Early childhood risk factors for rhinoconjunctivitis in adolescence: a prospective birth cohort study
© The Author(s) 2017
Received: 29 November 2016
Accepted: 10 March 2017
Published: 3 April 2017
Rhinoconjunctivitis is a global health problem and one of the most common chronic conditions in children. Development of rhinoconjunctivitis depends on both genetic and environmental factors. Many studies have investigated rhinoconjunctivitis, but only few studies have evaluated the risk factors for non-allergic rhinoconjunctivitis in children finding family history of atopic diseases and gender to be of importance. The aim of this study was to investigate possible risk factors in early life for rhinoconjunctivitis, allergic as well as non-allergic, in adolescence.
The children in the Danish Allergy Research Center cohort were examined eight times from birth to 14 years of age. Visits included questionnaire-based interview, clinical examination, skin prick test and specific IgE. We used univariate and multivariate logistic regression to investigate the relationship between early-life risk factors and the development of rhinoconjunctivitis, allergic as well as non-allergic, in adolescence.
Follow-up rate at 14-years was 66.2%. The prevalence of rhinoconjunctivitis was 32.8%. Family history of atopic diseases (aOR 2.25), atopic dermatitis (aOR 3.24), food allergy (aOR 3.89), early sensitization to inhalant and food allergens (aOR 2.92 and aOR 3.13) and male gender (aOR 1.90) were associated with allergic rhinoconjunctivitis but not with non-allergic rhinoconjunctivitis. Early environmental tobacco exposure was inversely associated with rhinoconjunctivitis (aOR 0.42), allergic (aOR 0.47) as well as non-allergic (aOR 0.43).
Different patterns of associations were revealed when stratifying rhinoconjunctivitis in allergic and non-allergic suggesting that allergic rhinoconjunctivitis and non-allergic-rhinoconjunctivitis are different phenotypes.
KeywordsRhinoconjunctivitis Risk factor Adolescence Logistic regression Predictors Birth cohort
Rhinoconjunctivitis (RC) is a global health problem and one of the most common chronic conditions in children  with a prevalence that is still increasing . When symptoms occur as a result of exposure to an allergen to which the individual is sensitized, the term allergic-rhinoconjunctivitis is used, but few longitudinal studies have used the combination of symptoms and measurement of sIgE .
Development of RC including allergic RC depends on both genetic and environmental factors . Studies have indicated that gender [5, 6], family atopy [2, 4–6], early sensitization [4, 7, 8], food allergy  and atopic dermatitis [4, 9] are risk factors for subsequent development of rhinoconjunctivitis. The association between breastfeeding [2, 5], having pets , early exposure to tobacco smoke [2, 11, 12], social class , early wheeze , obesity , older sibling(s) [15–17] and allergic RC in adolescence is more contradictory.
The Danish Allergy Research Center (DARC) cohort is a prospective birth cohort study with 6 follow-up examinations during the first 3 years of life and further two at 6 and 14 years. This gives a unique opportunity to explore risk factors in early childhood for the development of RC in adolescence. The aim of this study is to investigate possible risk factors in early life for RC, allergic as well as non-allergic, in adolescence.
The DARC cohort is a prospective non-interventional birth cohort study comprising 562 of 1095 consecutively enrolled full-term children born in the first two weeks of each month at Odense University Hospital, Denmark from November 1998 to November 1999. The children were evaluated during the first month of life and follow-up investigations were performed at 3, 6, 12, 18 months and 3, 6 and 14 years of age. All visits included questionnaire-based interviews, clinical examination, skin prick test (SPT), specific IgE (s-IgE), and at 6 and 14 years also spirometry. A detailed description was published previously .
Rhinoconjunctivitis (RC) at 14 years was defined as: At least two separate episodes in the previous 12 months with one or more of the following symptoms: sneezing, runny, blocked nose, or itchy, red, watery eyes apart from a upper airway infection.
Allergic rhinoconjunctivitis (allergic RC) at 14 years was defined as having symptoms of RC and s-IgE ≥ 0.35 kU/l (ImmunoCAP, Thermo Fisher Scientific, Sweden) and/or a positive SPT (ALK-ABELLO, Copenhagen, Denmark) with a mean wheal diameter ≥3 mm larger than the negative control to at least one of the inhalant allergens: grass, birch, mugwort, horse, dog, cat, Dermatophagoides pteronyssinus, Dermatophagoides farinae, Cladosporium herbarum and Alternaria alternata.
