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Maternal and neonatal 25‐hydroxyvitamin D concentrations and school‐age lung function, asthma and allergy. The Generation R Study
Author(s) -
MensinkBout Sara M.,
Meel Evelien R.,
Jongste Johan C.,
Voortman Trudy,
Reiss Irwin K.,
Jong Nicolette W.,
Jaddoe Vincent W. V.,
Duijts Liesbeth
Publication year - 2019
Publication title -
clinical and experimental allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.462
H-Index - 154
eISSN - 1365-2222
pISSN - 0954-7894
DOI - 10.1111/cea.13384
Subject(s) - medicine , asthma , spirometry , vital capacity , vitamin d and neurology , allergy , population , odds ratio , gestation , vitamin d deficiency , pregnancy , pediatrics , immunology , diffusing capacity , lung , lung function , environmental health , biology , genetics
Summary Background Vitamin D deficiency in early life might affect the developing lung and immune system, and subsequently influence the risk of asthma and allergy in later life. Objective We examined the associations of 25‐hydroxyvitamin D concentrations in mid‐gestation and at birth with lung function, asthma, inhalant allergic sensitization and inhalant allergy at school‐age. Methods This study among 4951 children and their mothers was embedded in a population‐based prospective cohort in Rotterdam, the Netherlands. Maternal venous blood samples in mid‐gestation and umbilical cord blood samples at birth were used to determine 25‐hydroxyvitamin D concentrations. At age 10 years, lung function was measured by spirometry, current asthma and physician‐diagnosed inhalant allergy by questionnaire, and inhalant allergic sensitization by skin prick tests. We used multivariable regression models to examine associations. Results Higher 25‐hydroxyvitamin D concentrations in mid‐gestation were associated with a higher forced vital capacity (FVC), but a lower forced expiratory volume in 1 second/FVC (FEV 1 /FVC) and a lower forced expiratory flow after exhaling 75% of FVC (FEF 75 ) ( Z ‐score differences [95% CI] 0.02 [0.00, 0.03], −0.02 [−0.03, −0.01] and −0.01 [‐0.03, −0.00], respectively, per 10 nmol/L 25‐hydroxyvitamin D), but not with asthma. Furthermore, higher 25‐hydroxyvitamin D concentrations in mid‐gestation were associated with an increased risk of inhalant allergy (Odds Ratio [95% CI] 1.07 [1.02, 1.12]), but not with inhalant allergic sensitization. After additional adjustment for child's 25‐hydroxyvitamin D concentrations at the age of 6 years, only the associations of 25‐hydroxyvitamin D concentrations in mid‐gestation with FEV 1 /FVC and FEF 75 remained. We did not find consistent associations of 25‐hydroxyvitamin D concentrations at birth with respiratory or allergy outcomes. Conclusion and clinical relevance Our results suggest that maternal 25‐hydroxyvitamin D concentrations in mid‐gestation may influence lung development. The clinical implications of the observed associations remain unclear.