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Objective: We aimed at evaluating the brain metabolic features of fused in sarcoma amyotrophic lateral sclerosis (FUS-ALS) compared with sporadic ALS (sALS), using 2-[fluorine-18] fluoro-2-deoxy-D-glucose positron emission tomography (2-[F]FDG-PET).
Methods: We employed the 2-sample t-test model of SPM12, implemented in MATLAB, to compare 12 FUS-ALS cases with 40 healthy controls (HC) and 48 sALS, randomly collected from the series of patients who underwent brain 2-[F]FDG-PET at the ALS Center of Turin (Italy) at diagnosis from 2009 to 2019. In the comparisons between cases and HC, we included age at PET and sex as covariates. Because FUS-ALS usually shows early onset in spinal regions, in the comparison between FUS-ALS and sALS, we included singularly the following covariates in a second step, to evaluate the determinants of eventual metabolic differences: age at PET, sex, and onset (spinal/bulbar).
Results: sALS patients showed significant relative hypometabolism in bilateral fronto-temporo-occipital cortex and right insula as compared with FUS-ALS. After adjusting for age, the relative hypometabolism remained in the bilateral precentral gyrus and in the right middle and inferior temporal gyrus. As compared with HC, FUS patients displayed a significant relative hypermetabolism in the pontobulbar region and right cerebellar tonsil, dentate nucleus, and uvula, while sALS showed relative hypometabolism in bilateral frontal and occipital cortices and in left temporal and parietal regions.
Interpretation: Patients with FUS-ALS show relative preservation of motor cortex metabolism compared with those with sALS, possibly reflecting the prevalence of lower motor neuron impairment in their phenotype. Prospective studies are necessary to investigate the possible role of 2-[F]FDG-PET as a biomarker to track disease spreading in clinical trials. ANN NEUROL 2025;97:1134-1143.
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http://dx.doi.org/10.1002/ana.27201 | DOI Listing |
Geroscience
September 2025
Department of Experimental and Clinical Biomedical Sciences, Nuclear Medicine Unit, University of Florence, Florence, Italy.
A growing body of evidence shows significant sex differences in Alzheimer's Disease (AD) epidemiology, clinical presentation, and pathology burden; however, sex differences in neuroimaging biomarkers remain underexplored, prompting recent calls to action for more targeted research in this field. We analyzed static brain positron emission tomography (PET) imaging with 2-[F] fluoro-2-deoxy-D-glucose (FDG) from 247 elderly individuals with AD dementia, including 151 women and 96 men. Voxel-based analysis was used to detect reductions in FDG uptake in each sex relative to a publicly shared normative database and to identify sex differences in FDG uptake within the AD cohort.
View Article and Find Full Text PDFEur J Nucl Med Mol Imaging
August 2025
Department of Neuroscience, Rehabilitation, Ophthalmology, Genetics, Maternal and Child Health, University of Genoa, Genoa, Italy.
Purpose: Recent advancements in autoimmune encephalitis (AE) have enhanced diagnosis and management, but predicting long-term outcomes remains challenging. This study aims to evaluate longitudinal changes in brain [F]FDG PET patterns in AE patients to identify specific regional metabolic variations and predict clinical outcomes.
Methods: This longitudinal study compared brain [F]FDG PET scans of 22 AE patients at baseline (BS) and after treatment follow-up (FU) using voxel-wise paired t-tests.
Alzheimers Dement
August 2025
Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.
Introduction: Primary age-related tauopathy (PART) is defined by neurofibrillary tangles (NFTs) with absent-minimal amyloid beta (Aβ) plaques. Currently, definitive diagnosis of PART occurs with autopsy. This study investigated whether [F]fluorodeoxyglucose positron emission tomography (FDG-PET) could detect PART-related metabolic changes and assessed the impact of common co-pathologies.
View Article and Find Full Text PDFZhonghua Yi Xue Za Zhi
August 2025
Department of Neurology, the Second Medical Centre and National Clinical Research Center for Geriatric Disease, Chinese PLA General Hospital, Beijing 100853, China.
To characterize the clinical and imaging features of Dementia with Lewy Bodies (DLB) through long-term follow-up. This study analyzed clinical and multimodal imaging data, including magnetic resonance imaging (MRI), dopamine transporter (DAT), C Pittsburgh compound B (C-PIB), and F-fluorodeoxyglucose (F-FDG) positron emission tomography (PET), from 11 probable DLB patients at the first and second medical center of PLA General Hospital from March 2012 to February 2025. Patients were longitudinally assessed for the following parameters: time from disease onset to bedridden status, time from onset to death, annual cognitive decline rate (measured by mini-mental state examination, MMSE), extent of cerebral atrophy, regions of hypometabolism, and areas of reduced DAT availability.
View Article and Find Full Text PDFJ Neurosci
August 2025
Sanders-Brown Center on Aging, University of Kentucky College of Medicine, Lexington, KY 40536, USA.
While cerebrovascular dysfunction and reactive astrocytosis are extensively characterized hallmarks of Alzheimer's disease (AD) and related dementias, the dynamic relationship between reactive astrocytes and cerebral vessels remains poorly understood. Here, we used jGCaMP8f and two photon microscopy to investigate calcium signaling in multiple astrocyte subcompartments, concurrent with changes in cerebral arteriole activity, in fully awake seven-to-eight-month-old male and female 5xFAD mice, a model for AD-like pathology, and wild-type (WT) littermates. In the absence of movement, spontaneous calcium transients in barrel cortex occurred more frequently in astrocyte somata, processes, and perivascular regions of 5xFAD mice.
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