Evidence map›Paper›PMID 36973952›Full record

ArticleClinical and translational allergy2023

Obese asthma phenotypes display distinct plasma biomarker profiles.

Sophia Björkander, Susanna Klevebro, Natalia Hernandez-Pacheco, Maura Kere, Sandra Ekström, Maria Sparreman Mikus, Marianne van Hage, Anna James, Inger Kull, Anna Bergström and 3 more

Open access · goldFull text read
In one paragraph

Article in Clinical and translational allergy, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 15 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
15citing papers in PubMed, 1 pooled it
3.3field-weighted citation impact, top 7% 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

15 citing papers in PubMed, 1 synthesis or guideline pooled it, 19 citations in OpenAlex.

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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

13 authors at 2 institutions in 2 countries.

Sophia BjörkanderDepartment of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
Susanna KlevebroDepartment of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.ORCID https://orcid.org/0000-0002-1261-6502
Natalia Hernandez-PachecoDepartment of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
Maura KereDepartment of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
Sandra EkströmInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Maria Sparreman MikusInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Marianne van HageDepartment of Medicine, Solna, Division of Immunology and Allergy, Karolinska Institutet and Karolinska University Hospital, Stockholm, Sweden.
Anna JamesInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Inger KullDepartment of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
Anna BergströmInstitute of Environmental Medicine, Karolinska Institutet, Stockholm, Sweden.
Jenny MjösbergDepartment of Medicine Huddinge, Centre for Infectious Medicine, Karolinska Institutet, Stockholm, Sweden.
Christopher Andrew TibbittDepartment of Medicine Huddinge, Centre for Infectious Medicine, Karolinska Institutet, Stockholm, Sweden.
Erik MelénDepartment of Clinical Science and Education, Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.
Karolinska Institutet · SEKarolinska University Hospital · SE

Funding

Astma- och AllergiförbundetEuropean Academy of Allergy and Clinical Immunology, Medium-Term Research Fellowship (NHP)European Respiratory Society (NHP) LTRF202101-00861Forskningsrådet om Hälsa, Arbetsliv och Välfärd 2017-00526H2020 European Research Council 757919Hjärt-LungfondenInsamlingsstiftelsen Cancer- och AllergifondenRegion Stockholm, ALF project, Clinical postdoctoral appointment (SK), and database maintenanceSvenska Forskningsrådet Formas 2016-01646Thermo Fisher Scientific, reagents for the allergen-specific IgE analysesVetenskapsrådet 2016-03086Vetenskapsrådet 2018-02524Vetenskapsrådet 2019-01060Vetenskapsrådet 2020-02170
6 · The paper itself

Abstract

backgroundObese asthma is a complex phenotype and further characterization of the pathophysiology is needed. This study aimed to explore inflammation-related plasma biomarkers in lean and overweight/obese asthmatics.

methodsWe elucidated levels of inflammation-related plasma proteins in obese asthma phenotypes in the population-based cohort BAMSE (Swedish: Children, Allergy, Milieu, Stockholm, Epidemiology) using data from 2069 24-26-year-olds. Subjects were divided into lean asthma (n = 166), lean controls (n = 1440), overweight/obese asthma (n = 73) and overweight/obese controls (n = 390). Protein levels (n = 92) were analysed using the Olink Proseek Multiplex Inflammation panel.

resultsOf the 92 included proteins, 41 were associated with lean and/or overweight/obese asthma. The majority of proteins associated with overweight/obese asthma also associated with overweight/obesity among non-asthmatics. Beta-nerve growth factor (BetaNGF), interleukin 10 (IL-10), and matrix metalloproteinase 10 (MMP10) were associated only with lean asthma while C-C motif chemokine 20 (CCL20), fibroblast growth factor 19 (FGF19), interleukin 5 (IL-5), leukemia inhibitory factor (LIF), tumor necrosis factor ligand superfamily member 9 (TNFRSF9), and urokinase-type plasminogen activator (uPA) were associated only with overweight/obese asthma. Overweight/obesity modified the association between asthma and 3 of the proteins: fibroblast growth factor 21 (FGF21), interleukin 4 (IL-4), and urokinase-type plasminogen activator (uPA). In the overweight/obese group, interleukin-6 (IL-6) was associated with non-allergic asthma but not allergic asthma.

conclusionThese data indicate distinct plasma protein phenotypes in lean and overweight/obese asthmatics which, in turn, can impact upon therapeutic approaches.

Indexed as

asthmabody mass indexinflammationobesityplasma biomarker

Identifiers

PMID36973952
PMCPMC10032201
OpenAlexW4353064986

What OpenQuestion holds

Textfull text, public
LicenceCC BY
measurements read29
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.