Sensitisation to airborne moulds and severity of asthma: cross sectional study from European Community respiratory health survey
a National Institute of Health and Medical Research (INSERM), Unit 408 Epidémiologie, Faculté de Médecine Xavier Bichat, BP 416, 75870 Paris CEDEX 18, France, b National Institute of Health and Medical Research (INSERM), Unit U454 Hôpital Arnaud de Villeneuve, 34295 Montpellier Cedex 05, France
Correspondence to: Mahmoud Zureik email@example.com
Objective: To assess whether the severity of asthma is
associated with sensitisation to airborne moulds rather than to
other seasonal or perennial allergens.
The severity of asthma varies widely between patients. Mild cases are characterised by normal lung function and patients are asymptomatic most of the time, whereas severe cases are characterised by permanently impaired lung function and frequent exacerbations. Little is known about the factors associated with severity, but the identification of such factors is necessary for management and prevention.
Sensitisation to airborne allergens might be involved in the underlying mechanisms of severity. The associations between exposure, sensitisation, and asthma have suggested that house dust mite, 1 2 animal dander, 3 4 cockroaches,5 pollens,6 and mould spores7 have a causal role in development. However, the associations between sensitisation to different allergens and the severity of asthma have been poorly explored.
Sensitisation to moulds has been suggested as a risk factor for life threatening asthma. In a study of 11 patients with episodes of respiratory arrest, 10 had positive results on skin prick testing for Alternaria alternata compared with only 31 of the 99 matched controls with asthma and no history of respiratory arrest.8 It was recently reported that 20 of 37 (54%) patients admitted to an intensive care unit for asthma had a positive result on skin testing for one or more fungal allergens (Alternaria tenuis, Cladosporium cladosporoides, Helminthosporium maydis, or Epicoccum nigrum) compared with 30% in patients not admitted to intensive care units. The patients admitted to intensive care units were no more likely than the other patients to have positive results on skin tests for grasses, cat dander, or house dust mites.9 Furthermore, a study of the effects of environmental moulds during the pollen season showed that mean concentrations of mould spores, but not of tree, grass, or ragweed pollen, were significantly higher on the days when there were deaths related to asthma than on the days when no such deaths occurred.10 Thus there is evidence for an association between sensitisation and exposure to moulds and life threatening exacerbations of asthma. However, the hypothesis that sensitisation to moulds is generally associated with the severity of asthma remains to be investigated.
In a preliminary study based on data from population samples of young adults collected in two French centres we found that sensitisation to Alternaria was associated with severity of asthma in a population of young adults. However, few participants had severe asthma (n=21) and there were not enough positive results on skin prick tests to investigate the effect of other moulds.11
We used data from 1132 people with asthma from the entire dataset of the
European Community respiratory health survey to assess whether
the severity of asthma is associated with sensitisation to
airborne moulds rather than to other seasonal or perennial
The methods of the survey have been fully described elsewhere. 12 13 Briefly, participating centres randomly selected samples of 20 to 44 year olds. Participants completed a short postal questionnaire about asthma and asthma-like symptoms (stage 1). At stage 2 about 20% random subsamples of responders were invited to attend a local test centre to complete a more detailed questionnaire administered by an interviewer and undergo skin prick and blood tests, assessment of lung function by spirometry, and airway challenge with methacholine. In addition, all participants who were not in the random subsamples but who reported in the postal questionnaire that they had been woken up by an attack of shortness of breath, had had at least one asthma attack in the past 12 months, or were currently taking medicine for asthma were also invited to participate in the stage 2 (symptomatic sample). The detailed questionnaire included questions about smoking, occupation, social status, home environment, medication, and use of services.13
Standardised skin prick tests were carried out with allergen coated lancets (Phazets, Pharmacia Diagnostics, Uppsala, Sweden). The allergens selected in all centres were A alternata, Cladosporium herbarum, Phleum pratense (timothy grass), birch, olive, Parietaria judaica (pellitory-of-the-wall), common ragweed (Ambrosia artemisifolia), Dermatophagoides pteronyssinus (house dust mite), and cat. An uncoated lancet was used as the negative control. Tests were performed on the volar surface of the forearm with a standard template. Weal size was recorded at 15 minutes as the biggest diameter and the diameter at 90° to its midpoint, each to the nearest whole millimetre. The mean weal diameter was calculated as the average of the two diameters. Results were regarded as positive if the mean weal diameter was at least 3 mm greater than that for the negative control. Baseline forced expiratory volume in one second and forced vital capacity were measured by standardised methods, most often with a Biomedin spirometer (Biomedin, Padua, Italy).14
Definitions of asthma and severity
We used the SAS-PC statistical package (SAS Institute, Cary, NC) for statistical analysis. We assessed the associations between severity of asthma (mild, moderate, severe) and categorical variables using 2 test and tested for trend with Mantel-Haenszel tests. We gathered data from the 30 centres within regions: United Kingdom and Republic of Ireland), northern Europe (Iceland, Norway, Sweden), central Europe (Belgium, France, the Netherlands), southern Europe (Italy and Spain), Australia and New Zealand, and United States (Portland was the only area in the United States). As we found no heterogeneity between regions in the association between severity and sensitisation to allergens (P>0.30 for all allergens except D pteronyssinus, for which P=0.13) we performed logistic regressions to estimate adjusted odds ratios for the associations between severity and sensitisation, taking potential confounding factors into account and with regions included in the model as an additional explanatory variable. We used nominal logistic regressions to assess odds ratios for moderate versus mild asthma and for severe versus mild asthma (without a linearity hypothesis). We used ordinal regression to test for linear trends of the associations between sensitisation and the three categories of severity.
