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Birth after preeclamptic pregnancies: association with allergic sensitization and allergic rhinoconjunctivitis in late childhood; a historically matched cohort study
© Byberg et al.; licensee BioMed Central Ltd. 2014
Received: 8 February 2013
Accepted: 10 April 2014
Published: 11 April 2014
The development of allergic sensitization and allergic disease may be related to factors during intrauterine life, but the role of maternal preeclampsia is not known.
We studied if maternal preeclampsia is associated with long-term allergic sensitization, allergic rhinoconjunctivitis, atopic dermatitis, asthma and with altered lung function in late childhood.
617 children participated in a 1:2 matched and controlled historical cohort study; 230 born after preeclamptic pregnancies and 387 born after normotensive pregnancies. Specific IgE in serum and lung function were measured at the age of 12.8 years and questionnaires on maternal and adolescent data were completed at the ages of 10.8 years (girls) and 11.8 years (boys), and at 12.8 years (both genders). The association between birth after preeclampsia and the main outcome measures allergic sensitization, allergic rhinoconjunctivitis, atopic dermatitis, asthma and lung function in late childhood were analysed with multiple regression analyses, including possible confounders.
Severe maternal preeclampsia was associated with high level allergic sensitization (sum of specific IgE in serum ≥ 3.9 kU/l; the 25 percentile for all children being sensitized); odds ratio (OR): 3.79; 95% confidence interval (CI): (1.54, 9.32); p = 0.015 and with allergic rhinoconjunctivitis in offspring; OR: 2.22, 95% CI: (1.19, 4.14), p = 0.047. Preeclampsia was not associated with atopic dermatitis, asthma or altered lung function in late childhood.
Maternal preeclampsia was associated with allergic sensitization and allergic rhinoconjunctivitis in offspring in late childhood, but not with other atopic diseases.
The prevalence of allergy and asthma has been increasing in both adults and children during the last decades . There is also increasing evidence that early life events including intrauterine factors are important for the development of atopic disease [2–4].
Atopic diseases are associated with an inhibition of the transition towards an increased T-helper cell type 1 (Th1)/Th2 balance after birth, resulting in Th2 cytokine predominance [4, 5]. Maternal inflammatory cytokines during pregnancy have been shown to correlate with corresponding cytokines in offspring at the age of one , and an association between an altered maternal cytokine profile and subsequent atopic disease in offspring has been suggested .
Preeclampsia is a common and potentially serious complication of the second half of pregnancy affecting both mother and child, characterised by maternal hypertension and proteinuria, and occasionally foetal growth restriction [8, 9]. Preeclampsia is associated with an increase in several circulating maternal cytokines, and a skewed maternal immune response towards an increased Th1/Th2 balance . This could potentially skew the child’s cytokine balance after birth in the same direction, and thereby protect against the development of atopic disease . However, clinical studies have suggested that complications during pregnancy may rather increase the risk of childhood asthma and allergic rhinoconjunctivitis [11, 12], and an association between maternal preeclampsia and subsequent allergic sensitization in offspring during adolescence has been suggested .
Preeclampsia has also been associated with an increased risk of RDS and BPD in preterm infants and to recurrent wheezing in a general population of pre-school children . This association might either be due to an increased soluble antiangiogenic factor , or a congenital reduction in airways calibre and compliance in particular in infants with intrauterine growth restriction . However, no studies have evaluated a possible long-term association between maternal preeclampsia and asthma or lung function in offspring.
In a long–term follow-up of children of preeclamptic and normal pregnancies, the aim was to study if maternal preeclampsia is associated with allergic sensitization, allergic rhinoconjunctivitis, atopic dermatitis, asthma, and lung function in late childhood.
Study population and design
The study was approved by the Norwegian Data Inspectorate, the Regional Committee for Ethics in medical research and the Institutional Review Board of the National Cancer Institute of the United States. Written consent was obtained from all participating children and mothers at follow-up.
Data collection and definitions
Preeclampsia was defined as a diastolic blood pressure increased by ≥ 25 mmHg to a persistent pressure of ≥ 90 mmHg and proteinuria with dipstick ≥ +1 present in at least one urine sample after 20 weeks of gestation. Preeclampsia was further divided into mild, moderate and severe. Moderate preeclampsia was defined as proteinuria with dipstick ≥ +2. Severe preeclampsia was defined as proteinuria with dipstick ≥ + 3 and diastolic blood pressure of ≥110 mmHg.
