Background: Approximately 10% to 30% of Alzheimer disease (AD) patients progress rapidly in severity and become more dependent on caregivers. Although several studies have investigated whether imaging biomarkers such as medial temporal atrophy (MTA) and posterior atrophy (PA) are useful for predicting the rapid progression of AD, their results have been inconsistent.
Objective: The study aims to investigate the association of visually rated MTA and PA with rapid disease progression in AD.
Methods: This was a retrospective cohort study of 159 AD patients who were initially diagnosed with mild AD and were followed for 1 year to determine whether they progressed rapidly (a decrease of three points or more on the Mini-Mental State Examination over 1 year). We used 5-point and 4-point visual rating scales to assess MTA and PA, respectively. MTA and PA scores for each patient were dichotomized as normal (without atrophy) or abnormal (atrophy). We performed a logistic regression analysis to determine the odds ratios (ORs) of MTA and PA for rapid disease progression with adjustment for covariates.
Results: Within the study population, 47 (29.6%) patients progressed rapidly. Visual assessment of the magnetic resonance imaging (MRI) scans revealed that 112 patients (70.4%) showed MTA, whereas 80 patients (50.3%) showed PA. The ORs with 95% confidence intervals for MTA and PA were 1.825 (0.819-4.070) and 2.844 (1.378-5.835), respectively. The association of visually assessed PA, but not MTA, with rapid progression was significant after adjustment for covariates.
Conclusion: In patients with mild AD, visual assessment of PA exhibits independent predictive value for rapid disease progression.
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http://dx.doi.org/10.1002/gps.5072 | DOI Listing |
Commun Biol
November 2024
Department of Medical Biology, Faculty of Medicine, University of Szeged, Szeged, Hungary.
The rapid advancements in sequencing technologies and bioinformatics have enabled metagenomic research of complex microbial systems, but reliable results depend on consistent laboratory and bioinformatics approaches. Current efforts to identify best practices often focus on optimizing specific steps, making it challenging to understand the influence of each stage on microbial population analysis and compare data across studies. This study evaluated DNA extraction, library construction methodologies, sequencing platforms, and computational approaches using a dog stool sample, two synthetic microbial community mixtures, and various sequencing data sources.
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October 2024
Gene and Stem Cell Therapy Program, Centenary Institute, University of Sydney, Sydney, NSW, Australia; University of Sydney, Central Clinical School, Faculty of Medicine and Health, Sydney, NSW, Australia; Department of Cell and Molecular Therapies, Royal Prince Alfred Hospital, Sydney, NSW, Australia. Electronic address:
NPJ Precis Oncol
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Danish Cancer Institute, Copenhagen, Denmark.
We analyzed genomic data from the prostate cancer of African- and European American men to identify differences contributing to racial disparity of outcome. We also performed FISH-based studies of Chromodomain helicase DNA-binding protein 1 (CHD1) loss on prostate cancer tissue microarrays. We created CHD1-deficient prostate cancer cell lines for genomic, drug sensitivity and functional homologous recombination (HR) activity analysis.
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Department of Microbiology, Faculty of Science and Informatics, University of Szeged, Szeged, Hungary.
BMC Ecol Evol
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'Lendület' Seed Ecology Research Group, Institute of Ecology and Botany, HUN-REN Centre for Ecological Research, Alkotmány str. 2-4, Vácrátót, 2163, Hungary.
Artificial linear landscape elements, including roads, pipelines, and drainage channels, are main sources of global habitat fragmentation. Restoration of natural habitats on unused linear landscape elements can increase habitat quality and connectivity without interfering with agricultural or industrial development. Despite that topsoil removal and transfer are widely applied methods in restoration projects, up to our knowledge these were previously not compared in the same study system.
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