Background Vitamin D is associated with lung function in adults, but its relation with childhood lung function is still unclear.
Objective To investigate whether prenatal and postnatal vitamin D supplementation and plasma level is associated with childhood lung function.
Methods In the KOALA Birth Cohort Study, children's lung function (n=436) was measured at age 6–7 years by means of spirometry and presented as forced expiratory volume in 1 s (FEV1) z scores and forced vital capacity z scores. The mother and child's 25-hydroxyvitamin D plasma level was determined around 36 weeks of pregnancy and at age 2 years. Vitamin D supplement intake during pregnancy was defined based on the amount of vitamin D in supplements, and trimester and duration of use. Data on child's vitamin D supplement use were collected through questionnaires at ages 1, 2 and 6–7 years.
Results 25-Hydroxyvitamin D level and vitamin D supplement use in childhood were not associated with lung function. Maternal use of vitamin D at <10 μg/day (adjusted beta (AdjB −0.37; 95% CI −0.69 to −0.05)), vitamin D containing multivitamin use in the second and/or third trimester (AdjB −0.26; 95% CI −0.49 to −0.03), and use for two trimesters (AdjB −0.25; 95% CI −0.49 to −0.02) were associated with a significantly lower FEV1 z score compared with no supplements. Maternal use of vitamin D at ≥10 μg/day and use in the first or all trimesters was not associated with significantly lower lung function levels.
Conclusion The authors found no association between 25-hydroxyvitamin D levels, vitamin D supplementation in childhood or recommended vitamin D dosage of ≥10 μg/day during pregnancy and lung function in children aged 6–7 years.
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What is the key question?
Is there an association between vitamin D supplement use and 25-hydroxyvitamin D level, during pregnancy and in childhood, and lung function level at school age?
What is the bottom line?
Vitamin D supplement use and 25-hydroxyvitamin D level during pregnancy and in childhood are not associated with lung function in school-aged children.
Why read on?
Although vitamin D has been positively associated with lung function in adults, its relation with childhood lung function is still unclear.
Determinants of pulmonary function in children are age, height and gender and it has become increasingly clear that antenatal and early life exposures are important influencing factors as well. Exposure to tobacco smoke, both prenatally and postnatally,1 2 and lower level of physical activity3 are well documented to reduce children's lung function. There is also evidence that a healthy maternal diet and high vitamin E levels during pregnancy,4 5 and a childhood diet consisting of a high intake of antioxidant vitamins, fruit and vegetables are associated with higher lung function levels.6
Lately the role of vitamin D in lung development and lung function is receiving increasing attention.7 Lung development begins in the uterus and continues through the first years of life. Postnatally, type II alveolar cells are responsible for proliferation of alveolar epithelium to maintain the integrity of the lung during growth, development, and in reaction to lung damage.8 Studies in fetal rat lung have identified alveolar type II cells as a target for vitamin D and have shown that vitamin D is important in surfactant production and lung maturation.9–11 There is evidence that low maternal vitamin D status during pregnancy is associated with disturbances in lung function in 50-day-old rats.12 From limited in vitro studies, vitamin D exposure, as early as 14 weeks' gestation, seems to be an important influencing factor for the developing and growing human lung as well, but these mechanisms are far more complex and it is not known what vitamin D levels are related to normal lung development.13–15 It is unknown how evidence from animal studies translates to human lung development but it is possible that (abnormal) vitamin D status during pregnancy and in childhood affects children's lung function as well.
Studies that investigated the relation between vitamin D and lung function levels are scarce. The cross-sectional study of Black and Scragg16 showed that serum 25-hydroxyvitamin D (25(OH)D) was positively associated with forced expiratory volume in 1 s (FEV1) and forced vital capacity (FVC) in human adults. Another study17 reported that higher 25(OH)D levels were associated with better lung function in adults with asthma.
No study to date has examined prospectively the 25(OH)D levels of mother and child during pregnancy and their relation to childhood lung function. Therefore the aim of this study is to investigate the association between 25(OH)D plasma levels and vitamin D supplement use, during pregnancy and in childhood, and lung function levels at school age.
