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Evaluation of the Sphingolipid Metabolite S1P as a Novel Biomarker in Food Allergy

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Medical University of Vienna

Status

Unknown

Conditions

Food Allergy
Anaphylaxis

Study type

Observational

Funder types

Other

Identifiers

NCT01776489
119/2011
KLI 284-B00 (Other Grant/Funding Number)

Details and patient eligibility

About

Food allergies represent an increasing health concern in the industrialized countries and especially affect pediatric patients. In this population adverse reactions against food compounds can lead to anaphylactic reactions. Despite substantial research efforts, clinical markers predicting disease severity and symptoms are missing to date.

Recent studies have revealed that sphingolipids, especially sphingosine-1-phosphate (S1P), play an essential role in allergy. It was reported that asthmatic patients have higher S1P levels in bronchiallavage fluids after allergen challenge. First experimental studies revealed a correlation of S1P and the outcome of anaphylaxis. Furthermore, we have shown in our recent mouse study that S1P homeostasis is pivotal for food allergy induction and effector cell response. Therefore, it is the aim of the presented pilot project to evaluate whether S1P serum titers are altered in food allergic children and if the S1P levels correlate with the outcome of anaphylaxis during double blind placebo controlled food challenges (DBPCFCs).

Enrollment

70 estimated patients

Sex

All

Ages

12 months to 17 years old

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients between 1-17 years who have been reported to suffer from food allergic reactions and who are subjected to DBPCFC or open provocation
  • Patients who are diagnosed by elevated allergen specific IgE and/or positive skin prick testing
  • Willingness to participate in the study

Exclusion criteria

  • Refusal to participate in the study
  • Non-IgE-mediated food allergy

Trial design

70 participants in 2 patient groups

food allergic
Description:
positive reaction during DBPCFC
Non-food allergic
Description:
no reaction during DBPCFC

Trial contacts and locations

1

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Central trial contact

Susanne C. Diesner, MD, PhD; Zsolt Szépfalusi, MD

Data sourced from clinicaltrials.gov

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