Different risk factor patterns for adult asthma, rhinitis and eczema: results from West Sweden Asthma Study

The West Gothia region of Sweden (Fig. 1) has a population of 1.6 million, approximately one-sixth of the total Swedish population. In 2008, a large population based questionnaire survey was dispatched by mail to 30,000 randomly selected subjects in this area. From the metropolitan area of Gothenburg 15,000 subjects were selected and 15,000 subjects from the rest of the county. Response rate was 62 % (18,087 participants). The population study and a study on effects of late and non-response has previously been described in detail [18, 19]. Among the responders, 2000 randomly selected participants were invited to clinical examinations and 1172 (59 %) individuals participated. Figure 2 shows the study set-up and participation.

The questionnaire consisted of three parts administered at the same time. The first part was the Swedish OLIN study questionnaire [20, 21] covering asthma, rhinitis, COPD, respiratory symptoms and possible risk factors of disease such as smoking and family history of airway diseases. The second part included questions regarding occupational exposures, environmental exposures and health status. The third part consisted of the Swedish Global Allergy and Asthma (GA²LEN) questionnaire [22] which further assessed respiratory symptoms and diseases and added questions about eczema. The clinical examinations included objective measures of height and weight, a structured interview and a drawn blood sample. Sixty-nine subjects did not participate in the blood sampling either due to unwillingness or technical difficulties but completed the other parts of the examination. The presence of serum Immunoglobulin E (IgE) was assessed using a mixture of 11 common airborne allergens and included timothy, birch, mugwort, olive, parietaria, cat, dog, horse, D. pteronyssinus, D. farinae and C. herbarum (ImmunoCAP^® Phadiatop, Thermo Scientific). A value of ≥0.35 kU_A/l was considered a positive test. Body Mass Index (BMI) was calculated by weight_(kg)/(height_(m))². BMI was defined as normal if 20–25 kg/m², underweight <20 kg/m², overweight 25–30 kg/m² and more than 30 kg/m² considered as obesity.

Current asthma: Asthma ever and a report of either use of asthma medication or recurrent wheeze or attacks of shortness of breath in the last 12 months.

Rhinitis ever: Either “Have you ever had nasal allergies or hay fever?”, or nasal blockage: “Do you have nasal blockage more or less constantly?’, or runny nose: “Do you have a runny nose more or less constantly?”

Current rhinitis: Either nasal blockage or runny nose, or both of the following: “Have you had sneezing, runny nose or nasal blockage apart from colds during the last 12 months?” and “Have these nasal symptoms occurred simultaneously with itching and running eyes?”

Allergic sensitization: Serum IgE to ImmunoCAP^® Phadiatop ≥0.35 kU_A/l

Statistical analyses were performed using IBM SPSS version 20.0.0. The significance level was set to 0.05. Tests for in group differences in proportions were calculated with Fisher’s exact test. Tests for trend were computed with a Mantel–Haenszel test where appropriate. Pearson Chi² was performed for in group differences in contingency tables larger than two by two. Crude Odds ratios (OR) and 95 % confidence intervals (CI) were calculated for the variables current asthma, current rhinitis and current eczema. Models of multiple logistic regressions were calculated with adjusted ORs and 95 % CIs. Independent covariates were: age divided in three categories, sex, family history of asthma and rhinitis, exposure to gas, dust and fumes at work, raised on a farm, BMI, allergic sensitization, number of siblings and childhood daycare.

Mean age ± SD of the participants was 50.4 ± 15.4 years with 54 % women. The prevalence of current asthma was 11.8 %, current rhinitis 42.8 % and current eczema 13.5 % (Table 1). Prevalence of asthma ever, eczema ever, rhinitis ever and current rhinitis were all inversely associated with increasing age, as was family history of asthma and rhinitis. Eczema was more common among women and women were also more likely to report a family history of asthma or rhinitis. Usage of rhinitis medications in the last 12 months was more common among younger subjects (P < 0.001). BMI increased by age. Men tended to have a higher BMI and were more exposed to gas, dust or fumes at work compared to women. The prevalence of allergic sensitization was 29.7 %, decreased by age and was more common among men (Table 1).

Figure 3 show the relationship between current asthma, current rhinitis and current eczema. Of all subjects, a similar proportion had both current asthma and current rhinitis as current eczema and current rhinitis, 8.5 % and 7.3 % respectively, while 2.6 % had current asthma and current eczema. Only 2.3 % had all three conditions and current rhinitis was the most common single condition (Fig. 3). The relationship between asthma ever, rhinitis ever and eczema ever showed a similar pattern and is available in the appendix (Additional file 1: Figure S1).

