950 resultados para Flat foot
Resumo:
L’adroterapia è un tipo di terapia oncologica in cui il tumore è irraggiato con particelle cariche (adroni) quali protoni e ioni carbonio. Il vantaggio principale rispetto alla radioterapia convenzionale a raggi X consiste nel fatto che l’irraggiamento con adroni non coinvolge i tessuti sani circostanti quelli malati. Tuttavia, si conosce ancora poco sui processi di frammentazione nucleare che avvengono tra gli adroni del fascio usato nel trattamento e i nuclei presenti nel corpo umano. Così, nel 2017 nasce l’esperimento FOOT (FragmentatiOn Of Target) con lo scopo di misurare le sezioni d’urto differenziali dei frammenti nucleari prodotti nell’interazione a energie di 200-400 MeV/u (tipicamente impiegate in adroterapia). Attualmente l’apparato sperimentale di FOOT è in grado di compiere misure accurate solo per frammenti carichi, ma nell’ultimo anno si è cominciata ad esplorare la possibilità di rivelare anche i neutroni. Per questa operazione è necessario servirsi di scintillatori liquidi affiancati ad un sistema di veto costituito da scintillatori plastici sottili accoppiati a sensori che segnalano il passaggio di eventuali frammenti carichi. In una precedente campagna di misure con la collaborazione FOOT, si sono utilizzati come sensori dei tubi fotomoltiplicatori (PMT). Per migliorare le prestazioni del sistema di veto si è reso necessario l’utilizzo di scintillatori plastici veloci, letti da sensori fotomoltiplicatori al silicio (SiPM). In questa tesi mi sono occupato della risoluzione temporale dei segnali acquisiti con scintillatori plastici EJ-204 di 3 mm di spessore, letti da SiPM SenseL®.
Resumo:
L’adroterapia è una tecnica di cura tumorale basata sull’irraggiamento della zona cancerosa tramite ioni pesanti e particelle cariche. Queste permettono di massimizzare il danno nella zona tumorale e limitare invece quello subito dalle cellule sane. Il più grande ostacolo risiede nella limitata reperibilità di informazioni in letteratura sulla frammentazione del target. I frammenti così prodotti infatti hanno una mobilità di µm e per questo motivo sono molto difficili da rivelare. In questo contesto nel 2017 l’esperimento FOOT, approvato dall’INFN nasce con l’obiettivo di misurare la sezione d’urto differenziale di tutti i prodotti emessi dalla frammentazione nucleare fra il fascio ed il paziente. Operando in condizione di cinematica inversa l’esperimento riesce a rivelare questi frammenti ed a misurarne l’abbondanza e l’energia. E’ stata effettuata a questo proposito, un’analisi dati volta ad eliminare le frammentazioni in aria precedenti ed interne al rivelatore MSD per poter ottenere misure più accurate delle sezioni d’urto di frammentazione.
Resumo:
L’adroterapia è una terapia medica oncologica che consiste nell’irraggiamento della massa tumorale tramite un fascio di particelle cariche, come protoni o ioni pesanti. Ad oggi però, non è ancora stata fatta una stima completa degli effetti causati dagli eventi di frammentazione nucleare tra le particelle del fascio e i nuclei del corpo umano. A tale scopo è nato nel 2017 l’esperimento FOOT (FragmentatiOn Of Target), con l’obiettivo di misurare la sezione d’urto differenziale di tutti i prodotti emessi nella frammentazione nucleare tra il fascio e il paziente. In questa tesi sono stati analizzati i dati acquisiti relativi all’interazione tra un fascio di ioni ossigeno a 400MeV/n su un bersaglio di grafite. Per ottenere una misura quanto migliore delle sezioni d’urto è necessario eliminare gli eventi di frammentazione che avvengono tra il fascio e i nuclei dell’aria posta tra i rivelatori dell’apparato sperimentale. Confrontando l’energia rilasciata in due rivelatori consecutivi si può capire se nell’aria posta fra questi vi sono stati tali eventi.
