Next Article in Journal
Legal Immigration Status is Associated with Depressive Symptoms among Latina Transgender Women in Washington, DC
Next Article in Special Issue
Maternal Serum and Breast Milk Adiponectin: The Association with Infant Adiposity Development
Previous Article in Journal
Physical Activity-Related Injury and Its Associated Factors among Middle School Students in Southern China
Previous Article in Special Issue
Prenatal Perfluorooctyl Sulfonate Exposure and Alu DNA Hypomethylation in Cord Blood
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
IJERPH
Volume 15
Issue 6
10.3390/ijerph15061245
ijerph-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Vitamins A and E during Pregnancy and Allergy Symptoms in an Early Childhood—Lack of Association with Tobacco Smoke Exposure

by
Jolanta Gromadzinska
1,*,
Kinga Polanska
2,
Lucyna Kozlowska
3,
Karolina Mikolajewska
1,
Iwona Stelmach
4,
Joanna Jerzynska
4,
Wlodzimierz Stelmach
5,
Mariusz Grzesiak
6,
Wojciech Hanke
2 and
Wojciech Wasowicz
1
1
Department of Biological and Environmental Monitoring, Nofer Institute of Occupational Medicine, 91-348 Lodz, Poland
2
Department of Environmental Epidemiology, Nofer Institute of Occupational Medicine, 91-348 Lodz, Poland
3
Department of Dietetics, Faculty of Human Nutrition, 02-776 Warsaw, Poland
4
Department of Pediatrics and Allergy, Medical University of Lodz, 90-329 Lodz, Poland
5
Department of Social and Preventive Medicine, Medical University of Lodz, 90-647 Lodz, Poland
6
Polish Mother’s Memorial Hospital—Research Institute change into Polish Mother’s Memorial Hospital Research Institute
*
Author to whom correspondence should be addressed.
Int. J. Environ. Res. Public Health 2018, 15(6), 1245; https://doi.org/10.3390/ijerph15061245
Submission received: 24 April 2018 / Revised: 30 May 2018 / Accepted: 7 June 2018 / Published: 12 June 2018
(This article belongs to the Special Issue Maternal and Child Health 2018)
Versions Notes

Abstract

:
Epidemiological studies have suggested an association between maternal antioxidant levels during pregnancy and development of allergic diseases in their offspring. The aim of the study was to determine plasma vitamins A and E concentration in the 1st trimester of pregnancy, at delivery and in cord blood and to search for a relationship with allergy in up to 2-year-old children who were prenatally exposed or not exposed to tobacco smoke. The study participants included 252 mother-child pairs from Polish Mother and Child Cohort. Vitamin concentrations were measured using the HPLC-UV method, smoking status—as saliva cotinine level using the HPLC-MS/MS technique. Children’s health status was assessed using a questionnaire and pediatricians/allergists examination. Cord plasma vitamin concentrations were significantly lower than their levels in maternal plasma in the 1st trimester and at delivery (p < 0.001). Significantly higher concentrations of vitamin E have been shown to occur during the 1st trimester of pregnancy in plasma of the women who have actively/passively smoked cigarettes compared to the non-smokers (p < 0.02). Multivariate analysis with inclusion of a variety of confounding factors have not indicated any statistically significant associations between β-carotene, vitamins A and E and the risk of food allergy, atopic dermatitis and wheezing in their children up to 2 years of age. The interaction between smoking during pregnancy and vitamins levels on the risk of allergy was not statistically significant (p > 0.4). The relationship between plasma concentration of vitamins A and E, and the risk of allergy in their young children has not been demonstrated.

1. Introduction

Allergic diseases constitute an increasing health problem; from year to year their frequency is increasing. Numerous studies on that subject have been undertaken and a large number of risk factors have been identified [1]. It is believed that the development of allergic diseases is a result of interaction between genetic predispositions, air pollution, lifestyle and environmental chemical exposure [2,3]. Exposure of pregnant women to air pollutants (particulate matter: PM2.5, PM10, nitrogen oxides, ozone, diesel exhaust), environmental irritants (titanium oxide) or skin sensitization (toluene diisocyanate) can affect the risk of allergy development in their children [4]. It is believed that prenatal and postnatal exposure to tobacco smoke is a factor that contributes to the development of not only respiratory but also dermal allergies in infants and young children [5].
Pregnancy is potentially associated with an increasing risk of oxidative stress [6]. Increased reactive oxygen species (ROS) production is normal in the second and third trimesters of pregnancy and is accompanied by elevated markers of oxidative stress [7,8]. Overproduction of ROS has been suggested to be involved in pregnancy-related disorders, such as: decreased lung function, hypertension, preeclampsia, spontaneous abortion, low for gestational age, preterm delivery or fetal death [9,10]. There are a few studies suggesting that cigarette smoking during pregnancy is an additional source of oxidative stress for mothers and their children [11]. There is plenty of evidence that allergic and inflammatory skin diseases are mediated by oxidative stress, and that development of respiratory allergy is associated with generation of oxidative stress [12,13,14].
Cook-Mills, when analyzing a number of both epidemiological and experimental animal studies, indicates that in humans and in animal models development of allergic diseases may start in the prenatal or early postnatal life. A link has been shown to occur between the increased risk of eczema, wheezing and lower respiratory tract infections in the first months after birth and the presence of acute phase proteins in the venous blood of an allergic mother and in umbilical cord blood [4].
The role of some vitamins intake by pregnant women with a diet or in a form of dietary supplements in the development of allergies in their children has not been completely explained. Vitamins A, C and E have a proven antioxidant activity. Their role in the development of allergy has been widely studied; however, it has not been completely explained [15,16]. Literature reviews show that pregnant women who smoke have lower concentrations of low-molecular-weight antioxidants than non-smokers [17]. Allergic diseases associated with the respiratory tract (asthma, rhinitis) develop in younger children, while the risk of eczema development usually occurs in older age, up to 16 years of age [18]. Since contribution of low molecular antioxidants to the development of young children allergy is considered, it seemed advisable to evaluate the potential link between development of allergies and the level of antioxidants twice—separately for children in the first year of life and for the two-year-old.
The aim of the study was to determine concentration of β-carotene (a precursor of vitamin A), vitamins A and E in the venous blood collected in the 1st trimester of pregnancy, at delivery and in cord and to search for a relationship with dermal, respiratory and food allergy in up to 2-year-old children who were prenatally exposed and were not exposed to tobacco smoke.

