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Allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study

BACKGROUND: Classical allergy diagnostic workup “from symptoms to molecules” comprises 1) clinical investigation, 2) skin prick- and IgE- testing, and recently, 3) molecular allergy testing. We aimed to examine the diagnostic fidelity of the alternative approach “from molecules to symptoms”, which w...

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Autores principales: Mothes-Luksch, N., Jordakieva, G., Hinterhölzl, L., Jensen, A. N., Hallmann, P. K., Kundi, M., Jensen-Jarolim, E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131881/
https://www.ncbi.nlm.nih.gov/pubmed/30214659
http://dx.doi.org/10.1186/s40413-018-0199-y
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author Mothes-Luksch, N.
Jordakieva, G.
Hinterhölzl, L.
Jensen, A. N.
Hallmann, P. K.
Kundi, M.
Jensen-Jarolim, E.
author_facet Mothes-Luksch, N.
Jordakieva, G.
Hinterhölzl, L.
Jensen, A. N.
Hallmann, P. K.
Kundi, M.
Jensen-Jarolim, E.
author_sort Mothes-Luksch, N.
collection PubMed
description BACKGROUND: Classical allergy diagnostic workup “from symptoms to molecules” comprises 1) clinical investigation, 2) skin prick- and IgE- testing, and recently, 3) molecular allergy testing. We aimed to examine the diagnostic fidelity of the alternative approach “from molecules to symptoms”, which was recently suggested in the EAACI Molecular Allergology User’s Guide, in a retrospective clinical study. METHODS: Records from 202 patients with clinically suspected allergic sensitizations were extracted from files at two sites applying either the “ISAC-first” workup with IgE-testing by immuno-solid phase allergen chip ISAC112 followed by selected skin prick tests (SPT) or the “SPT-first” starting with SPT followed by the microarray test. RESULTS: In the ISAC-first procedure significantly less SPTs were performed during allergy diagnosis (median 4 vs. 14). By SPT in 19% of patients in the ISAC-first group and in 34% in the SPT-first group additional respiratory allergens (p = 0.014) were detected not positive in ISAC microarray. By ISAC microarray test 18% additional sensitizations were found in the ISAC-first, and 32% in SPT-first cohort (p = 0.016). For food allergens 13 and 12% additional sensitizations were detected by the microarray not detected by SPT in the two groups (p = 0.800). No additional food allergen was found by SPT in the ISAC-first group, while in 6% of the cases in the SPT-first group detected sensitizations were negative in the microarray. DISCUSSION: The ISAC-first approach followed by (fewer) SPTs meets the demands for a patient’s tailored diagnostic work-up and therefore can be considered equivalent to the conventional way using the skin prick test as first screening tool, followed by IgE diagnosis. CONCLUSIONS: For the diagnostic verification of clinically suspected allergy, the novel concept “from molecules to clinic” offers a reliable diagnostic workup in shorter time. Due to lower skin test numbers it is especially applicable for young children and seniors, in atopic patients, and whenever skin tests get difficult or unreliable. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40413-018-0199-y) contains supplementary material, which is available to authorized users.
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spelling pubmed-61318812018-09-13 Allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study Mothes-Luksch, N. Jordakieva, G. Hinterhölzl, L. Jensen, A. N. Hallmann, P. K. Kundi, M. Jensen-Jarolim, E. World Allergy Organ J Original Research BACKGROUND: Classical allergy diagnostic workup “from symptoms to molecules” comprises 1) clinical investigation, 2) skin prick- and IgE- testing, and recently, 3) molecular allergy testing. We aimed to examine the diagnostic fidelity of the alternative approach “from molecules to symptoms”, which was recently suggested in the EAACI Molecular Allergology User’s Guide, in a retrospective clinical study. METHODS: Records from 202 patients with clinically suspected allergic sensitizations were extracted from files at two sites applying either the “ISAC-first” workup with IgE-testing by immuno-solid phase allergen chip ISAC112 followed by selected skin prick tests (SPT) or the “SPT-first” starting with SPT followed by the microarray test. RESULTS: In the ISAC-first procedure significantly less SPTs were performed during allergy diagnosis (median 4 vs. 14). By SPT in 19% of patients in the ISAC-first group and in 34% in the SPT-first group additional respiratory allergens (p = 0.014) were detected not positive in ISAC microarray. By ISAC microarray test 18% additional sensitizations were found in the ISAC-first, and 32% in SPT-first cohort (p = 0.016). For food allergens 13 and 12% additional sensitizations were detected by the microarray not detected by SPT in the two groups (p = 0.800). No additional food allergen was found by SPT in the ISAC-first group, while in 6% of the cases in the SPT-first group detected sensitizations were negative in the microarray. DISCUSSION: The ISAC-first approach followed by (fewer) SPTs meets the demands for a patient’s tailored diagnostic work-up and therefore can be considered equivalent to the conventional way using the skin prick test as first screening tool, followed by IgE diagnosis. CONCLUSIONS: For the diagnostic verification of clinically suspected allergy, the novel concept “from molecules to clinic” offers a reliable diagnostic workup in shorter time. Due to lower skin test numbers it is especially applicable for young children and seniors, in atopic patients, and whenever skin tests get difficult or unreliable. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s40413-018-0199-y) contains supplementary material, which is available to authorized users. BioMed Central 2018-09-11 /pmc/articles/PMC6131881/ /pubmed/30214659 http://dx.doi.org/10.1186/s40413-018-0199-y Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Original Research
Mothes-Luksch, N.
Jordakieva, G.
Hinterhölzl, L.
Jensen, A. N.
Hallmann, P. K.
Kundi, M.
Jensen-Jarolim, E.
Allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study
title Allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study
title_full Allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study
title_fullStr Allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study
title_full_unstemmed Allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study
title_short Allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study
title_sort allergy diagnosis from symptoms to molecules, or from molecules to symptoms: a comparative clinical study
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6131881/
https://www.ncbi.nlm.nih.gov/pubmed/30214659
http://dx.doi.org/10.1186/s40413-018-0199-y
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