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    <title>DSpace Communidade:</title>
    <link>https://ri.ufs.br/jspui/handle/riufs/2416</link>
    <description />
    <pubDate>Thu, 09 Apr 2026 05:19:25 GMT</pubDate>
    <dc:date>2026-04-09T05:19:25Z</dc:date>
    <image>
      <title>DSpace Communidade:</title>
      <url>http://ri.ufs.br:80/retrieve/bada6a0e-e914-42f3-a481-bc6ebd218f46/ppgcs.jpg</url>
      <link>https://ri.ufs.br/jspui/handle/riufs/2416</link>
    </image>
    <item>
      <title>Adaptação transcultural do Skin Cancer Index para o português e avaliação da qualidade de vida em pacientes com câncer de pele não melanoma cervicofacial</title>
      <link>https://ri.ufs.br/jspui/handle/riufs/24195</link>
      <description>Título: Adaptação transcultural do Skin Cancer Index para o português e avaliação da qualidade de vida em pacientes com câncer de pele não melanoma cervicofacial
Autor(es): Hora, Evânia Curvelo
Abstract: Non-melanoma skin cancer (NMSC) is the most frequent malignant neoplasm in Brazil.&#xD;
NMSCs occur mostly in the cervicofacial region, are associated with high morbidity, and often&#xD;
require surgical management. This causes functional, aesthetic, and emotional sequelae&#xD;
impacting the patient's quality of life (QoL). The Skin Cancer Index (SCI) was created to&#xD;
measure the QoL of NMSC patients. This study aimed to perform a cross-cultural adaptation of&#xD;
the SCI to the Portuguese language and the culture of northeastern Brazil, and measure its&#xD;
psychometric properties of reliability, validity, and responsiveness in assessing the QoL of&#xD;
patients with cervicofacial NMSC. This way, a specific instrument was developed to measure&#xD;
the QoL of this population. This study was performed in two stages. The first stage consisted&#xD;
of methodological research on the cross-cultural adaptation of the SCI through five steps: initial&#xD;
translation, synthesis of translations, back-translation, expert committee approval, and testing&#xD;
of the pre-final version (n=40). The second stage was a cross-sectional study on the clinical&#xD;
validation and assessment of the QoL of these patients (n= 182). The first stage resulted in an&#xD;
adapted version of the SCI. This version reached a Content Validity Index level significantly&#xD;
higher than 80% (p&lt;0.05), evaluated through the Exact Binomial test. Temporal stability of the&#xD;
SCI during the test and retest periods was observed. Moreover, the Pearson’s correlations, as&#xD;
well as the Intraclass Correlation Coefficient, showed coefficients higher than 0.9, indicating&#xD;
excellent reliability. In the second stage, the adapted version was administered together with&#xD;
the Brazilian version of the Dermatology Life Quality Index (DLQI), during the pre-and post-&#xD;
operative periods (4 months postoperatively). Reliability in the subscales, and the total&#xD;
instrument, guaranteed by McDonald's ω, were considered ideal (&gt;0.8) in all sub- dimensions.&#xD;
Moreover, α was considered ideal in the “emotional” and “social” sub-dimensions.Construct&#xD;
validity was obtained in all sub-dimensions and on the scale using the criteria (χ2) p-value &gt;&#xD;
0.05, RMSEA &lt; 0.08, CFI ≥ 0.9, and SRMR ≤ 0.08. QoL and responsiveness were assessed by&#xD;
the student’s t-test in a paired sample at T0 (preoperatively) and T1 (4 monthspostoperatively).&#xD;
Significant results were observed with an increase in the SCI scale scores in all its dimensions&#xD;
and the total instrument (p &lt; 0.001), and a decrease in the DLQI scale (p = 0.001). This showed&#xD;
that the adapted scale demonstrated a better postoperative QoL. The variables that presented&#xD;
significant results in the total scale, which indicated better QoL, were “men” (p = 0.002),&#xD;
“without children” (p = 0.019), “income above 4 minimun wages (p &lt; 0.001), “from the private&#xD;
sector” (p &lt; 0.001), “did not report itching” (p = 0.021), and “no scalp lesions” (p=0.012). The&#xD;
