ECEESPE2025 Poster Presentations Adrenal and Cardiovascular Endocrinology (169 abstracts)
1Department of Endocrinology, Odense University Hospital, Odense, Denmark, Odense, Denmark; 2Department of Clinical Pharmacology, Pharmacy and Environmental Medicine, University of Southern Denmark, Odense, Denmark, Odense, Denmark; 3Odense Child Cohort, Hans Christian Andersen Childrens Hospital, Odense University Hospital, Odense, Denmark, Odense, Denmark; 4Clinic for Cardiology and Angiology, University Heart Center FreiburgBad Krozingen, Medical CenterUniversity of Freiburg, Faculty of Medicine, University of Freiburg, Germany, Freiburg, Germany; 5Experimental and Clinical Research Center, a cooperation between the Max-Delbrück-Center for Molecular Medicine in the Helmholtz Association and the CharitéUniversitätsmedizin Berlin, Germany (R.D.). HELIOS Clinic Berlin-Buch, Department of Cardiology and Nephrology, Berlin, Germany (R.D.), Berlin, Germany; 6Institute for Molecular Medicine, University of Southern Denmark, Odense, Denmark, Odense, Denmark
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Background: Offspring blood pressure (OBP) may be programmed during pregnancy. Accordingly, maternal third trimester 24-hour (24 h) urine (u-) aldosterone levels are associated with feto-placental trophic effects. Furthermore, high potassium and low sodium intakes are generally recommended in adults with normal renal function. We hypothesized that maternal 24 h u-aldosterone levels were positively associated with OBP and maternal intake of potassium and sodium may influence the association.
Objectives: To investigate associations between maternal third trimester 24 h u-aldosterone, potassium and sodium intakes and OBP.
Methods: In the prospective Odense Child Cohort, 475 motherchild dyads had 24 h u-aldosterone from gestational week 29 and OBP (systolic (SBP) and diastolic (DBP)), at ages 3 and 18 months and 3 and 5 years. Maternal potassium and sodium intakes were calculated from 24 h u-potassium and u-sodium excretions.
Results: Increased maternal 24 h u-aldosterone associated with higher SBP in offspring at ages 3 months (β=0.54 mmHg (95% CI: 0.29; 0.79)) and 18 months (β=0.24 mmHg (95% CI: 0.03; 0.44)). One thousand mg/day increase in maternal potassium intake was associated with an average increase in offspring SBP of 0.68 mmHg (95% CI: 0.02; 1.34) up to 5 years of age (pooled), with significant associations only in girls (β=1.14 mmHg (95% CI: 0.21; 2.08)). No significant association was seen between maternal sodium intake and OBP.
Conclusions: Elevated maternal 24 h u-aldosterone and higher dietary potassium intake were associated with higher OBP, but within normal range, in young children, and girls were more susceptible to maternal potassium intake.