Material and methods
Study population and data collection
This cohort study is conducted within the prospective KOALA Birth Cohort Study in the Netherlands. The study design has previously been described in detail.18 In brief, from October 2000, healthy pregnant women with a conventional lifestyle (N=2343) were recruited from a prospective cohort study on pregnancy-related pelvic girdle pain (N=7020).19 In addition, pregnant women with an alternative lifestyle (N=491) with regard to child-rearing practices, diet (organic, vegetarian), vaccination programs and/or use of antibiotics were recruited through several ‘alternative’ channels like organic food shops and anthroposophic doctors' practices. All participants (N=2834) were enrolled between 14 and 18 weeks of gestation.
Women recruited from January 2002 onwards (conventional and alternative) were asked to consent to maternal blood sampling at 36 (±1) weeks of pregnancy (N=1365). Children of women from this group in whom blood collection was successful (N=1356) were eligible for venous blood sampling at age 2 years and lung function measurement at age 6–7 years. Information on vitamin D supplementation during pregnancy and in childhood was collected by questionnaires at 34 weeks of gestation, and when the child was aged 1, 2 and 6–7 years. Data on potential confounders were collected by questionnaires at 14 and 34 weeks of pregnancy and when the child was aged 1, 2, 4–5, and 6–7 years.
All parents signed informed consent forms. Ethical approval was obtained from the medical ethics committee of the Maastricht University/University Hospital Maastricht and the Netherlands Central Committee for Medical Studies on Human Subjects (CCMO).
Inclusion criteria were availability of biosamples, availability of questionnaire data at 34 weeks of pregnancy, and written informed consent. Exclusion criteria were birth at less than 37 weeks of pregnancy and congenital abnormalities related to immunity (such as Down's syndrome). Ultimately, 436 children were included in the study (figure 1).
Assessment of plasma 25-hydroxyvitamin D level
After collection by trained research assistants, the blood samples were centrifuged immediately, transported at 4°C and stored at −80°C in a biobank until further analysis. Plasma levels of 25(OH)D were determined with an ELISA kit from Immuno Diagnostic Systems (IDS, Boldon, UK).
Assessment of vitamin D supplement use
Maternal multivitamin supplement use was assessed in the 34th week of pregnancy by questionnaire. Data on the brand and type of multivitamins, duration and trimester of use were collected and vitamin D dosage in the supplements was estimated using a comprehensive list of dietary supplements used at that time in the Netherlands.20 Vitamin D intake through supplements was calculated and categorised (0 μg/day, <10 μg/day, ≥10 μg/day). Multivitamin use was also classified into trimester(s) of use during pregnancy (no supplement use, in first trimester, in second and/or third trimester, in all trimesters) to see if this affected outcome. Also, the duration of vitamin D containing multivitamin use in pregnancy was categorised (no supplement use, during one trimester, two trimesters, or all trimesters).
Data on vitamin D supplement use during childhood were collected using questionnaires at ages 1, 2, and 6–7 years. At age 1 year, vitamin D supplement use was defined as use in the 11th and/or 12th month (no, yes). Vitamin D supplementation at age 2 years was defined as use of vitamin D and/or AD supplements (no, yes) in the second year of life. During the home visits at age 6–7 years, information on the brand and type of vitamin D supplements and the amount taken was collected. Based on these data, vitamin D intake through supplements was calculated and categorised (0 μg/day, >0 to ≤2.5 μg/day, >2.5 μg/day). Cod liver oil supplements were not included because at age 1 and 2 years only two children (0.5%) used these supplements and at age 6–7 years none of the children used these supplements.
Assessment of lung function
Children's lung function was assessed at age 6–7 years by trained research assistants during home visits using the hand-held Medikro Spirostar USB spirometer (Medikro, Kuopio, Finland) according to the American Thoracic Society/European Respiratory Society (ATS/ERS) guidelines.21 22 Testing was performed after 10 min rest in an upright seated position. Each child performed forced expiratory manoeuvres that continued until three acceptable curves were achieved, with a maximum of eight attempts. Curves were acceptable if they met the reproducibility criteria defined by the ATS/ERS.21 22 FEV1 and FVC measures were collected and z scores were computed using Stanojevic prediction equations,23 taking into account the child's sex, age, weight and height, ambient temperature, humidity and barometric pressure measured by the assistant during the home visit.
Data analysis was performed using SPSS 15.0 for Windows. Linear regression models were used to analyse the association between 25(OH)D level, vitamin D supplementation and the lung function outcomes. Because women taking part in the KOALA study were recruited from two different channels (conventional and alternative), the effect of vitamin D exposure and recruitment group on lung function was assessed. Because the interaction terms did not reach statistical significance (p values ranged between 0.24 and 0.87), participants from both recruitment sources were pooled for analyses.
