02.311 SN - 0006-3223 SN - 1873-2402 VL - 83 IS - 9 SP - S118 EP - S118 PB - Elsevier CY - New York ER - TY - GEN A1 - Kaminski, Jakob A. A1 - Schlagenhauf, Florian A1 - Rapp, Michael Armin A1 - Awasthi, Swapnil A1 - Ruggeri, Barbara A1 - Deserno, Lorenz A1 - Banaschewski, Tobias A1 - Bokde, Arun L. W. A1 - Bromberg, Uli A1 - Büchel, Christian A1 - Quinlan, Erin Burke A1 - Desrivières, Sylvane A1 - Flor, Herta A1 - Frouin, Vincent A1 - Garavan, Hugh A1 - Gowland, Penny A1 - Ittermann, Bernd A1 - Martinot, Jean-Luc A1 - Paillère Martinot, Marie-Laure A1 - Nees, Frauke A1 - Papadopoulos Orfanos, Dimitri A1 - Paus, Tomáš A1 - Poustka, Luise A1 - Smolka, Michael N. A1 - Fröhner, Juliane H. A1 - Walter, Henrik A1 - Whelan, Robert A1 - Ripke, Stephan A1 - Schumann, Gunter A1 - Heinz, Andreas T1 - Epigenetic variance in dopamine D2 receptor BT - a marker of IQ malleability? T2 - Postprints der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe N2 - Genetic and environmental factors both contribute to cognitive test performance. A substantial increase in average intelligence test results in the second half of the previous century within one generation is unlikely to be explained by genetic changes. One possible explanation for the strong malleability of cognitive performance measure is that environmental factors modify gene expression via epigenetic mechanisms. Epigenetic factors may help to understand the recent observations of an association between dopamine-dependent encoding of reward prediction errors and cognitive capacity, which was modulated by adverse life events. The possible manifestation of malleable biomarkers contributing to variance in cognitive test performance, and thus possibly contributing to the "missing heritability" between estimates from twin studies and variance explained by genetic markers, is still unclear. Here we show in 1475 healthy adolescents from the IMaging and GENetics (IMAGEN) sample that general IQ (gIQ) is associated with (1) polygenic scores for intelligence, (2) epigenetic modification of DRD2 gene, (3) gray matter density in striatum, and (4) functional striatal activation elicited by temporarily surprising reward-predicting cues. Comparing the relative importance for the prediction of gIQ in an overlapping subsample, our results demonstrate neurobiological correlates of the malleability of gIQ and point to equal importance of genetic variance, epigenetic modification of DRD2 receptor gene, as well as functional striatal activation, known to influence dopamine neurotransmission. Peripheral epigenetic markers are in need of confirmation in the central nervous system and should be tested in longitudinal settings specifically assessing individual and environmental factors that modify epigenetic structure. T3 - Zweitveröffentlichungen der Universität Potsdam : Mathematisch-Naturwissenschaftliche Reihe - 950 KW - genome-wide association KW - reward anticipation KW - human intelligence KW - human brain KW - stress KW - metaanalysis KW - striatum KW - psychopathology KW - prediction KW - volume KW - epigenetics and behaviour KW - human behaviour KW - learning and memory Y1 - 2020 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-425687 SN - 1866-8372 IS - 950 ER - TY - JOUR A1 - Kaminski, Jakob A. A1 - Schlagenhauf, Florian A1 - Rapp, Michael Armin A1 - Awasthi, Swapnil A1 - Ruggeri, Barbara A1 - Deserno, Lorenz A1 - Banaschewski, Tobias A1 - Bokde, Arun L. W. A1 - Bromberg, Uli A1 - Büchel, Christian A1 - Quinlan, Erin Burke A1 - Desrivieres, Sylvane A1 - Flor, Herta A1 - Frouin, Vincent A1 - Garavan, Hugh A1 - Gowland, Penny A1 - Ittermann, Bernd A1 - Martinot, Jean-Luc A1 - Martinot, Marie-Laure