Resumo:
L'adroterapia è una delle tecniche utilizzate ad oggi per trattare i tumori ed è basata sull'utilizzo di fasci di particelle cariche, come protoni e ioni carbonio, accelerati sulla zona da trattare. A differenza dei fotoni, utilizzati in radioterapia, le particelle cariche permettono un rilascio di energia più mirato, danneggiando il DNA delle cellule tumorali fino ad impedirne la duplicazione, senza intaccare i tessuti sani circostanti. Per sfruttare al meglio questa tecnica è necessario conoscere a fondo i processi di frammentazione nucleare che possono avere luogo durante il trattamento, sui quali si hanno ancora insufficienti dati sperimentali, in particolare a proposito della frammentazione del bersaglio. L'esperimento FOOT (FragmentatiOn Of Target) nasce proprio per poter misurare le sezioni d'urto differenziali dei processi di frammentazione nucleare alle tipiche energie dell'adroterapia, dai 60 MeV/u ai 400 MeV/u. Allo stato attuale l'esperimento è dotato di un apparato per la rivelazione di frammenti carichi pesanti e uno per quelli leggeri, mentre non ha un sistema di rivelazione per le particelle neutre. Si sta quindi valutando la possibilità di aggiungere rivelatori di neutroni, per esempio gli scintillatori liquidi BC-501A, i quali permettono di discriminare fotoni da neutroni grazie alla diversa forma del segnale prodotto (Pulse Shape Discrimination). Per studiare le prestazioni di questi rivelatori, essi si stanno attualmente testando alla facility n_TOF del CERN con diverse sorgenti di particelle. In questo lavoro di tesi mi sono occupata di analizzare i segnali raccolti da due BC-501A con una sorgente AmBe di raggi γ e neutroni, con schermo in piombo, e con una sorgente 88Y di soli raggi γ, evidenziando le buone capacità di questi rivelatori di identificare correttamente neutroni e fotoni.
Resumo:
Hadrontherapy is a medical treatment based on the use of charged particles beams accelerated towards deep-seated tumors on clinical patients. The reason why it is increasingly used is the favorable depth dose profile following the Bragg Peak distribution, where the release of dose is almost sharply focused near the end of the beam path. However, nuclear interactions between the beam and the human body constituents occur, generating nuclear fragments which modify the dose profile. To overcome the lack of experimental data on nuclear fragmentation reactions in the energy range of hadrontherapy interest, the FOOT (FragmentatiOn Of Target) experiment has been conceived with the main aim of measuring differential nuclear fragmentation cross sections with an uncertainty lower than 5\%. The same results are of great interest also in the radioprotection field, studying similar processes. Long-term human missions outside the Earth’s orbit are going to be planned in the next years, among which the NASA foreseen travel to Mars, and it is fundamental to protect astronauts health and electronics from radiation exposure .\\ In this thesis, a first analysis of the data taken at the GSI with a beam of $^{16}O$ at 400 $MeV/u$ impinging on a target of graphite ($C$) will be presented, showing the first preliminary results of elemental cross section and angular differential cross section. A Monte Carlo dataset was first studied to test the performance of the tracking reconstruction algorithm and to check the reliability of the full analysis chain, from hit reconstruction to cross section measurement. An high agreement was found between generated and reconstructed fragments, thus validating the adopted procedure. A preliminary experimental cross section was measured and compared with MC results, highlighting a good consistency for all the fragments.
