TY - JOUR
T1 - Pharmacokinetic modeling of prenatal vitamin D exposure and the impact on offspring asthma and pulmonary function
AU - Shadid, Iskander L C
AU - Brustad, Nicklas
AU - Chawes, Bo L
AU - Moes, Dirk Jan A R
AU - Weiss, Scott T
AU - Guchelaar, Henk-Jan
AU - Mirzakhani, Hooman
N1 - Copyright © 2025. Published by Elsevier Masson SAS.
PY - 2025/2
Y1 - 2025/2
N2 - Gestational 25-hydroxyvitamin D (25[OH]D) is important in fetal lung development and may influence offspring respiratory outcomes, making accurate exposure assessment essential to understand clinical associations. Therefore, we used the combined data from two large RCTs investigating prenatal vitamin D supplementation, which included early and late prenatal 25(OH)D measurements, to refine a population pharmacokinetic model of vitamin D-25(OH)D and estimate individual area under the curve (AUC) Z-scores. The primary outcome was physician-diagnosed offspring asthma/wheezing at ages 3 and 6 years, and lung function, as a secondary outcome, was evaluated by spirometry at the ages 6 and 8 years. In total, 1319 mother-child pairs were included. We found that clearance of 25(OH)D increased with gestational age and bodyweight, and decreased with higher baseline 25(OH)D levels. Prenatal 25(OH)D AUC Z-scores were negatively associated with asthma/wheezing at age 3 years (aOR = 0.75, 95 % CI = 0.64-0.88, p < 0.001) and 6 years (aOR = 0.83, 95 % CI = 0.72-0.95, p = 0.008). Longitudinal analysis of lung function from age 6-8 years showed that AUC Z-scores were positively associated with percent-predicted FEV1 (β = 1.21%, 95 % CI = 0.30-2.11; p = 0.009), FVC (β = 0.79 %, 95 % CI = 0.13-1.46; p = 0.021), FEV1/FVC ratio (β = 0.56 %, 95 % CI = 0.11-1.01; p = 0.015) and FEF25-75 % (β = 2.18 %, 95 % CI = 0.46-3.91; p = 0.009). These results together indicate an exposure-outcome relationship where higher gestational 25(OH)D exposure, estimated by AUC, is associated with reduced childhood asthma/recurrent wheeze and improved lung function.
AB - Gestational 25-hydroxyvitamin D (25[OH]D) is important in fetal lung development and may influence offspring respiratory outcomes, making accurate exposure assessment essential to understand clinical associations. Therefore, we used the combined data from two large RCTs investigating prenatal vitamin D supplementation, which included early and late prenatal 25(OH)D measurements, to refine a population pharmacokinetic model of vitamin D-25(OH)D and estimate individual area under the curve (AUC) Z-scores. The primary outcome was physician-diagnosed offspring asthma/wheezing at ages 3 and 6 years, and lung function, as a secondary outcome, was evaluated by spirometry at the ages 6 and 8 years. In total, 1319 mother-child pairs were included. We found that clearance of 25(OH)D increased with gestational age and bodyweight, and decreased with higher baseline 25(OH)D levels. Prenatal 25(OH)D AUC Z-scores were negatively associated with asthma/wheezing at age 3 years (aOR = 0.75, 95 % CI = 0.64-0.88, p < 0.001) and 6 years (aOR = 0.83, 95 % CI = 0.72-0.95, p = 0.008). Longitudinal analysis of lung function from age 6-8 years showed that AUC Z-scores were positively associated with percent-predicted FEV1 (β = 1.21%, 95 % CI = 0.30-2.11; p = 0.009), FVC (β = 0.79 %, 95 % CI = 0.13-1.46; p = 0.021), FEV1/FVC ratio (β = 0.56 %, 95 % CI = 0.11-1.01; p = 0.015) and FEF25-75 % (β = 2.18 %, 95 % CI = 0.46-3.91; p = 0.009). These results together indicate an exposure-outcome relationship where higher gestational 25(OH)D exposure, estimated by AUC, is associated with reduced childhood asthma/recurrent wheeze and improved lung function.
KW - Humans
KW - Asthma
KW - Female
KW - Pregnancy
KW - Vitamin D/blood
KW - Child
KW - Child, Preschool
KW - Prenatal Exposure Delayed Effects
KW - Lung/physiopathology
KW - Male
KW - Models, Biological
KW - Respiratory Function Tests
KW - Adult
KW - Dietary Supplements
KW - Gestational Age
UR - http://www.scopus.com/inward/record.url?scp=85216091559&partnerID=8YFLogxK
U2 - 10.1016/j.biopha.2025.117859
DO - 10.1016/j.biopha.2025.117859
M3 - Journal article
C2 - 39874780
SN - 0753-3322
VL - 183
SP - 117859
JO - Biomedicine & Pharmacotherapy
JF - Biomedicine & Pharmacotherapy
M1 - 117859
ER -