Paillere A1 - Nees, Frauke A1 - Orfanos, Dimitri Papadopoulos A1 - Paus, Tomas A1 - Poustka, Luise A1 - Smolka, Michael N. A1 - Fröhner, Juliane H. A1 - Walter, Henrik A1 - Whelan, Robert A1 - Ripke, Stephan A1 - Schumann, Gunter A1 - Heinz, Andreas T1 - Epigenetic variance in dopamine D2 receptor BT - a marker of IQ malleability? JF - Translational Psychiatry N2 - Genetic and environmental factors both contribute to cognitive test performance. A substantial increase in average intelligence test results in the second half of the previous century within one generation is unlikely to be explained by genetic changes. One possible explanation for the strong malleability of cognitive performance measure is that environmental factors modify gene expression via epigenetic mechanisms. Epigenetic factors may help to understand the recent observations of an association between dopamine-dependent encoding of reward prediction errors and cognitive capacity, which was modulated by adverse life events. The possible manifestation of malleable biomarkers contributing to variance in cognitive test performance, and thus possibly contributing to the "missing heritability" between estimates from twin studies and variance explained by genetic markers, is still unclear. Here we show in 1475 healthy adolescents from the IMaging and GENetics (IMAGEN) sample that general IQ (gIQ) is associated with (1) polygenic scores for intelligence, (2) epigenetic modification of DRD2 gene, (3) gray matter density in striatum, and (4) functional striatal activation elicited by temporarily surprising reward-predicting cues. Comparing the relative importance for the prediction of gIQ in an overlapping subsample, our results demonstrate neurobiological correlates of the malleability of gIQ and point to equal importance of genetic variance, epigenetic modification of DRD2 receptor gene, as well as functional striatal activation, known to influence dopamine neurotransmission. Peripheral epigenetic markers are in need of confirmation in the central nervous system and should be tested in longitudinal settings specifically assessing individual and environmental factors that modify epigenetic structure. Y1 - 2018 U6 - https://doi.org/10.1038/s41398-018-0222-7 SN - 2158-3188 VL - 8 PB - Nature Publ. Group CY - New York ER - TY - GEN A1 - Rodriguez-Sillke, Yasmina A1 - Steinhoff, U. A1 - Bojarski, Christian A1 - Lissner, Donata A1 - Schumann, Michael A1 - Branchi, F. A1 - Siegmund, Britta A1 - Glauben, Rainer T1 - Deep immune profiling of human Peyer´s Patches in patients of inflammatory bowel diseases T2 - European journal of immunology Y1 - 2019 U6 - https://doi.org/10.1002/eji.201970300 SN - 0014-2980 SN - 1521-4141 VL - 49 SP - 203 EP - 204 PB - Wiley CY - Weinheim ER - TY - CHAP A1 - Rolf, Arno A1 - Berges, Marc A1 - Hubwieser, Peter A1 - Kehrer, Timo A1 - Kelter, Udo A1 - Romeike, Ralf A1 - Frenkel, Marcus A1 - Karsten, Weicker A1 - Reinhardt, Wolfgang A1 - Mascher, Michael A1 - Gül, Senol A1 - Magenheim, Johannes A1 - Raimer, Stephan A1 - Diethelm, Ira A1 - Dünnebier, Malte A1 - Gabor, Kiss A1 - Susanne, Boll A1 - Rolf, Meinhardt A1 - Gronewold, Sabine A1 - Krekeler, Larissa A1 - Jahnke, Isa A1 - Haertel, Tobias A1 - Mattick, Volker A1 - Lettow, Karsten A1 - Hafer, Jörg A1 - Ludwig, Joachim A1 - Schumann, Marlen A1 - Laroque, Christoph A1 - Schulte, Jonas A1 - Urban, Diana ED - Engbring, Dieter ED - Keil, Reinhard ED - Magenheim, Johannes ED - Selke, Harald T1 - HDI2010 – Tagungsband der 4. Fachtagung zur "Hochschuldidaktik Informatik" N2 - Mit der 4. Tagung zur Hochschuldidaktik Informatik wird eine Reihe fortgesetzt, die ihren Anfang 1998 in Stuttgart unter der Überschrift „Informatik und Ausbildung“ genommen hat. Seither dienen diese Tagungen den Lehrenden im Bereich der Hochschulinformatik als Forum der Information und des Diskurses über aktuelle didaktische und bildungspolitische Entwicklungen im Bereich der Informatikausbildung. Aktuell zählen dazu insbesondere Fragen der Bildungsrelevanz informatischer Inhalte und der Herausforderung durch eine stärkere Kompetenzorientierung in der Informatik. Die eingereichten Beiträge zur HDI 2010 in Paderborn veranschaulichen unterschiedliche Bemühungen, sich mit relevanten Problemen der Informatikdidaktik an Hochschulen in Deutschland (und z. T. auch im Ausland) auseinanderzusetzen. Aus der Breite des Spektrums der Einreichungen ergaben sich zugleich Probleme bei der Begutachtung. Letztlich konnten von den zahlreichen Einreichungen nur drei die Gutachter so überzeugen, dass sie uneingeschränkt in ihrer Langfassung akzeptiert wurden. Neun weitere Einreichungen waren trotz Kritik überwiegend positiv begutachtet worden, so dass wir diese als Kurzfassung bzw. Diskussionspapier in die Tagung aufgenommen haben. T3 - Commentarii informaticae didacticae (CID) - 4 Y1 - 2010 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus-49167 SN - 978-3-86956-100-4 PB - Universitätsverlag Potsdam CY - Potsdam ER - TY - THES A1 - Schumann, Michael T1 - Extraterrestrische Ex-zentriker T1 - Extraterrestrial Ec-centrics BT - zur theoriestrukturellen Einarbeitung des Außerirdischen bei Helmuth Plessner als Grundlage einer Philosophischen Anthropologie des Raumfahrtzeitalters BT - about the theoretic-structural inclusion of the Extraterrestrial in Helmuth Plessner, as the basis for a philosophical anthropology of the space age N2 - Seit ihrem Beginn ist die Raumfahrt Untersuchungsgegenstand verschiedenster Disziplinen. Auch die Philosophie hat seither eine kritische Perspektive auf diese Aktivität eingenommen. Und doch fehlt es bislang eines philosophisch-systematischen Zugangs, mit einem genuin ‚anthropologischen‘ Gesichtspunkt. Diese Lücke wird immer offensichtlicher, seitdem sich, nach Entdeckung der ersten Exoplaneten, neue ‚Astro-wissenschaften‘ (z.B. Astrobiologe, Astrokognition, Astrosoziologie) gebildet haben, die explizit Menschen als Raumfahrer voraussetzen bzw. menschliche Eigenschaften auf ihre ‚Ablösbarkeit‘ hin diskutieren. Mit vorliegender Masterarbeit soll der Versuch gemacht werden, die notwendigen Präsuppositionen, für das Verständnis von Menschen als ‚raumfahrende Lebewesen‘, aufzudecken, ohne naturalistische oder kulturalistische Verkürzungen zu betreiben. Zu diesem Zweck wird der systematische Rahmen von Helmuth Plessners Philosophischer Anthropologie gewählt, da dieser eine umfassende ‚spezies-neutrale‘ (d.h. es erlaubt über Menschen, Tiere und Extraterrestriker gleichermaßen nachzudenken, ohne ‚anthropozentrische‘ oder ‚speziesistische‘ Vorurteile zu machen) Untersuchung des infrage stehenden Sachverhaltes bietet. Um diesen Rahmen zu exemplifizieren, und währenddessen den philosophisch-systematischen Ansatz zur Raumfahrt zu elaborieren, der raumfahrende Extraterrestriker ohne Anthropomorphisierung konzeptualisieren, wie auch den Umgang mit Extraterrestrikern in ethischer und politischer Hinsicht berücksichtigen kann, werden die Themenkreise der Astrobiologie, Astroethik und Astropolitik in einzelnen Kapiteln besprochen. Abschließend ist, entgegen aller Erwartung, der gewählte Ansatz als ‚kritisch-posthumanistische‘ Option zu verteidigen. N2 - Since its beginning, space travel is examined by different disciplines. Likewise, philosophy has taken a critical look on this activity ever since. Though, until now a philosophic-systematic approach, with genuine ‘anthropological’ viewpoint, is lacking. This gap is getting obvious, since, after the discovery of the first exoplanets, new ‘astro-sciences’ (e.g. astrobiology, astrocognition, astrosociology) were established, for which ‘the human as space traveler’ is an explicit prerequisite, or for which the ‘detachability’ of human capacities is under discussion. The present master thesis is trying to uncover the necessary presuppositions, for the understanding of the human as a ‘space traveling life form’, without the narrow-minded perspective of naturalistic or culturalistic approaches. For this purpose, the systematic frame of Helmuth Plessners philosophical anthropology is selected, because, it offers a comprehensive ‘species-neutralized’ (i.e. it allows to contemplate about humans, animals and extraterrestrials equally, without ‘anthropocentric’ and ‘speciecist’ prejudices) examination of the matter in question. To exemplify these frame, and to elaborate in the course of this a philosophic-systematic approach to space travel, which is equally able to conceptualize the spacefaring extraterrestrial without anthropomorphization and to problematize the dealings with extraterrestrials in ethical and political regard, the topics of astrobiology, astroethics and astropolitics are discussed in separate chapters. At last, against all the odds, the approach is to defend as a new ‘critical-posthumanist’ option. KW - Philosophische Anthropologie KW - Helmuth Plessner KW - Raumfahrt KW - Extraterrestriker KW - Posthumanismus KW - Philosophical anthropology KW - Helmuth Plessner KW - space travel KW - extraterrestrials KW - posthumanism Y1 - 2019 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-434203 ER - TY - GEN A1 - Rodríguez Sillke, Yasmina A1 - Schumann, Michael A1 - Lissner, Donata A1 - Branchi, Frederica A1 - Glauben, Rainer A1 - Siegmund, Britta T1 - Small intestinal inflammation but not colitis drives pro-inflammatory nutritional antigen-specific T-cell response T2 - Journal of Crohn's and Colitis N2 - Background: Inflammatory bowel disease (IBD) represents a dysregulation of the mucosal immune system. The pathogenesis of Crohn’s disease (CD) and ulcerative colitis (UC) is linked to the loss of intestinal tolerance and barrier function. The healthy mucosal immune system has previously been shown to be inert against food antigens. Since the small intestine is the main contact surface for antigens and therefore the immunological response, the present study served to analyse food-antigen-specific T cells in the peripheral blood of IBD patients. Methods: Peripheral blood mononuclear cells of CD, with an affected small intestine, and UC (colitis) patients, either active or in remission, were stimulated with the following food antigens: gluten, soybean, peanut and ovalbumin. Healthy controls and celiac disease patients were included as controls. Antigen-activated CD4+ T cells in the peripheral blood were analysed by a magnetic enrichment of CD154+ effector T cells and a cytometric antigen-reactive T-cell analysis (‘ARTE’ technology) followed by characterisation of the ef- fector response. Results: The effector T-cell response of antigen-specific T cells were compared between CD with small intestinal inflammation and UC where inflammation was restricted to the colon. Among all tested food antigens, the highest frequency of antigen-specific T cells (CD4+CD154+) was found for gluten. Celiac disease patients were included as control, since gluten has been identified as the disease- causing antigen. The highest frequency of gluten antigen-specific T cells was revealed in active CD when compared with UC, celiac disease on a gluten-free diet (GFD) and