Maternal body mass index (BMI, kg/m2) was calculated using weight measurement at the first antenatal visit at primary healthcare examination during the first trimester of pregnancy and height measurement from FU1. Maternal smoking in pregnancy was recorded at the same antenatal visit. Data on gestational age at birth and mode of delivery were extracted from hospital records. Birth weight for gestational age was calculated as z-scores based on Scandinavian normal standards . Weight and height in offspring were recorded at FU1, and z-scores for BMI were calculated using the latest growth references for Norwegian children .
At FU1, the questions included the birth order of the child, parental asthma, and atopic disease of the child. The mothers were asked as follows: Has your child ever had asthma (diagnosed by physician), allergy in nose/eyes (hay fever) or atopic dermatitis (childhood eczema)?
At FU2, the children answered a questionnaire from the International Study of Asthma and Allergies in Childhood (ISAAC) translated into Norwegian . Reported asthma symptoms and asthma medication during the last year and asthma diagnosis ever were recorded. Missing answers were interpreted as negative. Current asthma at FU2 was defined as asthma ever, in addition to asthma symptoms or the use of asthma medication during the last 12 months.
At FU2 blood was drawn from the children, centrifuged and aliquoted, and serum stored at -80°C. Allergic sensitization was determined by serum specific immunoglobulin E (IgE) antibodies using Phadiatop® and fx5E® (ImmunoCAP® 250, Phadia AB, Uppsala, Sweden). If Phadiatop® was positive, serum was further analysed for specific IgE against Dermatophagoides pteronyssinus, cat, horse, dog, timothy, common silver birch, mugwort and Cladosporium herbarum. If fx5E® was positive, serum was further analysed for specific IgE against egg white, milk, fish (cod), wheat, peanut and soya bean. Allergic sensitization was defined as specific IgE ≥ 0.35 kU/l for at least one allergen. The levels of specific IgE ≥ 0.35 were added together, and high level allergic sensitization was defined as a sum > 3.9 kU/l; the 25 percentile for all children being sensitized.
At FU2, lung function measures were performed by spirometry according to standard quality criteria  with a Vmax Encore spirometer (Sensor Medics Inc., Anaheim, USA).
Groups were compared with Pearson’s chi-square exact test for the dichotomous outcomes and independent t-tests (Gosset’s t-test) and one way analysis of variance for the continuous outcomes. Bonferroni-correction of p-values was applied to adjust for multiple testing.
Before analyses, the variable preeclampsia was categorised into none, mild/moderate (combined) and severe. Risk associations between preeclampsia and related pregnancy variables with outcomes in late childhood were analysed by multiple logistic and linear regression analyses, including the covariates gender, birthweight z-score for gestational age, being firstborn, maternal smoking during pregnancy, maternal age at birth, caesarean section, gestational age, maternal BMI and maternal asthma. Paternal asthma was not included as a covariate due to low response rate. Each variable was first entered separately into simple regression models. Covariates significant at the 10% level and those considered important were included in backward stepwise logistic and linear regression analyses. Final models included the remaining covariates significant at the 5% level and the covariates gender and maternal asthma, considered as biologically important. Analysing the ordinal variable preeclampsia as were it a continuous variable with scores 0, 1 and 2 for the three levels, ORs showing a trend have been calculated by multiple logistic regression analysis.
From logistic regression odds ratios (OR) with 95% confidence interval (CI) and likelihood ratio p-value (LR-p) for each exposure are reported. From linear regression the estimated coefficients (b), 95% CI and F-test p-value are reported. Interactions between preeclampsia and all other risk factors remaining in the final models were tested. Also interactions between preeclampsia and gender were tested.
All tests were 2-tailed and p-values ≤ 0.05 were considered statistically significant. Due to missing data, matching was not included in the analyses, but the matching variables were adjusted for. SPSS for Windows (version 18.0.0, Chicago, Ill., USA) was used for all analyses.
Characteristics of the participants
Initial characteristics of 1025 Norwegian children born in 1993–1995 and invited to the Stavanger study according to consenting or not to the first follow-up 11–12 years later a)
Consented (n = 617)
Did not consent (n = 409)
Gender: boys, n (%)
Preeclampsia, n (%)
Maternal age, years, mean, 95% CI
Gestational age, weeks; mean, 95% CI
Birth weight z-scored)
At FU1, the age of the girls was 10.8 (±0.22) years (mean, SD), and for boys 11.8 (±0.18) years. At FU2 the age for both genders was 12.8 (±0.19) years.
