Publications by authors named "Cristina Carrazzone"

Article Synopsis
  • * A study of 402 Brazilian CD patients analyzed genetic polymorphisms in genes related to CD and its progression to determine associations with CARD severity, using logistic regression to adjust for factors like age and treatment.
  • * Although some genetic variants suggested potential links to CARD severity, no strong associations were confirmed after adjusting for multiple comparisons, while a specific haplotype showed protective effects against severe CARD progression.
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It is well documented that Chagas disease (CD) can pose a public health problem to countries. As one of the World Health Organization Neglected Tropical Diseases undoubtedly calls for comprehensive healthcare, transcending a restricted biomedical approach. After more than a century since their discovery, in 1909, people affected by CD are still frequently marginalised and/or neglected.

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Chagas disease is among the 21 neglected diseases according to the World Health Organization. This study aimed to investigate the morbidity and mortality distribution of Chagas disease for identifying areas with greater prevalences and deaths of the disease in Northeast Brazil. A population-based ecological study was performed from 2016 to 2018 using data on acute Chagas disease patients from the Disease Notification Information System, chronic cases from the Chagas Disease and the referral Heart Failure Outpatient Clinic in Pernambuco, and Chagas disease-related mortality from the Mortality Information System.

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Article Synopsis
  • Soluble TNF receptors (sTNFR1 and sTNFR2) inhibit TNF and their levels are elevated in various diseases, including Chagas disease, where TNF plays a crucial role in immune response and pathology.
  • In a study of 132 chronic Chagas disease patients, it was found that levels of sTNFR1 and sTNFR2 were higher in infected individuals compared to non-infected controls, indicating they may help regulate TNF activity.
  • A moderate correlation was observed between sTNFR1 and TNF in patients with the indeterminate form of the disease, suggesting a protective mechanism against progression to more severe conditions like heart disease.
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Introduction: Chagas disease (CD) is a neglected disease caused by the parasite Trypanosoma cruzi. One-third of infected patients will develop the cardiac form, which may progress to heart failure (HF). However, the factors that determine disease progression remain unclear.

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Background: The severity of chronic chagasic cardiomyopathy (CCC), the most frequent clinical outcome of Chagas disease (CD), has been associated with cytokine-enriched heart tissue inflammation, and high serum levels of transforming growth factor (TGFβ), interferon-gamma (IFNγ), and tumour necrosis factor (TNF). Conversely, increased interleukin (IL)-10 serum concentrations have been associated with asymptomatic CD. Cytokines and cytokine-related gene polymorphisms may control cytokine expression and have been proposed to contribute to CCC outcomes.

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Chronic cardiomyopathy is the main clinical manifestation of Chagas disease (CD), a disease caused by infection. A hallmark of chronic chagasic cardiomyopathy (CCC) is a fibrogenic inflammation mainly composed of CD8 and CD4 T cells and macrophages. CC-chemokine ligands and receptors have been proposed to drive cell migration toward the heart tissue of CD patients.

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