Evidence map›Paper›PMID 37010667›Full record

ArticleMikrochimica acta2023

Reversed-phase allergen microarrays on optical discs for multiplexed diagnostics of food allergies.

Luis A Tortajada-Genaro, Natalia Casañ-Raga, Salva Mas, Ethel Ibañez-Echevarria, Sergi Morais, Ángel Maquieira

Open access · hybridAbstract read
In one paragraph

Article in Mikrochimica acta, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.9field-weighted citation impact, top 15% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 8 citations in OpenAlex.

  1. Review
  2. Article
  3. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

6 authors at 2 institutions in 1 country.

Luis A Tortajada-GenaroInstituto Interuniversitario de Investigación de Reconocimiento Molecular Y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Camino de Vera S/N, 46022, Valencia, Spain. luitorge@qim.upv.es.ORCID http://orcid.org/0000-0003-4021-5607
Natalia Casañ-RagaInstituto Interuniversitario de Investigación de Reconocimiento Molecular Y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Camino de Vera S/N, 46022, Valencia, Spain.
Salva MasInstituto Interuniversitario de Investigación de Reconocimiento Molecular Y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Camino de Vera S/N, 46022, Valencia, Spain.
Ethel Ibañez-EchevarriaHospital Universitari I Politènic La Fe, Servicio de Alergología, Avinguda de Fernando Abril Martorell, 106, 46026, Valencia, Spain.
Sergi MoraisInstituto Interuniversitario de Investigación de Reconocimiento Molecular Y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Camino de Vera S/N, 46022, Valencia, Spain.
Ángel MaquieiraInstituto Interuniversitario de Investigación de Reconocimiento Molecular Y Desarrollo Tecnológico (IDM), Universitat Politècnica de València, Universitat de València, Camino de Vera S/N, 46022, Valencia, Spain.
Universitat de València · ESHospital Universitari i Politècnic La Fe · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A high percentage of the population suffers from multiple food allergies justifying  the importance of reliable diagnostic methods. Single-analyte solutions based on the determination of specific immunoglobulins E (sIgE) are safe and fast but are generally time-consuming and expensive. Thus sustainable microanalytical methods that provide multianalyte profiling information are highly demanded. This work presents the in vitro biosensing of specific IgE levels based on a reversed-phase allergen array. The approach consists of optical biosensing supported by direct multiplex immunoassays and on-disc technology. It identifies 12 sIgE associated with food allergies in a single analysis with a low serum sample volume (25 µL). After processing captured images, specific signals for each target biomarker correlate to their concentration. The assay analytically performs well with 0.3 IU/mL and 0.41 IU/mL as the detection and quantification limits in serum, respectively. This novel method achieves excellent clinical specificity (100%) and high sensitivity (91.1%), considering the diagnosis obtained by clinical history and ImmunoCAP analysis. The results demonstrate that microanalytical systems based on allergen arrays can potentially diagnose multiple food allergies and are easily implemented in primary care laboratory settings.

Indexed as

AllergensFood HypersensitivityHumansImmunoassayImmunoglobulin EMicroarray AnalysisAllergensImmunoglobulin EFood allergy,Micro-immunoassayImmunoglobulin EOptical biosensorProtein array

Identifiers

PMID37010667
PMCPMC10070211
OpenAlexW4362523873

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.