2. Material and Methods

2.1. Study Design and Population

The study subjects constituted a sample of the population from Polish Mother and Child Cohort (REPRO_PL). A complete description of the design, aim and methodology of the cohort was published in previous papers [19,20].
The study subjects included 252 pregnant women in single pregnancy, not assisted with reproductive technology, recruited from the central part of Poland. All the women with the chronic diseases (including diabetes, hypertension, nephropathy, epilepsy or cancer) and pregnancy complications were excluded from the study. The study subjects were interviewed once in each trimester of pregnancy in order to collect and update sociodemographic data, medical, and reproductive history as well as information about environmental, occupational and lifestyle factors. In addition, during each visit and at delivery, biological samples (saliva and blood) were collected.
One and two years after the children’s birth, the mothers were invited to the medical center where their children’s health status was examined by pediatricians and allergists. For the appropriate recognition of the children’s health status, a questionnaire was administered to the mothers and it was supplemented with information from the medical chart of each child [20,21]. The questionnaire was developed by an allergist based on the recommendations from the International Study of Asthma and Allergies in Childhood. The children were included either to individual allergy type groups or to a healthy group depending on the answer to the following questions: “Has your child ever diagnosed by a doctor with atopic dermatitis?”, “Has your child ever been diagnosed by a doctor with food allergy?”, “Has your child ever wheezed?”
The study was approved by the Ethical Committee of the Nofer Institute of Occupational Medicine, Lodz, Poland (Decision No. 7/2007 and 3/2008). All the women who had agreed to participate in the study were informed about the aims and procedures of the study and were asked to sign an informed consent form.

2.2. Sample Collection and Processing

At each time-point (the 1st trimester of pregnancy, at delivery), 10-mL blood samples were collected into S-MONOVETTE test tubes with lithium heparin as anticoagulant. The blood samples were centrifuged, plasma was collected and stored at −70 °C until the analysis.
Carotenoids (β-carotene, vitamin A) and E levels were determined by the use of an HPLC system integrated with a 190–800 nm UV-VIS detector [22]. NIST-968e (USA, Fat soluble vitamins, carotenoids in human serum) were used as a standard.
Cotinine levels in saliva of the pregnant women (a biomarker of tobacco smoke exposure) were determined using the high performance liquid chromatography coupled with tandem mass spectrometry (HPLC-ESI + MS/MS) as described and optimized by Stragierowicz et al. [23]. Cotinine concentration of 10 ng/mL was a cut-off value for active smoking and 1.5 ng/mL for passive smoking [24].

2.3. Covariates

The following covariates (based on existing literature and our previous assessments within REPRO_PL cohort) were considered: living area (urban, rural), housing condition (molds at home, home dampness, cleaning frequency, pets at home, cockroaches), parental atopy, child gender, birth outcomes, breastfeeding, and socio-demographic variables (parental age and education, marital status, socio-economic status). The detailed description of the variables was published previously [25].

2.4. Statistical Analysis

The statistical analysis was performed using the Statistica data analysis software system, version 12 (StatSoft, Tulsa, OK, USA). Before the statistical analysis, normality of the data was tested using the Shapiro–Wilk statistic. Variables with normal distribution are presented as mean and standard deviation (SD). Statistical analyses were performed using the one-way analysis of variance (ANOVA) test, and the least significant difference (LSD) post hoc test to compare differences between all the groups.
A simple linear correlation between some analyses was evaluated by the Pearson correlation. p value less than 0.05 was considered to be statistically significant.
Finally, the multivariable logistic regression stratified by smoking status during pregnancy was applied. The following variables (significant at 0.1 level) were included into the multivariable model: molds at home, cleaning frequency, pets at home, socio-economic status, maternal education, child gender, atopy in the family, breast feeding and living area.

3. Results

3.1. Maternal and Child Characteristics

Table 1 shows characteristic of the pregnant women and their neonates. Mean age of the women at birth was 29 ± 4 years, more than 80% of the women lived in urban areas. Most of the women were highly educated (69%) and with a medium to high socio-economic status (92%). Based on the cotinine level in saliva, about 13% of the women were classified as active and 31% as passive smokers. Maternal smoking resulted in a lower birth weight (3314 ± 480 g vs. 3444 ± 487 g, p < 0.05), lower child length (54.3 ± 2.7 cm vs. 55.3 ± 2.8 cm, p < 0.009) and lower head circumference (34.1 ± 1.6 cm vs. 34.6 ± 1.6 cm, p < 0.025). Visible molds at home were declared by about 9% of the mothers. About 30% of the families kept some animals at home.
Table 2 shows the children’s health status. About 19% of the children were diagnosed with food allergy and 13% of them with atopic dermatitis. Wheezing was identified in 11% of the children at 1 and 16% of the children at 2 years of age. The allergy symptoms at the age of 1 and 2 was identified for 11%, 7% and 5% of children for food allergy, atopic dermatitis and wheezing, respectively.

3.2. Vitamin Concentration

Cord plasma vitamin concentrations were significantly lower than their levels in maternal plasma in the 1st trimester and at delivery (p < 0.001) (Table 3). Significantly higher concentrations of vitamin E have been shown to occur during the 1st trimester of pregnancy in plasma of the women who have actively/passively smoked cigarettes compared to the non-smokers (p < 0.02).
Significant linear correlations were found between concentrations of vitamins in plasma collected at different studied periods (Table 4).

3.3. Vitamin Levels and Child Allergy

The mean levels of markers of oxidative stress in the 1st trimester of pregnancy, at delivery and umbilical cord blood in mothers whose children had been diagnosed in the 1st or the 2nd year of life with atopic dermatitis, food allergy or wheezing and healthy children is presented in the Supplementary Materials (Table S1). Table S2 presents the results stratified by maternal smoking status during pregnancy (active/passive smokers and non-smokers).
A significantly higher concentration of β-carotene in the 1st trimester of pregnancy was detected in plasma of the women who were active/passive smokers as compared to the non-smokers with healthy children (0.30 ± 0.20 μg/mL vs. 0.23 ± 0.16 μg/mL, p < 0.02) (Table S2). In the perinatal period (maternal blood at delivery), β-carotene concentration was significantly lower in the passive/active smokers whose children developed food allergy in the 1st and 2nd year of their life, compared to the mothers of healthy children (0.25 ± 0.20 μg/mL vs. 0.40 ± 0.25 μg/mL p < 0.03 and 0.19 ± 0.14 μg/mL vs. 0.36 ± 0.27 μg/mL p < 0.05). The mothers who smoked at any time during pregnancy and whose children developed food allergy in the 2nd year of their life had significantly lower levels of β-carotene than the non-smoking mothers of unhealthy children both in the 1st trimester of pregnancy (0.15 ± 0.08 μg/mL vs. 0.30 ± 0.19 μg/mL, p < 0.01) and at delivery (0.19 ± 0.14 μg/mL vs. 0.43 ± 0.22 μg/mL, p < 0.02).
Significantly lower levels of vitamin A were found in the 1st trimester of pregnancy in the non-smoking women whose 2-year-old children developed atopic dermatitis (0.82 ± 0.21 μg/mL vs. 0.99 ± 0.30 μg/mL, p < 0.004) as compared to the healthy children. In the perinatal period, regardless of tobacco smoke exposure of the pregnant women, significantly lower concentrations of vitamin A have been reported in the women whose children at 2 years of age were diagnosed with atopic dermatitis (maternal blood at delivery: for the non-smokers: 0.76 ± 0.23 μg/mL vs. 0.94 ± 0.36 μg/mL, p < 0.02, for the smokers: 0.64 ± 0.29 μg/mL vs. 0.91 ± 0.30 μg/mL, p < 0.04; cord blood: for the non-smokers: 0.47 ± 0.20 μg/mL vs. 0.59 ± 0.20 μg/mL, p < 0.008; for the smokers: 0.39 ± 0.20 μg/mL vs. 0.60 ± 0.39 μg/mL, p < 0.008). Significantly lower plasma levels of vitamin A were detected in the 1st trimester of pregnancy in the women who smoked and whose children developed wheezing during the first year of life, compared to those who did not smoke and whose children were diagnosed with wheezing (0.81 ± 0.25 μg/mL vs. 1.08 ± 0.26 μg/mL, p < 0.03).
In the perinatal period (maternal blood at delivery), significantly higher levels of vitamin E were detected in plasma of the pregnant non-smoking women whose children developed atopic dermatitis as compared to the mothers of healthy children (15.65 ± 4.980 μg/mL vs. 11.68 ± 6.66 μg/mL, p < 0.006). The concentrations of vitamin E in the active/passive smoking pregnant women, whose one-year-old children developed food allergy were significantly lower than in the mothers of children without allergies (9.59 ± 6.36 μg/mL vs. 14.67 ± 6.05 μg/mL, p < 0.01). Significantly higher levels of vitamin E were found in the perinatal period in the non-smoking mothers of children diagnosed with food allergy at 2 years of age than in those mothers whose children were not diagnosed with allergy at 2 years of age (15.78 ± 5.01 μg/mL vs. 11.83 ± 6.83 μg/mL, p < 0.03).During the perinatal period (maternal blood at delivery), in plasma of the active/passive smoking pregnant women whose children developed wheezing at the age of 2, levels of vitamin E were significantly higher compared to the mothers of healthy children (16.45 ± 4.80 μg/mL vs. 11.29 ± 6.48 μg/mL, p < 0.02).