Quintiles of 25(OH)D were computed based on the distribution in the cohort, for the mothers and 2-year-old children separately, with the first quintile assigned as a reference group. All analyses were adjusted for recruitment group, maternal age at delivery, maternal education level, maternal smoking at 14 weeks and 34 weeks of pregnancy, alcohol consumption at 14 weeks and 34 weeks of pregnancy, maternal body mass index (BMI) before pregnancy, child's BMI at age 2 years, birth weight, exposure to environmental tobacco smoke in first 6–7 years of life, multivitamin use at age 2 years, season of blood sampling for determining 25(OH)D level, physical activity at age 4–5 years and age 6–7 years.
The results are presented as regression coefficients beta (B), unadjusted (crudeB) or adjusted (adjB) for all potential confounders, with corresponding 95% CI. Test for trend over the quintiles of 25(OH)D and over the different groups of vitamin D dosage/day was calculated in the univariable and multivariable regression models. p<0.05 was considered statistically significant.
In 440 out of 2834 children included in the KOALA study, FEV1 and FVC at age 6–7 years were measured and approved. Four children were excluded because they were born at less than 37 weeks. Of the remaining 436 children, the mother and child's 25(OH)D levels were available for 415 children (95.2%) and 287 children (65.8%) respectively. Information was available for all children on maternal vitamin D dosage/day, period and duration of vitamin D containing supplementation during pregnancy. Data on the child's vitamin D use at age 1, 2, and 6–7 years were available for 435 children (99.8%), 433 children (99.3%) and 433 children (99.3%) respectively (figure 1).
The distribution of population characteristics for the total cohort at birth, the cohort who provided biosamples, and the study population with lung function measurements at age 6–7 years is outlined in table 1 (see also appendix table A1). The recruitment period for blood sampling coincided with the period in which women were recruited from ‘alternative’ channels and so the subgroup that provided biosamples included proportionally more families with an alternative lifestyle than a conventional lifestyle. At age 6–7 years, mainly families with a conservative lifestyle were visited for lung function testing. The number of smokers in this group was lower compared with the total cohort.
The mean (±SD) 25(OH)D plasma level for mothers at 36 weeks of pregnancy was 46.0 (±18.2) nmol/litre and for children at age 2 years, 73.1 (±22.0) nmol/litre. The mother and child's 25(OH)D levels were not associated with lung function at age 6–7 years (table 2). Analysing 25(OH)D level as a continuous variable instead of computing quintiles did not significantly change the results (results not shown).
Use of vitamin D supplementation at <10 μg/day was associated with a significantly lower FEV1 z score compared with the reference group (0 μg/day) (AdjB −0.37; 95% CI −0.69 to −0.05) (table 3). No such association was found between vitamin D intake at ≥10 μg/day and FEV1 z score or FVC z score. Also, no significant trend was found towards lower lung function levels with increasing vitamin D dosage/day during pregnancy (adjusted pfor trend=0.16 and 0.83, respectively).
When vitamin D containing multivitamins were used during the second and/or third trimesters of pregnancy the FEV1 z score (AdjB −0.26; 95% CI −0.49 to −0.03) was significantly lower compared with no use at all. Vitamin D containing multivitamins used in the first trimester or during all trimesters were not associated with lung function levels. Overall, duration of vitamin D containing multivitamin use in pregnancy was not associated with FVC z scores or FEV1 z scores. Only when mothers used these supplements during two trimesters was a significantly lower FEV1 z score seen compared with the reference group (AdjB −0.25, 95% CI −0.49 to −0.02) (table 3).
Vitamin D use at age 1, 2, and 6–7 years was not associated with higher lung function levels in childhood (table 4). Also, when analysing vitamin D dosage/day at age 6–7 years as a continuous variable no significant associations were found (results not shown).
The results did not change significantly when only children without asthma were included in the analyses. Because of the small number of children with asthma in this study, it was not possible to analyse these children separately.
The relationship between vitamin D supplement use (yes, no) and plasma 25(OH)D level during pregnancy and at age 2 years is outlined in table 5. Vitamin D supplement use was associated with 25(OH)D level, especially when vitamin D production through sunlight exposure is low (low season).
