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• Gaiser, Carolin; Vliet, Rick van der; Boer, Augustijn A. A. de; Donchin, Opher; Berthet, Pierre Guillaume Raphael & Devenyi, Gabriel A. [Vis alle 11 forfattere av denne artikkelen] (2024). Population-wide cerebellar growth models of children and adolescents. Nature Communications. 15. doi: 10.1038/s41467-024-46398-2. Fulltekst i vitenarkiv Vis sammendrag

  In the past, the cerebellum has been best known for its crucial role in motor function. However, increasingly more findings highlight the importance of cerebellar contributions in cognitive functions and neurodevelopment. Using a total of 7240 neuroimaging scans from 4862 individuals, we describe and provide detailed, openly available models of cerebellar development in childhood and adolescence (age range: 6–17 years), an important time period for brain development and onset of neuropsychiatric disorders. Next to a traditionally used anatomical parcellation of the cerebellum, we generated growth models based on a recently proposed functional parcellation. In both, we find an anterior-posterior growth gradient mirroring the age-related improvements of underlying behavior and function, which is analogous to cerebral maturation patterns and offers evidence for directly related cerebello-cortical developmental trajectories. Finally, we illustrate how the current approach can be used to detect cerebellar abnormalities in clinical samples.

• Gaiser, C.; Berthet, Pierre Guillaume Raphael; Kia, S.M.; Frens, M.A.; Beckmann, C.F. & Muetzel, R.L. [Vis alle 7 forfattere av denne artikkelen] (2024). Estimating cortical thickness trajectories in children across different scanners using transfer learning from normative models. Human Brain Mapping. ISSN 1065-9471. 45(2). doi: 10.1002/hbm.26565. Fulltekst i vitenarkiv Vis sammendrag

  This work illustrates the use of normative models in a longitudinal neuroimaging study of children aged 6–17 years and demonstrates how such models can be used to make meaningful comparisons in longitudinal studies, even when individuals are scanned with different scanners across successive study waves. More specifically, we first estimated a large-scale reference normative model using Hierarchical Bayesian Regression from N = 42,993 individuals across the lifespan and from dozens of sites. We then transfer these models to a longitudinal developmental cohort (N = 6285) with three measurement waves acquired on two different scanners that were unseen during estimation of the reference models. We show that the use of normative models provides individual deviation scores that are independent of scanner effects and efficiently accommodate inter-site variations. Moreover, we provide empirical evidence to guide the optimization of sample size for the transfer of prior knowledge about the distribution of regional cortical thicknesses. We show that a transfer set containing as few as 25 samples per site can lead to good performance metrics on the test set. Finally, we demonstrate the clinical utility of this approach by showing that deviation scores obtained from the transferred normative models are able to detect and chart morphological heterogeneity in individuals born preterm.

• Worker, Amanda; Berthet, Pierre Guillaume Raphael; Lawrence, Andrew J.; Kia, Seyed Mostafa; Arango, Celso & Dinga, Richard [Vis alle 18 forfattere av denne artikkelen] (2023). Extreme deviations from the normative model reveal cortical heterogeneity and associations with negative symptom severity in first-episode psychosis from the OPTiMiSE and GAP studies. Translational Psychiatry. 13(1). doi: 10.1038/s41398-023-02661-6. Fulltekst i vitenarkiv Vis sammendrag

  Abstract There is currently no quantifiable method to predict long-term clinical outcomes in patients presenting with a first episode of psychosis. A major barrier to developing useful markers for this is biological heterogeneity, where many different pathological mechanisms may underly the same set of symptoms in different individuals. Normative modelling has been used to quantify this heterogeneity in established psychotic disorders by identifying regions of the cortex which are thinner than expected based on a normative healthy population range. These brain atypicalities are measured at the individual level and therefore potentially useful in a clinical setting. However, it is still unclear whether alterations in individual brain structure can be detected at the time of the first psychotic episode, and whether they are associated with subsequent clinical outcomes. We applied normative modelling of cortical thickness to a sample of first-episode psychosis patients, with the aim of quantifying heterogeneity and to use any pattern of cortical atypicality to predict symptoms and response to antipsychotic medication at timepoints from baseline up to 95 weeks (median follow-ups = 4). T1-weighted brain magnetic resonance images from the GAP and OPTiMiSE samples were processed with Freesurfer V6.0.0 yielding 148 cortical thickness features. An existing normative model of cortical thickness ( n  = 37,126) was adapted to integrate data from each clinical site and account for effects of gender and site. Our test sample consisted of control participants ( n  = 149, mean age = 26, SD = 6.7) and patient data ( n  = 295, mean age = 26, SD = 6.7), this sample was used for estimating deviations from the normative model and subsequent statistical analysis. For each individual, the 148 cortical thickness features were mapped to centiles of the normative distribution and converted to z-scores reflecting the distance from the population mean. Individual cortical thickness metrics of +/– 2.6 standard deviations from the mean were considered extreme deviations from the norm. We found that no more than 6.4% of psychosis patients had extreme deviations in a single brain region (regional overlap) demonstrating a high degree of heterogeneity. Mann-Whitney U tests were run on z-scores for each region and significantly lower z-scores were observed in FEP patients in the frontal, temporal, parietal and occipital lobes. Finally, linear mixed-effects modelling showed that negative deviations in cortical thickness in parietal and temporal regions at baseline are related to more severe negative symptoms over the medium-term. This study shows that even at the early stage of symptom onset normative modelling provides a framework to identify individualised cortical markers which can be used for early personalised intervention and stratification.