healthy controls. Ovalbuminspecific T cells were almost undetectable, whereas the reaction to soybean and peanut was slightly higher. But again, the strong- est reaction was observed in CD with small intestinal involvement compared with UC. Remarkably, in celiac disease on a GFD only antigen-specific cells for gluten were detected. These gluten-specific T cells were characterised by up-regulation of the pro-inflammatory cytokines IFN-γ, IL-17A and TNF-α. IFN-g was exclusively elevated in CD patients with active disease. Gluten-specific T-cells expressing IL-17A were increased in all IBD patients. Furthermore, T cells of CD patients, independent of disease activity, revealed a high expression of the pro-inflammatory cytokine TNF-α. Conclusion: The ‘ARTE’-technique allows to analyse and quantify food antigen specific T cells in the peripheral blood of IBD patients indicating a potential therapeutic insight. These data provide evidence that small intestinal inflammation in CD is key for the development of a systemic pro-inflammatory effector T-cell response driven by food antigens. Y1 - 2020 U6 - https://doi.org/10.1093/ecco-jcc/jjz203.172 SN - 1873-9946 SN - 1876-4479 VL - 14 SP - S154 EP - S155 PB - Oxford Univ. Press CY - Oxford ER - TY - JOUR A1 - Holz, Nathalie E. A1 - Boecker-Schlier, Regina A1 - Buchmann, Arlette F. A1 - Blomeyer, Dorothea A1 - Jennen-Steinmetz, Christine A1 - Baumeister, Sarah A1 - Plichta, Michael M. A1 - Cattrell, Anna A1 - Schumann, Gunter A1 - Esser, Günter A1 - Schmidt, Martin A1 - Buitelaar, Jan A1 - Meyer-Lindenberg, Andreas A1 - Banaschewski, Tobias A1 - Brandeis, Daniel A1 - Laucht, Manfred T1 - Ventral striatum and amygdala activity as convergence sites for early adversity and conduct disorder JF - Frontiers in human neuroscience N2 - Childhood family adversity (CFA) increases the risk for conduct disorder (CD) and has been associated with alterations in regions of affective processing like ventral striatum (VS) and amygdala. However, no study so far has demonstrated neural converging effects of CFA and CD in the same sample. At age 25 years, functional MRI data during two affective tasks, i.e. a reward (N = 171) and a face-matching paradigm (N = 181) and anatomical scans (N = 181) were acquired in right-handed currently healthy participants of an epidemiological study followed since birth. CFA during childhood was determined using a standardized parent interview. Disruptive behaviors and CD diagnoses during childhood and adolescence were obtained by diagnostic interview (2–19 years), temperamental reward dependence was assessed by questionnaire (15 and 19 years). CFA predicted increased CD and amygdala volume. Both exposure to CFA and CD were associated with a decreased VS response during reward anticipation and blunted amygdala activity during face-matching. CD mediated the effect of CFA on brain activity. Temperamental reward dependence was negatively correlated with CFA and CD and positively with VS activity. These findings underline the detrimental effects of CFA on the offspring's affective processing and support the importance of early postnatal intervention programs aiming to reduce childhood adversity factors. KW - childhood adversity KW - conduct disorder KW - amygdala KW - ventral striatum KW - fMRI Y1 - 2016 U6 - https://doi.org/10.1093/scan/nsw120 SN - 1749-5016 SN - 1749-5024 VL - 12 IS - 2 SP - 261 EP - 272 PB - Oxford Univ. Press CY - Oxford ER - TY - GEN A1 - Xie, Chao A1 - Jia, Tianye A1 - Rolls, Edmund T. A1 - Robbins, Trevor W. A1 - Sahakian, Barbara J. A1 - Zhang, Jie A1 - Liu, Zhaowen A1 - Cheng, Wei A1 - Luo, Qiang A1 - Zac Lo, Chun-Yi A1 - Schumann, Gunter A1 - Feng, Jianfeng