Hot spots and labyrinths: Why neuromodulation devices for episodic migraine should be personalized

Department of Physics, Humboldt University Berlin, Germany, Berlin, Germany
Department of Biological Physik, Max Planck Institute for the Physics of Complex Systems, Dresden, Germany
School of Systems Engineering, University of Reading, Reading, UK
Department of Mathematics, The University of Auckland, Auckland, New Zealand
Department of Software Engineering and Theoretical Computer Science, Technische Universität Berlin, Berlin, Germany
Martinos Center for Biomedical Imaging, Massachusetts General Hospital, Harvard Medical School, Boston, USA
Gillberg Neuropsychiatry Centre, University of Gothenburg, Gothenburg, Sweden
Research Domain Transdisciplinary Concepts & Methods, Potsdam Institute for Climate Impact Research, Potsdam, Germany
DOI
10.7287/peerj.preprints.515v1
Subject Areas
Biotechnology, Computational Biology, Mathematical Biology, Neuroscience, Neurology
Keywords
reaction-diffusion, migraine, spreading depression, neuromodulation, gyrification
Copyright
© 2014 Dahlem et al.
Licence
This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, reproduction and adaptation in any medium and for any purpose provided that it is properly attributed. For attribution, the original author(s), title, publication source (PeerJ PrePrints) and either DOI or URL of the article must be cited.
Cite this article
Dahlem MA, Schmidt B, Bojak I, Boie S, Kneer F, Hadjikhani N, Kurths J. 2014. Hot spots and labyrinths: Why neuromodulation devices for episodic migraine should be personalized. PeerJ PrePrints 2:e515v1

Abstract

Stimulation protocols for medical devices should be rationally designed. For episodic migraine with aura we outline model-based design strategies towards preventive and acute therapies using stereotactic neuromodulation. To this end, we regard a localized spreading depression (SD) wave segment as a central element in migraine pathophysiology. To describe nucleation and propagation features of the SD wave segment, we define the new concepts of cortical hot spots and labyrinths, respectively. In particular, we firstly focus exclusively on curvature-induced dynamical properties by studying a generic reaction-diffusion model of SD on the folded cortical surface. This surface is described with increasing level of details, including finally personalized simulations using patient's magnetic resonance imaging (MRI) scanner readings. At this stage, the only relevant factor that can modulate nucleation and propagation paths is the Gaussian curvature, which has the advantage of being rather readily accessible by MRI. We conclude with discussing further anatomical factors, such as areal, laminar, and cellular heterogeneity, that in addition to and in relation to Gaussian curvature determine the generalized concept of cortical hot spots and labyrinths as target structures for neuromodulation.Our numerical simulations suggest that these target structures are like fingerprints, they are individual features of each migraine sufferer. The goal in the future will be to provide individualized neural tissue simulations. These simulations should predict the clinical data and therefore can also serve as a test bed for exploring stereotactic neuromodulation.

Author Comment

This is a manuscript submitted to Frontiers with the special Research Topic: Driving innovation in therapeutic brain stimulation with biophysical models.