Atopic dermatitis has increased four-fold over the recent decades in developed countries, indicating that changes in environmental factors associated with lifestyle may play an important role in this epidemic. It has been proposed that alcohol consumption may be one contributing risk factor in this development.
To analyze the impact of alcohol intake during pregnancy on the development of atopic dermatitis during the first 7 years of life.
The COPSAC cohort is a prospective, longitudinal, birth cohort study of 411 children born to mothers with a history of asthma, followed up for 7 years with scheduled visits every 6 months as well as visits for acute exacerbations of atopic dermatitis. Risk of atopic dermatitis from any alcohol consumption during pregnancy was analyzed as time-to-diagnosis and adjusted for known risk factors.
177 of 411 children developed atopic dermatitis before age 7 years. We found a significant effect of alcohol intake during pregnancy on atopic dermatitis development (HR 1.44, 95% CI 1.05–1.99 p = 0.024). This conclusion was unaffected after adjustment for smoking, mother's education and mother's atopic dermatitis.
The selection of a high-risk cohort, with all mothers suffering from asthma, and all children having a gestational age above 35 weeks with no congenital abnormality, systemic illness, or history of mechanical ventilation or lower airway infection.
Citation: Carson CG, Halkjaer LB, Jensen SM, Bisgaard H (2012) Alcohol Intake in Pregnancy Increases the Child's Risk of Atopic Dermatitis. The COPSAC Prospective Birth Cohort Study of a High Risk Population. PLoS ONE7(8): e42710. https://doi.org/10.1371/journal.pone.0042710
Editor: Claire Thorne, UCL Institute of Child Health, University College London, United Kingdom
Received: March 8, 2012; Accepted: July 11, 2012; Published: August 15, 2012
Copyright: © Carson et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Funding: Copenhagen Prospective Studies on Asthma in Childhood is funded by private and public research funds. The Lundbeck Foundation; the Pharmacy Foundation of 1991; Augustinus Foundation; the Danish Medical Research Council and The Danish Pediatric Asthma Centre provided the core funding. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Atopic dermatitis (AD) has increased fourfold over the last five decades in western countries–, indicating that changes in environmental factors associated with western lifestyle may play an important role–. It has been proposed that alcohol consumption may be one contributing factor to the rise in atopic diseases,  as alcohol consumption is part of the western lifestyle and has increased in the same period with an annual consumption nearly tripling in Denmark since 1955, . Also, alcohol consumption during pregnancy is frequent in westernized countries–.
We previously reported a cross-sectional analysis of a comprehensive range of potential risk factors for the development of AD by age 3 suggesting mother's AD, father's allergic rhinitis, child's FLG status, dog exposure at birth and baby's birth length as significant risk factors. Furthermore, breast feeding and mother's intake of alcohol during pregnancy was found to be marginally significant risk factors for AD in the child. Recently, we reported a longitudinal analysis of age-at-onset showing that breast feeding increased the risk of AD.
In this 7-year follow-up study we have used close longitudinal observations to re-test our initial observation of a borderline significant risk from alcohol intake by the pregnant mother on the development of AD in the child.
The Copenhagen Study on Asthma in Childhood (COPSAC) was conducted in accordance with the guiding principles of the Declaration of Helsinki, approved by the Ethics Committee for Copenhagen (KF 01–289/96) and The Danish Data Protection Agency (2002–41–2434), and in compliance with “Good Clinical Practice” (GCP) guidelines. Informed, written consent was obtained from all parents.
The COPSAC cohort is a prospective longitudinal birth cohort, including 411 children born to mothers with asthma. Mother's asthma was defined as doctor diagnosed asthma with a history of medication during two seasons. The main recruiting area of the cohort was greater Copenhagen, Denmark and all children were born between August 1998 and December 2001. The children were enrolled at one month of age and visited the COPSAC clinic at scheduled visits every six months thereafter, as well as for any acute complaints from skin or airways. Skin examinations, diagnoses and treatment of AD were handled in accordance with predefined standard operating procedures by trained medical doctors employed for this purpose in the COPSAC clinic. The enrolled children were primarily cared for at the COPSAC clinic. Data validity was assured by quality control procedures. Data were collected on-line and locked after external monitoring and with an automated audit trail showing operations on the database after locking. The study was previously described in details elsewhere, . See Table S1 for baseline characteristics.