• Rutherford, Saige; Kia, Seyed Mostafa; Wolfers, Thomas; Fraza, Charlotte; Zabihi, Mariam & Dinga, Richard [Vis alle 12 forfattere av denne artikkelen] (2022). The normative modeling framework for computational psychiatry. Nature Protocols. ISSN 1754-2189. 17(7), s. 1711–1734. doi: 10.1038/s41596-022-00696-5. Fulltekst i vitenarkiv
• Rutherford, Saige; Fraza, Charlotte; Dinga, Richard; Kia, Seyed Mostafa; Wolfers, Thomas & Zabihi, Mariam [Vis alle 32 forfattere av denne artikkelen] (2022). Charting brain growth and aging at high spatial precision. eLIFE. 11. doi: 10.7554/ELIFE.72904. Fulltekst i vitenarkiv Vis sammendrag

  Defining reference models for population variation, and the ability to study individual deviations is essential for understanding inter-individual variability and its relation to the onset and progression of medical conditions. In this work, we assembled a reference cohort of neuroimaging data from 82 sites (N=58,836; ages 2–100) and used normative modeling to characterize lifespan trajectories of cortical thickness and subcortical volume. Models are validated against a manually quality checked subset (N=24,354) and we provide an interface for transferring to new data sources. We showcase the clinical value by applying the models to a transdiagnostic psychiatric sample (N=1985), showing they can be used to quantify variability underlying multiple disorders whilst also refining case-control inferences. These models will be augmented with additional samples and imaging modalities as they become available. This provides a common reference platform to bind results from different studies and ultimately paves the way for personalized clinical decision-making.

• Kia, Seyed Mostafa; Huijsdens, Hester; Rutherford, Saige; Boer, Augustijn de; Dinga, Richard & Wolfers, Thomas [Vis alle 12 forfattere av denne artikkelen] (2022). Closing the life-cycle of normative modeling using federated hierarchical Bayesian regression. PLOS ONE. 17:e0278776(12), s. 1–29. doi: 10.1371/journal.pone.0278776. Fulltekst i vitenarkiv Vis sammendrag

  Clinical neuroimaging data availability has grown substantially in the last decade, providing the potential for studying heterogeneity in clinical cohorts on a previously unprecedented scale. Normative modeling is an emerging statistical tool for dissecting heterogeneity in complex brain disorders. However, its application remains technically challenging due to medical data privacy issues and difficulties in dealing with nuisance variation, such as the variability in the image acquisition process. Here, we approach the problem of estimating a reference normative model across a massive population using a massive multi-center neuroimaging dataset. To this end, we introduce a federated probabilistic framework using hierarchical Bayesian regression (HBR) to complete the life-cycle of normative modeling. The proposed model provides the possibilities to learn, update, and adapt the model parameters on decentralized neuroimaging data. Our experimental results confirm the superiority of HBR in deriving more accurate normative ranges on large multi-site neuroimaging datasets compared to the current standard methods. In addition, our approach provides the possibility to recalibrate and reuse the learned model on local datasets and even on datasets with very small sample sizes. The proposed method will facilitate applications of normative modeling as a medical tool for screening the biological deviations in individuals affected by complex illnesses such as mental disorders.

• Pedersen, Mads Lund; Alnæs, Dag; Meer, Dennis van der; Fernandez-Cabello, Sara; Berthet, Pierre Guillaume Raphael & Dahl, Andreas [Vis alle 12 forfattere av denne artikkelen] (2022). Computational Modeling of the n-Back Task in the ABCD Study: Associations of Drift Diffusion Model Parameters to Polygenic Scores of Mental Disorders and Cardiometabolic Diseases. Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. ISSN 2451-9022. doi: 10.1016/j.bpsc.2022.03.012. Fulltekst i vitenarkiv Vis sammendrag

