scholarly journals Fractal analysis of neuroimaging: comparison between control patients and patients with the presence of Alzheimer’s disease

2022 ◽  
Vol 2159 (1) ◽  
pp. 012011
Author(s):  
J Villamizar ◽  
L Uribe ◽  
A Cerquera ◽  
E Prada ◽  
D Prada ◽  
...  

Abstract Alzheimer’s disease is a neurodegenerative cognitive, affective, and behavioral disorder aligned to the aging process and other coronary diseases. To contribute to the early diagnosis of the disease, a neuroimaging treatment is implemented through a preprocessing to subsequently calculate the fractal dimension associated with these images in order to propose an alternative to the one proposed in medical physics through positron emission tomography. In this work, a comparative analysis is made of a previous work using the Box Counting methodology versus the calculation of the fractal dimension by means of software developed by the researchers based on the same method. The differences between the fractal dimensions of the neuroimages of control patients and patients with the presence of the disease are maintained showing a lower value of fractal dimension in patients with the disease due to the physical deterioration of the brain.

10.14311/1785 ◽  
2013 ◽  
Vol 53 (2) ◽  
Author(s):  
Václav Hubata-Vacek ◽  
Jaromír Kukal ◽  
Robert Rusina ◽  
Marie Buncová

Estimated entropies from a limited data set are always biased. Consequently, it is not a trivial task to calculate the entropy in real tasks. In this paper, we used a generalized definition of entropy to evaluate the Hartley, Shannon, and Collision entropies. Moreover, we applied the Miller and Harris estimations of Shannon entropy, which are well known bias approaches based on Taylor series. Finally, these estimates were improved by Bayesian estimation of individual probabilities. These methods were tested and used for recognizing Alzheimer’s disease, using the relationship between entropy and the fractal dimension to obtain fractal dimensions of 3D brain scans.


Fractals ◽  
2008 ◽  
Vol 16 (02) ◽  
pp. 103-107 ◽  
Author(s):  
A. L. KARPERIEN ◽  
H. F. JELINEK ◽  
A. M. BUCHAN

In pathological brain, a variety of morphological forms exist that reflect differences in functional requirements. To better understand microglia function in neurological disease, it is important to identify and quantify microglia morphology associated with specific neuropathologies. Traditional feature parameters such as area or cell diameter are not sufficient. In this study microglia were quantified by the box-counting fractal dimension (DB). One hundred and four cells from post-mortem tissue were analyzed comprising cells of controls, Alzheimer's disease, schizophrenia and affective disorder. The DBwas significantly different from the control (1.36) compared to schizophrenia (1.41), Alzheimer's disease (1.41) and affective disorder (1.43) with p < 0.01. Thus fractal analysis provides a useful quantitative and objective measure of microglial form associated with normal function and diverse neuropathology. The distribution of fractal dimensions associated with microglia structure and activation with disease progression also differs, suggesting a different etiology for these diseases.


Gels ◽  
2021 ◽  
Vol 7 (2) ◽  
pp. 46
Author(s):  
Pedram Nasr ◽  
Hannah Leung ◽  
France-Isabelle Auzanneau ◽  
Michael A. Rogers

Complex morphologies, as is the case in self-assembled fibrillar networks (SAFiNs) of 1,3:2,4-Dibenzylidene sorbitol (DBS), are often characterized by their Fractal dimension and not Euclidean. Self-similarity presents for DBS-polyethylene glycol (PEG) SAFiNs in the Cayley Tree branching pattern, similar box-counting fractal dimensions across length scales, and fractals derived from the Avrami model. Irrespective of the crystallization temperature, fractal values corresponded to limited diffusion aggregation and not ballistic particle–cluster aggregation. Additionally, the fractal dimension of the SAFiN was affected more by changes in solvent viscosity (e.g., PEG200 compared to PEG600) than crystallization temperature. Most surprising was the evidence of Cayley branching not only for the radial fibers within the spherulitic but also on the fiber surfaces.


2010 ◽  
Vol 30 (11) ◽  
pp. 1883-1889 ◽  
Author(s):  
Allyson R Zazulia ◽  
Tom O Videen ◽  
John C Morris ◽  
William J Powers

Studies in transgenic mice overexpressing amyloid precursor protein (APP) demonstrate impaired autoregulation of cerebral blood flow (CBF) to changes in arterial pressure and suggest that cerebrovascular dysfunction may be critically important in the development of pathological Alzheimer's disease (AD). Given the relevance of such a finding for guiding hypertension treatment in the elderly, we assessed autoregulation in individuals with AD. Twenty persons aged 75±6 years with very mild or mild symptomatic AD (Clinical Dementia Rating 0.5 or 1.0) underwent 15O-positron emission tomography (PET) CBF measurements before and after mean arterial pressure (MAP) was lowered from 107±13 to 92±9 mm Hg with intravenous nicardipine; 11C-PIB-PET imaging and magnetic resonance imaging (MRI) were also obtained. There were no significant differences in mean CBF before and after MAP reduction in the bilateral hemispheres (−0.9±5.2 mL per 100 g per minute, P=0.4, 95% confidence interval (CI)=−3.4 to 1.5), cortical borderzones (−1.9±5.0 mL per 100 g per minute, P=0.10, 95% CI=−4.3 to 0.4), regions of T2W-MRI-defined leukoaraiosis (−0.3±4.4 mL per 100 g per minute, P=0.85, 95% CI=−3.3 to 3.9), or regions of peak 11C-PIB uptake (−2.5±7.7 mL per 100 g per minute, P=0.30, 95% CI=−7.7 to 2.7). The absence of significant change in CBF with a 10 to 15 mm Hg reduction in MAP within the normal autoregulatory range demonstrates that there is neither a generalized nor local defect of autoregulation in AD.


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