Of the 1132 people with asthma in this study, 564 (50%) had mild asthma, 333 (29%) had moderate asthma, and 235 (21%) had severe asthma. Severity was not related to age, sex, smoking, passive smoking, or parental history of asthma (table 1). Table 1 also shows the features of severity that we used to classify participants into categories.
The proportion of people with mild asthma varied according to geographical area, ranging from 63% in southern Europe to 42% in Australia and New Zealand. The proportion with severe asthma was 15% in southern Europe, 17% in central Europe, 17% in northern Europe, 21% in the United Kingdom and Republic of Ireland, 28% in Australia and New Zealand, and 26% in Portland.
Over 73% of participants were sensitised to at least one allergen and 65% were sensitised to two or more. Sensitisation to moulds alone was extremely rare: nine people were sensitised to Alternaria only and two to Cladosporium only. The proportion of people with asthma with sensitisation to the various allergens varied according to the regions (table 2). Sensitisation to moulds was the lowest in southern Europe and the highest in Portland and in the United Kingdom and Republic of Ireland.
Table 3 shows that sensitisation to moulds was significantly associated with severity of asthma. For both Alternaria and Cladosporium the proportion of sensitised people increased with increasing severity (P<0.001 for trend). For Alternaria the odds ratio was 1.64 for moderate versus mild asthma and 2.05 for severe versus mild asthma. These remained unchanged in the multivariable models after we adjusted for possible confounding factors. For Cladosporium the odds ratio was >3 for severe versus mild asthma. When we considered sensitisation to either mould, the odds ratio was 2.34 for severe versus mild asthma (P<0.001). We observed similar patterns for the association between sensitisation to moulds and severity of asthma (severe versus mild asthma) in all regions (fig 2).
We found no association between severity of asthma and sensitisation to pollens. Table 4 shows the results for timothy grass and birch and sensitisation to at least one of the pollens tested. The latter results were identical when we excluded P judaica and ragweed, which are not ubiquitous, from the definition of sensitisation to any pollen.
Severity of asthma was positively associated with sensitisation to D pteronyssinus but not with sensitisation to cats (table 5). To assess the independent relations between the various allergens and severity of asthma we carried out simultaneous logistic regressions including sensitisation to moulds, pollens, D pteronyssinus, and cats (table 6). For moulds (Alternaria or Cladosporium, or both) the odds ratios were 1.48 for moderate versus mild asthma and 2.16 for severe versus mild asthma.
Our study of asthma from large population based samples of adults living in different countries showed that the severity of asthma is associated with sensitisation to Alternaria and Cladosporium but not to pollens. As expected the severity of asthma was also associated with sensitisation to D pteronyssinus.
Comparison with other studies
The definition of severity of asthma in a population study is a difficult issue.21 We based our classification on a score that included some features considered as the most relevant.22 It is necessary to consider the use of drugs to control asthma in the classification of currently treated patients because otherwise participants would be classified according to control of asthma rather than severity.23 The inclusion of the use of corticosteroids in our definition may have influenced the distribution of severity in different areas because of variation in prescription from country to country. 16 17 Such variations do not allow international comparisons for the prevalence of severe asthma. However, similar patterns of results for the association between severity and sensitisation to moulds were observed in the different areas. Because it has been suggested that long term use of oral corticosteroids may modify results of skin prick tests24 we reanalysed the data after excluding the 110 patients taking oral corticosteroids. The multivariate adjusted odds ratios for the association between moulds (either Alternaria or Cladosporium) and severity were 1.65 (95% confidence interval 1.08 to 2.50) for moderate versus mild asthma and 2.49 (1.55 to 3.99) for severe versus mild asthma. These results are similar to those presented in table 3.
