Serial Diurnal Salivary Cortisol Profiles in 667 Pregnant Women—Association With Cardiometabolic Complications

Author:

Schowe Alicia M12ORCID,Czamara Darina1,Lahti-Pulkkinen Marius3,Girchenko Polina3,Castro-Quintas Águeda45,Fañanas Lourdes45,Binder Elisabeth B1,Räikkönen Katri36ORCID

Affiliation:

1. Department of Genes and Environment, Max Planck Institute of Psychiatry , 80804 Munich , Germany

2. Graduate School of Systemic Neuroscience, Ludwig-Maximilian-Universität , 80804 Munich , Germany

3. Department of Psychology and Logopedics, University of Helsinki , 00014 Helsinki , Finland

4. Department of Evolutionary Biology, Ecology and Environmental Sciences (BEECA), Faculty of Biology, University of Barcelona, Institute of Biomedicine of the University of Barcelona (IBUB) , 08007 Barcelona , Spain

5. Network Centre for Biomedical Research in Mental Health (CIBER of Mental Health, CIBERSAM), Institute of Health Carlos III , 28029 Madrid , Spain

6. Department of Obstetrics and Gynecology, HUS Helsinki University Hospital , 00260 Helsinki , Finland

Abstract

Abstract Context Maternal obesity, hypertensive pregnancy disorders, and gestational diabetes (GDM) are linked to an increased risk of negative offspring health outcomes. This association may be mediated by maternal hypothalamic-pituitary-adrenal axis (HPA axis) activity, resulting in elevated maternal cortisol levels and fetal exposure, but evidence remains scarce. Objective We (1) examined maternal diurnal cortisol profiles longitudinally across gestation, and (2) explored associations with maternal cardiometabolic complications. Methods Women in the InTraUterine sampling in early pregnancy (ITU) study (n = 667) provided 7 salivary cortisol samples from awakening to bedtime up to 3 times during pregnancy (median gestational week 19.3, 25.7, and 38.1; n = 9356 samples). Changes in cortisol awakening response (CAR) and diurnal slope (indicative of HPA axis activity) and their associations with maternal body mass index (BMI), hypertensive pregnancy disorders and GDM were examined using linear mixed models. Results The CAR declined in 60% to 67% of women, and the diurnal slope attenuated from early to late pregnancy (b = 0.006; P = .001). Higher BMI was associated with less decline in CAR (b = 0.031; P = .0004) and less attenuation in diurnal slope from early to late pregnancy (b = −0.001; P = .006). Hypertensive pregnancy disorders and GDM were not significantly associated with diurnal cortisol profiles. Conclusion The attenuation in CAR and diurnal slope support HPA axis hyporesponsivity during pregnancy. Less attenuation of both markers in women with a higher BMI may indicate reduced adaption of the HPA axis to pregnancy, presenting a mechanistic link to offspring health outcomes.

Publisher

The Endocrine Society

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