  Background Cognitive dysfunction is common in mental disorders and represents a potential risk factor in childhood. The nature and extent of associations between childhood cognitive function and polygenic risk for mental disorders is unclear. We applied computational modeling to gain insight into mechanistic processes underlying decision making and working memory in childhood and their associations with polygenic risk scores (PRSs) for mental disorders and comorbid cardiometabolic diseases. Methods We used the drift diffusion model to infer latent computational processes underlying decision making and working memory during the n-back task in 3707 children ages 9 to 10 years from the Adolescent Brain Cognitive Development (ABCD) Study. Single nucleotide polymorphism–based heritability was estimated for cognitive phenotypes, including computational parameters, aggregated n-back task performance, and neurocognitive assessments. PRSs were calculated for Alzheimer’s disease, bipolar disorder, coronary artery disease (CAD), major depressive disorder, obsessive-compulsive disorder, schizophrenia, and type 2 diabetes. Results Heritability estimates of cognitive phenotypes ranged from 12% to 38%. Bayesian mixed models revealed that slower accumulation of evidence was associated with higher PRSs for CAD and schizophrenia. Longer nondecision time was associated with higher PRSs for Alzheimer’s disease and lower PRSs for CAD. Narrower decision threshold was associated with higher PRSs for CAD. Load-dependent effects on nondecision time and decision threshold were associated with PRSs for Alzheimer’s disease and CAD, respectively. Aggregated neurocognitive test scores were not associated with PRSs for any of the mental or cardiometabolic phenotypes. Conclusions We identified distinct associations between computational cognitive processes and genetic risk for mental illness and cardiometabolic disease, which could represent childhood cognitive risk factors.

• Wolfers, Thomas; Rokicki, Jaroslav; Alnæs, Dag; Berthet, Pierre; Agartz, Ingrid & Kia, Seyed Mostafa [Vis alle 14 forfattere av denne artikkelen] (2021). Replicating extensive brain structural heterogeneity in individuals with schizophrenia and bipolar disorder. Human Brain Mapping. ISSN 1065-9471. 42(8), s. 2546–2555. doi: 10.1002/hbm.25386. Fulltekst i vitenarkiv Vis sammendrag

  Identifying brain processes involved in the risk and development of mental disorders is a major aim. We recently reported substantial interindividual heterogeneity in brain structural aberrations among patients with schizophrenia and bipolar disorder. Estimating the normative range of voxel-based morphometry (VBM) data among healthy individuals using a Gaussian process regression (GPR) enables us to map individual deviations from the healthy range in unseen datasets. Here, we aim to replicate our previous results in two independent samples of patients with schizophrenia (n1 = 94; n2 = 105), bipolar disorder (n1 = 116; n2 = 61), and healthy individuals (n1 = 400; n2 = 312). In line with previous findings with exception of the cerebellum our results revealed robust group level differences between patients and healthy individuals, yet only a small proportion of patients with schizophrenia or bipolar disorder exhibited extreme negative deviations from normality in the same brain regions. These direct replications support that group level-differences in brain structure disguise considerable individual differences in brain aberrations, with important implications for the interpretation and generalization of group-level brain imaging findings to the individual with a mental disorder.

• Buccino, Alessio Paolo; Kuchta, Miroslav; Jæger, Karoline Horgmo; Ness, Torbjørn V; Berthet, Pierre & Mardal, Kent-Andre [Vis alle 8 forfattere av denne artikkelen] (2019). How does the presence of neural probes affect extracellular potentials? Journal of Neural Engineering. ISSN 1741-2560. 16(2). doi: 10.1088/1741-2552/ab03a1. Fulltekst i vitenarkiv Vis sammendrag

  Objective. Mechanistic modeling of neurons is an essential component of computational neuroscience that enables scientists to simulate, explain, and explore neural activity. The conventional approach to simulation of extracellular neural recordings first computes transmembrane currents using the cable equation and then sums their contribution to model the extracellular potential. This two-step approach relies on the assumption that the extracellular space is an infinite and homogeneous conductive medium, while measurements are performed using neural probes. The main purpose of this paper is to assess to what extent the presence of the neural probes of varying shape and size impacts the extracellular field and how to correct for them. Approach. We apply a detailed modeling framework allowing explicit representation of the neuron and the probe to study the effect of the probes and thereby estimate the effect of ignoring it. We use meshes with simplified neurons and different types of probe and compare the extracellular action potentials with and without the probe in the extracellular space. We then compare various solutions to account for the probes' presence and introduce an efficient probe correction method to include the probe effect in modeling of extracellular potentials. Main results. Our computations show that microwires hardly influence the extracellular electric field and their effect can therefore be ignored. In contrast, multi-electrode arrays (MEAs) significantly affect the extracellular field by magnifying the recorded potential. While MEAs behave similarly to infinite insulated planes, we find that their effect strongly depends on the neuron-probe alignment and probe orientation. Significance. Ignoring the probe effect might be deleterious in some applications, such as neural localization and parameterization of neural models from extracellular recordings. Moreover, the presence of the probe can improve the interpretation of extracellular recordings, by providing a more accurate estimation of the extracellular potential generated by neuronal models.

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• Berthet, Pierre; Hagen, Espen; Ness, Torbjørn V & Einevoll, Gaute (2018). Selectivity and sensitivity of cortical neurons to electric stimulation using ECoG electrode arrays. Fulltekst i vitenarkiv

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