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      Chronotype differences in cortical thickness: grey matter reflects when you go to bed.

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          Abstract

          Based on individual circadian cycles and associated cognitive rhythms, humans can be classified via standardised self-reports as being early (EC), late (LC) and intermediate (IC) chronotypes. Alterations in neural cortical structure underlying these chronotype differences have rarely been investigated and are the scope of this study. 16 healthy male ECs, 16 ICs and 16 LCs were measured with a 3 T MAGNETOM TIM TRIO (Siemens, Erlangen) scanner using a magnetization prepared rapid gradient echo sequence. Data were analysed by applying voxel-based morphometry (VBM) and vertex-wise cortical thickness (CTh) analysis. VBM analysis revealed that ECs showed significantly lower grey matter volumes bilateral in the lateral occipital cortex and the precuneus as compared to LCs, and in the right lingual gyrus, occipital fusiform gyrus and the occipital pole as compared to ICs. CTh findings showed lower grey matter volumes for ECs in the left anterior insula, precuneus, inferior parietal cortex, and right pars triangularis than for LCs, and in the right superior parietal gyrus than for ICs. These findings reveal that chronotype differences are associated with specific neural substrates of cortical thickness, surface areas, and folding. We conclude that this might be the basis for chronotype differences in behaviour and brain function. Furthermore, our results speak for the necessity of considering "chronotype" as a potentially modulating factor in all kinds of structural brain-imaging experiments.

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          Author and article information

          Journal
          Brain Struct Funct
          Brain structure & function
          Springer Science and Business Media LLC
          1863-2661
          1863-2653
          Sep 2018
          : 223
          : 7
          Affiliations
          [1 ] Institute of Neuroscience and Medicine (INM-4), Medical Imaging Physics, Forschungszentrum Jülich GmbH, 52425, Jülich, Germany. j.rosenberg@fz-juelich.de.
          [2 ] JARA-Translational Brain Medicine, RWTH Aachen University, 52074, Aachen, Germany. j.rosenberg@fz-juelich.de.
          [3 ] Department of Neurology, University Clinic Aachen, 52074, Aachen, Germany. j.rosenberg@fz-juelich.de.
          [4 ] Institute of Neuroscience and Medicine (INM-3), Forschungszentrum Juelich GmbH, 52425, Jülich, Germany.
          [5 ] Alzheimer Centre Limburg, School for Mental Health and Neuroscience (MHeNS), Faculty of Health, Medicine and Life Sciences, Maastricht University Medical Centre, PO Box 616, 6200 MD, Maastricht, The Netherlands.
          [6 ] Department of Cognitive Neuroscience, Faculty of Psychology and Neuroscience, Maastricht University, PO BOX 616, 6200 MD, Maastricht, The Netherlands.
          [7 ] Institute of Neuroscience and Medicine (INM-4), Medical Imaging Physics, Forschungszentrum Jülich GmbH, 52425, Jülich, Germany.
          [8 ] Experimental Physics III, TU Dortmund University, 44221, Dortmund, Germany.
          [9 ] JARA-Translational Brain Medicine, RWTH Aachen University, 52074, Aachen, Germany.
          [10 ] Institute of Neuroscience and Medicine (INM-6), Computational and Systems Neuroscience, and Institute for Advanced Simulation (IAS-6), Theoretical Neuroscience, Forschungszentrum Jülich GmbH, 52425, Jülich, Germany.
          [11 ] Department of Neurology, University Clinic Aachen, 52074, Aachen, Germany.
          [12 ] Department of Electrical and Computer Systems Engineering, and Monash Biomedical Imaging, School of Psychological Sciences, Monash University, Melbourne, VIC, Australia.
          Article
          10.1007/s00429-018-1697-y
          10.1007/s00429-018-1697-y
          29948193
          29b910c3-2d85-451f-bf2b-5e8ebaa8ed57
          History

          Chronotype,Circadian,Cortical thickness,Grey matter,Voxel-based morphometry

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