Table 2 shows unadjusted associations for the conditions expressed as odds ratios. Younger age was a significant risk factor for current rhinitis but not for current asthma. For current eczema, only the 40–59 years of age category had an increased risk compared to the oldest. Female sex only increased the risk of current eczema. Family history of both asthma and rhinitis had the strongest positive association with current asthma (OR 5.4 CI 3.4–8.6) but also significantly increased the risk for current rhinitis and current eczema. Allergic sensitization was a strong risk factor for both current asthma (OR 4.0 CI 2.8–5.4) and current rhinitis (OR 5.8 CI 4.3–7.7) but not significantly so for current eczema (OR 1.4 CI 0.9–1.9). Exposure to gas, dust or fumes at work was a significant risk factor for both current eczema and current asthma (both OR 1.7). Obesity was associated with an increased risk of current rhinitis and current asthma but not of current eczema, while degree of urbanization and metropolitan domicile was not associated with any of the three conditions.

Subjects that grew up on a farm had a lower risk of both current eczema and current rhinitis (OR 0.5 CI 0.2–0.9 and 0.5 CI 0.4–0.8) respectively (Table 3). Childhood smoke exposure and maternal smoking in pregnancy was associated with an increased risk of current eczema, while current smoking status was not significantly associated with any of the three conditions. Childhood airway infection increased the risk of asthma. Having one or more sibling increased the risk of current asthma whereas childhood daycare increased the risk of current eczema. Birth weight and educational level were not associated with any of the three conditions (Table 3). Risk factors for eczema ever, asthma ever and rhinitis ever were similar with a few exceptions; most notably allergic sensitization was also positively associated with eczema ever (Additional file 2: Table S1).

Age was not a risk factor for any of the conditions when adjusted odds ratios were calculated in multiple regression models (Table 4). Female sex was a risk factor for both current asthma (OR 1.8 CI 1.2–2.7) and current eczema (OR 1.7 CI 1.2–2.5). Family history of asthma and rhinitis significantly increased the risk of current rhinitis, and the risk of current asthma was of an even greater magnitude, while it was not significantly associated with current eczema. Allergic sensitization was the strongest risk factor for current rhinitis (OR 5.1 CI 3.8–6.9) and the second strongest for current asthma (OR 4.1 2.7–6.3) but was not associated with current eczema.

Exposure to gas dust or fumes as work remained a stable risk factor for current eczema and current asthma after adjustment. Growing up on a farm remained similarly associated with a protective effect on current eczema (OR 0.5 CI 0.3–0.99) and current rhinitis (OR 0.6 CI 0.4–0.96). Obesity was a risk factor for current asthma and current rhinitis but not for current eczema. Having siblings was a risk factor for current asthma but childhood daycare showed no effect in the multivariate models. Maternal smoking in pregnancy, childhood smoke exposure and smoking status were added separately to the model but were not significantly associated with any of the conditions and did not alter the other risk estimates (not shown). Childhood airway infection was a risk factor for current asthma, OR 2.6 (95 % CI 1.7–4.1) when added separately to the models but did not alter the magnitude of the other risk factors. An additional multivariate analysis was performed to assess the risk factor pattern of subjects with the combination of current asthma and current rhinitis. The results showed that the risk factor pattern in this group was close to identical to subjects with current asthma (data not shown).

Adjusted odds ratios for eczema ever, rhinitis ever and asthma ever showed similar results for most risk factors with some exceptions. Most notably, exposure to gas dust or fumes was not a risk factor for any of the conditions and growing up on a farm had no significant protective on rhinitis ever and eczema ever. However, allergic sensitization was a risk factor for all of eczema ever, rhinitis ever and asthma ever (Additional file 3: Table S2).

In this population based study of 1172 adults we found that family history of both asthma and allergy was the strongest risk factor for current asthma and it also increased the risk of current rhinitis but not for current eczema after adjustment. Allergic sensitization was an important risk factor for current asthma and current rhinitis, but for not current eczema, and obesity showed the same pattern. Occupational exposure to gas, dust and fumes was positively associated with both current asthma and current eczema but not with current rhinitis. Growing up on a farm had a protective effect on both current eczema and current rhinitis but not on current asthma. Female sex was associated with an increased risk for current asthma and current eczema but not for current rhinitis.

Comparisons with other studies should be interpreted with caution due to varying definitions of disease. The prevalence of current eczema in our study was 13.5 %. Earlier studies addressing eczema in adults have found similar magnitudes of prevalence with 11.6 % in Sweden [23], 8.1 % in Italy [24], 14.3 % in Denmark [25], 11.5 % in Colombia [26] and 10.2–10.7 % in the United States [16, 17]. Earlier studies of rhinitis have mainly focused on either allergic rhinitis or symptoms of chronic rhinosinusitis. Our definition of current rhinitis included subjects with either allergic rhinitis or other chronic nasal symptoms. The observed prevalence of current rhinitis in our study was 42.8 %. This high prevalence of rhinitis may seem remarkable; however, another recent study in Sweden found that the prevalence of rhinitis symptoms was 51 % [27]. Further, 28.1 % in our study reported use of medication against rhinitis in the last year. Allergic rhinitis has also seen a significant increase in prevalence during the last thirty years [28‐30]. The prevalence in Italy has been estimated at 26 % [31] and in southern Finland it has exceeded 40 % [32].

