Cadastramento de doadores voluntários de Medula Óssea no REDOME

Anais do 35º Seminário de Extensão Universitária da Região Sul - Área temática: SaúdeO transplante de medula óssea consiste na substituição de uma medula óssea doente ou deficitária por células normais, com o objetivo de reconstituição de uma nova medula. Um fator que dificulta a realização do procedimento é a falta de doador compatível. Assim, quanto maior o número de novos doadores voluntários cadastrados no REDOME (Registro Brasileiro de Doadores Voluntários de Medula Óssea), maiores são as possibilidades de o paciente encontrar um doador compatível. Nosso projeto de extensão tem como objetivo a conscientização da população sobre o cadastramento de doadores voluntários de medula óssea nas regiões de Maringá, Cianorte e Paranavaí, por meio de campanhas de captação de doadores, palestras de conscientização e divulgação sobre a doação e o transplante de medula óssea. O projeto vem colaborando no crescimento do REDOME com doadores mais conscientes sobre a responsabilidade do cadastro no banco. Assim, nossa equipe deve continuar realizando o trabalho de conscientização da população, pois quanto maior o número de doadores, maior é a possibilidade de se encontrar um doador compatíve

Prestimulus functional connectivity reflects attention orientation in a prospective memory task: A magnetoencephalographic (MEG) study.

Prospective Memory (PM) is the ability to encode an intention in memory and retrieve it at the right time in the future. After the intention is formed, it must be maintained in memory while simultaneously monitoring the environment until the occurrence of the stimulus associated with its retrieval. Therefore, monitoring and maintenance processes must work in conjunction to subserve PM processing (monitoring/maintenance phase). Several brain regions play a role in PM, such as the anterior prefrontal cortex, inferior parietal lobules, and precuneus. Notably, these regions belong to different brain networks and are differently involved depending on the memory and attentional requests of the PM task. In this study, we investigate the neural bases of PM from a network perspective, using functional connectivity (FC) analysis to identify the networks involved in the attentional and memory mechanisms underlying PM. To this end, we analyzed MEG data collected in two different PM conditions, enhancing either the monitoring (i.e., attention) or the maintenance (i.e., memory) loads of the PM task. To disentangle the neural correlates of these mechanisms from other processes occurring after stimulus presentation, the analysis focused on the prestimulus time window (monitoring/maintenance phase). The monitoring-load condition was characterized by increased inter-network FC of the Dorsal Attention Network (DAN) in the alpha band, a marker of increased top-down monitoring. In contrast, the maintenance-load condition was associated with increased connectivity of the Ventral Attention Network (VAN) with the FrontoParietal Control and the Default-Mode Networks (FPCN and DMN, respectively). Additionally, response times were found to correlate with prestimulus alpha connectivity of different networks in the two conditions. These differences in connectivity within and between networks support the hypothesis that different networks (DAN, or VAN and DMN) and mechanisms (top-down or bottom-up, respectively) are involved in PM processing depending on the features of the PM task

Metacontrast masking of symmetric stimuli.

This study investigated whether symmetry perception is vulnerable to metacontrast masking and whether such masking selectively disrupts feedback-dependent visual processes. Across four experiments, we employed a metacontrast paradigm with briefly presented targets (20 ms) followed by masks at varying stimulus onset asynchronies (SOAs), manipulating both target-mask configuration and task demands. All experiments produced the classic U-shaped accuracy-by-SOA curve associated with Type B masking, where performance is lowest at intermediate SOAs. Critically, performance at 0 ms SOA varied depending on the perceptual compatibility of the stimuli. In Experiments 1 and 2, the target and mask were spatially complementary and could be perceptually grouped into a unified figure. Under these conditions, performance at 0 ms SOA exceeded the no-mask baseline, reflecting facilitation due to perceptual integration. In contrast, in Experiments 3 and 4-where the stimuli and mask had no complementary shape and could not be integrated into a coherent object-performance at 0 ms SOA was slightly suppressed, indicating that integration failed to occur. These findings suggest that facilitation at short SOAs depends on the rapid formation of a coherent perceptual object, whereas symmetry detection-requiring temporally extended, feedback-supported integration-is more susceptible to early interruption by masking. Together, these results support both dual-channel and recurrent models of visual masking. Type B suppression reflects interactions between fast feedforward and slower feedback signals, while the presence or absence of early facilitation serves as an index of perceptual organization. These findings underscore how stimulus structure and task context affect the temporal dynamics of shape perception