3.4. Association between Markers of Oxidative Stress during Pregnancy and the Risk of Child Allergy—The Multivariable Analysis Stratified by Maternal Smoking Status

The results of multivariable logistic regression analysis for the association between markers of oxidative stress and the risk of allergy at the age of 1 and 2 stratified by maternal active/passive smoking status during pregnancy are presented in Table 5. After inclusion of a variety of confounding factors such as: molds at home, cleaning frequency, pets at home, maternal socio-economic status and education, child gender, parental atopy, breast feeding and living area none of the results were statistically significant (p > 0.05). There was no interaction between smoking (active/passive) during pregnancy and vitamins levels on the risk of allergy (p > 0.4).

4. Discussion

The study investigated the levels of β-carotene and vitamins A and E in plasma of the pregnant women in the 1st trimester of pregnancy and at delivery in relation to allergy development in their children up to 2 years of age. After inclusion of a variety of confounding factors such as: molds at home, cleaning frequency, pets at home, maternal socio-economic status and education, child gender, parental atopy, breast feeding and living area none of the results were statistically significant. The interaction between smoking during pregnancy and vitamins levels on the risk of allergy was not statistically significant.
Oxidative stress accompanies many pathological conditions, including those involving many inflammatory conditions, such as allergies. Oxidative stress is generated during normal physiological processes, but can be also a result of exposure to chemical, biological or physical agents. It is believed that a number of environmental factors affecting pregnant women may contribute to the development of allergy in their children. The potential role of antioxidants, especially those with low molecular weight and provided with a diet, as factors that reduce the risk of developing allergies has been extensively discussed. It has been a subject of numerous studies and raised interest among researchers on the relationship between the intake of low-molecular-weight antioxidants such as vitamins A, C, E and allergy development.
The results of epidemiological studies are not conclusive: most research confirms beneficial associations between maternal dietary antioxidants intake during pregnancy or maternal plasma levels and allergy outcomes in their children (wheezing, asthma, atopic sensitization), but reports on potentially adverse associations are also accessible [26]. Currently, two contradictory hypotheses concerning the relationship between antioxidants and development of allergies are proposed: too low consumption of vitamins resulting from a change of dietary habits, the way of storing food or preparing meals and the second one: using vitamin supplements or consuming antioxidant rich foods [2,26]. The crucial point in that type of analyses is the inclusion of confounding factors which can be responsible of the observed associations. As it was demonstrated in current study after inclusion of covariates the results were not statistically significant.
Vitamin E is a major lipid-soluble antioxidant directly involved in inhibiting propagation of lipid peroxidation. Changes in plasma concentration of vitamin E during pregnancy are not clearly defined; Chechlowska et al. have shown a significant increase in the concentration of vitamin E during the perinatal period in relation to the first trimester of pregnancy [27]. Smedts et al. have reported that vitamin E significantly increased throughout pregnancy [28]. In our study we found significantly higher concentrations of vitamin E in plasma of the tobacco smoke exposed women in the first trimester of pregnancy compared to the non-exposed women. However, in the perinatal period, there was no difference in the plasma concentration of vitamin E between the tobacco smoke exposed and non-exposed women. Chechlowsk et al. have reported significantly higher levels of vitamin E in the third trimester of pregnancy in smoker women [27]. Other authors have reported lower concentrations of vitamin E in smokers only in the third trimester [29] or no differences [11].
Carotenoids (β-carotene and vitamin A) are also involved in the antioxidant defense, but their contribution to removing ROS is less effective. There were no differences in concentrations of carotenoids between the 1st trimester of pregnancy and the perinatal period and, depending on tobacco smoke exposure, Chechlowska et al. have reported significantly lower vitamin A levels in plasma of the smoker women in all trimesters of pregnancy [27].
During pregnancy, all necessary nutrients are transported through the placenta to a developing fetus [30]. Probably they are immediately transferred to actively metabolizing tissues of the fetus, hence concentrations of the substances essential for proper functioning of the fetus are much lower in the cord than in the maternal blood. Cord blood levels of β-carotene, vitamins A and E are significantly lower (20%, 59% and 40%) than the respective maternal blood plasma levels. Similar findings have been reported by other authors [30,31].
In our study, concentration of the cord plasma vitamin A is equal to 59% of vitamin A concentration in the plasma of the women at birth. This is in agreement with the data reported by other authors which indicates that the cord vitamin A level varies from 50–60% of the maternal values [32].
Exposure to tobacco smoke during pregnancy has been an important public health problem for many decades. Analysis of the data published throughout nearly 20 years indicates that, despite some geographical and cultural differences, approx. up to 30% of female smokers continue to smoke cigarettes during pregnancy and after childbirth [33]. The analysis on Polish Mother and Child Cohort conducted in a group of 1771 pregnant women indicated that about 15% of pregnant women smoked cigarettes, while about 35% was exposed to tobacco smoke at home [24]. Maternal smoking during pregnancy is associated with an elevated risk of pregnancy (pregnancy induced hypertension, preeclampsia, gestational diabetes etc.) and with adverse fetal outcomes (intrauterine fetal growth retardation and with disturbances in postnatal growth and development) [34,35]. Analysis of pre- and postnatal tobacco smoke exposure and development of respiratory illness during childhood points to the origins of respiratory disease during fetal life [33]. Tobacco smoke contains more than 5000 chemicals, many of which have proven adverse effects on human health [36]. Their association with an increased risk of developing asthma and other respiratory diseases is also proven [37]. Research carried out nearly 20 years ago showed no association between parental smoking during pregnancy and an increased positive response to allergen skin prick tests (OR = 0.87, 95% CI 0.62–1.24) [38]. However, a multicenter study carried out in Germany has shown that children prenatally exposed to environmental tobacco smoke had a higher probability of sensitization to food allergens (OR = 2.3, 95% CI 1.1–4.6) [39].
Lee has found that adult onset of atopic dermatitis was associated with gestational and prenatal exposure to tobacco smoke [40]. Tobacco smoke may affect immunological processes—newborns of smoking mothers have a diminished innate immune response.
Based on the analysis of the studied population and changes in the concentration of antioxidant vitamins during pregnancy and their relationship with the occurrence of allergies in young children, it was concluded that lower concentrations of vitamin A were observed in the women whose children developed respiratory and skin allergies. It is characteristic that statistically significant differences were found in maternal blood during the perinatal period and only respiratory allergies were associated with exposure to tobacco smoke.
Vitamin A and pro-vitamin A carotenoids (e.g., α-carotene, β-carotene, lutein, zeaxantin) are necessary for normal growth and homeostasis of organisms. Vitamin A plays a crucial role in immune functions. In vitro studies suggest that deficiency of antioxidants interferes with differentiation and promotion of T-helper cells, i.e., cells responsible for safeguarding the immune function [41]. The research of Maslova et al. shows that high maternal intake of vitamin A reduces the risk of allergy in children [42]. However, this inverse relationship is associated with natural sources of vitamin A: vegetables and fruit, milk, and not vitamin A itself. So the risk of allergy is reduced by the intake of carotenoids, and not of chemically pure vitamin A. Therefore, the immune response is responsible for a path of metabolism, in which carotenoids are incorporated. The Polish study group of pregnant women had higher levels of vitamin A and β-carotene than pregnant cohort study in Scotland [30]. Women in Poland often use multivitamin dietary supplements. The concentrations determined in our population are the sum of vitamins supplied with a diet (vitamin A, pro-vitamin A, other carotenoids) and supplements (probably vitamin A). Supplements may contain vitamin A, with a small amount of pro-vitamin A carotenoids, hence, they cannot fulfill a protective role against allergy development. It is also important that the concentration of carotenoids in plasma that is needed to decrease inflammation in target organs during pregnancy is variable [43]. Therefore, they constitute a labile pool used for the current metabolic needs. Also results of the analysis of the relationship between vitamin E in the life of prenatal allergies in the children of 2 years of age are ambiguous. High maternal intake of vitamin E during pregnancy reduces the risk of asthma and wheezing in children at the age 1–2 years. No association has been found with eczema [44,45].
The impact of vitamins intake during pregnancy and the incidence of allergies in children depends certainly on basal vitamins intake. Research shows that the average intake of vitamins E is 7.8 mg/d in Japan, 30.7 mg/d in the US, 8.2 mg/d in the UK and 12.3 mg/d in Sweden [41]. In Poland the recommended daily intake of vitamin E is 10 mg/d. In the studies from 2011–2012 it was demonstrated that about 15% of the general population use dietary supplements. Concentration of vitamin E in supplement users may amount even up to 300% of the daily recommended dose [46]. Frequently neither this supplementation is justified by medical issues nor does it result from medical indications. The same concerns pregnant women. Analysis of vitamin intake in pregnant women living in central Poland assessed by a 24-h recall interview repeated 3 times for each study woman, has indicated that the intake of vitamin E exceeded the recommended daily allowance level by 70%, vitamin A—by 30%. This is probably due to the widespread use of vitamin supplements by pregnant women. Vitamin and mineral supplementation is practiced by 80–90% of pregnant women, both in the period immediately before pregnancy and during pregnancy itself [47]. Probably such a different vitamin E intake can be a critical factor contributing to the risk of allergies development in children. The differences concerning timing of assessment of dietary intake have small effect on the risk of allergies in small children [48]. As a result there are discrepancies in the results of the studies published by various research centers looking for a relationship between vitamins A and E intake and the allergy risk in small children. Therefore, it seems that assessment of concentrations of antioxidant vitamins in plasma is a more appropriate marker serving for the purpose of the study of the role of antioxidants and allergy development [49]. Finally as it was stated above the inclusion of variety confounding factors is the crucial point in the analysis of the impact of vitamins on the risk of child allergy.
The strength of the study is the prospective study design and assessment of vitamins concentrations at different time points (1st trimester, maternal blood at delivery, cord blood). In addition, active/passive smoking status of pregnant women was assessed based on a biomarker of exposure. The main limitation of the present study is the fact that we looked only at prenatal exposure and were not able to evaluate vitamins levels in children. Taking into account children’s age (up to 2 years of age) neither skin prick testing nor pulmonary function testing were performed. However, it needs to be pointed out that the children from REPRO_PL cohort are currently the subjects of assessment at the age of 7 years (with these tests included in children’s health status examination). This will allow a more objective outcome evaluation in future research.

5. Conclusions

Multivariate analysis with inclusion of a variety of confounding factors have not indicated any statistically significant associations between β-carotene and vitamins A and E in plasma of the pregnant women in the 1st trimester of pregnancy and at delivery in and the risk of food allergy, atopic dermatitis and wheezing in their children up to 2 years of age. There was no interaction between smoking during pregnancy and vitamins levels on the risk of allergy.

Supplementary Materials

The following are available online at https://www.mdpi.com/1660-4601/15/6/1245/s1, Table S1: Markers of oxidative stress in the 1st trimester of pregnancy, at delivery and umbilical cord blood in mothers whose children had been diagnosed in the 1stor the 2nd year of lifewith atopic dermatitis, food allergy or wheezing and healthy children (t test), Table S2: Markers of oxidative stress in the 1st trimester of pregnancy, at delivery and umbilical cord blood in smoking and non-smoking mothers whose children had been diagnosed in the 1st or the 2nd year of lifetime with atopic dermatitis, food allergy or wheezing and healthy children (t test).

Author Contributions

J.G. conceived the original idea for the analysis and drafted the manuscript; K.P. coordinated Polish Mother and Child Cohort and participated in the manuscript preparation, L.K. performed the statistical analysis and participated in the manuscript preparation, K.M. performed cotinine analysis, I.S., J.J. and W.S. performed literature search and interpretation of the results focusing on children’s health, M.G. performed literature search and interpretation of the results focusing on vitamins levels during pregnancy, W.H. and W.W. participated in the interpretation of the results and the manuscript preparation; All the authors have read and approved the final paper.

Acknowledgments

The analysis was performed as part of the grant no. DEC-2014/15/B/NZ7/00998 funded by the National Science Centre, Poland, grant no. 603946 HEALS by FP7, grant no. 3068/7.PR/2014/2 by the Ministry of Science and Higher Education and internal grant IMP1.23/2014-16.

