Evidence map›Paper›PMID 36294955›Full record

ArticleLife (Basel, Switzerland)2022

Atopy and Multisensitizations in Specific IgE Microarrays and Their Impact on Severe Asthma.

Jan Romantowski, Aleksandra Górska, Grażyna Moszkowska, Julia Kulczycka, Karolina Minkowska, Agata Rolewicz, Marita Nittner-Marszalska, Marek Niedoszytko

Open access · goldAbstract read
In one paragraph

Article in Life (Basel, Switzerland), 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.1field-weighted citation impact, top 53% 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

1 citing paper in PubMed, 1 citations in OpenAlex.

  1. 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

8 authors at 3 institutions in 1 country.

Jan RomantowskiDepartment of Allergology, Medical University of Gdansk, 80-214 Gdansk, Poland.ORCID 0000-0002-0487-0957
Aleksandra GórskaDepartment of Allergology, Medical University of Gdansk, 80-214 Gdansk, Poland.
Grażyna MoszkowskaLaboratory of Clinical Immunology and Transplantology, University Clinical Centre of Gdansk, 80-952 Gdańsk, Poland.
Julia KulczyckaLaboratory of Clinical Immunology and Transplantology, University Clinical Centre of Gdansk, 80-952 Gdańsk, Poland.
Karolina MinkowskaDepartment of Allergology, Medical University of Gdansk, 80-214 Gdansk, Poland.
Agata RolewiczDepartment of Allergology, Medical University of Gdansk, 80-214 Gdansk, Poland.
Marita Nittner-MarszalskaDepartment of Internal Medicine Pneumology and Allergology, Wroclaw Medical University, 50-425 Wrocław, Poland.
Marek NiedoszytkoDepartment of Allergology, Medical University of Gdansk, 80-214 Gdansk, Poland.
Gdańsk Medical University · PLUniversity Clinical Centre · PLWroclaw Medical University · PL

Funding

Gdańsk Medical University ST 02-141/07/231
6 · The paper itself

Abstract

(1) Asthma is a chronic inflammatory airway disease. Around 3-10% of patients experience severe refractory asthma. These patients with high symptom intensity and frequent exacerbations present a challenge for allergologists. Their allergic vs. non-allergic profile might be different from the standard asthmatic group and this difference is vital in qualifying for anti-IgE biologicals. The aim of the study was to analyze multiple sensitizations in patients with severe asthma and assess their impact on the course of the disease. (2) Forty-two patients with severe asthma according to GINA were enrolled. They experienced at least two exacerbations during the past year and had uncontrolled asthma despite high inhaled steroid use. A microarray serum Alex test (allergen-specific IgE to 295 extracts and components) was performed together with Complete Blood Count tests, the Asthma Control Questionnaire (ACQ), the Mini Asthma Quality of Life Questionnaire (MiniAQLQ), and spirometry. (3) There were 29 female and 13 male patients. The patient mean age was 50.4 (22-70). In 25 (60%) patients, inhalant sensitizations were detected. In 9 (21%) cases, a new perennial allergen was discovered that might enable anti-IgE treatment in the future. In the entire studied group, 8 patients (19%) would still not qualify for anti-IgE, anti-IL4, or anti-IL5 treatment. A linear regression analysis revealed that a C

Indexed as

ALEX 1asthma 4IgE 3microarray 2

Identifiers

PMID36294955
PMCPMC9604971
OpenAlexW4297982817

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.