A linear regression model was constructed and included factors associated with 25(OH)D level. In the season with high cutaneous vitamin D production, vitamin D containing multivitamin use, maternal obesity, and recruitment group were associated with maternal 25(OH)D level. In the low season multivitamin use increased the 25(OH)D level but maternal overweight was not statistically significantly associated with 25(OH)D level. Maternal education was not associated with maternal 25(OH)D level and was therefore not included in the final model.
For children, only vitamin D supplement use was associated with increased 25(OH)D level at age 2 years. Multivitamin use, child's overweight, maternal education, gender and recruitment group were not associated with child's 25(OH)D level and therefore were excluded from the final model.
In this birth cohort study we found no association between the mother and child's 25(OH)D level or vitamin D supplementation at age 1, 2, and 6–7 years and FEV1 z scores and FVC z scores at age 6–7 years. Maternal use of vitamin D at <10 μg/day, multivitamin use in the second and/or third trimester and use for two trimesters in pregnancy were associated with decreased FEV1 z scores. However, there was no consistent trend towards lower lung function levels with increasing maternal vitamin D dosage/day or duration of multivitamin use in pregnancy.
In line with our results, Devereux et al24 reported that maternal dietary vitamin D intake during pregnancy and child's dietary vitamin D intake were not associated with better lung function levels at age 5 years old. To our knowledge, no studies to date have examined 25(OH)D levels during pregnancy and early childhood in relation to childhood lung function, although two cross-sectional studies in adults (with asthma)16 17 found, in contrast to our results, that higher 25(OH)D levels were associated with better lung function. Because the range of 25(OH)D level in our study was comparable to the other studies,16 17 this could not explain the different results. However, these studies measured vitamin D level and lung function cross-sectionally, making the results prone to reverse causation because healthier people with better lung function may spend more time outdoors and consequently have higher 25(OH)D levels. Furthermore, these studies were conducted in adult populations. After early adult life, lung growth ceases and tissue damage accumulates, and vitamin D may influence lung function by effects on a variety of cell types important in lung tissue repair and remodelling. This study found no evidence of an effect of vitamin D on still developing lungs in mainly healthy school-aged children. However, this may only be apparent in healthy children if vitamin D status is outside the normal range or only in children with asthma or atopic predisposition. The literature reports positive effects of vitamin D on wheeze at age 3 years25 and 5 years,24 and on asthma.26 Xystrakis et al27 found that in patients with corticosteroid-resistant asthma, supplementation of the active form of vitamin D3 could reverse steroid resistance through induction of interleukin -10 secreting T-regulatory cells, suggesting vitamin D is clinically relevant for asthma. However, others reported that vitamin D supplementation in infancy may increase the risk of asthma and allergies.28 29 Gale et al reported that a high maternal 25(OH)D level during pregnancy was associated with an increased risk of asthma at age 9 years.30 Ginde et al31 found that vitamin D decreases risk of respiratory infections (and wheeze). This can lead to less cumulate airway damage in predisposed children and may prevent clinical asthma in some cases.
This study did not consider dietary vitamin D intake because it is naturally present in very few foods we eat, for example oily fish, fish liver oil, egg yolk and offal.32 Also, vitamin D supplements contain significantly more vitamin D than vitamin D-containing foods33 and the bioavailability of vitamin D from food is less than from supplements (50% vs 55–99%).34
This study was not able to investigate vitamin D supplementation in pregnancy as a standalone supplement. Therefore the possibility that the findings were confounded by other vitamins used cannot be completely excluded. For example, vitamin A and D both bind to the retinoid X receptor and therefore may antagonise each other's action. It has also been suggested that vitamin A and E in pregnancy may improve childhood lung function.4 However, in the Netherlands, the regular multivitamin supplements contain only a limited amount of vitamin A (and the pregnancy supplements contain none because of teratogenicity). Also, the vitamin E amount in the multivitamin supplements in the Netherlands is about 30–50% less compared with the study described above,4 making a possible influence on our findings small.