A1 - Wang, He A1 - Banaschewski, Tobias A1 - Barker, Gareth J. A1 - Bokde, Arun L.W. A1 - Büchel, Christian A1 - Quinlan, Erin Burke A1 - Desrivières, Sylvane A1 - Flor, Herta A1 - Grigis, Antoine A1 - Garavan, Hugh A1 - Gowland, Penny A1 - Heinz, Andreas A1 - Hohmann, Sarah A1 - Ittermann, Bernd A1 - Martinot, Jean-Luc A1 - Paillère Martinot, Marie-Laure A1 - Nees, Frauke A1 - Papadopoulos Orfanos, Dimitri A1 - Paus, Tomáš A1 - Poustka, Luise A1 - Fröhner, Juliane H. A1 - Smolka, Michael N. A1 - Walter, Henrik A1 - Whelan, Robert T1 - Reward versus nonreward sensitivity of the medial versus lateral orbitofrontal cortex relates to the severity of depressive symptoms T2 - Zweitveröffentlichungen der Universität Potsdam : Humanwissenschaftliche Reihe N2 - BACKGROUND: The orbitofrontal cortex (OFC) is implicated in depression. The hypothesis investigated was whether the OFC sensitivity to reward and nonreward is related to the severity of depressive symptoms. METHODS: Activations in the monetary incentive delay task were measured in the IMAGEN cohort at ages 14 years (n = 1877) and 19 years (n = 1140) with a longitudinal design. Clinically relevant subgroups were compared at ages 19 (high-severity group: n = 116; low-severity group: n = 206) and 14. RESULTS: The medial OFC exhibited graded activation increases to reward, and the lateral OFC had graded activation increases to nonreward. In this general population, the medial and lateral OFC activations were associated with concurrent depressive symptoms at both ages 14 and 19 years. In a stratified high-severity depressive symptom group versus control group comparison, the lateral OFC showed greater sensitivity for the magnitudes of activations related to nonreward in the high-severity group at age 19 (p = .027), and the medial OFC showed decreased sensitivity to the reward magnitudes in the high-severity group at both ages 14 (p = .002) and 19 (p = .002). In a longitudinal design, there was greater sensitivity to nonreward of the lateral OFC at age 14 for those who exhibited high depressive symptom severity later at age 19 (p = .003). CONCLUSIONS: Activations in the lateral OFC relate to sensitivity to not winning, were associated with high depressive symptom scores, and at age 14 predicted the depressive symptoms at ages 16 and 19. Activations in the medial OFC were related to sensitivity to winning, and reduced reward sensitivity was associated with concurrent high depressive symptom scores. T3 - Zweitveröffentlichungen der Universität Potsdam : Humanwissenschaftliche Reihe - 860 KW - adolescents KW - depression KW - monetary incentive delay task KW - nonreward sensitivity KW - orbitofrontal cortex KW - reward anticipation KW - reward sensitivity KW - ventral striatum Y1 - 2021 U6 - http://nbn-resolving.de/urn/resolver.pl?urn:nbn:de:kobv:517-opus4-557882 SN - 1866-8364 IS - 3 ER - TY - JOUR A1 - Xie, Chao A1 - Jia, Tianye A1 - Rolls, Edmund T. A1 - Robbins, Trevor W. A1 - Sahakian, Barbara J. A1 - Zhang, Jie A1 - Liu, Zhaowen A1 - Cheng, Wei A1 - Luo, Qiang A1 - Zac Lo, Chun-Yi A1 - Schumann, Gunter A1 - Feng, Jianfeng A1 - Wang, He A1 - Banaschewski, Tobias A1 - Barker, Gareth J. A1 - Bokde, Arun L.W. A1 - Büchel, Christian A1 - Quinlan, Erin Burke A1 - Desrivières, Sylvane A1 - Flor, Herta A1 - Grigis, Antoine A1 - Garavan, Hugh A1 - Gowland, Penny A1 - Heinz, Andreas A1 - Hohmann, Sarah A1 - Ittermann, Bernd A1 - Martinot, Jean-Luc A1 - Paillère Martinot, Marie-Laure A1 - Nees, Frauke A1 - Papadopoulos Orfanos, Dimitri A1 - Paus, Tomáš A1 - Poustka, Luise A1 - Fröhner, Juliane H. A1 - Smolka, Michael N. A1 - Walter, Henrik A1 - Whelan, Robert T1 - Reward versus nonreward