COPSAC provides comprehensive assessments of the prenatal, perinatal and postnatal milieu, aiming to elucidate critical factors driving atopic disease expression. In this study we analyzed alcohol intake during pregnancy for development of AD during the first 7 years of life.
Childhood asthma was diagnosed based on preasthma (recurrent episodes of troublesome wheezing, breathlessness and/or cough) and the response and subsequent relapse to a 3-month trial of inhaled corticosteroids.
Rhinitis was defined as troublesome sneezing, blocked or runny nose in the past 12 months in periods without accompanying cold or flu. All diagnoses were performed by the doctors in the COPSAC clinic.
Alcohol intake during pregnancy was determined at the interview at the 1-month visit. The mothers were interviewed about their drinking habits, and the average alcohol intake pr. week pr. trimester was entered online. Mothers drinking minimum one unit of alcohol pr. week in minimum one of the 3 trimesters were defined as having an intake of alcohol during pregnancy. One unit of alcohol was defined as 15 ml or 12 g of alcohol, explained to the mothers as e.g. one beer or one glass of wine. Information about mother's education (high school/medium-long education/university), smoking habits in the 3rd trimester (smoking yes/no) and AD (doctor diagnosed) was also recorded at the 1-month scheduled visits in the COPSAC clinic.
The association between alcohol intake during pregnancy and development of AD during the first 7 years of life was examined by survival analysis. The children were retained in the analysis from birth, until age at first diagnosis of AD, drop-out, or 7 years of age whichever came first.
Kaplan-Meier curves were estimated for alcohol drinking during pregnancy. The plots were used as a descriptive presentation of the results, illustrating the cumulative risk of developing AD with respect to mother's alcohol intake during pregnancy. Survival analyses were performed by use of Cox proportional-hazards regression, supporting the Kaplan-Meier curves with information about hazard ratios (HR), 95% confidence intervals (CI) and p-values. The dependent variable was the time to first event (AD diagnosis, dropout or 7 years). The confounders, mother's education, smoking habits in 3rd trimester and AD, were placed in the regression models simultaneously. Tests for functional form and proportional hazards were based on martingales.
The overall significance level used was 0.05. The analyses were done using PROC TPHREG in SAS version 9.1 as well as R version 2.6.1.
COPSAC enrolled 411 infants out of which 77 were lost to follow-up before debut of AD symptoms and/or before the age of 7 years. There was no difference in alcohol consumption between the group lost to follow-up and the remaining families (Table S1). Forty eight percent of the mothers had a history of AD, 16% and 13% of the fathers had a history of asthma and AD, respectively. There were 16 siblings and 18 twins in the cohort, thus totaling 8.3% of the participants. All 411 children were included in the univariate analysis. Data for mother's education were missing for 34 children, leaving 377 children for the confounder adjusted analysis (92% of the enrolled cohort).
108 mothers in the cohort (26%) had an intake of one or more units of alcohol pr. week in minimum one of the 3 trimesters, respectively 88, 73 and 73 women in the 1st, 2nd and 3rd trimester. The quantity of alcohol intake was distributed as follows (in units of alcohol pr. trimester):
- 1st trimester: range 1–7, median: 1, mean: 1.55, interquartile range: 1–2
- 2nd trimester: range 1–7, median: 1, mean: 1.44, interquartile range: 1–2
- 3rd trimester: range 1–7, median: 1, mean: 1.51, interquartile range: 1–2
One hundred seventy-seven children of the 411 participating infants (43%) had an AD diagnosis before age 7 years. In the group of children developing AD 31% (55) of the mothers had been drinking alcohol at some point during pregnancy, i.e. more than an average of one unit of alcohol pr. week in minimum one of the three trimesters. Of the 234 children who did not develop AD, 23% (53) of the mothers had been drinking alcohol at some point during pregnancy. This difference in prevalence of mother's alcohol drinking in the two groups of children (31% vs. 23%) was marginally statistically significant (p = 0.055)
The age-at-onset analysis confirmed an increased risk of AD associated with alcohol intake during pregnancy, with the effect persisting throughout the whole 7 years follow-up period (Figure 1) (HR 1.44, 95% CI 1.05–1.99, p = 0.024).