IL17F: A Possible Risk Marker for Spondyloarthritis in HLA-B*27 Negative Brazilian Patients

HLA-B*27 is an important marker for spondyloarthritis (SpA), however, many SpA patients are HLA-B*27 negative. Thus, the aim of this study was to investigate the influence of IL17, TNF and VDR gene polymorphisms in SpA patients who were HLA-B*27 negative. This case-control study was conducted in 158 patients [102 patients with ankylosing spondylitis (AS) and 56 with psoriatic arthritis (PsA)] and 184 controls. HLA-B*27 genotyping was performed using PCR-SSP and IL17A (rs2275913), IL17F (rs763780), TNF-308 (rs1800629), TNF-238 (rs361525), FokI C>T (rs2228570), TaqI C>T (rs731236), ApaI A>C (rs7975232), and BsmI C>T (rs1544410) using PCR-RFLP. Statistical analyses were performed by Chi-square and logistic regression using OpenEpi and SNPStats software. The IL17F C allele frequency was higher in patients with SpA, AS and PsA compared to controls. The IL17F T/C genotype frequency was higher in SpA patients in an overdominant inheritance model and when men and women were separately analyzed. IL17A_IL17F AC haplotype was significantly associated to the risk for SpA patients. As for VDR, the ApaI a/a was a potential risk factor for SpA in men. In conclusion, IL17F C variant contributed to the risk of SpA in Brazilian patients who were HLA-B*27 negative and could be a potential marker for SpA

IL17F: A Possible Risk Marker for Spondyloarthritis in HLA-B*27 Negative Brazilian Patients

HLA-B*27 is an important marker for spondyloarthritis (SpA), however, many SpA patients are HLA-B*27 negative. Thus, the aim of this study was to investigate the influence of IL17, TNF and VDR gene polymorphisms in SpA patients who were HLA-B*27 negative. This case-control study was conducted in 158 patients [102 patients with ankylosing spondylitis (AS) and 56 with psoriatic arthritis (PsA)] and 184 controls. HLA-B*27 genotyping was performed using PCR-SSP and IL17A (rs2275913), IL17F (rs763780), TNF-308 (rs1800629), TNF-238 (rs361525), FokI C&gt;T (rs2228570), TaqI C&gt;T (rs731236), ApaI A&gt;C (rs7975232), and BsmI C&gt;T (rs1544410) using PCR-RFLP. Statistical analyses were performed by Chi-square and logistic regression using OpenEpi and SNPStats software. The IL17F C allele frequency was higher in patients with SpA, AS and PsA compared to controls. The IL17F T/C genotype frequency was higher in SpA patients in an overdominant inheritance model and when men and women were separately analyzed. IL17A_IL17F AC haplotype was significantly associated to the risk for SpA patients. As for VDR, the ApaI a/a was a potential risk factor for SpA in men. In conclusion, IL17F C variant contributed to the risk of SpA in Brazilian patients who were HLA-B*27 negative and could be a potential marker for SpA.</jats:p