Non-allergic rhinoconjunctivitis (non-allergic RC) at 14 years was defined as symptoms of RC and s-IgE ≤ 0.35 kU/l and a negative SPT.
Potential risk factors for rhinoconjunctivitis (RC), allergic RC and non-allergic RC, at 14 years
Risk factors 0–3 years
Family history of atopic diseases at baselinea (FH)
Early sensitization to inhalant allergensb
Early sensitization to food allergensc
Food allergyd (FA)
Atopic dermatitise (AD)
Early wheeze: at least two episodes of wheezing
Elevated cord blood IgE ≥ 0.3 kU/l (CB-IgE)
CB IgE < 0.3 kU/l
Daily exposure to tobacco smoke from parents or others in the household at more than two visits (ETS)
Maternal tobacco smoking in pregnancy
No ETS in utero
Cat and/or dog keeping (pets)
Exclusive breastfeeding ≥3 months (eBF)
eBF ≤ 3 months
Overweight at 3 years (BMI girls ≤17.6 and boys ≤17.8) 
Older siblings (siblings)
No older siblings
Risk factors are described and defined in Table 1.
Crude and adjusted effect estimates were analyzed with (multiple) logistic regression and given as crude odds ratio (cOR) and adjusted odds ratio (aOR) with 95% confidence interval (95% CI). P values ≤0.05 were considered significant.
Based on knowledge from the literature the variables gender, family history (FH), early sensitization, food allergy (FA) and atopic dermatitis (AD) were identified as risk factors [4, 5, 7, 9, 13] for developing RC and allergic RC and included in the multiple logistic regression model without further analysis. Gender  and FH [17, 19] were identified as risk factors for non-allergic RC and therefore included in this model without further analysis.
All other potential risk factors in Table 1 were tested individually with RC, allergic RC and non-allergic RC using univariate logistic regression analysis and included in the final model for RC, allergic RC and non-allergic RC if P value was <0.10.
Correlation between risk factors were tested using Spearman’s correlation coefficients and negligible correlation was found (r ≤ 0.3) except between the variables maternal smoke in pregnancy and exposure to tobacco smoke (ETS) where the correlation was moderate (r = 0.34). Therefore, all variables were retained for further analysis.
All analyses were performed using STATA/SE (Stata Corporation, College Station, TX, USA).
Symptoms score and use of medication in those with symptoms of allergic and non-allergic RC
Allergic RC % (n)
Non-allergic RC % (n)
Allergic symptoms at least 1 h daily for at least 2 weeks from eyes and nose
Use of oral antihistamines
Use of nasal sodium cromoglicate
Use of intranasal corticosteroids
Use of other antiallergic medication
Use of any of the above medication
Crude effect estimates for the associations between risk factor in early childhood and RC, allergic RC and non-allergic RC at 14 years of age
cOR (CI 95%)
cOR (CI 95%)
cOR (CI 95%)
Boys (n = 178)
Girls (n = 194)
FH (n = 174)
Early sensitization to inhalant allergens (n = 113)
Early sensitization to foods (n = 204)
s-IgE > 4.00 SU/ml to inhalant allergens (n = 56)
s-IgE > 4.00 SU/ml to food allergens (n = 57)
FA (n = 18)
AD (n = 87)
Early wheeze (n = 59)
CB IgE 0.3 (n = 62)
ETS (n = 192)
Maternal tobacco smoking in pregnancy (n = 110)
Breast feed (n = 247)
Pets (n = 231)
Social class (n = 305)
Overweight at 3 years (n = 25)
Cesarean section (n = 44)
Older siblings (n = 182)
Crude odds estimates for all risk factors are giving in Table 3.
RC and allergic RC
Adjusted effect estimates (aOR CI 95%) for associations with RC, allergic RC and non-allergic RC at 14 years of age
RC inc. s-IgE ≥ 4.00 SU/ml
Allergic RC inc s-IgE ≥ 4.00 SU/ml
aOR (CI 95%)
aOR (CI 95%)
aOR (CI 95%)
aOR (CI 95%)
aOR (CI 95%)
Early sensitization to inhalant allergens
Early sensitization to foods
s-IgE ≥ 4.00 SU/ml to inhalant allergens
s-IgE ≥ 4.00 SU/ml to food allergens
Maternal tobacco smoking in pregnancy
We found no association between early wheeze, maternal smoking in pregnancy, pets, breastfeeding, elevated CB-IgE, social class, overweight at 3 years, cesarean section and RC and allergic RC in adolescence.
