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Janssen, N.

Publications and source records attributed to Janssen, N..

4 recordsLinked to original sources

Scale-dependent brain age with higher-order statisticsfrom structural magnetic resonance imaging

Inferring chronological age from magnetic resonance imaging (MRI) brain data has become a valuable tool for the early detection of neurodegenerative diseases. We present a method inspired by cosmological techniques for analyzing galaxy surveys, utilizing higher-order summary statistics with multivariate two- and three-point analyses in 3D Fourier space. This method offers physiological interpretability during the inference, allowing the detection of scales where brain anatomy differs across age groups, providing insights into brain aging processes. Similarly to the evolution of cosmic structures, the brain structure also evolves naturally but displays contrasting behaviors at different scales. On larger scales, structure loss occurs with age, possibly due to ventricular expansion, while smaller scales show increased structure, likely related to decreased cortical thickness and gray/white matter volume. Using MRI data from the OASIS-3 database of 869 sessions, our method predicts chronological age with a Mean Absolute Error (MAE) of 3.1 years, while providing information as a function of scale. A posterior density estimation shows that the 1-{sigma} uncertainty for each individual varies between [~] 2 and 8 years, suggesting that, beyond sample variance, complex genetic or lifestyle-related factors may influence brain aging. We perform a twofold validation of the method. First, we apply the method to the Cam-CAN dataset, yielding a MAE of [~] 5.9 years for the age range from 18 to 88 years. Second, we apply the method to thousands of simulated MRI images generated with a state-of-the-art Latent Diffusion model. This work demonstrates the utility of interdisciplinary research, bridging cosmological methods and neuroscience. PACS87.19.lf, 87.61.Jc, 02.50.Tt, 87.19.lo

neuroscience↗

Dynamic fMRI networks of emotion

The experience of emotions is that of dynamic, time changing processes. Yet, many fMRI studies of emotion average across time to focus on maps of static activations, overlooking the temporal dimension of emotional responses. In this study, we used time-resolved fMRI, group spatial independent component analysis (ICA), dual regression, and Gaussian curve fitting to examine both the spatial and temporal properties of whole-brain networks during a behavioral task. This task included trials that spanned over 25 seconds of watching short, emotionally evocative movie clips, making emotion-related decisions, and an intertrial rest period. We identified four whole-brain networks with unique spatial and temporal features that mapped onto different stages of the task. A network activated early in the course of the task included perceptual and affective evaluation regions, while two later networks supported semantic interpretation and decision-making, and a final network aligned with default mode activity. Both spatial and temporal properties of all four networks were modulated by the emotional content of the movie clips. Our findings extend current models of emotion by integrating temporal dynamics with large-scale network activity, offering a richer framework for understanding how emotions unfold across distributed circuits. Such temporal-spatial markers of emotional processing may prove valuable for identifying and tracking alterations in clinical populations.

neuroscience↗

Age-related constraints on the spatial geometry of the brain

Age-related structural brain changes may be better captured by assessing complex spatial geometric differences rather than isolated changes to individual regions. We applied a novel analytic method to quantify age-related changes to the spatial anatomy of the brain by measuring expansion and compression of global brain shape and the distance between cross-hemisphere homologous regions. To test how global brain shape and regional distances are affected by aging, we analyzed 2,603 structural MRIs (range: 30-97 years). Increasing age was associated with global shape expansion across inferior-anterior gradients, global compression across superior-posterior gradients, and regional expansion between frontotemporal homologues. Specific patterns of global and regional expansion and compression were further associated with clinical impairment and distinctly related to deficits in various cognitive domains. These findings suggest that changes to the complex spatial anatomy and geometry of the aging brain may be associated with reduced efficiency and cognitive dysfunction in older adults.

neuroscience↗

Heterogeneity of morphometric similarity networks in health and schizophrenia

IntroductionMorphometric similarity is a recently developed neuroimaging phenotype of inter-regional connectivity by quantifying the similarity of a region to other regions based on multiple MRI parameters. Altered average morphometric similarity has been reported in psychotic disorders at the group level, with considerable heterogeneity across individuals. We used normative modeling to address cross-sectional and longitudinal inter-individual heterogeneity of morphometric similarity in health and schizophrenia. MethodsMorphometric similarity for 62 cortical regions was obtained from baseline and follow-up T1-weighted scans of healthy individuals and patients with chronic schizophrenia. Cortical regions were classified into seven predefined brain functional networks. Using Bayesian Linear Regression and taking into account age, sex, image quality and scanner, we trained and validated normative models in healthy controls from eleven datasets (n = 4310). Individual deviations from the norm (z-scores) in morphometric similarity were computed for each participant for each network and region at both timepoints. A z-score [greater double equals] than 1.96 was considered supra-normal and a z-score [less double equals] -1.96 infra-normal. As a longitudinal metric, we calculated the change over time of the total number of infra- or supra-normal regions per participant. ResultsAt baseline, patients with schizophrenia had decreased morphometric similarity of the default mode network and increased morphometric similarity of the somatomotor network when compared with healthy controls. The percentage of patients with infra- or supra-normal values for any region at baseline and follow-up was low (<6%) and did not differ from healthy controls. Mean intra-group changes over time in the total number of infra- or supra-normal regions were small in schizophrenia and healthy control groups (<1) and there were no significant between-group differences. ConclusionsIn a case-control setting, a decrease of morphometric similarity within the default mode network may be a robust finding implicated in schizophrenia. However, normative modeling suggests that significant reductions and changes over time of regional morphometric similarity are evident only in a minority of patients.

neuroscience↗