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Multiple sclerosis (MS) is an autoimmune and neurodegenerative disease that affects young adults. It is characterized by generating a chronic demyelinating autoimmune inflammation in the central nervous system. An experimental model for studying MS is the experimental autoimmune encephalomyelitis (EAE), induced by immunization with antigenic proteins from myelin. The present study investigated the evolution of EAE in pregabalin treated animals up to the remission phase. The results demonstrated a delay in the onset of the disease with statistical differences at the 10th and the 16th day after immunization. Additionally, the walking track test (CatWalk) was used to evaluate different parameters related to motor function. Although no difference between groups was obtained for the foot print pressure, the regularity index was improved post treatment, indicating a better motor coordination. The immunohistochemical analysis of putative synapse preservation and glial reactivity revealed that pregabalin treatment improved the overall morphology of the spinal cord. A preservation of circuits was depicted and the glial reaction was downregulated during the course of the disease. qRT-PCR data did not show immunomodulatory effects of pregabalin, indicating that the positive effects were restricted to the CNS environment. Overall, the present data indicate that pregabalin is efficient for reducing the seriousness of EAE, delaying its course as well as reducing synaptic loss and astroglial reaction.
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To characterize cumulative joint damage (CJD) patterns in rheumatoid arthritis (RA) and determine their associations with demographic/clinical features and HLA-DRB1 gene polymorphism. Hand and foot radiographs were obtained from 404 patients with RA. CJD patterns were determined by 3 derivations from Sharp/van der Heijde scores, obtained by the mathematical division of scores for hands/feet (Sharp-h/f score), fingers/wrists (Sharp-f/w score), and erosion/space narrowing (Sharp-e/sn score), respectively. DNA and serum were obtained for determination of HLA-DRB1 polymorphism, rheumatoid factor (RF), and anticitrullinated protein antibodies (ACPA). Patients with wrist-dominant CJD pattern were more likely to have severe RA than those with finger-dominant pattern (68.4% vs 46.0%; p = 0.036) as were those with foot-dominant vs hand-dominant CJD pattern (76.5% vs 56.4%; p = 0.044). HLA-DRB1 shared epitope (SE) alleles were associated with erosion-dominant CJD pattern (p = 0.021). Patients with erosion-dominant CJD pattern had higher levels of RF and ACPA than those with space-narrowing-dominant CJD pattern (median RF 71.35 U/ml vs 22.05 U/ml, respectively; p = 0.003; median ACPA 187.9 U/ml vs 143.2 U/ml, respectively; p < 0.001). The majority of triple-positive patients (SE+, RF+, ACPA+) had erosion-dominant CJD pattern (62.3%) while the majority of triple-negative patients (SE-, FR-, ACPA-) had space narrowing-dominant CJD pattern (75%; p = 0.017). ACPA was associated with HLA-DRB1 SE alleles (p < 0.05). Patients with foot-dominant CJD pattern were taller than those with hand-dominant CJD pattern (p = 0.002); those with erosion-dominant CJD pattern had higher weight and body mass index than those with space narrowing-dominant CJD pattern (p = 0.014, p = 0.001). CJD patterns were associated with disease severity, HLA-DRB1 SE status, presence and titer of ACPA and RF, and morphometric features.
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In diabetes mellitus (DM), podocyte apoptosis leads to albuminuria and nephropathy progression. Low-density lipoprotein receptor-related protein 6 (LRP6) is WNT pathway receptor that is involved in podocyte death, adhesion and motility. Glycogen synthase kinase 3 (GSK3) interaction with p53 (GSK3-p53) promotes apoptosis in carcinoma cells. It is unknown if GSK3-p53 contributes to podocyte apoptosis in DM. In experimental DM, green tea (GT) reduces albuminuria by an unknown mechanism. In the present study, we assessed the role of the GSK3β-p53 in podocyte apoptosis and the effects of GT on these abnormalities. In diabetic spontaneously hypertensive rats (SHRs), GT prevents podocyte's p-LRP6 expression reduction, increased GSK3β-p53 and high p53 levels. In diabetic SHR rats, GT reduces podocyte apoptosis, foot process effacement and albuminuria. In immortalized mouse podocytes (iMPs), high glucose (HG), silencing RNA (siRNA) or blocking LRP6 (DKK-1) reduced p-LRP6 expression, leading to high GSK3β-p53, p53 expression, apoptosis and increased albumin influx. GSK3β blockade by BIO reduced GSK3β-p53 and podocyte apoptosis. In iMPs under HG, GT reduced apoptosis and the albumin influx by blocking GSK3β-p53 following the rise in p-LRP6 expression. These effects of GT were prevented by LRP6 siRNA or DKK-1. In conclusion, in DM, WNT inhibition, via LRP6, increases GSK3β-p53 and podocyte apoptosis. Maneuvers that inactivate GSK3β-p53, such as GT, may be renoprotective in DM.
