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Eikeland, R.

Publications and source records attributed to Eikeland, R..

3 recordsLinked to original sources

The within-subject stability of cortical thickness, surface area, and brain volumes across one year

T1-weighted (T1w) imaging is widely used to examine brain structure based on image-derived phenotypes (IDPs) such as cortical thickness, surface area, and brain volumes. The reliability of these IDPs has been extensively explored, mainly focusing on the inter-subject variations, whereas the stability of the within-subject variations has often been overlooked. Additionally, how environmental factors such as time of day and daylight hours impact the structural brain is poorly understood. Therefore, we aimed to address the stability of T1w-derived phenotypes and explore the effecting factors including processing stream, brain region size, time of day, daylight hours, and head movement. Three subjects in their late 20s, early 30s, and early 40s were scanned repeatedly on the same scanner over one year, from which a densely sampled dataset was acquired with 38, 40, and 25 sessions for subjects 1, 2, and 3, respectively. The temporal stability was evaluated using within-subject percentage change and coefficients of variation (CV). The effects of time of day and daylight hours were assessed by fitting general linear models, aggregating the effect size with meta-analysis, and equivalent analysis. The longitudinal processing stream generates more stable results than the cross-sectional processing stream, hence the following results are all derived from the longitudinal processing stream. First and foremost, most IDPs demonstrated percentage changes within 5% and CVs within 2% for almost all brain regions, indicating high stability. Interestingly, we found that the brain region size negatively correlates with the CVs. Specifically, several small brain regions, including the temporal pole, frontal pole, pericalcarine, entorhinal cortex, and accumbens area, showed low stability. In addition, cortical thickness change was strongly and positively correlated with that of volume change while being negatively correlated with change in surface area, illustrating their distinct roles in brain anatomy. Moreover, the time of day could be ignored when evaluating the total surface area and total cortical brain volume but not the average cortical thickness and total subcortical brain volume. Furthermore, daylight hours could be left out when evaluating IDPs since there was no appreciable effect of daylight hours on the IDPs stability. Lastly, apparent head motion causes cortical thickness and volume underestimated and surface area overestimated.

neuroscience↗

The Bergen Breakfast Scanning Club dataset: a deep brain imaging dataset

Populational brain imaging methods based on group averages provide valuable insights into the general functions of the brain. However, they often overlook the inherent inter- and intra-subject variability, limiting our understanding of individual differences. To address this limitation, researchers have turned to big datasets and deep brain imaging datasets. Big datasets enable the exploration of inter-subject variations, while deep brain imaging datasets, involving repeated scanning of multiple subjects over time, offer detailed insights into intra-subject variability. Despite the availability of numerous big datasets, the number of deep brain imaging datasets remains limited. In this article, we present a deep brain imaging dataset derived from the Bergen Breakfast Scanning Club (BBSC) project. The dataset comprises data collected from three subjects who underwent repeated scanning over the course of approximately one year. Specifically, three types of data chunks were collected: behavioral data, functional brain data, and structural brain data. Functional brain images, encompassing magnetic resonance spectroscopy (MRS) and resting-state functional magnetic resonance imaging (fMRI), along with their anatomical reference T1-weighted brain images, were collected twice a week during the data collection period. In total, 38, 40, and 25 sessions of functional data were acquired for subjects 1, 2, and 3, respectively. On the other hand, structural brain images, including T2-weighted brain images, diffusion-weighted images (DWI), and fluid-attenuated inversion recovery (FLAIR) images, were obtained once a month. A total of 10, 9, and 6 sessions were collected for subjects 1, 2, and 3, respectively. The primary objective of this article is to provide a comprehensive description of the data acquisition protocol employed in the BBSC project, as well as detailed insights into the preprocessing steps applied to the acquired data.

neuroscience↗

Brain age predictions in longitudinal data reveal the importance of scan quality and field strength

IntroductionBrain age, the estimation of a persons age from magnetic resonance imaging (MRI) parameters, has been used as a general indicator of health. The marker requires however further validation for application in clinical contexts. Here, we show how brain age predictions perform for for the same individual at various time points and validate our findings with age-matched healthy controls. MethodsWe used densly sampled T1-weighted MRI data from four individuals (from two datasets) to observe how brain age corresponds to age and is influenced by acquision and quality parameters. For validation, we used two cross-sectional datasets. Brain age was predicted by a pre-trained deep learning model. ResultsWe find small within-subject correlations between age and brain age. We also find evidence for the influence of field strength on brain age which replicated in the cross-sectional validation data, and inconclusive effects of scan quality. ConclusionThe absence of maturation effects for the age range in the presented sample, brain age model-bias (including training age distribution and field strength) and model error are potential reasons for small relationships between age and brain age in longitudinal data. Future brain age models should account for differences in field strength and intra-individual differences.

neuroscience↗