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Moreno-Macias, H.; Romieu, I. Effects of antioxidant supplements and nutrients on patients with asthma and allergies. J. Allergy Clin. Immunol. 2014, 133, 1237–1244. [Google Scholar] [CrossRef] [PubMed]
  2. Murr, C.; Schroecksnadel, K.; Winkler, C.; Ledochowski, M.; Fuchs, D. Antioxidants may increase the probability of developing allergic diseases and asthma. Med. Hypotheses 2005, 64, 973–977. [Google Scholar] [CrossRef] [PubMed]
  3. Bowatte, G.; Lodge, C.; Lowe, A.J.; Erbas, B.; Perret, J.; Abramson, M.J.; Matheson, M.; Dharmage, S.C. The influence of childhood traffic-related air pollution exposure on asthma, allergy and sensitization: A systematic review and meta-analysis of birth cohort studies. Allergy 2015, 70, 245–256. [Google Scholar] [CrossRef] [PubMed]
  4. Cook-Mills, J. Maternal influence over offspring allergic responses. Curr. Allergy Asthma Rep. 2015, 15, 501–519. [Google Scholar] [CrossRef] [PubMed]
  5. Feleszko, W.; Ryszczynski, M.; Jaworska, J.; Strzelak, A.; Zalewski, B.M.; Kulus, M. Environmental tobacco smoke exposure and risk of allergic sensitisation in children: A systematic review and meta-analysis. Arch. Dis. Child. 2014, 99, 985–992. [Google Scholar] [CrossRef] [PubMed]
  6. Tara, F.; Rayman, M.P.; Boskabadi, H.; Ghayour-Mobarhan, M.; Sahebkar, A.; Alamdari, D.H.; Razavi, B.S.; Tavallaie, S.; Azimi-Nezhad, M.; Shakeri, M.T.; et al. Prooxidant-antioxidant balance in pregnancy: A randomized double-blind placebo-controlled trial of selenium supplementation. J. Perinat. Med. 2010, 38, 473–478. [Google Scholar] [CrossRef] [PubMed]
  7. Fait, V.; Sela, S.; Ophir, E.; Khoury, S.; Nissimov, J.; Tkach, M.; Hirsh, Y.; Khotaba, S.; Tarasova, L.; Oettinger, M. Hyperemesis gravidarum is associated with oxidative stress. Am. J. Perinatol. 2002, 19, 93–98. [Google Scholar] [CrossRef] [PubMed]
  8. Wasowicz, W.; Gromadzinska, J.; Szram, K.; Rydzynski, K.; Wolkanin, P.; Pietrzak, Z.; Tomczak, J. Relationship between Trace Elements, Activities of Antioxidant Enzymes in Maternal and Umbilical Cord Blood in Poland. W: “Trace Elements in Man and Animals 10”; Roussel, A.M., Anderson, R.A., Favier, A.E., Eds.; Kluver Academic/Plenum Publishers: New York, NY, USA, 2000. [Google Scholar]
  9. Gupta, P.; Narang, M.; Banerjee, B.D.; Basu, S. Oxidative stress in term small for gestational age neonates born to undernourished mothers: A case control study. Biomed. Cent. Pediatr. 2004, 4, 14–23. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  10. Gupta, S.; Agarwal, A.; Banerjee, J.; Alvarez, J. The role of oxidative stress in spontaneous abortion and recurrent pregnancy loss: A systemic review. Obstet. Gynaecol. Surv. 2007, 62, 335–347. [Google Scholar] [CrossRef] [PubMed]
  11. Orhon, F.S.; Ulukol, B.; Kahya, D.; Cengiz, B.; Baskan, S.; Tezcan, S. The influence of maternal smoking on maternal and newborn oxidant and antioxidant status. Eur. J. Pediatr. 2009, 168, 975–981. [Google Scholar] [CrossRef] [PubMed]
  12. Chang, H.Y.; Suh, D.I.; Yang, S.I.; Kang, M.J.; Lee, S.-Y.; Lee, E.; Choi, I.A.; Lee, K.-S.; Shin, Y.-J.; Shin, Y.H.; et al. Prenatal maternal distress affects atopic dermatitis in offspring mediated by oxidative stress. J. Allergy Clin. Immunol. 2016, 138, 468–475. [Google Scholar] [CrossRef] [PubMed]
  13. Hüls, A.; Klümper, C.; MacIntyre, E.A.; Brauer, M.; Melén, E.; Bauer, M.; Berdel, D.; Bergström, A.; Brunekreef, B.; Chan-Yeung, M.; et al. Atopic dermatitis: Interaction between genetic variants of GSTP1, TNF, TLR2 & TLR4 and air pollution in early life. Pediatr. Allergy Immunol. 2018. [Google Scholar] [CrossRef]
  14. Corsini, E.; Galbiati, V.; Nikitopvic, D.; Tsatsakis, A.M. Role of oxidative stress in chemical allergens induced skin cells activation. Food Chem. Toxicol. 2013, 61, 74–81. [Google Scholar] [CrossRef] [PubMed]
  15. Junge, K.M.; Lehmann, I.; Borte, M. Can vitamin D and E intake during pregnancy affect the risk of allergy in children? Expert Rev. Clin. Immunol. 2013, 9, 699–701. [Google Scholar] [CrossRef] [PubMed]
  16. Cook-Mills, J.M.; Abdala-Valencia, H.; Hartert, T. Two faces of vitamin E in the lung. Am. J. Respir. Crit. Care Med. 2013, 188, 279–284. [Google Scholar] [CrossRef] [PubMed]
  17. Silva, S.S.B.; Rondo, P.H.C.; Erzinger, G.S. β-carotene concentrations in maternal and cord blood of smokers and non-smokers. Early Hum. Dev. 2005, 81, 313–317. [Google Scholar] [CrossRef] [PubMed]
  18. Thacher, J.D.; Gruzieva, O.; Pershang, G.; Nueman, A.; Wickman, M.; Kull, I.; Melen, E.; Bergstrom, E. Pre- and postnatal exposure to parental smoking and allergic disease through adolescence. Pediatrics 2014, 134, 428–434. [Google Scholar] [CrossRef] [PubMed]
