Eva Östblom
Karolinska Institutet
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Publication
Featured researches published by Eva Östblom.
Allergy | 2012
Natalia Ballardini; Inger Kull; Tomas Lind; Eva Hallner; Catarina Almqvist; Eva Östblom; Erik Melén; Göran Pershagen; G. Lilja; Anna Bergström; Magnus Wickman
Allergy‐related diseases are a public health issue, but knowledge on development and comorbidity among children is scarce. The aim was to study the development of eczema, asthma and rhinitis in relation to sex and parental allergy, in a population‐based cohort, during childhood.
Allergy | 2010
Anna Asarnoj; Robert Movérare; Eva Östblom; Maryam Poorafshar; G. Lilja; Gunilla Hedlin; M. van Hage; Staffan Ahlstedt; Magnus Wickman
To cite this article: Asarnoj A, Movérare R, Östblom E, Poorafshar M, Lilja G, Hedlin G, van Hage M, Ahlstedt S, Wickman M. IgE to peanut allergen components: relation to peanut symptoms and pollen sensitization in 8‐year‐olds. Allergy 2010; 65: 1189–1195.
Clinical Immunology | 2009
Magdalena Janzi; Inger Kull; Ronald Sjöberg; Jinghong Wan; Erik Melén; Narges Bayat; Eva Östblom; Qiang Pan-Hammarström; Peter Nilsson; Lennart Hammarström
Selective IgA deficiency in early life is quite common in Caucasian populations, but it is unclear whether it increases the risk of infections and allergic diseases during childhood. Serum IgA levels were measured in 2423 children at 4 years of age in a Swedish population based birth cohort (BAMSE). Parental questionnaires were repeatedly sent out during the childs first 8 years of life, collecting information about infections and allergic diseases. 14 children (1:173) were found to be IgA deficient at 4 years of age. These children had an increased risk of pseudocroup at year 1 (p<0.01) and food hypersensitivity at year 4 (p<0.05) as compared to IgA sufficient children. No increased risk was observed in the partial IgA deficiency group. The findings suggest that selective IgA deficiency may increase the risk of parentally reported pseudocroup and food hypersensitivity during early childhood.
Clinical & Experimental Allergy | 2012
Mirja Vetander; C. Flodström; Eva Östblom; Tobias Alfvén; D. H. Ly; Gunilla Hedlin; G. Lilja; Caroline Nilsson; Magnus Wickman
Information about acute reactions to foods among children is limited.
The Journal of Allergy and Clinical Immunology | 2012
Anna Asarnoj; Caroline Nilsson; Jonas Lidholm; Susanne Glaumann; Eva Östblom; Gunilla Hedlin; Marianne van Hage; G. Lilja; Magnus Wickman
BACKGROUND Isolated Ara h 8 sensitization is suggested to be associated with no or mild symptoms among peanut-sensitized subjects. OBJECTIVE We sought to investigate the occurrence of systemic reactions in children with isolated sensitization to Ara h 8. METHODS Participants were 144 children sensitized to Ara h 8 (≥ 0.35 kU(A)/L) but not to Ara h 1, Ara h 2, or Ara h 3 (<0.35 kU(A)/L). An open oral challenge with peanut was performed in those subjects who did not consume peanut regularly, and an extended IgE reactivity profile was obtained. If the child had a documented history of systemic reactions up to grade I anaphylaxis, double-blind, placebo-controlled food challenges were performed. RESULTS One hundred twenty-nine (89.5%) children were either peanut consumers or did not react to peanut challenge. Another 14 (9.7%) children experienced oral cavity symptoms at the first 2 but not subsequent challenge doses. At the time of the double-blind, placebo-controlled food challenge, 1 boy with a previous mild systemic reaction to peanut experienced lip swelling, stomach cramping, and objective tiredness. Reanalysis of IgE levels showed an increase in peanut IgE levels from 1.5 to 8.8 kU(A)/L, but IgE levels to Ara h 8 remained stable and IgE levels to Ara h 1, Ara h 2, and Ara h 3 were all still less than 0.35 kU(A)/L. The IgE level to Ara h 6 was 0.45 kU(A)/L. CONCLUSION Isolated Ara h 8 sensitization indicates tolerance to peanuts in almost all cases. However, sensitization against thus far unidentified determinants in peanut might cause symptoms in rare cases.
Allergy | 2008
Eva Östblom; Ann-Charlotte Egmar; Ann Gardulf; G. Lilja; Magnus Wickman
Background: There are only a few studies on the impact of food hypersensitivity (FHS) in children on health‐related quality of life (HRQL). The present study was designed to examine this impact in a population‐based birth cohort (BAMSE).
Clinical & Experimental Allergy | 2008
Eva Östblom; G. Lilja; Göran Pershagen; M. van Hage; Magnus Wickman
Background Longitudinal data from population‐based studies on the development and persistence of food hypersensitivity (FHS) during childhood are almost absent.
Allergy | 2010
Anna Asarnoj; Eva Östblom; Staffan Ahlstedt; Gunilla Hedlin; G. Lilja; M. van Hage; Magnus Wickman
To cite this article: Asarnoj A, Östblom E, Ahlstedt S, Hedlin G, Lilja G, van Hage M, Wickman M. Reported symptoms to peanut between 4 and 8 years among children sensitized to peanut and birch pollen – results from the BAMSE birth cohort. Allergy 2010; 65: 213–219.
Allergy | 2008
Eva Östblom; G. Lilja; Staffan Ahlstedt; M. van Hage; Magnus Wickman
Background: Diagnosis of food hypersensitivity (FHS) is difficult and interpretation of food allergy tests is complicated.
Clinical & Experimental Allergy | 2008
Anna Asarnoj; Eva Östblom; Inger Kull; G. Lilja; Göran Pershagen; Gunilla Hedlin; M. van Hage; Magnus Wickman
Background There is limited knowledge of the development of IgE‐antibody levels over time in childhood, with respect to persistency and co‐sensitization to specific inhalant allergens.