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1.
J Alzheimers Dis ; 65(1): 89-97, 2018.
Article in English | MEDLINE | ID: mdl-30056421

ABSTRACT

BACKGROUND: Pittsburgh Compound B (PiB) positron emission tomography (PET) is used to visualize in vivo amyloid plaques in the brain. Frequently the PiB examinations are complemented with a fluorodeoxyglucose (FDG) PET scan to further assess neurodegeneration. OBJECTIVE: Our goal is to identify alternative correlates of FDG images by assessing which kinetic methods originate PiB derived relative delivery ratio (R1) images that can be correlated with the FDG images, and to compare them with PiB perfusion (pPiB) images obtained from the early-phase of PiB acquisition. METHODS: We selected 52 patients with cognitive impairment who underwent a dynamic PiB and FDG acquisitions. To compute the R1 images, two simplified reference tissue models (SRTM and SRTM2) and two multi-linear reference tissue models (MRTM and MRTM2) were used. The pPiB images were obtained in two different time intervals. RESULTS: All six types of images were of good quality and highly correlated with the FDG images (mean voxelwise within-subjects r > 0.92). The higher correlation was found for FDG-R1(MRTM). Regarding the voxelwise regional correlation, the higher mean all brain correlations was r = 0.825 for FDG-R1(MRTM) and statistically significant in the whole brain analysis. CONCLUSION: All R1 and pPiB images here tested have potential to assess the metabolic impact of neurodegeneration almost as reliably as the FDG images. However, this is not enough to validate these images for a single-subject analysis compared with the FDG image, and thus they cannot yet be used clinically to replace the FDG image before such evaluation.


Subject(s)
Brain/diagnostic imaging , Carbon Radioisotopes/metabolism , Cognition Disorders/diagnostic imaging , Fluorodeoxyglucose F18/metabolism , Positron-Emission Tomography , Aged , Aged, 80 and over , Algorithms , Alzheimer Disease/diagnostic imaging , Brain/drug effects , Female , Humans , Male , Middle Aged , Neurodegenerative Diseases/diagnostic imaging , Tomography Scanners, X-Ray Computed
2.
Acta Medica Philippina ; : 261-267, 2018.
Article in English | WPRIM (Western Pacific) | ID: wpr-959693

ABSTRACT

@#<p style="text-align: justify;"><strong>OBJECTIVE:</strong> The study aimed to evaluate the sound pressure levels of selected traffic enforcer sites in the City of Manila.</p><p style="text-align: justify;"><strong>METHODOLOGY:</strong> A Brüel & Kjær Integrating Sound Level Meter type 2225 was used to measure sound pressure levels in dB(A) to estimate personal noise exposure of traffic enforcers designated at Quezon Boulevard near Quiapo Church and Recto - Rizal Avenue on a weekday and a weekend. Graphs were generated while appropriate measures were calculated for the noise exposure levels. The mean exposure levels were compared with the Philippine Occupational Safety and Health standards by computing the corresponding permissible exposure limit for each work shift using the Equal Energy Principle.17</p><p style="text-align: justify;"><strong>RESULTS:</strong> Noise exposure levels at Quezon Boulevard ranged from 75.0 dB(A) to 91.5 dB(A) with mean noise exposure level of 84.3 ± 3.7 dB(A) and 82.5 ± 2.6 dB(A) for the weekday AM and PM shift, respectively. The mean noise exposure level at Quezon Boulevard for the weekend AM shift was 82.4 ± 2.6, whereas 80.4 ± 2.8 for the PM shift. The noise exposure levels at Recto - Rizal Avenue ranged from 81.5 dB(A) to 99.3 dB(A) with mean noise exposure level of 86.7 ± 2.6 dB(A) and 86.0 ± 2.1 dB(A) for the weekday AM and PM shift, respectively. The mean noise exposure level at Recto - Rizal Avenue for the weekend AM shift was 86.7 ± 2.3, whereas 89.0 ± 4.0 for the PM shift.</p><p style="text-align: justify;"><strong>CONCLUSION:</strong> The study showed that traffic enforcers designated at Quezon Boulevard and Recto - Rizal Avenue are exposed to noise levels that do not exceed the Philippine Occupational Safety and Health standards.</p>


Subject(s)
Humans , Noise, Occupational , Occupational Health
3.
Nucl Med Biol ; 37(2): 125-32, 2010 Feb.
Article in English | MEDLINE | ID: mdl-20152711

ABSTRACT

Colorectal cancer is one of the most common malignancies in the Western world and is an example of a solid tumour in which hypoxia is a common feature and develops because of the inability of the vascular system to supply adequate amounts of oxygen to growing tumours. Hypoxia effects on tumour cell biology can be detected and characterized using different methods. The use of imaging with gamma-emitting radionuclides to detect hypoxic tissue was first suggested by Chapman in 1979 [N Engl J Med 301 (1979) 1429-1432]. (99m)Tc-4,9-diaza-3,3,10,10-tetramethyldodecan-2,11-dione dioxime, also known as (99m)Tc-HL-91, has been among the most studied hypoxia markers. The objective of this study was to correlate the uptake of (99m)Tc-HL-91 and (99m)Tc-MIBI in colon cancer cells under normoxic and hypoxic conditions and to compare this information with some parameters such as oxidative stress and mitochondrial dysfunction of the cells analyzed by flow cytometry. Our results show that the in vitro (99m)Tc-HL-91 uptake is higher in hypoxic conditions, which is confirmed by the decreased uptake of (99m)Tc-MIBI. Flow cytometry results demonstrate that hypoxic conditions used are not enough to induce cellular death, but are responsible for the alterations in the intracellular redox environment, namely, increase of ROS production, proteic pimonidazol-derived adduct formation and alteration in the mitochondrial membrane permeability. Therefore, these results confirm that (99m)Tc-HL-91 is a radiopharmaceutical with favourable characteristics for detecting hypoxia.


Subject(s)
Colonic Neoplasms/metabolism , Colonic Neoplasms/pathology , Organotechnetium Compounds/metabolism , Oximes/metabolism , Technetium Tc 99m Sestamibi/metabolism , Animals , Biological Transport , Cell Death , Cell Hypoxia , Cell Line, Tumor , Cell Survival , Flow Cytometry , Humans , Membrane Potential, Mitochondrial , Oxidation-Reduction , Oxidative Stress , Reactive Oxygen Species/metabolism
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