BMI z-score at FU1 was higher in children who only consented to FU1 than in children who consented to both FU1 and FU2 (mean difference BMI z-score: 0.31 kg/m2; 95% CI: 0.13 to 0.49; p = 0.001). When analysed separately for girls and boys, the difference persisted for girls only (mean difference BMI: 0.44 kg/m2; 95% CI: 0.20 to 0.68; p < 0.001). More children had atopic dermatitis of those who only consented to FU1 (48/150; 32%), than those who consented to both FU1 and FU2 (100/445; 22.5%); p = 0.022. No other variables differed significantly between those who consented to FU1 only and those who consented to both FU1 and FU2.
Preeclampsia and outcomes
Atopy, asthma and lung function in late childhood in 586 Norwegian children according to mother’s preeclampsia status
Severe vs. no preeclampsia
Mild/moderate vs. no preeclampsia
Allergic rhinoconjunctivitis, n (%)
Atopic dermatitis, n (%)
Asthma, n (%)
Allergic sensitization, n (%)
High level allergic sensitization, n (%)c)
Current asthma, n (%)
FEV1%, mean, 95% CI
FVC%, mean, 95% CI
FEV1/FVC, mean, 95% CI
FEF25–75%, mean, 95% CI
FEF25–75/FVC, mean, 95% CI
Among children with any allergic sensitization, 50% had symptoms of allergic rhinoconjunctivitis, whereas 5.6% of children with allergic rhinoconjunctivitis did not have any allergic sensitization.
Summary of logistic regression analyses of atopic diseases in late childhood in 586 Norwegian children according to mother’s preeclampsia status
Effects of maternal preeclampsia
High level allergic sensitizationc)
In the backward stepwise regression analysis of high level allergic sensitization the final model included preeclampsia as a significant risk factor, in addition to male gender, maternal smoking during pregnancy, gestational age in weeks and maternal asthma (Table 3). Specifically, birth after severe preeclampsia gave 4.05 times higher odds for high level allergic sensitization than birth after non-preeclampsia, adjusted for the other variables.
In a backward stepwise regression analysis of allergic rhinoconjunctivitis the final model included preeclampsia in addition to male gender and maternal asthma (Table 3). Specifically, severe preeclampsia gave 2.23 times higher odds for allergic rhinoconjunctivitis than no preeclampsia, adjusted for the other variables.
Adjusted for the same covariates as in final analysis, there was a trend of an increasing effect of preeclampsia (none, mild/moderate, severe) on both high level allergic sensitization (OR = 1.88; 95% CI: (1.23, 2.86); LR-p = 0.003) and on allergic rhinoconjunctivitis (OR = 1.42; 95% CI: (1.07, 1.89); LR-p = 0.018).
Preeclampsia was not a significant risk factor for other outcomes of atopic disease in the final models.
Summary of linear regression analyses of lung function in late childhood in 395 Norwegian children according to mother’s preeclampsia status
Effects of maternal preeclampsia
In the present study we found positive associations between severe maternal preeclampsia and both high level allergic sensitization and allergic rhinoconjunctivitis in adolescent offspring. This is to our knowledge showed for the first time. Preeclampsia was not associated with subsequent atopic dermatitis, asthma or alterations in lung function.
Preeclampsia and atopic disease
Few other studies have evaluated preeclampsia as a possible risk factor for subsequent allergic sensitization or atopic disease in a long-term perspective. Keski-Nisula et al. found an association between maternal preeclampsia and severe atopy in children. However, in that study only women who underwent caesarean section were included, and a very high percentage of children were sensitized . Nafstad et al. found a relation between uterus-related complications during pregnancy and allergic rhinoconjunctivitis and asthma, but not for children born after preeclamptic pregnancies . To our knowledge, no other studies have evaluated the risk for allergic rhinoconjunctivitis after preeclamptic pregnancies.
A possible causal relation between preeclampsia and atopic disease in offspring could be linked to the inflammatory changes observed during preeclampsia. If the tendency for preeclampsia to skew the cytokine profile of the mother towards an increased Th1/Th2 ratio is reflected in the cytokine pattern of the offspring during pregnancy and early life, it could potentially protect the child from the development of Th2 driven atopic disease [6, 22]. However, preeclampsia is a complex inflammatory condition characterised by a variety of pro-inflammatory cytokines beyond the Th1 type of cytokines [10, 23]. Pro-inflammatory cytokines, chemokines and adhesion molecules appear to be increased in maternal circulation during preeclampsia , and could potentially initiate the development of immunological conditions in the foetus, such as atopic sensitization or diseases .
