Publications by authors named "A Malet Llado"

Background And Objectives: Pathogenic variants in the gene cause frontotemporal dementia (FTD-) with marked brain asymmetry. This study aims to assess whether the disease progression of FTD- depends on the initial side of the atrophy. We also investigated the potential use of brain asymmetry as a biomarker of the disease.

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  • The study focuses on a modified script training intervention called Video-Implemented Script Training for Aphasia (VISTA) aimed at improving speech in people with Primary Progressive Aphasia (PPA), a disorder that affects language skills.
  • Thirteen bilingual participants (Spanish-Catalan) with different variants of PPA underwent the training over 8 weeks, with evaluations on their script accuracy and production quality at multiple time points.
  • Results indicated significant improvements in various speech measures regardless of whether the training was conducted via teletherapy or in-person, highlighting the effectiveness and acceptability of the intervention for individuals with different PPA variants.
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  • Neuroimaging and fluid biomarkers, like MRI and cerebrospinal fluid (CSF) analysis, help distinguish frontotemporal dementia (FTD) from Alzheimer's disease (AD).
  • A machine learning algorithm was developed to calculate individual probabilistic scores, yielding an 82% accuracy rate for differentiating between AD and FTD using MRI alone.
  • Combining MRI data with CSF biomarkers improved diagnostic accuracy and confidence, making the algorithm a promising tool for clinical use, especially in scenarios with limited access to expert diagnoses.
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  • Early-onset Alzheimer's disease (EOAD) has more severe neuropsychiatric symptoms and lower integrity of the locus coeruleus (LC) compared to late-onset Alzheimer's disease (LOAD).
  • A study involving 104 subjects with AD and 32 healthy controls used MRI and other measurements to analyze the differences in LC integrity and symptoms between EOAD and LOAD.
  • Results showed that EOAD's lower LC integrity correlates with increased neuropsychiatric symptoms, and its greater degeneration may explain these severe symptoms compared to LOAD.
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  • Wasteosomes (or corpora amylacea) are polyglucosan bodies linked to aging and neurodegenerative diseases, potentially serving a brain cleaning function.
  • A study examined wasteosomes in 124 post-mortem FTLD patients across three proteinopathies (tau, TDP, and FUS), finding a higher accumulation in FTLD patients compared to controls, particularly in FTLD-FUS cases.
  • Results indicated that while wasteosomes increased with disease duration in FTLD-TDP, they did not show this trend in FTLD-tau and FTLD-FUS, suggesting varying roles in disease progression among the proteinopathies.
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