An association between male gender, FA and sibling were only found in those with allergic RC (Table 4).
Among the 38 children with non-allergic RC no association with FH, early sensitization to inhalant and food allergens, FA, and AD was found, while ETS was significantly associated with less non-allergic RC in adolescence (Table 4).
In this study, different patterns of associations were revealed by stratifying RC in allergic and non-allergic. It appears that atopic heredity and early atopic manifestations are important for the development of allergic RC in adolescence but less important for the development of non-allergic RC. Furthermore, early ETS was inversely associated with RC (aOR 0.42), allergic-RC (aOR 0.47) and non-allergic RC (aOR 0.43), in adolescence.
Family atopy (FH) was associated with allergic RC (aOR 2.25). The relation between FH and the development of rhinitis are well established in cohort studies [2, 4, 5, 9, 19]. Some argue that maternal atopy are more important than paternal atopy , but in the MAAS (Manchester Asthma and Allergy Study) study  both maternal asthma (OR 2.38) and paternal hayfever (OR 1.96) were significantly associated with RC at age 5. Having two parents with allergy was associated with allergic rhinitis at 13 years in the MAS (Multi-center Allergy Study) study  (OR 3.1) as was parental isolated hay fever with allergic rhinitis at 8 years in the Swedish BAMSE (Children Allergy Milieu Stockholm study) study  (OR 2.2), whereas parental isolated asthma or eczema was not. Our study did not have the sufficient power to differentiate between the different parental atopic diseases.
Food allergy (FA) was associated with allergic RC in adolescence (aOR 3.89). Among those participating at 14 years of age, 54.8% were sensitized to food allergens early but only 4.8% had verified FA up to 3 years, which may reflect the transient and often benign nature of food sensitization in infancy . The association between food allergy in infancy and RC in adolescence is less investigated. In the Isle of Wight cohort an increased risk of nasal symptoms in those with FA at 1 and 4 years was found in the univariate analysis but this association disappeared in the multivariate analysis . Using a higher cut-off value both early sensitization to inhalant allergens and foods reach significance, while the association between FA and allergic RC disappeared. This probably reflects sensitization in those with FA. Thus, weak sensitization to food and inhalant allergens in early life might be less important as a risk factor for subsequent development of allergic RC.
No association was found between FH, early sensitization to inhalant allergens or foods, AD and FA and non-allergic RC. Though analyzed in another way (time-to-event analysis) the same patterns were found in the German MAS study  while other studies of non-allergic RC found an association between FH and non-allergic RC [17, 19]. An explanation of the different patterns of association seen in the two diseases might be that allergic RC and non-allergic RC are different phenotypes with non-allergic RC not being driven by atopy but environmental factors. Another explanation might be that the children with non-allergic RC had milder symptoms and therefore may outgrow RC.
AD was in our study associated with both RC (aOR 2.44) and allergic-RC (aOR 3.24). Of 87 children that had AD up to 3 years, 48 developed RC in adolescence. Thus these children might follow a trajectory of the atopic march, whereas in two English cohort studies MAAS and ALSPAC (Avon Longitudinal Study of Parents and Children)  only a small proportion of children followed trajectory profiles similar to the atopic march.
In our study boys had a higher risk of allergic-RC in adolescence (aOR 1.90). A consistent male predominance in the prevalence of allergic rhinitis was seen in all ages in the German MAS cohort but only in those with allergic parents . In the Isle of Wight cohort a male predominance was seen at 18 years in those with allergic rhinitis  while there was female predominance in non-allergic-rhinitis. Though not reaching statistical significance a tendency to female predominance in those with non-allergic RC was found in our study.
We found that having older siblings were inversely associated with allergic-RC (aOR 0.53). The relation between large family size and less hayfever was described by Strachan in 1989  and summarized in the “hygiene hypothesis”  suggesting that allergic diseases were prevented by infections in early childhood transmitted by contact with older siblings. Other cohort studies report similar associations, the German MAS cohort  for allergic rhinitis and the Tucson cohort  for asthma. Though studies of the association between having older siblings and the development of RC are fairly consistent in the conclusions of the possible beneficial effect [5, 16] we found such an association for allergic RC, but not for non-allergic RC.
