Evidence map›Paper›PMID 33900050›Full record

ArticleClinical and translational allergy2021

Combinations of self-reported rhinitis, conjunctivitis, and asthma predicts IgE sensitization in more than 25,000 Danes.

Susan Mikkelsen, Khoa Manh Dinh, Jens Kjaergaard Boldsen, Ole Birger Pedersen, Gitte Juel Holst, Mikkel Steen Petersen, Kathrine Agergård Kaspersen, Bjarne Kuno Møller, Kaspar Rene Nielsen, Helene Martina Paarup and 10 more

Open access · goldAbstract read
In one paragraph

Article in Clinical and translational allergy, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

7 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
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  4. Cohort Profile: The Danish Blood Donor Study.International journal of epidemiology · 2023
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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

20 authors at 9 institutions in 1 country.

Susan MikkelsenDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.ORCID https://orcid.org/0000-0001-7806-1143
Khoa Manh DinhDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Jens Kjaergaard BoldsenDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Ole Birger PedersenDepartment of Clinical Immunology, Zealand University Hospital, Køge, Denmark.
Gitte Juel HolstThe Danish Clinical Quality Program-National Clinical Registries (RKKP), Central Denmark Region, Aarhus, Denmark.
Mikkel Steen PetersenDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Kathrine Agergård KaspersenDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Bjarne Kuno MøllerDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Kaspar Rene NielsenDepartment of Clinical Immunology, Aalborg University Hospital, Aalborg, Denmark.
Helene Martina PaarupDepartment of Clinical Immunology, Odense University Hospital, Odense, Denmark.ORCID https://orcid.org/0000-0003-1281-1567
Klaus RostgaardDepartment of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
Henrik HjalgrimDepartment of Epidemiology Research, Statens Serum Institut, Copenhagen, Denmark.
Erik SørensenDepartment of Clinical Immunology, Copenhagen University Hospital, Copenhagen, Denmark.
Linda Jenny HandgaardDepartment of Clinical Immunology, Copenhagen University Hospital, Copenhagen, Denmark.
Thomas Folkmann HansenDepartment of Neurology, Danish Headache Center, Copenhagen University Hospital, Glostrup, Denmark.
Karina BanasikFaculty of Health and Medical Sciences, Novo Nordisk Foundation Center for Protein Research, University of Copenhagen, Copenhagen, Denmark.
Kristoffer Sølvsten BurgdorfDepartment of Clinical Immunology, Copenhagen University Hospital, Copenhagen, Denmark.
Henrik UllumDepartment of Clinical Immunology, Copenhagen University Hospital, Copenhagen, Denmark.
Torben SigsgaardDanish Big Data Centre for Environment and Health (BERTHA), Aarhus University, Roskilde, Denmark.
Christian ErikstrupDepartment of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark.
Aarhus University · DKAarhus University Hospital · DKCopenhagen University Hospital · DKStatens Serum Institut · DKUniversity of Copenhagen · DKAalborg University Hospital · DKCentral Denmark Region · DKOdense University Hospital · DKZealand University Hospital Køge · DK

Funding

Aarhus University 12073Bloddonorernes Forskningsfond FF4, 2016-02Kong Christian den Tiendes Fond 93/2016The A.P. Møller Foundation for the Advancement of Medical Science 17-L-0496The Danish Administrative Regions (http://www.regioner.dk)The Danish Bio- and Genome Bank (http://www.regioner.dk/rbgben)The Danish Council for Independent Research-Medical Sciences 09-069412The Danish Medical Association Research Foundation 2016-1840/111The Novo Nordisk Foundation NNF17OC0027594
6 · The paper itself

Abstract

backgroundAllergic rhinitis (AR), allergic conjunctivitis (AC), and asthma composing multiple phenotypes and improved understanding of these phenotypes and their respective risk factors are needed.

objectivesThe objective of this study was to define the prevalence of AR, AC, and asthma and their association with allergen-specific immunoglobulin E (sIgE) sensitization in a large cohort of blood donors and identify risk factors.

methodsFrom the nationwide population-based Danish Blood Donor Study, 52,976 participants completed an electronic questionnaire including AR, AC, asthma, allergic predisposition, and childhood residence. Of these, 25,257 were additionally tested for sIgE to inhalation allergens (Phadiatop).

resultsThe prevalence of sIgE sensitization, AR, AC, and asthma was 30%, 19%, 15%, and 9%, respectively. The youngest birth cohorts had the highest prevalence of sIgE sensitization and symptoms of asthma, AR, and AC, and for asthma, they apparently experienced symptoms at an earlier age. The sIgE sensitization was positively associated with male sex. The sIgE seroprevalence was higher in participants with both AR and AC (ARC) than in participants with either AR or AC. Allergic predisposition and sIgE sensitization increased the risk of the diseases, while farm upbringing was associated with reduced prevalence of ARC, however, only in sIgE sensitized participants.

conclusionBirth year, childhood residence, sIgE sensitization, and allergic predisposition were associated with asthma, AR, and AC prevalence. Individuals with self-reported ARC represent a primarily sIgE-positive phenotype, while those with either AR or AC represent more diverse phenotypes.

Indexed as

allergic IgE sensitizationasthmaconjunctivitisenvironmentrhinitis

Identifiers

PMID33900050
PMCPMC8099331
OpenAlexW3149541008

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.