  19. Polanska, K.; Hanke, W.; Gromadzinska, J.; Ligocka, D.; Gulczynska, E.; Sobala, W.; Wasowicz, W. Polish mother and child cohort study—Defining the problem. The aim of the study and methodological assumptions. Int. J. Occup. Med. Environ. Health 2009, 22, 383–391. [Google Scholar] [CrossRef] [PubMed]
  20. Polanska, K.; Hanke, W.; Jurewicz, J.; Sobala, W.; Madsen, C.; Nafstad, P.; Magnus, P. Polish Mother and Child Cohort Study (REPRO_PL)—Methodology of follow-up of the children. Int. J. Occup. Med. Environ. Health 2011, 24, 391–398. [Google Scholar] [CrossRef] [PubMed]
  21. Stelmach, I.; Grzelewski, T.; Bobrowska-Korzeniowska, M.; Kopka, M.; Majak, P.; Jerzynska, J.; Stelmach, W.; Polanska, K.; Sobala, W.; Gromadzińska, J.; et al. The role of zinc, copper, plasma glutathione peroxidase enzyme and vitamins in the development of allergic diseases in early childhood: The Polish mother and child cohort study. Allergy Asthma Proc. 2014, 35, 227–232. [Google Scholar] [CrossRef] [PubMed]
  22. Grzelinska, Z.; Gromadzinska, J.; Swiercz, R.; Wasowicz, W. Plasma concentration of vitamin E, vitamin A and b-carotene in healthy men. Pol. J. Environ. Study 2007, 16, 209–213. [Google Scholar]
  23. Stragierowicz, J.; Mikołajewska, K.; Zawadzka-Stolarz, M.; Polanska, K.; Ligocka, D. Estimation of cutoff values of cotinine in urine and saliva for pregnant women in Poland. Biomed. Res. Int. 2013. [Google Scholar] [CrossRef] [PubMed]
  24. Polanska, K.; Krol, A.; Kaluzny, P.; Ligocka, D.; Mikolajewska, K.; Shaheen, S.; Walton, R.; Hanke, W. Estimation of saliva cotinine cut-off points for active and passive smoking during pregnancy-polish mother and child cohort (REPRO_PL). Int. J. Environ. Res. Public Health 2016, 13, 1216. [Google Scholar] [CrossRef] [PubMed]
  25. Stelmach, I.; Bobrowska-Korzeniowska, M.; Smejda, K.; Majak, P.; Jerzynska, J.; Stelmach, W.; Polańska, K.; Sobala, W.; Krysicka, J.; Hanke, W. Risk factors for the development of atopic dermatitis and early wheeze. Allergy Asthma Proc. 2014, 35, 382–389. [Google Scholar] [CrossRef] [PubMed]
  26. Allan, K.; Kelly, F.J.; Devereux, G. Antioxidants and allergic disease: A case of too little or too much. Clin. Exp. Allergy 2009, 40, 370–380. [Google Scholar] [CrossRef] [PubMed]
  27. Chechlowska, M.; Ambroszkiewicz, J.; Gajewska, J.; Laskowska-Klita, T.; Leibschang, J. The effect of tobacco smoking during pregnancy on plasma oxidant and antioxidant status in mother and newborn. Eur. J. Obstet. Gynecol. Reprod. Biol. 2011, 155, 132–136. [Google Scholar]
  28. Smedts, H.P.; de Vries, J.H.; Rakhshandehroo, M.; Wildhagen, M.F.; Verkleij-Hagoort, A.C.; Steegers, E.A.; Steegers-Theunissen, R.P. High maternalvitamin Eintake by diet or supplements is associated with congenital heart defects in the offspring. BJOG 2009, 116, 416–423. [Google Scholar] [CrossRef] [PubMed]
  29. Fayol, L.; Gulian, J.M.; Dalmsasso, C.; Calf, R.; Simeoni, U.; Millet, V. Antioxidant status of neonates exposed in utero to tobacco smoke. Biol. Neonate 2005, 87, 121–126. [Google Scholar] [CrossRef] [PubMed]
  30. Scaife, A.R.; McNeill, G.; Campbell, D.M.; Martindale, S.; Devereux, G.; Seaton, A. Maternal intake of antioxidant vitamins in pregnancy in relations to maternal and fetal plasma levels at delivery. Br. J. Nutr. 2006, 95, 771–778. [Google Scholar] [CrossRef] [PubMed]
  31. Vahamiko, S.; Isolauri, E.; Poussa, T.; Laitinen, K. The impact of dietary counseling during pregnancy on vitamin intake and status of women and their children. Int. J. Food Sci. Nutr. 2013, 64, 551–560. [Google Scholar] [CrossRef] [PubMed]
  32. Kiely, M.; Cogan, P.F.; Kearny, P.J.; Morrissey, P.A. Concentrations of tocopherols and carotenoids in maternal and cord blood plasma. Eur. J. Clin. Nutr. 1999, 53, 711–715. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Stocks, J.; Dezateux, C. The effect of parental smoking on lung function and development during infancy. Respirology 2003, 8, 266–285. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  34. Meyer, S.; Raisig, A.; Gortner, L.; Ong, M.F.; Bucheler, M.; Tutdibi, E. In utero tobacco exposure: The effects of heavy and very heavy smoking on the rate of SGA infants in the Federal State Saarland, Germany. Eur. J. Obstet. Gynecol. Rep. Biol. 2009, 146, 37–40. [Google Scholar] [CrossRef] [PubMed]
  35. Murthy, P.; Mishra, S. Tobacco use in pregnancy-global evidence and relevance to LMIC. J. Subst. Abuse Alcohol. 2017, 5, 1069. [Google Scholar]
  36. Talhout, R.; Schulz, T.; Florek, E.; van Benthem, J.; Wester, P.; Opperhuizen, A. Hazardous compounds in tobacco smoke. Int. J. Environ. Res. Public Health 2011, 8, 613–628. [Google Scholar] [CrossRef] [PubMed]
  37. Wegienka, G.; Zoratti, E.; Johnson, C.C. The role of the early-life environment in the development of allergic disease. Immunol. Allergy Clin. N. Am. 2015, 35, 1–17. [Google Scholar] [CrossRef] [PubMed]
  38. Ciaccio, C.E.; DiDonna, A.C.; Kennedy, K.; Barnes, C.S.; Portnoy, J.M.; Rosenwasser, L.J. Association of tobacco smoke exposure and atopic sensitization. Ann. Allergy Asthma Immunol. 2013, 111, 387–390. [Google Scholar] [CrossRef] [PubMed]
