Background: The extent and severity are two important parameters when describing a regional defect in myocardial single-photon emission computed tomography (SPECT) perfusion imaging. Intuitively, these two parameters should be independent of each other, but we have shown in a previous study that there is an interdependence. This interdependence has been investigated in two commercially available analysis programs (AutoQUANT and 4D-MSPECT) using Monte Carlo-simulated SPECT data.
Methods: An anthropomorphic digital computer phantom and a Monte Carlo program were used to generate SPECT data. Several defects of different volumes and lesion activity uptake reductions were simulated and evaluated. Comparison of the measures of extent and severity with their corresponding known values led to the development of a correction model based on least-squares parameter estimation. This model was then applied to a test group consisting of 10 different computer-simulated patients.
Results: Our results showed that the interdependence was reduced significantly for most of our test cases after applying the correction method. The application of the correction model to the test group demonstrated that the model was robust with respect to different patient geometries. A further test with projections that simulated a perfect SPECT system revealed that the interdependence between the extent and severity was not caused by the limited spatial resolution of the SPECT system, but rather the inherent design of the algorithms of the analysis programs.
Conclusions: A model has been developed to take into account the interdependence of the extent and severity.
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http://dx.doi.org/10.1097/01.mnm.0000195673.68040.d7 | DOI Listing |
Cureus
November 2024
Neonatology, Souss Massa University Hospital Center, Agadir, MAR.
Holoprosencephaly (HPE) is a severe and complex congenital brain malformation caused by a defect in the midline cleavage of the prosencephalon during early embryonic development. It is the most common prosencephalic malformation in humans and is categorized into three classical forms based on the severity of this cleavage defect: alobar, semilobar, and lobar HPE. A milder interhemispheric variant, called syntelencephaly, is also considered a form of HPE.
View Article and Find Full Text PDFMol Autism
December 2024
Neuroscience Center, University of North Carolina at Chapel Hill, Chapel Hill, NC, USA.
Background: Angelman syndrome (AS), a severe neurodevelopmental disorder resulting from the loss of the maternal UBE3A gene, is marked by changes in the brain's white matter (WM). The extent of WM abnormalities seems to correlate with the severity of clinical symptoms, but these deficits are still poorly characterized or understood. This study provides the first large-scale measurement of WM volume reduction in children with AS.
View Article and Find Full Text PDFPharmacol Res
December 2024
Translational Neurodegeneration Research and Neuropathology Lab, Department of Clinical Medicine (KlinMed), Medical Faculty, University of Oslo (UiO) and Section of Neuropathology Research, Department of Pathology, Clinics for Laboratory Medicine (KLM), Oslo University Hospital (OUS), Sognsvannsveien 20, N-0372 Oslo, Norway; Institute of Nutritional Medicine (INUM) and Lübeck Institute of Dermatology (LIED), University of Lübeck (UzL) and University Medical Center Schleswig-Holstein (UKSH), Ratzeburger Allee 160, D-23538 Lübeck, Germany; Faculty of Medicine and Life Sciences, University of Latvia, Jelgavas iela 3, LV-1004 Rīga, Latvia; School of Neurobiology, Biochemistry and Biophysics, The Georg S. Wise Faculty of Life Sciences, Tel Aviv University, Ramat Aviv, IL-6997801, Israel. Electronic address:
Huntington's disease (HD) is a debilitating neurodegenerative disorder characterized by severe motor deficits, cognitive decline and psychiatric disturbances. An early and significant morphological hallmark of HD is the activation of astrocytes triggered by mutant huntingtin, leading to the release of inflammatory mediators. Fingolimod (FTY), an FDA-approved sphingosine-1-phosphate (S1P) receptor agonist is used to treat multiple sclerosis (MS), a neuroinflammatory disease, and has shown therapeutic promise in other neurological conditions.
View Article and Find Full Text PDFInt J Legal Med
December 2024
Victorian Institute of Forensic Medicine, 65 Kavanagh Street, Melbourne, VIC, 3006, Australia.
Jurors rely on evidence presented in court to find the facts of a case. Consequently, the manner in which evidence is delivered may significantly impact the extent to which jurors comprehend and interpret the evidence. Building on a pilot study, the aim of this research was to further investigate which format for presenting forensic medical evidence in court was best for laypersons (i.
View Article and Find Full Text PDFEnviron Sci Technol
December 2024
The Swire Institute of Marine Science and School of Biological Sciences, The University of Hong Kong, Hong Kong SAR, Hong Kong, China.
Global changes can profoundly affect the sex determination and reproductive output of marine organisms, disrupting the population structure and ecosystems. High COdriven low pH in the context of ocean acidification (OA) has been shown to severely affect various calcifiers, but less is known about the extent to which low pH influences sex determination and reproduction of marine organisms, particularly mollusks. This study is the first to report a biased sex ratio over multiple generations toward females, driven by exposure to high CO-induced low pH environments, using the ecologically and economically important Portuguese oyster () as a model.
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