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Biphasic Glucocorticoid Rhythm in One-Month-Old Infants: Reflection of a Developing HPA-Axis?
Jonneke J Hollanders1, Bibian van der Voorn2, Paul de Goede3,4
1Pediatric Endocrinology, Emma Children's Hospital, Amsterdam University Medical Center, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
Insights
One-month-old infants show a biphasic glucocorticoid (GC) rhythm, with morning and evening peaks. Breast milk GC levels may influence infant GC patterns, offering insights into early HPA axis development.
Area of Science:
- Endocrinology
- Developmental Biology
- Neonatal Research
Background:
- The hypothalamus-pituitary-adrenal (HPA) axis regulates the stress response and exhibits diurnal patterns.
- Understanding the development of the HPA axis in early life is crucial for assessing infant health.
- Limited data exists on HPA axis rhythmicity in the first month of life.
Purpose of the Study:
- To characterize the diurnal rhythm of glucocorticoids (GCs) in 1-month-old infants.
- To investigate potential influencing factors on infant HPA axis activity, including maternal distress and breast milk GCs.
Main Methods:
- Observational study involving 55 mother-infant pairs.
- Collection of infant saliva and maternal breast milk at 1 month postpartum.
- Analysis of cortisol and cortisone concentrations using liquid chromatography-tandem mass spectrometry.
Main Results:
- Infants exhibited a significant biphasic GC rhythm with peaks in the morning and evening.
- No association was found between infant GC rhythm and maternal psychological distress, season, or infant sex.
- Breast milk cortisol and cortisone levels were associated with infant GC rhythmicity and timing.
Conclusions:
- A group-level biphasic GC rhythm is present in 1-month-old infants.
- Breast milk GCs may play a role in establishing infant GC rhythm, potentially through signaling or enhanced mother-infant synchrony.
- This study enhances understanding of early-life HPA axis development.
Context:
The hypothalamus-pituitary-adrenal (HPA) axis displays a diurnal rhythm. However, little is known about its development in early life.
Objective:
To describe HPA-axis activity and study possible influencing factors in 1-month-old infants.
Design:
Observational.
Setting:
Amsterdam University Medical Center, location VU University Medical Center (VUMC), and Onze Lieve Vrouwe Gasthuis (OLVG), Amsterdam.
Participants:
Fifty-five mother-infant pairs.
Interventions:
Collection of breast milk and infants' saliva 1 month postpartum for analysis of glucocorticoids (GCs; ie, cortisol and cortisone) using liquid chromatography- tandem mass spectrometry.
Main Outcome Measure:
GC rhythm in infants' saliva and associations with vulnerability for maternal psychological distress (increased Hospital Anxiety and Depression Scale [HADS] score) or consultation at the Psychiatric Obstetric Pediatric (POP clinic), season at sampling, sex, and breast milk GC rhythmicity analyzed with SigmaPlot 14.0 software (Systat Software, San Jose, CA, USA) and regression analyses.
Results:
A significant biphasic GC rhythm was detected in infants, with mean peaks [standard error of the mean, SEM] at 6:53 am [1:01] and 18:36 pm [1:49] for cortisol, and at 8:50 am [1:11] and 19:57 pm [1:13] for cortisone. HADS score, POP consultation, season at sampling, and sex were not associated with the infants' GC rhythm. Breast milk cortisol maximum was positively associated with infants' cortisol area-under-the-curve (AUC) increase and maximum. Higher breast milk cortisone AUC increase, AUC ground, and maximum were associated with an earlier maximum in infants. Breast milk and infant GC concentrations were associated between 6:00 am and 9:00 am.
Conclusions:
A biphasic GC rhythm, peaking in the morning and evening, was seen in 1-month-old infants at a group level. Breast milk GC parameters might be associated with the infants' GC rhythm, possibly caused by a signaling effect of breast milk GCs, or as an associative effect of increased mother-infant synchrony. These results contribute to an increased understanding of early life HPA-axis development.
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