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A Modified Trier Social Stress Test for Vulnerable Mexican American Adolescents
Published on: July 10, 2017
Hyper-responsiveness to acute stress, emotional problems and poorer memory in former preterm children
Andrea A Quesada1, Rosana M Tristão, Riccardo Pratesi
1Department of Cognitive Psychology, Institute of Cognitive Neuroscience, Ruhr-University Bochum , Bochum , Germany .
Insights
Preterm birth (PTB) survivors show altered stress hormone profiles and heightened emotional difficulties, impacting memory and behavior into childhood. These long-term effects are more pronounced in girls, suggesting early adversity impacts neurodevelopment.
Area of Science:
- Neuroscience
- Endocrinology
- Developmental Psychology
Background:
- Preterm birth (PTB) affects neurodevelopment and hormonal systems, with long-term childhood outcomes poorly understood.
- Early life stress in preterm infants can lead to lasting negative health consequences.
Purpose of the Study:
- Compare cortisol and alpha-amylase (sAA) profiles, including cortisol awakening response (CAR), between preterm and full-term children.
- Evaluate stress responsiveness in preterm children using the Trier Social Stress Test for Children (TSST-C).
- Assess memory skills and emotional/behavioral profiles in preterm children.
Main Methods:
- Measured basal and stress-induced cortisol and sAA levels in 30 preterm and 30 full-term children (aged 6-10).
- Administered the Wide Range Assessment of Memory and Learning and the Strengths and Difficulties Questionnaire.
- Compared physiological and psychological data between preterm and control groups.
Main Results:
- Preterm children exhibited higher awakening cortisol, a blunted CAR, and exaggerated TSST-C response.
- Alterations in stress response were more pronounced in girls.
- Preterm children showed more emotional problems and poorer memory performance.
Conclusions:
- Preterm birth has lasting, sex-dependent effects on the hypothalamic-pituitary-adrenal (HPA) axis, behavior, and memory.
- Early adversity may alter HPA axis set-point, creating a vulnerable phenotype.
- Findings highlight the need for continued monitoring of preterm children's neuroendocrine and psychosocial development.
Abstract:
The prevalence of preterm birth (PTB) is high worldwide, especially in developing countries like Brazil. PTB is marked by a stressful environment in intra- as well as extrauterine life, which can affect neurodevelopment and hormonal and physiological systems and lead to long-term negative outcomes. Nevertheless, little is known about PTB and related outcomes later on in childhood. Thus, the goals of the current study were threefold: (1) comparing cortisol and alpha-amylase (sAA) profiles, including cortisol awakening response (CAR), between preterm and full-term children; (2) evaluating whether preterm children are more responsive to acute stress and (3) assessing their memory skills and emotional and behavioral profiles. Basal cortisol and sAA profiles, including CAR of 30 preterm children, aged 6 to 10 years, were evaluated. Further, we assessed memory functions using the Wide Range Assessment of Memory and Learning, and we screened behavior/emotion using the Strengths and Difficulties Questionnaire. The results of preterm children were compared to an age- and sex-matched control group. One week later, participants were exposed to a standardized laboratory stressor [Trier Social Stress Test for Children (TSST-C)], in which cortisol and sAA were measured at baseline, 1, 10 and 25 min after stressor exposure. Preterm children had higher cortisol concentrations at awakening, a flattened CAR and an exaggerated response to TSST-C compared to full-term children. These alterations were more pronounced in girls. In addition, preterm children were characterized by more emotional problems and poorer memory performance. Our findings illustrate the long-lasting and in part sex-dependent effects of PTB on the hypothalamic-pituitary-adrenal (HPA) axis, internalizing behavior and memory. The findings are in line with the idea that early adversity alters the set-point of the HPA axis, thereby creating a more vulnerable phenotype.
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