IgE sensitization to food allergens and airborne allergens in relation to biomarkers of type 2 inflammation in asthma

Summary Background We have recently reported that sensitization to food allergens and sensitization to airborne allergens had independent associations with increased fraction of exhaled nitric oxide (FeNO) and blood eosinophils in middle‐aged adults and in young subjects with asthma. Objective To in...

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Published inClinical and experimental allergy Vol. 48; no. 9; pp. 1147 - 1154
Main Authors Patelis, A., Alving, K., Middelveld, R., James, A., Ono, J., Ohta, S., Izuhara, K., Borres, M. P., Forsberg, B., Janson, C., Malinovschi, A.
Format Journal Article
LanguageEnglish
Published England Wiley Subscription Services, Inc 01.09.2018
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ISSN0954-7894
1365-2222
1365-2222
DOI10.1111/cea.13165

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Summary:Summary Background We have recently reported that sensitization to food allergens and sensitization to airborne allergens had independent associations with increased fraction of exhaled nitric oxide (FeNO) and blood eosinophils in middle‐aged adults and in young subjects with asthma. Objective To investigate the relation between IgE sensitization and several type 2 inflammation biomarkers in adult asthmatics. Methods FeNO, urinary eosinophil‐derived neurotoxin (U‐EDN), serum eosinophil cationic protein (S‐ECP) and periostin were measured in 396 asthmatics, aged 17‐76 years, from the Swedish GA2LEN study. Sensitization to airborne allergens was examined with skin prick tests (≥3 mm wheal) and sensitization to food allergens with measurement of specific IgE (≥0.35 kU/L). Results Asthmatics sensitized to food allergens had higher FeNO, 22.3 ppb (18.6, 26.7) vs 16.1 ppb (14.2, 18.2) (P = .005), S‐ECP, 17.7 mg/L (14.8, 21.1) vs 12.8 mg/L (10.9, 14.9) (P = .01), and periostin, 73.7 (67.5, 80.3) ng/mL vs 59.9 (55.8, 64.2) ng/mL (P = .003), than non‐sensitized subjects. Periostin levels in this group were also significantly higher than in the group sensitized only to airborne allergens (P = .01). Sensitization to food allergens related independently to FeNO (P = .02), S‐ECP (P = .006) and periostin (P = .004), whereas sensitization only to airborne allergens related only to FeNO (P = .02) after adjustments for age, sex, height, weight and smoking history. FeNO correlated weakly with S‐ECP (r = .17, P < .001), periostin (r = .19, P < .001) and U‐EDN (0.16, P < .001). S‐ECP also correlated weakly with U‐EDN (r = .12, P = .02). None of the correlations between the remaining pairs of markers of type 2 inflammation were significant. Conclusions & Clinical Relevance Sensitization to food allergens related to several local and systemic type 2 inflammation markers, such as FeNO, S‐ECP and periostin. Assessing the profile of allergic sensitization, including to food allergens, might improve the understanding and interpretation of inflammatory markers and potentially improve asthma management.
Bibliography:Funding information
The study was funded by Västerbotten County Council (ALF), Uppsala University Hospital, Hesselman's Research Foundation, the EU FP6 project GA2LEN (EU contract number FOOD‐CT‐2004‐506378), The Centre for Allergy Research at the Karolinska Institute, The Swedish Heart‐Lung Foundation, The Swedish Heart and Lung Association, The Swedish Asthma and Allergy Association, The Centre for Allergy Research at Karolinska Institutet, the Medical Research Council, the Vårdal Foundation, Stockholm County Council (ALF), the Swedish Foundation for Strategic Research, Konsul Th C Berghs Foundation, the Karolinska Institutet SciLifeLab Collaborations on Translational Medicine (ChAMP) project and Karolinska Institutet. Thermo Fischer Scientific has kindly provided reagents for serum eosinophil cationic protein and IgE measurements in this study.
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ISSN:0954-7894
1365-2222
1365-2222
DOI:10.1111/cea.13165