QoL measurement indicated a change from the baseline and postoperative improvement in all&#xD;
subscales and in the total instrument. The final version of the SCI adapted to the Portuguese&#xD;
language was called “SCI-versão brasileira” and proved to be a valid, reliable, and responsive&#xD;
instrument that allows health professionals to identify changes in the QoL of patients with&#xD;
NMSC.</description>
      <pubDate>Sun, 01 Jan 2023 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://ri.ufs.br/jspui/handle/riufs/24195</guid>
      <dc:date>2023-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Perfil fenotípico e funcional de neutrófilos em paciente COVID-19 após vacinação</title>
      <link>https://ri.ufs.br/jspui/handle/riufs/23631</link>
      <description>Título: Perfil fenotípico e funcional de neutrófilos em paciente COVID-19 após vacinação
Autor(es): Oliveira, Yrna Lorena Matos de
Abstract: Introduction: A dysregulation in the innate immune response against the SARS-CoV-2&#xD;
coronavirus may contribute to a worse prognosis in COVID-19. Serum biomarkers released by&#xD;
neutrophils such as the TREM-1 receptor and IL-6 are associated with the severity of&#xD;
inflammatory diseases. Different functional profiles of neutrophils have been described with an&#xD;
important role in antiviral defense and also in the inflammatory process triggered by the virus.&#xD;
With the advance of vaccination, it is important to understand how neutrophils are contributing&#xD;
to the pathogenesis of the disease. Aim: To evaluate the neutrophil profile in COVID1-9 after&#xD;
vaccination. Methods: This study was divided into two chapters, the first referring to a meta-&#xD;
analysis and the second to an experimental study. The meta-analysis was carried out in order to&#xD;
evaluate serum levels of the soluble form of TREM-1 (sTREM-1) in humans with viral&#xD;
pneumonia compared to healthy controls, according to the PRISMA guideline, and seven&#xD;
studies were included, four studies analyzed patients with COVID-19 and three studies&#xD;
evaluated other viruses. The cross-sectional study was carried out with severe COVID-19&#xD;
patients, 17 unvaccinated and 12 vaccinated, admitted to intensive care units. The phenotypic&#xD;
and functional profile of neutrophils and the dosage of serum proteins and cytokines were&#xD;
evaluated. The neutrophil phenotype was determined by flow cytometry using the following&#xD;
surface markers: CD11b (cell adhesion), CD16 (phagocytic capacity), CD182 (chemotaxis),&#xD;
TREM-1 (activation), HLA-DR (antigen presentation) and CD274 (suppressive activity),&#xD;
together with the dosage of serum proteins, IL-6 and sTREM-1 assessed using specific&#xD;
immunoassays and, the dosage of cytokines : GM-CSF; IFN-γ; IL-1β; IL-2; IL-4; IL-5; IL-12&#xD;
p70; IL-13; IL-18; and TNF-α by the LUMINEX method. Results: The meta-analysis found&#xD;
increased sTREM-1 levels in COVID-19 patients compared to healthy controls (SMD 1.53;&#xD;
95% CI 0.53-2.52). In addition, higher sTREM-1 levels were found in vaccinated severe&#xD;
COVID-19 patients compared to healthy patients. There was no significant difference between&#xD;
severe and non-severe COVID-19 patients. The cross-sectional study found that serum IL-6&#xD;
levels were significantly higher in unvaccinated severe COVID-19 patients compared to the&#xD;
vaccinated group. In vaccinated patients, neutrophils expressed more surface markers TREM-&#xD;
1, CD182, HLA-DR, MFI of HLA-DR and PD-L1, as well as an increase in the&#xD;
CD16+CD182+TREM-1+ population (p=0.0009) and the HLA-DR+PDL-1+ population&#xD;
(p&lt;0.0001). Correspondingly, vaccinated patients showed significant correlations mainly&#xD;
related to the number of PD-L1+ neutrophils and inflammatory cytokines, while in&#xD;
unvaccinated patients, inflammatory cytokines were negatively correlated with TREM-1 on the&#xD;
surface of neutrophils. Conclusion: From these data we can conclude that the TREM-1&#xD;
molecule participates in the pathogenesis of COVID-19 and that vaccination has favored a more&#xD;