  39. Kulig, M.; Luck, W.; Lau, S.; Niggemann, B.; Bergmann, R.; Klettke, U.; Guggenmoos-Holzmann, I.; Wahn, U. Effect of pre- and postnatal tobacco smoke exposure on specific sensitization to food and inhalant allergens during the first 3 years of life. Multicenter Allergy Study Group, Germany. Allergy 1999, 54, 220–228. [Google Scholar] [CrossRef] [PubMed]
  40. Lee, C.H.; Chuang, H.Y.; Hong, C.H.; Huang, S.K.; Chang, Y.C.; Ko, Y.C.; Yu, H.S. Lifetime exposure to cigarette smoking and the development of adult onset atopic dermatitis. Br. J. Dermatol. 2011, 164, 483–489. [Google Scholar] [CrossRef] [PubMed]
  41. Nwaru, B.I.; Erkkola, M.; Ahonen, S.; Kaila, M.; Kronberg-Kippila, C.; Ilonen, J.; Simell, O.; Knip, M.; Veijola, R.; Virtanen, S.M. Intake of antioxidants during pregnancy and the risk of allergies and asthma in the offspring. Eur. J. Clin. Nutr. 2011, 65, 937–943. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  42. Maslova, E.; Hansen, S.; Strom, M.; Halldorsson, T.I.; Olsen, S.F. Maternal intake of vitamins A, E and K in pregnancy and child allergic disease: A longitudinal study from the Danish National Birth Cohort. Br. J. Nutr. 2014, 111, 1096–1108. [Google Scholar] [CrossRef] [PubMed]
  43. Ruhl, R. Non-pro-vitamin A and pro-vitamin A carotenoids in atopy development. Int. Arch. Allergy Immunol. 2013, 161, 99–115. [Google Scholar] [CrossRef] [PubMed]
  44. Miyake, Y.; Sasaki, S.; Tanaka, K.; Hirota, Y. Consumption of vegetables, fruits and antioxidants during pregnancy and wheeze and eczema in infants. Allergy 2010, 65, 758–765. [Google Scholar] [CrossRef] [PubMed]
  45. Martindale, S.; McNeill, G.; Devereux, G.; Campbell, D.; Russell, G.; Seaton, A. Antioxidant intake in pregnancy in relations to wheeze and eczema in the first of two years of life. Am. J. Respir. Crit. Care Med. 2005, 171, 121–128. [Google Scholar] [CrossRef] [PubMed]
  46. Waśkiewicz, A.; Sygnowska, E.; Broda, G.; Chwojnowska, Z. The use of vitamin supplements among adults in Warsaw: Is there any nutritional benefit? Rocz. Panstw. Zakl. Hig. 2014, 65, 119–126. [Google Scholar] [PubMed]
  47. Hamułka, J.; Wawrzyniak, A.; Pawłowska, R. Assessment of vitamins and mineral intake with supplements in pregnant women. Rocz. Panstw. Zakl. Hig. 2010, 61, 269–275. [Google Scholar] [PubMed]
  48. Nwaru, B.I.; Virtanen, S.M.; Alfthan, G.; Karvonen, A.M.; Genuneit, J.; Lauener, R.P.; Dalphin, J.C. Serum vitamin E concentrations at 1 year and risk of atopy, atopic dermatitis, wheezing and asthma in childhood: The PASTURE study. Allergy 2014, 69, 87–94. [Google Scholar] [CrossRef] [PubMed]
  49. Patelarou, E.; Giourgouli, G.; Lykeridou, A.; Vrioni, E.; Fotos, N.; Siamanga, E.; Vivilaki, V.; Brokalaki, H. Association between biomarker-quantified antioxidant status during pregnancy and infancy and allergic disease during early childhood: A systemic review. Nutr. Rev. 2011, 69, 627–641. [Google Scholar] [CrossRef] [PubMed]
Table
Table 1. Characteristics of the pregnant women and anthropometric measures of their neonates.
Table 1. Characteristics of the pregnant women and anthropometric measures of their neonates.
Characteristicn = 252
Mothers’ age, years. (n = 248)29.1 ± 4.2
Fathers’ age, years. (n = 227)31.2 ± 5.3
Living area (n = 251)
 Rural47 (18.7%)
 Urban204 (81.32%)
Mothers’ education
 Primary10 (4.0%)
 Secondary69 (27.4%)
 University173 (68.6%)
Socio-economic status
 Low21 (8.3%)
 Medium198 (78.6%)
 High33 (13.1%)
Mothers’ BMI (kg/m2)
 Prepregnancy (n = 242)23.2 ± 3.7
 1st trimester (n = 233)23.2 ± 3.8
 2nd trimester (n = 227)224.7 ± 3.9
 3rd trimester (n = 209)226.8 ± 4.0
Parental atopy
 Yes45 (17.9%)
 No 207 (82.1%)
Maternal smoking
 Ever smokers90 (35.7%)
 Smokers during pregnancy (saliva cotinine level ≥10 ng/mL)32 (12.7%)
 Never smokers156(61.9%)
Passive smokers during  pregnancy(saliva cotinine level ≥1.5 ng/mL)78 (30.9%)
 No data 6 (2.4%)
Molds at home
 Yes 23 (9.1%)
 No229 (90.9%)
Pets at home (n = 237)
 Yes70 (29.5%)
 No167 (70.5%)
Child gender
 Male125 (49.6%)
 Female 127 (50.4%)
Breast feeding
 No26 (10.3%)
 Yes226 (89.7%)
  ≤6 months111 (49.4%)
  >6–≤12 months78 (34.7%)
  No data 35 (15.7%)
Gestational age (weeks) (n = 248)39.2 ± 1.4
Birthweight (g) (n = 237)3394 ± 486
Body length (cm) (n = 237)55 ± 3
Table
Table 2. The children’s health status.
Table 2. The children’s health status.
Total Number of the Examined Children 1-Year Old/2-Year OldNumber of the Children Diagnosed with Allergy within 1 Year of Their LifetimeNumber of the Children Diagnosed with Allergy within 2 Years of Their LifetimeNumber of the Children Diagnosed with Allergy within the 1st and 2nd Year of Their Lifetime
Food allergy221/16043 (19.5%)30 (18.7%)17 (10.6%)
Atopic dermatitis252/25234 (13.5%)32 (12.7%)18 (7.1)