The hazard ratio from the univariate analysis was largely unchanged after confounder adjusted analysis adjusting for mother's education, smoking habits 3rd trimester and AD (HR 1.45, 95% CI 1.04–2.02, p = 0.029).
There was no association between alcohol intake during pregnancy and other atopic endpoints (wheeze episodes, asthma, allergic rhinitis, blood eosinophil count, total IgE, sensitization (specific IgE≥0.35 kU/L), nasal eosinophilia and cord blood IgE (IgE≥0.5 kU/L)). Results are not shown.
In this prospective, longitudinal, birth cohort study we find alcohol intake during pregnancy to be associated with an increased risk of developing AD in the first 7 years of life, adjusted for possible confounders. The increased risk was persistent throughout the whole 7 years follow-up period.
Strengths and limitations
Recall bias is reduced from the prospective data collection, with half-yearly clinic visits and visits at any acute symptoms from the skin. The alcohol related questions were recorded before any onset of atopic diseases including AD.
Misclassification of AD is reduced by the participants being diagnosed and treated at the COPSAC clinic and not by their general practitioner. Furthermore, all mothers in the cohort have personal experience with atopic diseases, and should therefore be expected to be better at reporting symptoms. Ambiguities over the definition of AD, especially during infancy and early childhood, make the estimates of prevalence unreliable and render comparisons between studies difficult. In this cohort study the specificity of the AD diagnosis is high, since the diagnosis, detailed phenotype and management of skin lesions were controlled solely by the COPSAC clinic physicians from predefined standard operating procedures and included assessment of localization and severity at each visit. This reduces the risk of misclassification and is of particular importance in the clinical evaluation of AD where inter-observer variation is a problem. The specificity of the diagnosis in this study is illustrated by the observation that the cumulative incidence of seborrheic dermatitis capitis was not significantly different in children with AD and in children with skin lesions not fulfilling AD diagnosis, suggesting that there was no misclassification between AD and seborrheic dermatitis capitis.
We have used predefined questions concerning alcohol consumption, recording average alcohol intake per week per trimester. We are aware that alcohol histories are notoriously unreliable. However, this unreliability is not biased as it must be expected to be equal among mothers to children later developing AD and not. Therefore, it can only result in a type 2 and not a type 1 error, i.e. it could have obscured an effect but it could not cause a false effect to be seen.
We have chosen to present data as a binary variable just to determine whether alcohol intake during pregnancy correlates to AD at all. We found similar estimates in sub-analyses stratifying for alcohol amount or onset/duration of alcohol intake, but the number of individuals in each group was very small. Therefore, these results are not included in the article. This narrow definition of alcohol intake limits our results and future studies designed to determine quantity of alcohol ingested should be sought. The external validity of our study is limited from the selection of a high-risk cohort, with all mothers suffering from asthma, and all children having a gestational age above 35 weeks with no congenital abnormality, systemic illness, or history of mechanical ventilation or lower airway infection. Therefore, our results need replication in an unselected population.
