Methodologic aspects of the quantification of skin prick test responses: The EGEA study

Background: The expression of responses of allergy skin prick tests is not standardized. Usual definitions of atopy are not quantitative. Objective: We sought to perform a biometric analysis of responses to various allergens to propose synthetic, quantitative indices independent of the heterogeneity...

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Published inJournal of allergy and clinical immunology Vol. 111; no. 4; pp. 750 - 756
Main Authors Maccario, Jean, Oryszczyn, Marie-Pierre, Charpin, Denis, Kauffmann, Francine
Format Journal Article
LanguageEnglish
Published New York, NY Mosby, Inc 01.04.2003
Elsevier
Elsevier Limited
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ISSN0091-6749
1097-6825
DOI10.1067/mai.2003.1386

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Abstract Background: The expression of responses of allergy skin prick tests is not standardized. Usual definitions of atopy are not quantitative. Objective: We sought to perform a biometric analysis of responses to various allergens to propose synthetic, quantitative indices independent of the heterogeneity of responses to various allergens. Methods: Adults (N = 1286) from the Epidemiological Study on the Genetics and Environment of Asthma, Bronchial Hyperresponsiveness, and Atopy (EGEA) were included in the analysis. The first step, conducted for 678 subjects with at least 1 wheal >0, was to perform a standardization of wheal diameters to obtain comparable figures for 10 allergens through use of the means of the squares of wheal size as a scaling factor. The second step was a factor analysis of the standardized responses conducted not only for all subjects but also separately for asthmatic case and nonasthmatic control subjects. Finally, the strength of the link between various dichotomous and quantitative scores was assessed with multiRAST, total IgE, and asthma. Analyzed quantitative scores were based on the number of positive responses and on the nonstandardized and standardized sizes of the wheals. Results: The standardization was efficient. Among asthmatic subjects but not other subjects, factor analysis evidenced a pattern with 3 factors, corresponding to outdoor, indoor, and mold allergens. The link study showed that all scores performed very similarly. Conclusion: The number of positive tests is a quantitative score with valid biometric properties. It should be used more widely in clinical settings and in epidemiology to assess the severity of atopy.
AbstractList Background: The expression of responses of allergy skin prick tests is not standardized. Usual definitions of atopy are not quantitative. Objective: We sought to perform a biometric analysis of responses to various allergens to propose synthetic, quantitative indices independent of the heterogeneity of responses to various allergens. Methods: Adults (N = 1286) from the Epidemiological Study on the Genetics and Environment of Asthma, Bronchial Hyperresponsiveness, and Atopy (EGEA) were included in the analysis. The first step, conducted for 678 subjects with at least 1 wheal >0, was to perform a standardization of wheal diameters to obtain comparable figures for 10 allergens through use of the means of the squares of wheal size as a scaling factor. The second step was a factor analysis of the standardized responses conducted not only for all subjects but also separately for asthmatic case and nonasthmatic control subjects. Finally, the strength of the link between various dichotomous and quantitative scores was assessed with multiRAST, total IgE, and asthma. Analyzed quantitative scores were based on the number of positive responses and on the nonstandardized and standardized sizes of the wheals. Results: The standardization was efficient. Among asthmatic subjects but not other subjects, factor analysis evidenced a pattern with 3 factors, corresponding to outdoor, indoor, and mold allergens. The link study showed that all scores performed very similarly. Conclusion: The number of positive tests is a quantitative score with valid biometric properties. It should be used more widely in clinical settings and in epidemiology to assess the severity of atopy.
The expression of responses of allergy skin prick tests is not standardized. Usual definitions of atopy are not quantitative. We sought to perform a biometric analysis of responses to various allergens to propose synthetic, quantitative indices independent of the heterogeneity of responses to various allergens. Adults (N = 1286) from the Epidemiological Study on the Genetics and Environment of Asthma, Bronchial Hyperresponsiveness, and Atopy (EGEA) were included in the analysis. The first step, conducted for 678 subjects with at least 1 wheal >0, was to perform a standardization of wheal diameters to obtain comparable figures for 10 allergens through use of the means of the squares of wheal size as a scaling factor. The second step was a factor analysis of the standardized responses conducted not only for all subjects but also separately for asthmatic case and nonasthmatic control subjects. Finally, the strength of the link between various dichotomous and quantitative scores was assessed with multiRAST, total IgE, and asthma. Analyzed quantitative scores were based on the number of positive responses and on the nonstandardized and standardized sizes of the wheals. The standardization was efficient. Among asthmatic subjects but not other subjects, factor analysis evidenced a pattern with 3 factors, corresponding to outdoor, indoor, and mold allergens. The link study showed that all scores performed very similarly. The number of positive tests is a quantitative score with valid biometric properties. It should be used more widely in clinical settings and in epidemiology to assess the severity of atopy.
