23 research outputs found

    Artificial immune system and particle swarm optimization for electroencephalogram based epileptic seizure classification

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    Automated analysis of brain activity from electroencephalogram (EEG) has indispensable applications in many fields such as epilepsy research. This research has studied the abilities of negative selection and clonal selection in artificial immune system (AIS) and particle swarm optimization (PSO) to produce different reliable and efficient methods for EEG-based epileptic seizure recognition which have not yet been explored. Initially, an optimization-based classification model was proposed to describe an individual use of clonal selection and PSO to build nearest centroid classifier for EEG signals. Next, two hybrid optimization-based negative selection models were developed to investigate the integration of the AIS-based techniques and negative selection with PSO from the perspective of classification and detection. In these models, a set of detectors was created by negative selection as self-tolerant and their quality was improved towards non-self using clonal selection or PSO. The models included a mechanism to maintain the diversity and generality among the detectors. The detectors were produced in the classification model for each class, while the detection model generated the detectors only for the abnormal class. These hybrid models differ from each other in hybridization configuration, solution representation and objective function. The three proposed models were abstracted into innovative methods by applying clonal selection and PSO for optimization, namely clonal selection classification algorithm (CSCA), particle swarm classification algorithm (PSCA), clonal negative selection classification algorithm (CNSCA), swarm negative selection classification algorithm (SNSCA), clonal negative selection detection algorithm (CNSDA) and swarm negative selection detection algorithm (SNSDA). These methods were evaluated on EEG data using common measures in medical diagnosis. The findings demonstrated that the methods can efficiently achieve a reliable recognition of epileptic activity in EEG signals. Although CNSCA gave the best performance, CNSDA and SNSDA are preferred due to their efficiency in time and space. A comparison with other methods in the literature showed the competitiveness of the proposed methods

    Biomedical Signal and Image Processing

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    Written for senior-level and first year graduate students in biomedical signal and image processing, this book describes fundamental signal and image processing techniques that are used to process biomedical information. The book also discusses application of these techniques in the processing of some of the main biomedical signals and images, such as EEG, ECG, MRI, and CT. New features of this edition include the technical updating of each chapter along with the addition of many more examples, the majority of which are MATLAB based

    Epilepsy

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    With the vision of including authors from different parts of the world, different educational backgrounds, and offering open-access to their published work, InTech proudly presents the latest edited book in epilepsy research, Epilepsy: Histological, electroencephalographic, and psychological aspects. Here are twelve interesting and inspiring chapters dealing with basic molecular and cellular mechanisms underlying epileptic seizures, electroencephalographic findings, and neuropsychological, psychological, and psychiatric aspects of epileptic seizures, but non-epileptic as well

    Advances in Clinical Neurophysiology

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    Including some of the newest advances in the field of neurophysiology, this book can be considered as one of the treasures that interested scientists would like to collect. It discusses many disciplines of clinical neurophysiology that are, currently, crucial in the practice as they explain methods and findings of techniques that help to improve diagnosis and to ensure better treatment. While trying to rely on evidence-based facts, this book presents some new ideas to be applied and tested in the clinical practice. Advances in Clinical Neurophysiology is important not only for the neurophysiologists but also for clinicians interested or working in wide range of specialties such as neurology, neurosurgery, intensive care units, pediatrics and so on. Generally, this book is written and designed to all those involved in, interpreting or requesting neurophysiologic tests

    Dynamics of biologically informed neural mass models of the brain

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    This book contributes to the development and analysis of computational models that help brain function to be understood. The mean activity of a brain area is mathematically modeled in such a way as to strike a balance between tractability and biological plausibility. Neural mass models (NMM) are used to describe switching between qualitatively different regimes (such as those due to pharmacological interventions, epilepsy, sleep, or context-induced state changes), and to explain resonance phenomena in a photic driving experiment. The description of varying states in an ordered sequence gives a principle scheme for the modeling of complex phenomena on multiple time scales. The NMM is matched to the photic driving experiment routinely applied in the diagnosis of such diseases as epilepsy, migraine, schizophrenia and depression. The model reproduces the clinically relevant entrainment effect and predictions are made for improving the experimental setting.Die vorliegende Arbeit stellt einen Beitrag zur Entwicklung und Analyse von Computermodellen zum Verständnis von Hirnfunktionen dar. Es wird die mittlere Aktivität eines Hirnareals analytisch einfach und dabei biologisch plausibel modelliert. Auf Grundlage eines Neuronalen Massenmodells (NMM) werden die Wechsel zwischen Oszillationsregimen (z.B. durch pharmakologisch, epilepsie-, schlaf- oder kontextbedingte Zustandsänderungen) als geordnete Folge beschrieben und Resonanzphänomene in einem Photic-Driving-Experiment erklärt. Dieses NMM kann sehr komplexe Dynamiken (z.B. Chaos) innerhalb biologisch plausibler Parameterbereiche hervorbringen. Um das Verhalten abzuschätzen, wird das NMM als Funktion konstanter Eingangsgrößen und charakteristischer Zeitenkonstanten vollständig auf Bifurkationen untersucht und klassifiziert. Dies ermöglicht die Beschreibung wechselnder Regime als geordnete Folge durch spezifische Eingangstrajektorien. Es wird ein Prinzip vorgestellt, um komplexe Phänomene durch Prozesse verschiedener Zeitskalen darzustellen. Da aufgrund rhythmischer Stimuli und der intrinsischen Rhythmen von Neuronenverbänden die Eingangsgrößen häufig periodisch sind, wird das Verhalten des NMM als Funktion der Intensität und Frequenz einer periodischen Stimulation mittels der zugehörigen Lyapunov-Spektren und der Zeitreihen charakterisiert. Auf der Basis der größten Lyapunov-Exponenten wird das NMM mit dem Photic-Driving-Experiment überein gebracht. Dieses Experiment findet routinemäßige Anwendung in der Diagnostik verschiedener Erkrankungen wie Epilepsie, Migräne, Schizophrenie und Depression. Durch die Anwendung des vorgestellten NMM wird der für die Diagnostik entscheidende Mitnahmeeffekt reproduziert und es werden Vorhersagen für eine Verbesserung der Indikation getroffen