activated state or a more prepared immune system, in terms of regulation, antigen presentation,&#xD;
chemotaxis, inflammatory response and immune activation in the face of SARS-CoV-2&#xD;
infection.</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://ri.ufs.br/jspui/handle/riufs/23631</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Tendência secular de mortalidade e morbidade por câncer do colo do útero nas regiões do Brasil</title>
      <link>https://ri.ufs.br/jspui/handle/riufs/23629</link>
      <description>Título: Tendência secular de mortalidade e morbidade por câncer do colo do útero nas regiões do Brasil
Autor(es): Ferrari, Yasmim Anayr Costa
Abstract: Cervical cancer continues to be a significant public health challenge worldwide.&#xD;
Despite well-established prevention and screening methods, the disease still exhibits&#xD;
high rates of incidence, morbidity, and mortality among women. The objective of this&#xD;
research is to analyze the long-term trends in mortality and morbidity caused by&#xD;
cervical cancer in Brazil and its regions. This study utilizes a population and ecological&#xD;
approach with time series analysis, examining cases of cervical cancer-related deaths&#xD;
and hospitalizations across all age groups in the five Brazilian regions: Midwest,&#xD;
Northeast, North, Southeast, and South. The data used for analysis were obtained&#xD;
from the Department of Informatics of the Unified Health System. Information on&#xD;
deaths came from the Mortality Information System (SIM) and hospitalizations from the&#xD;
Hospital Information System (SIH). The specific codes employed to retrieve the data&#xD;
were 180 (Malignant neoplasm of the cervix) according to the International&#xD;
Classification of Diseases (ICD) 9 and C53 (Malignant neoplasm of the cervix)&#xD;
according to ICD-10. Crude rates, age-specific rates, and age-standardized rates were&#xD;
calculated for each year and age group, using both the Brazilian population and the&#xD;
world population as references. The age groups were categorized into 20 to 44 years,&#xD;
45 to 64 years, and 65 years or older, excluding women below 19 years of age due to&#xD;
their low representation (less than 0.5%). The mortality trend was calculated using the&#xD;
Joinpoint Regression Program, version 4.9.1.0, National Cancer Institute, USA. The&#xD;
statistical significance adopted was 5.0%, identified through the Monte Carlo&#xD;
Permutation test, and the Confidence Interval (CI) was 95.0%. There were 171,793&#xD;
thousand deaths recorded from 1980 to 2021 and 736,491 thousand hospitalizations&#xD;
from 1992 to 2021. Mortality rates from cervical cancer increased in the North and&#xD;
Northeast and decreased in other places. Hospitalization rates have reduced in Brazil&#xD;
and in all regions. Regarding mortality trends, there was a reduction in the Central-&#xD;
West (AAPC -1,3; CI -1,5; -1,1) and Southeast (AAPC -0,9; CI -1,4; -0,5), stability in&#xD;
Brazil (AAPC -0,3; CI -1,0; 0,4), North (AAPC 0,6; CI -0,1; 1,3) and South (AAPC 0,0;&#xD;
CI -0,5; 0,5) and an increase in the Northeast (AAPC 0,6; CI 0,3; 0,8). For&#xD;
hospitalizations, Brazil (AAPC -2,5; CI -3,9; -1,0), Northeast (AAPC -3,2; CI -4,5; -1,9)&#xD;
and Southeast (AAPC -2,9; CI -4,7; -1,2) showed decreasing trends and the Central-&#xD;
West (AAPC -2,6; CI -5,6; 0,4), North (AAPC -1,2; CI -5,0; 2,8) and South (AAPC -1,7;&#xD;
CI -3,6; 0,2) regions-maintained stability. Regional disparities were evident in this&#xD;
study, where the North and Northeast had the highest mortality rates. Despite&#xD;
decreasing and stationary trends, cervical cancer still represents an important cause&#xD;
of illness and death in Brazilian women.</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://ri.ufs.br/jspui/handle/riufs/23629</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
    </item>
    <item>