The expression of responses of allergy skin prick tests is not standardized. Usual definitions of atopy are not quantitative.BACKGROUNDThe expression of responses of allergy skin prick tests is not standardized. Usual definitions of atopy are not quantitative.We sought to perform a biometric analysis of responses to various allergens to propose synthetic, quantitative indices independent of the heterogeneity of responses to various allergens.OBJECTIVEWe sought to perform a biometric analysis of responses to various allergens to propose synthetic, quantitative indices independent of the heterogeneity of responses to various allergens.Adults (N = 1286) from the Epidemiological Study on the Genetics and Environment of Asthma, Bronchial Hyperresponsiveness, and Atopy (EGEA) were included in the analysis. The first step, conducted for 678 subjects with at least 1 wheal >0, was to perform a standardization of wheal diameters to obtain comparable figures for 10 allergens through use of the means of the squares of wheal size as a scaling factor. The second step was a factor analysis of the standardized responses conducted not only for all subjects but also separately for asthmatic case and nonasthmatic control subjects. Finally, the strength of the link between various dichotomous and quantitative scores was assessed with multiRAST, total IgE, and asthma. Analyzed quantitative scores were based on the number of positive responses and on the nonstandardized and standardized sizes of the wheals.METHODSAdults (N = 1286) from the Epidemiological Study on the Genetics and Environment of Asthma, Bronchial Hyperresponsiveness, and Atopy (EGEA) were included in the analysis. The first step, conducted for 678 subjects with at least 1 wheal >0, was to perform a standardization of wheal diameters to obtain comparable figures for 10 allergens through use of the means of the squares of wheal size as a scaling factor. The second step was a factor analysis of the standardized responses conducted not only for all subjects but also separately for asthmatic case and nonasthmatic control subjects. Finally, the strength of the link between various dichotomous and quantitative scores was assessed with multiRAST, total IgE, and asthma. Analyzed quantitative scores were based on the number of positive responses and on the nonstandardized and standardized sizes of the wheals.The standardization was efficient. Among asthmatic subjects but not other subjects, factor analysis evidenced a pattern with 3 factors, corresponding to outdoor, indoor, and mold allergens. The link study showed that all scores performed very similarly.RESULTSThe standardization was efficient. Among asthmatic subjects but not other subjects, factor analysis evidenced a pattern with 3 factors, corresponding to outdoor, indoor, and mold allergens. The link study showed that all scores performed very similarly.The number of positive tests is a quantitative score with valid biometric properties. It should be used more widely in clinical settings and in epidemiology to assess the severity of atopy.CONCLUSIONThe number of positive tests is a quantitative score with valid biometric properties. It should be used more widely in clinical settings and in epidemiology to assess the severity of atopy.
Author Kauffmann, Francine
Maccario, Jean
Charpin, Denis
Oryszczyn, Marie-Pierre
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Issue 4
Keywords Human
Immunopathology
Allergy
Prick test
Methodology
methods
Diagnosis
Epidemiology
Quantitative analysis
Skin test
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Snippet Background: The expression of responses of allergy skin prick tests is not standardized. Usual definitions of atopy are not quantitative. Objective: We sought...
The expression of responses of allergy skin prick tests is not standardized. Usual definitions of atopy are not quantitative. We sought to perform a biometric...
The expression of responses of allergy skin prick tests is not standardized. Usual definitions of atopy are not quantitative.BACKGROUNDThe expression of...
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SubjectTerms Adolescent
Adult
Aged
Allergens - immunology
Allergies
Allergological tests
Asthma
Asthma - diagnosis
Biological and medical sciences
Environment
Epidemiologic Studies
Female
Humans
Immunological methods for diagnosis and exploration
Immunopathology
Judaica
Male
Medical sciences
Middle Aged
Phenotype
Skin Tests - standards
Standardization
Statistical methods
Title Methodologic aspects of the quantification of skin prick test responses: The EGEA study
URI https://www.clinicalkey.com/#!/content/1-s2.0-S0091674903008480
https://dx.doi.org/10.1067/mai.2003.1386
https://www.ncbi.nlm.nih.gov/pubmed/12704353
https://www.proquest.com/docview/1504839865
https://www.proquest.com/docview/73211336
Volume 111
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