ETS before the age of 3 was inversely associated with RC (aOR 0.42), allergic-RC (aOR 0.47) and non-allergic RC (aOR 0.43) in adolescence. The same tendency was seen between maternal smoking during pregnancy and non-allergic RC though not reaching statistical significance. The inverse association between ETS and RC, allergic as well as non-allergic RC could be due to bias in different ways, firstly as report-bias, secondly that parents with atopy smoked less than parents without atopy and thirdly as a disease-related modification of exposure  if parents to symptomatic children quit smoking. Firstly, all follow-up investigations included measurement of parental expiratory carbon monoxide as an objective measurement of smoking which could enhance parents to report smoking more accurately. Secondly, ETS was reported in 51.6%, and 29.6% of the mothers smoked during pregnancy. Parental atopy at baseline was found in 46.8 and 46% of those reported smoking. Thirdly, parents to those developing allergic diseases are prone to stop smoking and among parents to children with atopic dermatitis and/or wheeze before 3 years only 24% were smokers at the 14 years follow-up. This indicates a possible reverse causation and that not only smoking exposure in early life, but also the long-lasting exposure was important. Another Danish study  found the same tendency with an inverse association for prenatal smoke exposure OR 0.8 and hayfever in adolescence and a large ISAAC study  found an inconsistent or weak association between ETS and RC. An explanation of a possible beneficial effect of ETS on RC could be an immunomodulatory effects of nicotine, which also indicates a possible beneficial effect of smoking in some inflammatory and neurodegenerative diseases .
Strengths and limitations
Our study has several limitations. First of all our study population are relative small and since the study included only 51.3% of those fulfilling the inclusion criteria, there is a risk for selection bias. However, this group did not differ from those that declined participation originally . Participants at 14 years belonged to a higher social class and were less exposed to maternal smoking during pregnancy and birth, which may influence the prevalence of atopic diseases. Besides, participants in a cohort study may have increased awareness of atopic diseases resulting in an overestimation of the prevalence and on the other hand in avoidance of possible risk factors, which may result in lowering the prevalence. Despite of this we found a high prevalence of RC in adolescence which was in line with finding of other cohorts [6, 23]. In our study we used symptoms within the last 12 months and diagnosis of RC by a doctor and sensitization was determined both by SPT and measurement of s-IgE.
Of the 372 children participating at 14 years of age, 353 attended at least 6 follow-up investigations. The DARC cohort had 6 study visits in the first 3 years which allow us to compensate for missing data from 1 or more visits. Most of the environmental risk factors were only included if these were present at two visits or more, e.g. ETS, to validate the outcome.
In this study we used a widely used model to estimate the association between early-life risk factors and RC. Different patterns of association were revealed when stratifying RC in allergic and non-allergic suggesting that allergic RC and non-allergic RC are different phenotypes. Early sensitization is a risk factor for developing allergic RC in adolescence and a higher cut-off value of s-IgE seems associated with a higher risk.
Non-allergic RC is not driven by atopic heredity or early atopic manifestations but possibly by other mechanism to intrinsic or environmental factors.
In the future it appears important to explore the nature and clinical characteristics and course of non-allergic-RC in order to find optimal treatment options.
Furthermore the pattern of early sensitization to specific allergens and the relation to later atopic diseases seem important to investigate focusing on possible preventive measures.
adjusted odds ratio
body mass index
- CB IgE:
cord blood IgE
crude odds ratio
The Danish Allergy Research Center
environmental tobacco smoke
skin prick test
ESC did the follow-up investigation, the data management and wrote the article. HFK, EE, CGM, SH, AH and CBJ critically reviewed the article. All authors read and approved the final manuscript.
We thank the children in the DARC cohort and their parents for their cooperation, and nurses Lis Lykkegaard and Joan Kramer and laboratory technicians Anni Larsen and Ulla Johannessen for skillful technical help. This work has been performed at The Allergy Center and Hans Christian Andersen Children’s Hospital, Odense University Hospital, Denmark.
The authors declare that they have no competing interests.
Availability of data and materials
All relevant raw data on which this article is based are available from the author.
Consent to publish
A written consent to publish was obtained from the parents of the participants in the DARC cohort.
Ethical approval, consent to participate
The study was conducted according to the latest version of the Declaration of Helsinki for biomedical research involving humans and approved by the Regional Scientific Ethical Committee for Southern Denmark: DARC cohort (S-VF-19980101). Before entering the study a written consent to participate and to publish was obtained from the parents of the participants in the DARC cohort.
The DARC trial has received funding from University of Southern Denmark, Odense University Hospital and ALK-Abelló, Denmark and Thermo Fisher Scientific, Uppsala, Sweden did the measurements of s-IgE.
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