Wheezing217/16723 (10.6%)27 (16.2%)8 (4.8)
Table
Table 3. β-Carotene, vitamin A and E concentrations in plasma in the pregnant women in the 1st trimester, at delivery and in umbilical cord plasma.
Table 3. β-Carotene, vitamin A and E concentrations in plasma in the pregnant women in the 1st trimester, at delivery and in umbilical cord plasma.
Plasma Vitamins LevelTotal, n = 252Passive and Active Smokers, n = 90Non-Smokers, n = 156
β-Carotene, μg/mL
1st trimester0.252 ± 0.1850.277 ± 0.1950.238 ± 0.174
at delivery0.330 ± 0.222 *0.337 ± 0.2400.329 ± 0.207
Cord blood0.051 ± 0.045 *,&0.053 ± 0.053 *,&0.050 ± 0.039 *,&
Vitamin A, μg/mL
1st trimester0.954 ± 0.2750.949 ± 0.2540.963 ± 0.290
at delivery0.896 ± 0.3340.888 ± 0.3060.908 ± 0.347
Cord blood0.569 ± 0.204 *,&0.578 ± 0.200 *,&0.571 ± 0.202 *
Vitamin E, μg/mL
1st trimester8.67 ± 3.659.38 ± 3.438.21 ± 3.71 #
at delivery12.50 ± 6.6312.94 ± 6.3312.37 ± 6.70
Cord blood3.44 ± 2.17 *,&3.73 ± 2.57 *,&3.33 ± 1.86 *,&
* statistically significant as compared with the 1st trimester, p < 0.001; & statistically significant as compared with maternal blood at delivery time, p < 0.001; # statistically significant as compared with the passive and active smokers, p < 0.02.
Table
Table 4. Correlation between plasma vitamins A, E and β-carotene during the 1st trimester of pregnancy, at delivery and in cord blood plasma.
Table 4. Correlation between plasma vitamins A, E and β-carotene during the 1st trimester of pregnancy, at delivery and in cord blood plasma.
Correlation Coefficient
1st Trimester/at Deliveryat Delivery/Cord Blood1st Trimester/Cord Blood
Vitamin A0.75; p < 0.00010.730; p < 0.00010.660; p < 0.0001
β-Carotene0.56; p < 0.00010.45; p < 0.00010.42; p < 0.0001
Vitamin E0.41; p < 0.00010.45; p < 0.00010.32; p < 0.0001
Table
Table 5. Association between markers of oxidative stress in the 1st trimester of pregnancy, at delivery and umbilical cord blood stratified by maternal smoking status (active/passive smokers, non-smokers) and the risk of atopic dermatitis, food allergy or wheezing at the age of 1 and 2—the multivariable model.
Table 5. Association between markers of oxidative stress in the 1st trimester of pregnancy, at delivery and umbilical cord blood stratified by maternal smoking status (active/passive smokers, non-smokers) and the risk of atopic dermatitis, food allergy or wheezing at the age of 1 and 2—the multivariable model.
One Year Old ChildrenTwo Year Old Children
Food AllergyAtopic DermatitisWheezingFood AllergyAtopic DermatitisWheezing
OR (95% CI)
Active or Passive Smokers during Pregnancy
β-Carotene, µg/mL
1st trimester1.14 (0.06–22.57)0.45 (0.01–13.14)0.06 (0.01–32.72)0.27 (0.01–48.36)0.55 (0.02–13.33)1.56 (0.01–487.3)
Delivery0.03 (0.01–1.75)1.55 (0.06–40.94)0.20 (0.01–1.50)0.09 (0.01–15.78)0.39 (0.02–9.44)16.94 (0.06–465.0)
Cord blood1.54 (0.28–8.29)3.67 (0.85–9.63)0.05 (0.01–40.75)6.43 (0.03–164.3)9.39 (0.21–48.01)0.14 (0.01–179.0)
Vitamin A, µg/mL
1st trimester1.02 (0.08–12.58)0.53 (0.06–15.08)0.47 (0.01–17.07)0.4 (0.01–25.55)0.27 (0.02–3.67)5.18 (0.06–485.0)
Delivery0.57 (0.05–1.99)0.86 (0.06–7.12)2.68 (0.12–61.09)1.98 (0.13–29.32)0.17 (0.02–1.74)1.56 (0.07–36.06)
Cord blood1.42 (0.04–45.12)0.29 (0.01–12.72)4.63 (0.02–12.18)5.85 (0.03–105.79)0.07 (0.01–2.52)16.92 (0.13–228.6)
Vitamin E, µg/mL
1st trimester1.03 (0.86–1.24)0.95 (0.78–1.16)0.99 (0.77–1.26)0.98 (0.80–1.21)0.91 (0.76–1.08)1.11 (0.87–1.41)
Delivery0.85 (0.74–1.12)1.05 (0.94–1.19)0.91 (0.75–1.09)1.07 (0.93–1.24)0.99 (0.89–1.10)1.02 (0.86–1.22)
Cord blood1.05 (0.75–1.45)1.55 (0.82–2.36)0.35 (0.12–1.09)4.95 (0.98–17.75)1.35 (0.96–1.89)1.18 (0.75–1.86)
Non-Smokers during Pregnancy
β-Carotene, µg/mL
1st trimester4.70 (0.30–74.00)6.29 (0.37–96.56)0.54 (0.01–22.42)0.29 (0.01–10.98)4,97 (0.22–113.8)0.02 (0.01–2.18)
Delivery1.18 (0.12–11.41)1.57 (0.13–19.76)0.75 (0.03–20.79)5.17 (0.26–103.9)2.87 (0.29–28.55)1.41 (0.07–29.38)
Cord blood0.18 (0.02–3.41)0.13 (0.04–9.16)0.71 (0.01–9.87)0.01 (0.01–485.0)0.03 (0.01–55.22)0.18 (0.01–32.36)
Vitamin A, µg/mL
1st trimester1.44 (0.21–9.63)0.38 (0.04–3.27)1.52 (0.17–13.92)0.12 (0.01–1.63)0.03 (0.01–1.36)0.47 (0.05–4.19)
Delivery0.59 (0.12–3.05)0.29 (0.05–1.73)0.18 (0.02–1.97)0.29 (0.03–3.10)0.08 (0.01–1.66)0.38 (0.05–3.22)
Cord blood0.09 (0.01–1.43)0.21 (0.01–4.35)0.15 (0.01–4.62)0.03 (0.01–1.68)0.06 (0.01–1.23)0.10 (0.01–4.23)
Vitamin E, µg/mL
1st trimester1.11 (0.93–1.28)1.18 (0.91–1.38)1.11 (0.94–1.32)1.14 (0.97–1.35)1.01 (0.86–1.18)1.00 (0.85–1.16)
Delivery1.01 (0.93–1.09)1.08 (0.98–1.18)1.04 (0.93.1.18)1.12 (1.00–1.27)1.03 (0.94–1.14)1.07 (0.96–1.20)
Cord blood0.88 (0.66–1.17)1.03 (0.79–1.33)1.52 (0.92–2.12)1.04 (0.74–1.47)1.04 (0.76–1.42)1.06 (0.74–1.52)
Adjusted for: molds at home, cleaning frequency, pets at home, maternal socio-economic status and education, child gender, parental atopy, breast feeding and living area. p for interaction >0.4.