The prevalence of current asthma was 11.8 %. This is of a similar magnitude to Australia where current asthma was present in 8.3–13.1 % depending on age and sex [33], and to Finland where 10.0 % reported asthma and an absolute majority also had symptoms [34]. Other studies have found lower prevalence with 6.6 % in Italy [31] and from 7 to 11 % in Denmark [35, 36]. Noteworthy, all of those studies did not involve older adults and had a more narrow definition of asthma with the Italian study excluding subjects not using medication against asthma.

In agreement with earlier studies [37] we found allergic sensitization to be a strong risk factor for current asthma and current rhinitis. Studies have established that allergic sensitization is a risk factor for childhood eczema [38] but published results among adults are scarce. One pooled study from Europe and the United States [39] found a weak positive association between allergic sensitization and eczema while a stronger association was found in a Danish study [40]. That our study did not show a significant association between eczema and allergic sensitization may reflect a weaker association in adults compared to children, yet also be attributed to the definition of eczema where studies presenting a stronger association often employ traditional definitions of eczema that are affected by asthma and rhinitis [41].

The finding that current asthma and current rhinitis are associated to family histories of those conditions is well known [42, 43], yet the impact of family history of other atopic diseases on adult eczema has not been fully established. One of very few studies on this subject did show an association [44], while in our study no association to either family history of asthma, family history of rhinitis or both was noted. The finding that more women than men suffer from current asthma is in agreement with earlier results [45, 46]. We could also replicate the positive association between female sex and current eczema that previously has been demonstrated in the few studies on this topic [15, 44]. The cause for this gender related difference is largely unknown but different expression of sex hormones may play a role at least for asthma [47].

Occupational exposure to gas, dust or fumes increased the risk for both current asthma and current eczema. In the case of asthma, this has previously been reported [48, 49] and it has been estimated that 14 % of adult onset asthma may be attributed to occupational exposure to GDF [50]. The effect of occupational exposure to GDF on eczema is relatively unknown because most studies on eczema to this date have focused on children. Earlier occupational studies regarding eczema have been limited to contact dermatitis. There are reports highlighting the importance of airborne particles for eczema. A Turkish study [51] found that using wood for house heating was associated with eczema, and in Germany [52] there was an increase in eczema after a large accidental airborne emission of chemicals.

Occupational agents can cause asthma by acting as antigens resulting in an IgE mediated allergic reaction and can also exert a direct effect on the respiratory epithelium with subsequent cell-mediated inflammation that is independent of IgE [53]. The mechanism by how airborne particles from an occupational setting may cause eczema is yet to be elucidated. Recent work with the skin the barrier disruption in focus has gained attention [54] which may explain a plausible mechanism for the role between eczema and occupational exposure.

We found that having lived on a farm during the first 5 years of life was associated with a protective effect on both current rhinitis and current eczema but not current asthma. This contrasts results from studies among children where a protective association with asthma has been shown [55]. The protective effect of farm childhood on rhinitis has been observed in young adults in Finland [56] Germany [57] and Sweden [43]. However, the association between farm living and eczema has not been found in populations of children [58]. In older subjects, a protective effect has been shown in Swedish military conscripts [59]. This is, to our knowledge, the first population based epidemiologic study showing a significant protective association between farm childhood and current eczema in adults.

Our observed positive association between obesity and current asthma has already been established in both cross-sectional [60, 61], case-referent [62] and longitudinal studies [63, 64]. We also found that current rhinitis, but not current eczema was positively associated with obesity. The effect of obesity on rhinitis and eczema is so far infrequently studied with conflicting results. In Japan, a study found that allergic rhinitis was associated with obesity only in conjunction with asthma or wheeze [65]. Another study in Poland found that asthma but not eczema or rhinitis was associated with obesity [66]. However, obese subjects in the United States were more likely to report eczema [15, 67].

There are several methodological strengths and weaknesses with cross-sectional studies of this type. The strength of the randomized population based approach of our study is that it decreases the risk of selection bias. Further, a non-response study comparing the responders to the non-responders of the postal survey has been carried out that did not show any significant differences in terms of diseases or symptoms [19]. While a participation rate of 59 % in the clinical examinations is satisfying and comparable to other international studies, there is a risk of bias with enrichment of subjects with the condition studied. An analysis was performed that compared participants and the non-participants in the clinical examination. No differences were seen in gender, smoking or reported use of asthma medication. However, prevalence was slightly higher for asthma and rhinitis but we do not believe that this had any major influence on the studied associations. The questions used in the survey were from internationally validated questionnaires and anthropometric parameters were objectively measured. The cross-sectional design of the study has a weakness in its inability to infer causality between the dependent and the independent variables. Associations must thus be regarded with uncertain causality. Recall bias is a concern where for an example individuals with asthma may be better informed of childhood infections compared to healthy subjects. Another weakness is that the questions on eczema may include other non-eczematous types of dermatitis. Validation studies on questions about eczema similar to ours in children have shown good sensitivity but lower specificity [68].