We have previously demonstrated risk factors in the development of AD in a cross-sectional analysis by age 3 in this birth cohort. We found that mother's AD, father's allergic rhinitis, child's FLG status, dog exposure at birth and higher birth length were significant factors predicting AD by 3 years of age. Duration of breastfeeding and mother's alcohol consumption during pregnancy also increased the risk of AD but were not statistical significant in this cross-sectional analysis. However, age-of-onset survival statistics was used in subsequent analyses to show, that both breast feeding and now also mother's alcohol intake in pregnancy were significant risk factors for AD in the off-spring.
AD has increased dramatically since the 1960's in Western countries–,  and genetic factors only cannot explain the recent rapid increase in the incidence. The exposure to early life style factors is thought to be crucial for the later development of AD, and suggestions about factors influencing the intra uterine milieu have been made–. A questionnaire based cohort study, reported a significant and dose-dependent effect from the mother's intake of alcohol during pregnancy in the risk of developing AD during the first 2 months of child life, but not beyond this period. This effect was mainly seen in high-risk infants (two parents with allergic disease).The authors interpreted their observations to be indirectly supported by a study investigating the influence of environmental factors on levels of total IgE in cord blood of 2631 newborn infants. They found an independent positive dose–response relationship between maternal alcohol consumption during pregnancy and the levels of cord blood IgE, and hypothized that the increased IgE synthesis may contribute to the immunologic sensitization. However, increased IgE is generally not believed to be directly associated to AD, but rather to illustrate a common mechanism for the atopic diseases. This is also supported by the paradox, that alcohol consumption is found associated with an increased risk of developing perennial allergic rhinitis, but not seasonal allergic rhinitis. In our study we do not find any association to other atopic diseases, including cord blood IgE, allergic rhinitis, total IgE and sensitization, and can therefore not support the hypothesis that the association between alcohol and AD are caused by a higher level of IgE.
In this study we adjusted for reasonable confounders including mother's education, smoking habits in 3rd trimester and AD. These confounders were chosen, because we believe them to be the only factors both affecting the child's risk of developing AD and the mother's alcohol intake. Other factors, such as prenatal behavior, pets in home at birth and breastfeeding were not included in the analysis as confounders, because we do not believe them to affect both the exposure (mother's alcohol intake during pregnancy) and the outcome (AD). We detect an association between alcohol intake during pregnancy and the child's risk of developing AD, but the underlying causal relationship is not clear and further studies are needed to confirm our findings and explore the reasons for our observed associations.
It has been suggested that factors, which influence cytokine production by the feto-placental unit, may be important determinants of atopic disease. This is further supported by findings that the effect of the maternal line on childhood AD is greater than that of the paternal line–, which are, however, not confirmed in all studies, . Alcohol may trigger hypersensitivity reactions, i.e. allergic, asthmatic or eczematous symptoms. The mechanisms underlying these reactions are unknown, but are hypothesized to be due to a histamine-releasing effect of acetaldehyde–. Gonzalez-Quintela et al have reported that alcohol intake may induce changes in the cytokine profile, including increasing level of some Th2-associated cytokines, and impairment of the Th1 lymphocyte response. This is supported by other studies, . However, such differences in cytokine profiles are most often found in alcohol abusers, and one should therefore be cautious in transferring these findings to our cohort's pregnant women. Still, it could be worth considering as a possible explanation for our observed association between mother's alcohol intake and the offspring's risk of developing AD, although further studies are needed to clarify this.
We found that alcohol intake during pregnancy in asthmatic women is associated with a statistically significantly higher risk of developing AD in the offspring. The increased risk is still significant after confounder adjustment for other known risk factors. However, the underlying mechanism is not clear.
The authors wish to thank the children and parent participating in the COPSAC cohorts as well as the COPSAC study teams.
The abstract from this manuscript has been presented as a poster at the European Respiratory Society's annual congress in Barcelona, September 2010. Data will not be presented in any other official form.
Conceived and designed the experiments: HB LBH CGC. Performed the experiments: HB LBH CGC. Analyzed the data: SMJ CGC HB. Contributed reagents/materials/analysis tools: SMJ CGC HB. Wrote the paper: SMJ CGC HB LBH.
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