We considered hospital admissions in the past 12 months in the classification of asthma severity, but in only a few participants (2.2%) was this relevant. Our results do not therefore duplicate those of previous studies of life threatening asthma.
To date, there has been little evidence that sensitisation to moulds is associated with severity of asthma. A study of 343 children aged 7 to 12 years recruited from a paediatric practice investigated the association between sensitisation to individual allergens and the frequency of episodes of wheezing. The proportion of children sensitised to A tenuis increased with the number of episodes. However, significant associations were also observed for sensitisation to mites and especially to cats.25 The relation between skin test reactivity and forced expiratory volume in one second was examined in children aged 6 to 12 years with asthma or frequent wheezing as part of the second national health and nutrition survey. Low forced expiratory volume in one second was associated with reactions to house dust, Alternaria, dogs, ragweed, oak, and Bermuda grass allergens.26
To our knowledge no population studies apart from the European Community respiratory health survey have investigated the association between severity of asthma and sensitisation to allergens in adults. In a study of the relative importance of sensitisation to individual allergens for bronchial hyper-responsiveness in the United Kingdom within the framework of the European survey, people with positive results to Cladosporium were considerably more responsive than those with positive results to cats or timothy grass.27 Analysis of Spanish data showed that sensitisation to Alternaria, cats, and timothy grass was associated with a decrease in forced expiratory volume in one second in women.28 In a preliminary study based on data from two French centres we found that sensitisation to Alternaria was associated with severity of asthma.11
As the importance of sensitisation to moulds as a risk factor for severe asthma may be dependent on area, the European survey was an unique opportunity to assess the consistency of the association. Data were collected with thoroughly standardised methods in comparable populations. Consistency of results across the survey areas has not always been observed for other issues. For example, the association between symptoms of asthma and lung function and the use of gas appliances varied considerably between areas. 29 30 In contrast, the association between severity and sensitisation to moulds was remarkably consistent, though there were differences in the distribution of severity and in the frequency of sensitisation to the various allergens in the various areas, despite the fact the gathering of centres into regions is necessarily arbitrary.
We observed a differential association between moulds and pollens and severity of asthma. Possibly the size of fungal spores allows them to reach the lower airways and also they may be inhaled by means of fragments and other amorphous bioaerosols. Pollens are larger and their effect on asthma requires exceptional situations such as thunderstorms, when pollen is concentrated by changes in air flow, grains are ruptured by osmotic shock, and each grain releases hundreds of starch granules that are small enough to be respired.31 Other explanations for the different effects of sensitisation to moulds and to pollens are possible. Unlike pollens, moulds are present all through the year with increase in the spore counts during the autumn months. Also, the level of mould exposure is probably greater because the exposure occurs indoors rather than outdoors and people spend most of their time indoors. The severity of asthma was associated with sensitisation to airborne moulds despite the fact that sensitisation to moulds alone was extremely rare. This might suggest a synergistic or additive effect of various sensitisations in determining severity. However, this is unlikely because when the number of positive test results was taken into account in the analysis the results did not change.
Our results of the associations between moulds and severity of asthma may be put together with results from studies on asthma incidence or outbreaks, where the role of moulds can be suspected for effects that were primarily attributed to other allergens. Moulds might be involved in the dramatic increase in incidence in Tucson that was initially attributed in part to a 10-fold increase in atmospheric pollen due to the widespread use of ornamental trees that produce pollen.32 More recently, it has been suggested that moulds may have had a role in the asthma epidemics in Barcelona that were attributed to soybean.33
In conclusion, our results show that sensitisation to moulds might be involved in the severity of asthma. Given the increase of asthma and the prevalence of severe asthma in the past decades these results may be relevant for many people. Those people with asthma who are sensitised to airborne moulds should be educated to pay careful attention to symptoms and comply with treatment, particularly during the seasonal increase in mould spore counts. Patients should be encouraged to decrease exposure by avoiding indoor conditions that facilitate the growth of mouldsfor example, by better ventilation and by decreasing dampness.
Project management group: P Burney (project leader), S Chinn, C Luczynska, D Jarvis, P Vermeire (Antwerp), H Kesteloot (Leuven), J Bousquet (Montpellier), D Nowak (Hamburg), the late J Prichard (Dublin), R De Marco (Verona), B Rijcken (Groningen), J M Anto (Barcelona), J Alves (Oporto), G Boman (Uppsala), N Nielsen (Copenhagen), P Paoletti (Pisa).
