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Bengtsson, T.

Publications and source records attributed to Bengtsson, T..

2 recordsLinked to original sources

MORPH2DIAG: Automated Structural MRI Preprocessing and Tissue Segmentation for Interpretable Machine and Deep Learning-Based Neuroanatomical Classification

Structural MRI provides a noninvasive window into brain morphology, yet the reproducibility and interpretability of morphometric analyses remain limited by inconsistent preprocessing, variable spatial alignment, and heterogeneous feature construction. We introduce MORPH2DIAG, a fully automated, atlas-free morphometric pipeline that integrates standardized preprocessing, tissue segmentation, spatial normalization, data-driven subtyping, and machine- and deep-learning classification within a single, modular framework. The pipeline performs intensity normalization, morphological cleanup, PCA-informed affine alignment, isotropic rescaling, and Gaussian Mixture Model (GMM) segmentation to generate quantitative gray-matter (GM), white-matter (WM), and cerebrospinal-fluid (CSF) maps. Global tissue fractions were used to derive latent neuroanatomical subtypes via unsupervised K-means clustering, revealing progressive GM-CSF gradients consistent with patterns commonly observed along normative-to-atrophic structural continua observed in neurodegeneration. To capture finer-grained spatial heterogeneity, a voxel-wise K-means parcellation yielded parcel-level intensity means and variances that served as regional morphometric descriptors. These global and parcel-level features were integrated into a unified evaluation suite comparing classical machine learning models (Random Forests, Logistic Regression, XGBoost) with lean, deep, and hybrid multilayer perceptrons (MLPs) trained using focal loss, label smoothing, stochastic weight averaging, and nested cross-validation with PCA-based dimensionality reduction. Across methods, the hybrid MLP achieved the highest macro-F1 and balanced accuracy, demonstrating strong discriminative performance for the discovered morphometric subtypes. Collectively, MORPH2DIAG establishes a fully automated, atlas-free framework that unites unsupervised structural subtype discovery with interpretable machine and deep learning, providing a reproducible foundation for MRI-based morphometric profiling and automated detection of neurodegenerative-like patterns.

neuroscience↗

The metabolically protective energy expenditure increase of Pik3r1-related insulin resistance is not explained by Ucp1-mediated thermogenesis

Human SHORT syndrome is caused by dominant negative human PIK3R1 mutations that impair insulin-stimulated phosphoinositide 3-kinase (PI3K) activity. This produces severe insulin resistance (IR) and often reduced adiposity, commonly described as lipodystrophy. However unlike human primary lipodystrophies, SHORT syndrome does not feature fatty liver or dyslipidaemia. Pik3r1Y657*/WT (Pik3r1Y657*) mice metabolically phenocopy humans, moreover exhibiting increased energy expenditure. We have hypothesised that this increased energy expenditure explains protection from lipotoxicity, and suggested that understanding its mechanism may offer novel approaches to mitigating the metabolic syndrome. We thus set out to determine whether increased Ucp1-dependent thermogenesis explains the increased energy expenditure in Pik3r1-related IR. Male and female Pik3r1Y657* mice challenged with a 45% fat diet for 3 weeks at 21{degrees}C showed reduced metabolic efficiency not explained by changes in food intake or physical activity. No changes were seen in thermoregulation, assessed by thermal imaging and a modified Scholander protocol. Ucp1-dependent thermogenesis, assessed by norepinephrine-induced oxygen consumption, was also unaltered. Housing at 30{degrees}C did not alter the metabolic phenotype of male Pik3r1Y657* mice, but led to lowered physical activity in female Pik3r1Y657* mice compared to controls. Nevertheless these mice still exhibited increased energy expenditure. Ucp1-dependent thermogenic capacity at 30{degrees}C was similar in Pik3r1Y657* and WT mice. We conclude that the likely metabolically protective energy leak in Pik3r1-related IR is not caused by Ucp1-mediated BAT hyperactivation, nor impaired thermal insulation. Further metabolic studies are required to seek alternative explanations such as non Ucp1-mediated futile cycling. New and NoteworthyUnderstanding how Pik3r1Y657* mice and humans are protected from lipotoxicity despite insulin resistance may suggest new ways to mitigate metabolic syndrome. We find reduced metabolic efficiency and increased energy expenditure in Pik3r1Y657* mice but no differences in locomotion, thermoregulation or Ucp1-dependent thermogenesis. Protective energy expenditure in Pik3r1-related insulin resistance has an alternative, likely metabolic, explanation

physiology↗