The Influence of Vitamin D Receptor Gene Polymorphisms in Spondyloarthritis

Spondyloarthritis (SpA) is an inflammatory rheumatic disease related to low bone mineral density. Because vitamin D plays an important role in bone metabolism and immune system modulation, the aim of this study was to evaluate the influence of polymorphisms in vitamin D receptor genes (VDR) in the development of SpA. In this case–control study, a total of 244 patients with SpA and 197 individuals with no SpA were included. Among the patients, 174 had ankylosing spondylitis (AS) and 66 had psoriatic arthritis (PsA). Genotyping of FokI (rs2228570 C > T), BsmI (rs1544410 C > T), ApaI (rs7975232 A > C), and TaqI (rs731236 T > C) was performed using PCR-RFLP, while genotyping of HLA-B∗27 was performed using PCR-SSP. Serum levels for hydroxy (OH) vitamin D and the clinical activity index of the disease (BASDAI) were also evaluated. SNPStats and OpenEpi software were used for statistical analysis. The ApaI a allele and ApaI a/a genotype were less frequent in PsA compared with controls. The ApaI a/a genotype was associated with a protecting factor for PsA in females, and ApaI A/a was associated with a protecting factor for the disease in HLA-B∗27 positive patients. Notwithstanding, the ApaI a/a genotype was a risk factor for SpA and AS in males. The FokI f/f genotype was associated with a better clinical activity in PsA. When considering the covariates, vitamin D sufficiency, and gender, the FokI F/F genotype was associated with a risk factor in males with SpA and AS compared with females with this same genotype. In conclusion, the ApaI rs7975232 polymorphism was associated with PsA, and the FokI rs2228570 polymorphism was associated with better clinical PsA activity. ApaI and FokI were associated with SpA and AS when considering gender and vitamin D sufficiency

Mobility of flumioxazin herbicide in a Dystrophic Red Yellow Latosol at Brazilian Southern Amazon

Herbicides are chemicals which can contaminate soil and water, if inadvertently used. In the soil, the herbicide may undergo adsorption and leaching or degradation by physical, chemical and biological processes in addition to being absorbed by the weeds and / or cultivation. The aim of this study was to determine the mobility of flumioxazin in Dystrophic Red Yellow Latosol, in the southern Amazon, using sorghum plant as test under different rainfall indexes. We used PVC pipes, which were filled with soil. The experimental design was completely randomized in a 2x2x5 factorial scheme, consisting of herbicide treatments [with or without flumioxazin (50 g i.a. ha-1)], rain (40 or 80 mm) and soil depths (2.5, 5, 10, 15 and 30 cm). After each rainfall simulation, the tubes were removed and sorghum seeds were placed in the depths 2.5, 5, 10, 15 and 30 cm from the top of the columns. It was observed a higher activity of flumioxazin in the initial 2.5 cm. In all depths where herbicide effect was observed, it was also observed the interruption of sorghum growth, being more intense in the simulations of 80 mm of rainfall. The herbicide presented high adsorptive capacity in Dystrophic Red Yellow Latosol, with mobility up to the first 2.5 cm along the profile.</jats:p

The Influence of Vitamin D Receptor Gene Polymorphisms in Spondyloarthritis

Spondyloarthritis (SpA) is an inflammatory rheumatic disease related to low bone mineral density. Because vitamin D plays an important role in bone metabolism and immune system modulation, the aim of this study was to evaluate the influence of polymorphisms in vitamin D receptor genes (VDR) in the development of SpA. In this case–control study, a total of 244 patients with SpA and 197 individuals with no SpA were included. Among the patients, 174 had ankylosing spondylitis (AS) and 66 had psoriatic arthritis (PsA). Genotyping of FokI (rs2228570 C &gt; T), BsmI (rs1544410 C &gt; T), ApaI (rs7975232 A &gt; C), and TaqI (rs731236 T &gt; C) was performed using PCR-RFLP, while genotyping of HLA-B ∗ 27 was performed using PCR-SSP. Serum levels for hydroxy (OH) vitamin D and the clinical activity index of the disease (BASDAI) were also evaluated. SNPStats and OpenEpi software were used for statistical analysis. The ApaI a allele and ApaI a/a genotype were less frequent in PsA compared with controls. The ApaI a/a genotype was associated with a protecting factor for PsA in females, and ApaI A/a was associated with a protecting factor for the disease in HLA-B ∗ 27 positive patients. Notwithstanding, the ApaI a/a genotype was a risk factor for SpA and AS in males. The FokI f/f genotype was associated with a better clinical activity in PsA. When considering the covariates, vitamin D sufficiency, and gender, the FokI F/F genotype was associated with a risk factor in males with SpA and AS compared with females with this same genotype. In conclusion, the ApaI rs7975232 polymorphism was associated with PsA, and the FokI rs2228570 polymorphism was associated with better clinical PsA activity. ApaI and FokI were associated with SpA and AS when considering gender and vitamin D sufficiency.</jats:p