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We characterized the functional consequences of intravesical bacillus Calmette-Guérin on the molecular mechanism of the AKT/mTOR signaling pathway in nonmuscle invasive bladder cancer. To our knowledge this has not been reported previously. At age 7 weeks female Fischer 344 rats received 1.5 mg/kg MNU intravesically every other week for 6 weeks. They were randomized at 10 per group to MNU (0.2 ml vehicle), bacillus Calmette-Guérin (10(6) cfu Connaught strain), rapamycin (15 μg/ml) and bacillus Calmette-Guérin plus simultaneous rapamycin, each intravesically for 6 weeks. At week 15 the bladders were collected for histopathology, immunohistochemistry and immunoblot to determine p-AKT, Rictor, Raptor, p-4E-BP1, p-p70S6K1, p-AMPK-α, p-mTOR and p-p53. Papillary carcinoma (pTa) and high grade intraepithelial neoplasia (pTis) predominated in the MNU group while normal urothelium, papillary and flat hyperplasia were more common in treated groups. Nonmuscle invasive bladder cancer treated with bacillus Calmette-Guérin showed suppression of p70S6K1 but not 4E-BP1 phosphorylation. This suggests that 4E-BP1 is regulated differently than p70S6K1, escaping the bacillus Calmette-Guérin action that occurs in a mTOR independent manner. The association of bacillus Calmette-Guérin with rapamycin but not rapamycin monotherapy affected p70S6K1 and 4E-BP1 phosphorylation with no features of in situ carcinoma (pTis). The activation status of p70S6K1 and 4E-BP1 might be used to stratify patients who could benefit from targeting such molecular elements with multitarget/multidrug intravesical therapy. In the future 4E-BP1 might be a worthwhile new target for bacillus Calmette-Guérin refractory nonmuscle invasive bladder cancer.
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Dental materials that release fluoride have been shown to be effective in caries inhibition around restorations. Adhesive materials would also be effective in caries inhibition by sealing and protecting cavity margins from acidic demineralization. This in vitro study tested the hypothesis that composite restorations with a dentin adhesive system have a caries preventive effect similar to that of an adhesive material with fluoride - glass-ionomer cement - on root surfaces. Twenty roots from extracted sound third molars were embedded in polystyrene resin and ground flat. Standardized cavities were prepared in leveled root surfaces and randomly restored with (a) Chelon-Fil (Espe) or (b) Z100/SingleBond (3M). Baseline indentations were measured at 100, 200 and 300 mum from the occlusal margins of each restoration and the surface microhardness values were obtained using a Knoop diamond indenter. A 2.0 mm wide margin around the restorations was submitted to a pH-cycling model, at 37ºC. After that, surface microhardness was measured again, as it was before. The differences between baseline and final surface microhardness were considered for statistical analysis. The median values of differences were (a): -3.8; -0.3; -1.0; and (b): 3.3; 2.5; 1.7, for the distances of 100, 200 and 300 mum, respectively. The Kruskal-Wallis test did not show statistically significant difference between 100, 200 and 300 mum distances in each tested group. There was no difference between the studied materials at the distances of 200 and 300 mum. Chelon-Fil was statistically different from Z100/SingleBond, at 100 mum (p<0.05). Under the studied conditions, the glass-ionomer cement had a higher caries preventive effect than the composite/dentin adhesive restorations.
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Universidade Estadual de Campinas . Faculdade de Educação Física
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Universidade Estadual de Campinas . Faculdade de Educação Física
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Universidade Estadual de Campinas . Faculdade de Educação Física
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Universidade Estadual de Campinas . Faculdade de Educação Física
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Universidade Estadual de Campinas . Faculdade de Educação Física