14 research outputs found
Extraction of features from sleep EEG for Bayesian assessment of brain development
Brain development can be evaluated by experts analysing age-related patterns in sleep electroencephalograms (EEG). Natural variations in the patterns, noise, and artefacts affect the evaluation accuracy as well as experts' agreement. The knowledge of predictive posterior distribution allows experts to estimate confidence intervals within which decisions are distributed. Bayesian approach to probabilistic inference has provided accurate estimates of intervals of interest. In this paper we propose a new feature extraction technique for Bayesian assessment and estimation of predictive distribution in a case of newborn brain development assessment. The new EEG features are verified within the Bayesian framework on a large EEG data set including 1,100 recordings made from newborns in 10 age groups. The proposed features are highly correlated with brain maturation and their use increases the assessment accuracy
Informativeness of sleep cycle features in Bayesian assessment of newborn electroencephalographic maturation
Clinical experts assess the newborn brain development by analyzing and interpreting maturity-related features in sleep EEGs. Typically, these features widely vary during the sleep hours, and their informativeness can be different in different sleep stages. Normally, the level of muscle and electrode artifacts during the active sleep stage is higher than that during the quiet sleep that could reduce the informative-ness of features extracted from the active stage. In this paper, we use the methodology of Bayesian averaging over Decision Trees (DTs) to assess the newborn brain maturity and explore the informativeness of EEG features extracted from different sleep stages. This methodology has been shown providing the most accurate inference and estimates of uncertainty, while the use of DT models enables to find the EEG features most important for the brain maturity assessment
Feature extraction from electroencephalograms for Bayesian assessment of newborn brain maturity
We explored the feature extraction techniques for Bayesian assessment of EEG maturity of newborns in the context that the continuity of EEG is the most important feature for assessment of the brain development. The continuity is associated with EEG âstationarityâ which we propose to evaluate with adaptive segmentation of EEG into pseudo-stationary intervals. The histograms of these intervals are then used as new features for the assessment of EEG maturity. In our experiments, we used Bayesian model averaging over decision trees to differentiate two age groups, each included 110 EEG recordings. The use of the proposed EEG features has shown, on average, a 6% increase in the accuracy of age differentiation
Bayesian Assessment of Newborn Brain Maturity from Two-Channel Sleep Electroencephalograms
Newborn brain maturity can be assessed by expert analysis of maturity-related patterns recognizable in polysomnograms. Since 36 weeks most of these patterns become recognizable in EEG exclusively, particularly, in EEG recorded via the two central-temporal channels. The use of such EEG recordings enables experts to minimize the disturbance of sleep, preparation time as well as the movement artifacts. We assume that the brain maturity of newborns aged 36 weeks and older can be automatically assessed from the 2-channel sleep EEG as accurately as by expert analysis of the full polysomnographic information. We use Bayesian inference to test this assumption and assist experts to obtain the full probabilistic information on the EEG assessments. The Bayesian methodology is feasibly implemented with Monte Carlo integration over areas of high posterior probability density, however the existing techniques tend to provide biased assessments in the absence of prior information required to explore a model space in detail within a reasonable time. In this paper we aim to use the posterior information about EEG features to reduce possible bias in the assessments. The performance of the proposed method is tested on a set of EEG recordings
Feature extraction with GMDH-type neural networks for EEG-based person identification
The brain activity observed on EEG electrodes is influenced by volume conduction and functional connectivity of a person performing a task. When the task is a biometric test the EEG signals represent the unique âbrain printâ, which is defined by the functional connectivity that is represented by the interactions between electrodes, whilst the conduction components cause trivial correlations. Orthogonalization using autoregressive modeling minimizes the conduction components, and then the residuals are related to features correlated with the functional connectivity. However, the orthogonalization can be unreliable for high-dimensional EEG data. We have found that the dimensionality can be significantly reduced if the baselines required for estimating the residuals can be modeled by using relevant electrodes. In our approach, the required models are learnt by a Group Method of Data Handling (GMDH) algorithm which we have made capable of discovering reliable models from multidimensional EEG data. In our experiments on the EEG-MMI benchmark data which include 109 participants, the proposed method has correctly identified all the subjects and provided a statistically significant (p<0.01) improvement of the identification accuracy. The experiments have shown that the proposed GMDH method can learn new features from multi-electrode EEG data, which are capable to improve the accuracy of biometric identification
Bayesian assessment of newborn brain maturity from sleep electroencephalograms
A thesis submitted to the University of Bedfordshire, in partial fulfilment of the requirements for the degree of Doctor of PhilosophyIn this thesis, we develop and test a technology for computer-assisted assessments of newborn brain maturity from sleep electroencephalogram (EEG). Brain maturation of newborns is reflected in rapid development of EEG patterns over a number of weeks after conception. Observing the maturational patterns, experts
can assess newbornâs EEG maturity with an accuracy ±2 weeks of newbornâs stated age. A mismatch between the EEG patterns and newbornâs physiological age alerts clinicians about possible neurological problems. Analysis of newborn
EEG requires specialised skills to recognise the maturity-related waveforms and patterns and interpret them in the context of newborns age and behavioural state. It is highly desirable to make the results of maturity assessment most
accurate and reliable. However, the expert analysis is limited in capability to estimate the uncertainty in assessments. To enable experts quantitatively evaluate risks of brain dysmaturity for each case, we employ the Bayesian model
averaging methodology. This methodology, in theory, provides the most accurate assessments along with the estimates of uncertainty, enabling experts to take into account the full information about the risk of decision making. Such
information is particularly important when assessing the EEG signals which are highly variable and corrupted by artefacts. The use of decision tree models within the Bayesian averaging enables interpreting the results as a set of rules
and finding the EEG features which make the most important contribution to assessments. The developed technology was tested on approximately 1,000 EEG recordings of newborns aged 36 to 45 weeks post conception, and the accuracy
of assessments was comparable to that achieved by EEG experts. In addition, it was shown that the Bayesian assessment can be used to quantitatively evaluate the risk of brain dysmaturity for each EEG recording
Amplitude variability over sleep stages.
<p>a) A 120-min sleep EEG recorded from a newborn at age of 44 weeks, b) <i>ÎŒ</i> (Red) and <i>Ï</i> (Black) are the parameters of the distribution of AV extracted from EEG.</p
Segmentation results.
<p>Segment rates, <i>sr</i>, for different EEG patterns: a) discontinuous pattern at 36 weeks, b) semi-discontinuous pattern at 38 weeks, c) and d) continuous patterns at 41 weeks.</p