Mu, beta, and gamma rhythms increase and decrease in amplitude during movement. This event-related synchronization (ERS) and desynchronization (ERD) can be readily recorded non-invasively using magneto- and electro-encephalography (M/EEG). In addition, event-related potentials and fields (i.e., evoked responses) can be elucidated during movement. There is some evidence that the frequency, amplitude and latency of the movement-related ERS/ERD changes with ageing, however the evidence surrounding this topic comes mainly from studies in sample sizes on the order of tens of participants. The objective of this study was to examine a large open-access MEG dataset for age-related changes in movement-related ERS/ERD and evoked responses. MEG data acquired at the Cambridge Centre for Ageing and Neuroscience during cued button pressing was used from 567 participants between the ages of 18 and 88 years. The characteristics movement-related ERD/ERS and evoked responses were calculated for each individual participant. Based on linear regression analysis, significant relationships were found between participant age and some response characteristics, although the predictive value of these relationships was low. Specifically, we conclude that peak beta rebound frequency and amplitude decreased with age, peak beta suppression amplitude increased with age, movement-related gamma burst amplitude decreased with age, and peak motor-evoked response amplitude increased with age. Given our current understanding of the underlying mechanisms of these responses, our findings suggest the existence of age-related changes in the neurophysiology of thalamocortical loops and local circuitry in the primary somatosensory and motor cortices.

Two techniques for analyzing human extracranial neurophysiological signals, namely the periodic/aperiodic parameterization of neural power spectra and the transient events framework of oscillatory activity, have recently emerged in the scientific literature. In this work, we integrate these two analysis perspectives to analyze extracranial neurophysiological signals as a series of transient rhythmic events disambiguated from the background aperiodic activity. We call this novel technique the periodic/aperiodic parametrization of transient oscillations (PAPTO). We demonstrate PAPTO by investigating resting-state sensorimotor magnetoencephalography recordings from the Cambridge Center for Ageing and Neuroscience cross-sectional study on healthy ageing (n = 600, ages 18-88). We show that PAPTO is more sensitive to neocortical transient beta rhythms compared to more conventional transient event detection algorithms and captures more variance in the resting-state occurrence rate of beta events across participants. The improved sensitivity of PAPTO reveals that the beta occurrence rate almost doubles over the adult lifespan which we discuss in terms of thalamocortical beta generation in the somatosensory cortex and the age-related decline of sensory perception.

Non-invasive neurophysiological recordings, such as those measured by magnetoencelography (MEG), provide insight into the behaviour of neural networks and how these networks change with factors such as task performance, disease state, and age. Recently, there has been a trend in describing neurophysiological recordings as a series of transient bursts of neural activity rather than averaged sustained oscillations as burst characteristics may be more directly correlated with the neurological generators of brain activity. In this work, we investigate how beta burst characteristics change with age in a large open access dataset. The objectives are (1) to detect and characterize transient beta bursts over the ipsilateral and contralateral primary sensorimotor cortices during a unilateral motor task performance and during wakeful resting, and (2) to identify age-related changes in beta burst characteristics, in the context of earlier reports of age-related changes in beta suppression and the post-movement beta rebound. MEG data, acquired at the Cambridge Centre for Ageing and Neuroscience, of roughly 600 participants with a nearly uniform distribution of ages between 18 and 88 years old was used for analysis. We found that burst rate is the predominant factor related to age-related changes in the amplitude of the induced beta rhythm responses associated with a button press task. Furthermore, we present a cross-validation of burst parameters detected at the sensor- (peak sensor and sensor ROI) and source-level (beamformer spatial filter). This work is as an important step in characterizing transient bursts in neuromagnetic signals in the temporal domain, towards a better understanding of the healthy aging human brain.

Accuracy in localizing the brain areas that generate neuromagnetic activity in magnetoencephalography (MEG) is dependent on properly co-registering MEG data to the participant’s structural magnetic resonance image (MRI). Effective MEG-MRI co-registration is, in turn, dependent on how accurately we can digitize anatomical landmarks on the surface of the head. In this study, we compared the performance of three devices —Polhemus electromagnetic system, NextEngine laser scanner and Microsoft Kinect for Windows — for source localization accuracy and MEG-MRI co-registration. A calibrated phantom was used for verifying the source localization accuracy. The Kinect improved source localization accuracy over the Polhemus and the laser scanner by 2.23 mm (137%) and 0.81 mm (50%), respectively. MEG-MRI co-registration accuracy was verified on data from five healthy human participants, who received the digitization process using all three devices. The Kinect device captured approximately 2000 times more surface points than the Polhemus in one third of the time (one minute compared to three minutes) and thrice as many points as the NextEngine laser scanner. Following automated surface matching, the calculated mean MEG-MRI co-registration error for the Kinect was improved by 2.85 mm with respect to the Polhemus device, and equivalent to the laser scanner. Importantly, the Kinect device automatically aligns 20-30 images per second in real-time, reducing the limitations on participant head movement during digitization that are implicit in NextEngine laser scan (~1 minute). We conclude that the Kinect scanner is an effective device for head digitization in MEG, providing the necessary accuracy in source localization and MEG-MRI co-registration, while reducing digitization time.

Interpreting neurophysiology recordings as a series of transient bursts with varying temporal and spectral characteristics provides meaningful insight into mechanisms underlying neural networks. Previous research has revealed age-related changes in the time-frequency dynamics of sensorimotor beta bursts, but to date, there has been little focus on the spatial localization of these beta bursts or how the localization patterns change with normal healthy ageing. The objective of the current study is to implement existing source localization algorithms for use in the detection of the cortical sources of transient beta bursts, and to uncover age-related trends in the resulting source localization patterns. Two well-established source localization algorithms (minimum-norm estimation and beamformer) were applied to localize beta bursts detected over the sensorimotor cortices in a cohort of 561 healthy participants between the ages of 18 and 88 (CamCAN open access dataset). Age-related trends were then investigated by applying regression analysis between participant age and average source power within several cortical regions of interest. This analysis revealed that beta bursts localized primarily to the sensorimotor cortex ipsilateral to the side of the sensor used for their detection. Region of interest analysis revealed that there were age-related changes in the beta burst localization pattern, with most substantial changes evidenced in frontal brain regions. In addition, regression analysis revealed a tendency of age-related trends to peak around 60 years of age suggesting that 60 is a potential critical age in this population. These results show for the first time that source localization techniques can be implemented for the identification of the sources of transient beta bursts. The exploration of these sources provides us with insight into the anatomical generators of transient beta activity and how they change across the lifespan.