The association between preeclampsia and atopy could be due to shared genetic or environmental factors in pregnancy. Preeclampsia is more common in nulliparous  and pregnancies with a male foetus , and atopic disease is more common in first-born-children  and boys up to adolescence . According to the hygiene hypothesis, the birth order effect on atopy may be explained by a reduced tendency for Th2 deviation due to greater exposure to pathogens from older siblings . However, recent studies have demonstrated a birth order effect on cord blood IgE and food allergy in very early life, suggesting a prenatal origin of this effect [29, 30]. Our analyses were controlled for birth order, suggesting that preeclampsia may be a risk factor for atopy in the offspring unrelated to birth order. However, as this is an observational study, the possibility of residual confounding cannot be excluded.
Finally, maternal conditions prior to pregnancy could increase the risk for both preeclampsia and atopic disease in offspring. Maternal asthma has been shown as a risk factor for preeclampsia . To our knowledge, no studies have shown any association between maternal allergy and preeclampsia.
There was a trend of an increased risk of atopic disease in the child by an increasing severity of the maternal preeclampsia. Moreover, preeclampsia was not associated with low level allergic sensitization, asthma or atopic dermatitis. Low level allergic sensitization may be unspecific and less related to clinical atopic disease compared to higher levels of sensitization . The pathophysiology of asthma and atopic dermatitis is more multifactorial than the specific allergy driven pathophysiology of rhinoconjunctivitis. Our results may therefore suggest that the association between severe preeclampsia and atopic disease in offspring is related to specific Th2-mediated mechanisms .
Preeclampsia, asthma, wheezing and lung function
Some studies have shown an association between different complications of pregnancy and asthma in offspring, but preeclampsia was not shown to be a risk factor in these studies [12, 33]. In a large population-based study using a questionnaire, an association between maternal preeclampsia and wheezing in the offspring was shown . A possible explanation for this association could be that hypertension in pregnancy is related to fetal growth restriction and hence altered airway function . Our results do not contradict this. Although we could not find any association between preeclampsia and asthma ever, current asthma or lung function in late childhood, we did not investigate wheezing disorders in the first years of life. However, the present study had a longer follow-up than in the studies mentioned above, and may therefore be better suited to study any long time effect of preeclampsia on asthma and lung function in late childhood.
One limitation of the study is the rather low rate of participation, especially in FU2. It is not known whether there was a difference in prevalence of asthma or atopy between those who consented and those who didn’t consent to overall follow-up. Especially for the outcomes of asthma, there was a rather low response rate which increases the risk of a type 2 error. Furthermore, children who participated in FU1 but not in FU2 had a higher BMI and more atopic dermatitis. This may have biased our results, as both overweight and atopic dermatitis may be associated with allergic sensitization and other atopic disease.
Another limitation may be that that allergic rhinoconjunctivitis, asthma and atopic dermatitis were defined only by questionnaire. However, allergic sensitization was found in 94.4% of children diagnosed with rhinoconjunctivitis, suggesting a high degree of diagnostic accuracy. Some children reported allergic rhinoconjunctivitis without having sensitization, but this is also seen in other studies and does not rule out allergic rhinoconjunctivitis . Due to study design, allergic rhinoconjunctivitis and allergic sensitization were assessed at two different ages. However, this should not affect that independent associations were found between preeclampsia pregnancies and allergic rhinoconjunctivitis and allergic sensitization respectively.
In the multivariate analyses we included a set of variables possibly influencing the outcomes. The covariates gestational age, birthweight z-score and caesarean section could be considered as intermediate variables between preeclampsia and the outcomes, but may also be independent risk factors for subsequent allergy and atopic disease and were therefore included as covariates in the analyses. Given the lack of complete ascertainment of causal links, one cannot exclude the possibility of collider bias and therefore biased associations between exposures and outcomes .
The only data on family atopy available were on maternal and paternal asthma. Paternal asthma was not considered to be a possible confounder for the relationship between maternal preeclampsia and subsequent atopy, asthma or lung function in offspring and not included as a covariate.
The results of this study suggest that severe maternal preeclampsia may be associated with allergic sensitization and allergic rhinoconjunctivitis in late childhood. This emphasizes the possible early origin of atopic disease, but larger studies are needed to further explore the role of preeclampsia in the development of atopic disease. No other significant associations between maternal preeclampsia and atopic dermatitis, asthma or lung function were found.
“The Stavanger Study” was funded by an internal grant from the National Cancer Institute, NIH and is a part of the MD Anderson Global Programme.
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