25(OH)D level is considered the most accurate measurement of short-term vitamin D status because it takes diet, supplements and sunlight exposure into account. However, this one-time measurement might not reflect a person's vitamin D status over the course of a year.33 Because blood samples were taken at 36 weeks of pregnancy in this study, the relationship between 25(OH)D levels in early pregnancy and childhood lung function could not be assessed. Measuring vitamin D intake through supplements is considered a more accurate assessment of long-term vitamin D status.33 Because information was collected on dosage and duration of supplement use for mothers in pregnancy and children aged 6–7 years, the intake of vitamin D from supplements could be accurately determined. In addition, 25(OH)D levels and questions about supplemental intake complement each other, and so a combination of these exposition factors was used to achieve vitamin D status throughout a person's lifetime.
This study had the advantage of a prospective follow-up with relatively short intervals between questionnaires, decreasing recall bias. Self-reporting questionnaires are a valid method for assessing supplement use.35 The study populations' characteristics after 6–7 years of follow-up were comparable to those at birth, making bias as a result of differential loss to follow-up unlikely. Missing data due to non-response could have influenced the results, but this is expected to be non-differential.
Measurement and assessment of lung function were performed in line with the ATS/ERS guidelines.21 22 According to Miller et al22 acceptable spirometry curves can be obtained in children as young as 5 years if these guidelines are followed.
In conclusion, the study found that, in contrast to previous studies in adults and adolescents, there was no association between 25(OH)D level, vitamin D supplement use in childhood or recommended vitamin D dosage of ≥10 μg/day during pregnancy and lung function levels at age 6–7 years.
We thank the children and their parents who participated in the KOALA Birth Cohort Study. In addition, we thank H. Cremers and P. Beekhof for their excellent assistance in the analysis of 25(OH)D level.
|Child's vitamin D status|
|Available (N=287)||Unavailable (N=149)|
|Recruitment group conventional||246 (85.7%)||134 (89.9%)|
|Maternal age at delivery (mean±SD)||32.5±3.6||32.2±3.6|
|Low||21 (7.3%)||12 (8.2%)|
|Middle||113 (39.5%)||56 (38.4%)|
|High||142 (49.7%)||76 (52.0%)|
|Other||10 (3.5%)||2 (1.4%)|
|Maternal smoking during early pregnancy†|
|Yes||13 (4.6%)||6 (4.0%)|
|Maternal smoking during late pregnancy‡|
|Yes||15 (5.2%)||7 (4.7%)|
|Maternal alcohol use during early pregnancy†|
|Yes||27 (11.4%)||19 (14.6%)|
|Maternal alcohol use during late pregnancy‡|
|Yes||45 (15.7%)||25 (16.8%)|
|Maternal BMI before pregnancy (mean±SD)||24.0±3.9||23.3±3.4|
|Boy||127 (44.3%)||71 (47.7%)|
|<2500 g||1 (0.3%)||2 (1.4%)|
|2500–4500 g||276 (96.2%)||141 (94.6%)|
|>4500 g||10 (3.5%)||6 (4.0%)|
|Child's BMI at 2 years (mean±SD)||16.4±1.3||16.8±1.6|
|Use of multivitamins/minerals at age 2 years|
|Yes||46 (16.1%)||22 (15.0%)|
|Exposure to environmental tobacco smoke in first 6–7 years of life|
|Yes||47 (16.4%)||24 (16.1%)|
|Physical activity at age 4–5 years (mean±SD)||13.5±6.6||13.2±6.0|
|Physical activity at age 6–7 years (mean±SD)||14.9±6.4||14.2±6.2|
BMI, body mass index.
↵* Low: primary school, preparatory vocational or lower general secondary school, middle: vocational, higher general secondary or pre-university education, high: higher vocational or academic education.
↵† Early pregnancy: 14th week of pregnancy.
↵‡ Late pregnancy: 34th week of pregnancy.
Funding This study was financially supported by grants from the Netherlands Asthma Foundation (grant numbers 3.2.07.022 and 3.2.03.48), the Netherlands Organization for Health Research and Development (ZonMw Prevention Program number 1.210-00-090), Royal Friesland Foods, Triodos Foundation, Phoenix Foundation, Raphaël Foundation, Iona Foundation, Foundation for the Advancement of Heilpedagogie, The Netherlands Brain Foundation, and the Netherlands Ministry of Public Health, Welfare and Sport.
Competing interests None
Ethics approval Ethical approval was obtained from the medical ethics committee of the Maastricht University/University Hospital Maastricht and the Netherlands Central Committee for Medical Studies on Human Subjects (CCMO).
Provenance and peer review Not commissioned; externally peer reviewed.
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