    HUMAN ELECTROENCEPHALOGRAM BASED BIOMARKERS FOR DETECTION OF ALZHEIMER’S DISEASE

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    File embargoed until 31.08.2021 at author's request.Alzheimer’s disease (AD) is a progressive disorder that affects cognitive brain functions and develops many years before there are any clinical manifestations. A biomarker that provides a quantitative measure of changes in the brain in the early stages of AD would therefore be useful for early diagnosis. However, this would involve dealing with large numbers of people because up to 50% of dementia sufferers do not receive a formal diagnosis. Thus, there is a need for accurate, low-cost, robust, and easy to use biomarkers that can be used to detect AD in its early stages. Recent guidelines promote the use of biochemical and neuroimaging biomarkers to improve the diagnosis of AD. Cerebral spinal fluid (CSF) testing for AD is not widely used in clinical practice because it involves an invasive lumbar puncture procedure. Neuroimaging (e.g., positron emission tomography-PET), on the other hand, is expensive, available only in specialist centres, and may be unsuitable for patients with pacemakers or certain other implants. Blood-based biomarkers have shown promising results in terms of AD diagnosis, but these are not yet fully developed and low-cost biosensors to detect such biomarkers do not yet exist. However, electroencephalogram (EEG) based biomarkers can potentially fulfil these needs and play a vital role in the early diagnosis of AD. AD causes changes in EEGs that are thought to be associated with functional disconnections among cortical areas due to the death of brain cells. EEG analysis may therefore provide valuable information about brain dynamics in AD. Potentially, the EEG could be used to detect changes in brain signals even in the preclinical stages of the disease. This means it could be used as a first line decision-support tool in AD diagnosis and complement other AD biomarkers. This thesis describes research into the development of EEG biomarkers that detect AD based on analysis of changes in the EEG. The most characteristic features in AD are slowing of the EEG activities, a decrease in coherence, and a reduction in complexity. These changes can be quantified as a biomarker of AD. In this study, we identified characteristic EEG features that have a significant association with AD. The most promising EEG features were then used to develop EEG biomarkers that can exhibit high diagnostic performance. Four measures of complexity were investigated and evaluated for their suitability as the basis for EEG-based biomarkers of AD: Tsallis entropy, Higuchi Fractal dimension, Lempel-Ziv complexity, and approximation entropy. Two EEG slowing measures were also investigated and evaluated: changes in zero-crossing intervals, and changes in the power spectrum of EEG. In addition, a new approach to quantifying the slowing of EEGs based on analysing changes in EEG amplitudes was developed and evaluated. The coherence of connections among cortical regions of the brain was also investigated to analyse EEG connectivity. A new biomarker was developed based on analysing changes in EEG amplitude (ΔEEGA). This is a marker for the subsequent rate of cognitive and functional decline in AD patients and provides high diagnostic performance. The performance of ΔEEGA measured 100% and 88.88% for sensitivity and specificity, respectively. Our results therefore show that EEG-based measures can potentially be a good biomarker for AD. An important contribution of the thesis is the development of a method to derive robust biomarkers from the EEG through selective band filtering and by combining key biomarkers. Thus, this study provides a framework for constructing robust EEG biomarkers that can be used to detect AD with high diagnostic performance (e.g., in terms of sensitivity and specificity).Ministry of Higher Education and Scientific Research (MoHESR

    Interictal Network Dynamics in Paediatric Epilepsy Surgery

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    Epilepsy is an archetypal brain network disorder. Despite two decades of research elucidating network mechanisms of disease and correlating these with outcomes, the clinical management of children with epilepsy does not readily integrate network concepts. For example, network measures are not used in presurgical evaluation to guide decision making or surgical management plans. The aim of this thesis was to investigate novel network frameworks from the perspective of a clinician, with the explicit aim of finding measures that may be clinically useful and translatable to directly benefit patient care. We examined networks at three different scales, namely macro (whole brain diffusion MRI), meso (subnetworks from SEEG recordings) and micro (single unit networks) scales, consistently finding network abnormalities in children being evaluated for or undergoing epilepsy surgery. This work also provides a path to clinical translation, using frameworks such as IDEAL to robustly assess the impact of these new technologies on management and outcomes. The thesis sets up a platform from which promising computational technology, that utilises brain network analyses, can be readily translated to benefit patient care
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