Participating centres: Austria: W Popp (Vienna); Australia: M
Abramson, J Kutin (Melbourne); Belgium: P Vermeire, F van
Bastelaer (Antwerp South, Antwerp Central); France: J Bousquet, J
Knani (Montpellier), F Neukirch, R Liard (Paris), I Pin, C Pison
(Grenoble), A Taytard (Bordeaux); Germany: H Magnussen, D Nowak
(Hamburg), H E Wichmann, J Heinrich (Erfurt); Greece: N
Papageorgiou, P Avarlis, M Gaga, C Marossis (Athens); Iceland: T
Gislason, D Gislason (Reykjavik); Ireland: the late J Prichard, S
Allwright, D MacLeod (Dublin); Italy: M Bugiani, C Bucca, C
Romano (Turin), R de Marco Lo Cascio, C Campello (Verona), A
Marinoni, I Cerveri, L Casali (Pavia); the Netherlands: B Rijcken,
A Kremer, (Groningen, Bergen-op-Zoom, Geleen); New Zealand: J
Crane, S Lewis, (Wellington, Christchurch, Hawkes Bay); Norway: A
Gulsvik, E Omenaas (Bergen); Portugal: J A Marques, J Alves (Oporto);
Spain: J M Antó, J Sunyer, F Burgos, J Castellsangué, J Roca, J B
Soriano, A Tobías (Barcelona), N Muniozguren, J Ramos Gonzáles, A
Capelastegui (Galdakao), J Castillo, J Rodriguez Portal
(Seville), J Martinez-Moratalla, E Almar (Albacete), J Maldonado
Pérez, A Pereira, J Sánchez (Huelva), J Quiros, I Huerta, F Pavo,
(Oviedo); Sweden: G Boman, C Janson, E Björnsson (Uppsala), L
Rosenhall, E Norrman, B Lundbäck (Umea), N Lindholm, P Plaschke
(Gothenburg,); Switzerland: U Ackermann-Liebrich, N Künzli, A
Perruchoud (Basle); United Kingdom: M Burr, J Layzell (Caerphilly),
R Hall (Ipswich), B Harrison (Norwich), J Stark (Cambridge);
United States: S Buist, W Vollmer, M Osborne (Portland).
Contributions: All authors conceived and initiated this study within the framework of the European Community respiratory health survey. MZ designed and performed the analysis, wrote the first draft of the paper, and is guarantor. CN helped with analysis, interpretation, and writing the paper. BL conducted part of the statistical analysis and helped in interpretation. RL gave substantial help to writing the paper. JB participated in study design and interpretation. FN was principal investigator and participated in study design, analysis, and interpretation. MZ and CN participated in the data collection for the Paris centre.
Funding: Australia: Allen & Hanbury, Australia; Belgium: Belgian Science Policy Office, National Fund for Scientific Research; France: Ministčre de la Santé, Glaxo France, Institut Pneumologique d'Aquitaine, Contrat de Plan Etat-Région Languedoc-Roussillon, CNMATS, CNMRT (90MR/10, 91AF/6), Ministre délégué de la santé, RNSP, Ministčre de l'Environnement (No 96115-EN96D4); Germany: GSF, Bundesminister für Forschung und Technologie, Bonn; Greece: Greek Secretary General of Research and Technology, Fisons, Astra, Boehringer-Ingelheim; India: Bombay Hospital Trust; Italy: Ministero dell'Univesitŕ e della Ricerca Scientifica e Tecnologica, CNR, Regione Veneto Grant RSF No 381/05.93; New Zealand: Asthma Foundation of New Zealand, Lotteries Grant Board, Health Research Council of New Zealand; Norway: Norwegian Research Council project No 101422/310; Portugal: Glaxo Farmacęutica Lda, Sandoz Portugesa; Spain: Ministero Sanidad y Consumo FIS (grants 91/0016060/OOE-05E, 92/0319, 93/0393), Hospital General de Albacete, Hospital General Juan Ramón Jiménenz, Consejeria de Sanidad Principado de Asturias; Sweden: Swedish Medical Research Council, Swedish Heart Lung Foundation, Swedish Association against Asthma and Allergy, Swedish Society of Medicine, Astra, Glaxo-Wellcome, Boehringer-Ingelheim; Switzerland: Swiss National Science Foundation Grant 4026-28099; United Kingdom: National Asthma Campaign, British Lung Foundation, Department of Health, South Thames Regional Health Authority; United States: US Department of Health, Education and Welfare Public Health Service Grant No 2 S07 RR05521-28.
Competing interests: None declared.
(Accepted 4 April 2002)
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