Share and Cite

MDPI and ACS Style

Gromadzinska, J.; Polanska, K.; Kozlowska, L.; Mikolajewska, K.; Stelmach, I.; Jerzynska, J.; Stelmach, W.; Grzesiak, M.; Hanke, W.; Wasowicz, W. Vitamins A and E during Pregnancy and Allergy Symptoms in an Early Childhood—Lack of Association with Tobacco Smoke Exposure. Int. J. Environ. Res. Public Health 2018, 15, 1245. https://doi.org/10.3390/ijerph15061245

AMA Style

Gromadzinska J, Polanska K, Kozlowska L, Mikolajewska K, Stelmach I, Jerzynska J, Stelmach W, Grzesiak M, Hanke W, Wasowicz W. Vitamins A and E during Pregnancy and Allergy Symptoms in an Early Childhood—Lack of Association with Tobacco Smoke Exposure. International Journal of Environmental Research and Public Health. 2018; 15(6):1245. https://doi.org/10.3390/ijerph15061245

Chicago/Turabian Style

Gromadzinska, Jolanta, Kinga Polanska, Lucyna Kozlowska, Karolina Mikolajewska, Iwona Stelmach, Joanna Jerzynska, Wlodzimierz Stelmach, Mariusz Grzesiak, Wojciech Hanke, and Wojciech Wasowicz. 2018. "Vitamins A and E during Pregnancy and Allergy Symptoms in an Early Childhood—Lack of Association with Tobacco Smoke Exposure" International Journal of Environmental Research and Public Health 15, no. 6: 1245. https://doi.org/10.3390/ijerph15061245

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop