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Crainiceanu, C. M.

Publications and source records attributed to Crainiceanu, C. M..

2 recordsLinked to original sources

Exploring Links between Brain Image-Derived Phenotypes and Accelerometer-Measured Physical Activity in the UK Biobank

A broad range of neurodegenerative disorders are associated with altered functional connectivity (FC) patterns and atrophy of gray matter volume (GMV). Similarly, there are links between physical activity (PA) and a number of neurodegenerative disorders. However, studies investigating the link between brain image-derived phenotypes (IDPs) and PA remain limited. Using data from the UK Biobank, we investigated the multivariate association between two sets of brain IDPs (related to FC and GMV) and PA using canonical correlation analysis (CCA). We further quantified the importance of individual PA variables in modeling each set of IDPs using both supervised and unsupervised approaches, and assessed their predictive performance for individual brain phenotypes. Finally, we evaluated the predictive performance of brain IDPs and PA variables for diabetes, stroke, coronary heart disease (CHD), and cancer using nested logistic regression models, with their relative contributions to explained variation in disease status quantified using a coefficient of determination specifically designed for logistic regression. Our analyses identified a statistically robust but low-dimensional axis of shared variation between PA and FC (canonical correlation r = 0.50), whereas the corresponding association between PA and GMV was weaker (r = 0.19). Brain features contributing most strongly to these associations were located in motor- and attention-related networks. Across predictive models, a small set of correlated PA measures reflecting activity intensity and circadian rhythm consistently emerged as representative predictors of both FC and GMV variation. Finally, we found that PA variables demonstrated greater predictive utility than either FC or GMV alone, particularly for CHD and diabetes, as assessed by both the area under the receiver operating characteristic (ROC) curve (AUC) and the proportion of explained variation. Together, these findings indicate that objectively measured PA is strongly associated with a set of motor-related brain features and provides substantial predictive information for cardiometabolic disease risk, while cross-sectional neuroimaging measures offer more modest incremental explanatory value.

neuroscience↗

MISPEL: A deep learning approach for harmonizingmulti-scanner matched neuroimaging data

Large-scale data obtained from aggregation of already collected multi-site neuroimaging datasets has brought benefits such as higher statistical power, reliability, and robustness to the studies. Despite these promises from growth in sample size, substantial technical variability stemming from differences in scanner specifications exists in the aggregated data and could inadvertently bias any downstream analyses on it. Such a challenge calls for data normalization and/or harmonization frameworks, in addition to comprehensive criteria to estimate the scanner-related variability and evaluate the harmonization frameworks. In this study, we propose MISPEL (Multi-scanner Image harmonization via Structure Preserving Embedding Learning), a supervised multi-scanner harmonization method that is naturally extendable to more than two scanners. We also designed a set of criteria to investigate the scanner-related technical variability and evaluate the harmonization techniques. As an essential requirement of our criteria, we introduced a multi-scanner matched dataset of 3T T1 images across four scanners, which, to the best of our knowledge is one of the few datasets of this kind. We also investigated our evaluations using two popular segmentation frameworks: FSL and segmentation in statistical parametric mapping (SPM). Lastly, we compared MISPEL to popular methods of normalization and harmonization, namely White Stripe, RAVEL, and CALAMITI. MISPEL outperformed these methods and is promising for many other neuroimaging modalities.

neuroscience↗