Background: Acquired brain injury (ABI) often produces heterogeneous cognitive and emotional outcomes that are not fully explained by conventional neuropsychological testing. Diffusion tensor imaging (DTI) tractography may capture patient-specific patterns of white matter connectivity and thereby complement clinical assessment. Methods: We conducted an exploratory case series of nine patients in the subacute phase of ABI (traumatic brain injury or subarachnoid hemorrhage). Each underwent a brief cognitive-emotional battery and 1.5 T DTI with deterministic tractography of major association tracts and the corpus callosum. Tract lateralization was quantified using the Structural Asymmetry Index (SAI), and individual profiles were compared with neuropsychological and emotional data. Results: Six patients met criteria for clinically significant anxiety, and four for depression, often dissociated from global cognitive screening. Tractography revealed heterogeneous asymmetry patterns, most often in the superior longitudinal fasciculus, uncinate fasciculus, and cingulum. In several cases, structural asymmetries diverged from neuropsychological findings, suggesting dissociations between behavioral testing and connectivity-based measures. Conclusions: Within-subject tract asymmetry analysis provided preliminary, potentially clinically relevant information not captured by tests alone. These findings indicate that individualized tractography could enrich the interpretation of cognitive and emotional profiles and help guide hypothesis generation for connectivity-informed neurorehabilitation.

Background: Acquired brain injury (ABI) leads to cognitive, emotional, and social impairments that substantially affect quality of life. Although cortical lesions have traditionally received more attention, increasing evidence highlights the importance of the integrity of major white matter association tracts. However, few studies have simultaneously examined cognitive, affective, and social domains within a tractography framework.Methods: In this exploratory pilot study, ten ABI patients underwent diffusion-based tractography of the principal association tracts—the superior and inferior longitudinal fasciculi, the uncinate fasciculus, the inferior fronto-occipital fasciculus, and the cingulum—together with a comprehensive neuropsychological battery covering global cognition, executive functions, memory, emotional symptoms, and empathy. Results: Marked interindividual variability was observed in both tract profiles and neuropsychological outcomes. Findings revealed paradoxical associations, such as larger volumes of the left superior longitudinal fasciculus being linked to poorer cognitive performance, suggesting maladaptive reorganization. Hemispheric lateralization patterns were also identified, with the uncinate fasciculus showing differential contributions to immediate memory and working memory across hemispheres. Notably, empathy scores consistently correlated with volumes of the inferior longitudinal fasciculus, the uncinate fasciculus, and the cingulum, in line with recent evidence on the structural basis of socio-emotional outcomes after ABI. Conclusions: Although limited by sample size, this study provides novel evidence regarding the structure–function paradox, hemispheric specialization, and the clinical relevance of empathy in ABI. Overall, the results support the integration of tractography of the main association tracts with neuropsychological assessment as complementary tools to advance personalized neurorehabilitation.

Background: Acquired brain injury (ABI) leads to cognitive, emotional, and social impairments that substantially affect quality of life. Although cortical lesions have traditionally received more attention, increasing evidence highlights the importance of the integrity of major white matter association tracts. However, few studies have simultaneously examined cognitive, affective, and social domains within a tractography framework. Methods: In this exploratory pilot study, ten ABI patients underwent diffusion-based tractography of the principal association tracts—the superior and inferior longitudinal fasciculi, the uncinate fasciculus, the inferior fronto-occipital fasciculus, and the cingulum—together with a comprehensive neuropsychological battery covering global cognition, executive functions, memory, emotional symptoms, and empathy. Results: Marked interindividual variability was observed in both tract profiles and neuropsychological outcomes. Findings revealed paradoxical associations, such as larger volumes of the left superior longitudinal fasciculus being linked to poorer cognitive performance, suggesting maladaptive reorganization. Hemispheric lateralization patterns were also identified, with the uncinate fasciculus showing differential contributions to immediate memory and working memory across hemispheres. Notably, empathy scores consistently correlated with volumes of the inferior longitudinal fasciculus, the uncinate fasciculus, and the cingulum, in line with recent evidence on the structural basis of socio-emotional outcomes after ABI. Conclusions: Although limited by sample size, this study provides novel evidence regarding the structure–function paradox, hemispheric specialization, and the clinical relevance of empathy in ABI. Overall, the results support the integration of tractography of the main association tracts with neuropsychological assessment as complementary tools to advance personalized neurorehabilitation.

Major depressive disorder pathophysiology involves complex gut-brain axis interactions, yet the systemic non-neurochemical impacts of selective serotonin reuptake inhibitors re-main poorly defined. This study evaluated the multidimensional effects of chronic fluoxe-tine administration in Sprague-Dawley rats. Male rats received fluoxetine (10 mg/kg/day) or water for 60 days, followed by behavioral phenotyping, fecal microbiological quantifi-cation, serum biochemistry, complete blood count analysis, and immunohistochemical assessment of the immediate-early gene product c-Fos (cellular proto-oncogene protein) in the striatum. Fluoxetine treatment significantly reduced immobility time in the forced swim test, whereas object recognition memory deteriorated without alterations in anxie-ty-like behavior. Pharmacological intervention markedly depleted fecal bacterial popula-tions and significantly decreased serum vitamin D concentrations. Hematologically, treated animals exhibited significant reductions in total leukocytes, red blood cells, and platelets, alongside elevated hematocrit and mean corpuscular volume. Concurrently, c-Fos-positive neuronal activation increased significantly within the striatal nucleus ac-cumbens. In conclusion, chronic fluoxetine exposure induces profound systemic disrup-tion, altering gut microbial homeostasis, depleting vitamin D, and modulating peripheral blood profiles while enhancing central striatal neuronal plasticity. These findings under-score the necessity of monitoring gut-brain axis integrity during prolonged antidepressant therapy.