sensitivity of the medial versus lateral orbitofrontal cortex relates to the severity of depressive symptoms JF - Biological Psychiatry: Cognitive Neuroscience and Neuroimaging N2 - BACKGROUND: The orbitofrontal cortex (OFC) is implicated in depression. The hypothesis investigated was whether the OFC sensitivity to reward and nonreward is related to the severity of depressive symptoms. METHODS: Activations in the monetary incentive delay task were measured in the IMAGEN cohort at ages 14 years (n = 1877) and 19 years (n = 1140) with a longitudinal design. Clinically relevant subgroups were compared at ages 19 (high-severity group: n = 116; low-severity group: n = 206) and 14. RESULTS: The medial OFC exhibited graded activation increases to reward, and the lateral OFC had graded activation increases to nonreward. In this general population, the medial and lateral OFC activations were associated with concurrent depressive symptoms at both ages 14 and 19 years. In a stratified high-severity depressive symptom group versus control group comparison, the lateral OFC showed greater sensitivity for the magnitudes of activations related to nonreward in the high-severity group at age 19 (p = .027), and the medial OFC showed decreased sensitivity to the reward magnitudes in the high-severity group at both ages 14 (p = .002) and 19 (p = .002). In a longitudinal design, there was greater sensitivity to nonreward of the lateral OFC at age 14 for those who exhibited high depressive symptom severity later at age 19 (p = .003). CONCLUSIONS: Activations in the lateral OFC relate to sensitivity to not winning, were associated with high depressive symptom scores, and at age 14 predicted the depressive symptoms at ages 16 and 19. Activations in the medial OFC were related to sensitivity to winning, and reduced reward sensitivity was associated with concurrent high depressive symptom scores. KW - adolescents KW - depression KW - monetary incentive delay task KW - nonreward sensitivity KW - orbitofrontal cortex KW - reward anticipation KW - reward sensitivity KW - ventral striatum Y1 - 2021 U6 - https://doi.org/10.1016/j.bpsc.2020.08.017 SN - 0006-3223 SN - 1873-2402 VL - 6 IS - 3 SP - 259 EP - 269 PB - Elsevier Science CY - Amsterdam ER - TY - GEN A1 - Awasthi, Swapnil A1 - Kaminski, Jakob A1 - Rapp, Michael Armin A1 - Schlagenhauf, Florian A1 - Walter, Henrik A1 - Ruggeri, Barbara A1 - Ripke, Stephan A1 - Schumann, Gunter A1 - Heinz, Andreas T1 - A neural signature of malleability BT - general intelligence correlates with ventral striatal activation and epigenetic makers of dopamine neurotransmission T2 - European neuropsychopharmacology : the journal of the European College of Neuropsychopharmacology N2 - General intelligence has a substantial genetic background in children, adolescents, and adults, but environmental factors also strongly correlate with cognitive performance as evidenced by a strong (up to one SD) increase in average intelligence test results in the second half of the previous century. This change occurred in a period apparently too short to accommodate radical genetic changes. It is highly suggestive that environmental factors interact with genotype by possible modification of epigenetic factors that regulate gene expression and thus contribute to individual malleability. This modification might as well be reflected in recent observations of an association between dopamine-dependent encoding of reward prediction errors and cognitive capacity, which was modulated by adverse life events. Y1 - 2019 U6 - https://doi.org/10.1016/j.euroneuro.2017.08.139 SN - 0924-977X SN - 1873-7862 VL - 29 SP - S858 EP - S859 PB - Elsevier CY - Amsterdam ER -