Publications by authors named "Veronica Euclydes"

We aimed to develop and validate a standardized, qualitative-quantitative protocol for digital IHC analysis to assess neurodevelopmental biomarkers in placental tissue. Placental tissues from 60 births were obtained from the Western Region Birth Cohort (ROC), and IHC staining was performed using Novolink Polymer System. The primary antibody against 11βHSD2 protein was used for protocol development, and ANXA1 was employed for validation.

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This paper reports the methods and preliminary findings of Germina, an ongoing cohort study to identify biomarkers and trajectories of executive functions and language development in the first 3 years of life. 557 mother-infant dyads (mean age of mothers 33.7 years, 65.

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Introduction: Interpersonal violence against women is a major global health problem that may have intergenerational effects. This study investigated associations between maternal experiences of interpersonal violence and other traumatic events and maternal and infant salivary diurnal cortisol in a cohort of adolescent mothers in São Paulo, Brazil.

Method: Adolescent mothers (14-19 years) participating in a home-visiting intervention were interviewed retrospectively about lifetime and pregnancy violence and trauma exposure.

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Article Synopsis
  • The study investigates how maternal immune responses during pregnancy, particularly through immune biomarkers, affect the neurodevelopment of children in their first two years of life.
  • It examines maternal psychosocial stress and childhood trauma, measuring various inflammatory markers at two gestational stages in 160 women.
  • Results indicate that specific immune profiles in late pregnancy can predict children's neurodevelopmental progress, while no direct correlation was found between maternal stress and immune markers, suggesting a complex interaction between stress and immune response in predicting neurodevelopment.
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  • Primary human trophoblast stem cells (TSCs) and those derived from human pluripotent stem cells (hPSCs) can be modeled in the lab, but how hPSCs differentiate into TSCs is not well understood.
  • This study shows that a specific primed pluripotent state can produce TSCs by activating certain pathways (like EGF and WNT) and inhibiting others (like TGFβ and ROCK), all without adding BMP4, referred to as the TS condition.
  • The researchers found that the TSCs generated under TS conditions can proliferate extensively and closely resemble first-trimester placental cells, suggesting that primed hPSCs can differentiate into TSCs through various
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  • Maternal prenatal psychosocial stress negatively impacts the hypothalamic-pituitary-adrenal axis function in infants, with unknown biological mechanisms possibly linked to altered DNA methylation.
  • A study was conducted with 80 pregnant adolescents, measuring maternal distress via depression and anxiety, and assessing infant DNA methylation and cortisol levels at 12 months.
  • Key findings indicated that elevated maternal anxiety and cortisol levels in late pregnancy were associated with lower DNA methylation of stress-related genes in infants, particularly the oxytocin receptor gene (OXTR), which may influence stress regulation.
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Background: Physiological maternal stress response, such as imbalance in the glucocorticoid pathway and immune system seems to be mediated by DNA methylation (DNAm) and might translate intrauterine stress exposures into phenotypic changes in a sex-specific manner. DNAm in specific sites can also predict newborn gestational age and gestational age acceleration (GAA). GAA occurs when the predicted biological age is higher than the chronological age.

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The crosstalk between maternal stress exposure and fetal development may be mediated by epigenetic mechanisms, including DNA methylation (DNAm). To address this matter, we collect 32 cord blood samples from low-income Brazilian pregnant adolescents participants of a pilot randomized clinical intervention study (ClinicalTrials.gov, Identifier: NCT02807818).

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Background: Gestational diabetes mellitus (GDM) is a common complication of pregnancy. It may predispose offspring to increased fat mass (FM) and the development of obesity, however few data from Latin America exist.

Objective: To investigate the influence of GDM on newborn FM in mother-newborn pairs recruited from a public maternity care center in São Paulo, Brazil.

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Objectives: Adipose tissue development starts in intrauterine life and cytokines are involved in this process. Therefore, understanding the role of cytokines in the fat mass gain of infants is crucial to prevent obesity later in life. Furthermore, recent evidence indicates a sex-specific link between cytokines and adipose tissue development.

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Sex differences in the prevalence of psychiatric disorders are well documented, with exposure to stress during gestation differentially impacting females and males. We explored sex-specific DNA methylation in the cord blood of 39 females and 32 males born at term and with appropriate weight at birth regarding their potential connection to psychiatric outcomes. Mothers were interviewed to gather information about environmental factors (gestational exposure) that could interfere with the methylation profiles in the newborns.

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Increased maternal blood concentrations of leptin and decreased adiponectin levels, which are common disturbances in obesity, may be involved in offspring adiposity by programming fetal adipose tissue development. The aim of this study was to assess the relationship between maternal leptin and adiponectin concentrations and newborn adiposity. This was a cross-sectional study involving 210 healthy mother-newborn pairs from a public maternity hospital in São Paulo, Brazil.

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