      <title>Presença de polimorfismos genéticos no receptor de vitamina D e padrão da reserva corporal de micronutrientes e suas relações com os marcadores do controle glicêmico, perfis lipídico e inflamatório de indivíduos com diabetes mellitus tipo 2</title>
      <link>https://ri.ufs.br/jspui/handle/riufs/23615</link>
      <description>Título: Presença de polimorfismos genéticos no receptor de vitamina D e padrão da reserva corporal de micronutrientes e suas relações com os marcadores do controle glicêmico, perfis lipídico e inflamatório de indivíduos com diabetes mellitus tipo 2
Autor(es): Santos, Ramara Kadija Fonseca
Abstract: Genetic single nucleotide polymorphisms (SNPs) and haplotypes in the vitamin D&#xD;
receptor (VDR), and deficiencies in vitamin D, magnesium (Mg), zinc (Zn), calcium (Ca)&#xD;
and potassium (K) are factors that alone contribute to inadequate metabolic control in&#xD;
individuals with type 2 diabetes mellitus (DM2). Thus, the aim of this study is to associate&#xD;
the presence of SNPs in the VDR, haplotypes and patterns of micronutrient body reserves&#xD;
with markers of glycemic control, lipid levels and inflammatory profile in individuals&#xD;
with DM2. To this end, a meta-analysis evaluated the association between the presence&#xD;
of SNPs in the VDR and markers of glycemic control, lipid levels and inflammatory&#xD;
profile in individuals with DM2, following the MOOSE guidelines and registered with&#xD;
PROSPERO (nºCRD42021268152). A systematic search of the data was carried out in&#xD;
the PubMed, EMBASE and SCOPUS databases. Studies comparing the values of markers&#xD;
of glycemic control, lipid profile and inflammation between the identified genotypes were&#xD;
included. The quality of the studies was assessed using the Newcastle-Ottawa scale.&#xD;
Effect sizes were tested using a random-effects model and reported as standardized mean&#xD;
difference (SMD) and 95% confidence interval (95%CI). In parallel, an observational,&#xD;
cross-sectional study was carried out with 160 adults with DM2, both sexes, living in&#xD;
Sergipe. Sociodemographic information was collected, anthropometric and body&#xD;
composition assessments were carried out, and blood was drawn to identify SNPs and&#xD;
assess biochemical markers of glycemic and lipid control. The frequency of SNPs,&#xD;
linkage disequilibrium and the Hardy-Weinberg test were calculated and SNPs with a&#xD;
frequency greater than 1% were inserted into the haplotype model. The SNPs and&#xD;
haplotypes, and the micronutrient body reserve patterns established by principal&#xD;
component analysis and stratified into quartiles, were entered into the binary logistic&#xD;
regression model tests (dependent variables therapeutic target values for fasting glycemia,&#xD;
percent of glycated hemoglobin (%HbA1c) and Homeostasis Model Assessment - Insulin&#xD;
Resistance (HOMA-IR) adjusted for gender, age, time of diagnosis and BMI, significance&#xD;
p&lt;0.05. The meta-analysis identified four SNPs: Fokl (rs2228570); BsmI (rs1544410);&#xD;
Taql (rs731236) and Apal (rs7975232). The Fokl and BsmI SNPs were associated with&#xD;
higher %HbA1c (SMD=0.409, p=0.002) and triacylglycerol (SMD=0.206, p=0.023),&#xD;
respectively. In the observational study, the Bsml SNP was associated with increased&#xD;
%HbA1c (OR=2.071, p=0.045), but the haplotypes did not contribute to inadequate&#xD;
glycemic control. Two patterns of body micronutrient reserve were established. The&#xD;
lowest quartile of Pattern 1 (Mg, Zn, Ca and K) and Pattern 2 (25(OH)D and Zn) were&#xD;
4.319 (p=0.019) and 3.970 (p=0.038) times more likely to increase HOMA-IR and&#xD;
%HbA1c values, respectively. It is concluded that SNPs in the VDR and the pattern of&#xD;
micronutrient body reserves explained by the lower concentration of 25(OH)D, Zn, Mg,&#xD;
Ca and K contribute to poor metabolic control in individuals with DM2.</description>
      <pubDate>Mon, 01 Jan 2024 00:00:00 GMT</pubDate>
      <guid isPermaLink="false">https://ri.ufs.br/jspui/handle/riufs/23615</guid>
      <dc:date>2024-01-01T00:00:00Z</dc:date>
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