Evidence map›Paper›PMID 40541274›Full record

ArticleBMJ open respiratory research2025

Asthma and extrapulmonary comorbidities in a middle-aged general population: results from the SCAPIS study.

Juan Wang, Anders Blomberg, Magnus Ekström, Hans Lennart Persson, Magnus Sköld, Kjell Torén, Xingwu Zhou, Andrei Malinovschi, Christer Janson

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Article in BMJ open respiratory research, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Juan WangDepartment of Medical Sciences, Respiratory-, Allergy- and Sleep Research, Uppsala University, Uppsala, Sweden juan.wang@medsci.uu.se.ORCID http://orcid.org/0000-0003-4435-097X
Anders BlombergDepartment of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Magnus EkströmDepartment of Clinical Sciences Lund, Respiratory Medicine, Allergology and Palliative Medicine, Faculty of Medicine, Lund University, Lund, Sweden.ORCID http://orcid.org/0000-0002-7227-5113
Hans Lennart PerssonDepartment of Respiratory Medicine in Linköping, Department of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.ORCID http://orcid.org/0000-0002-5700-7284
Magnus SköldRespiratory Medicine Unit, Department of Medicine Solna and Center for Molecular Medicine, Karolinska Institute, Stockholm, Sweden.
Kjell TorénDepartment of Occupational and Environmental Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden.ORCID http://orcid.org/0000-0001-8509-7603
Xingwu ZhouDepartment of Medical Sciences, Respiratory-, Allergy- and Sleep Research, Uppsala University, Uppsala, Sweden.
Andrei MalinovschiDepartment of Medical Sciences, Clinical Physiology, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0002-4098-7765
Christer JansonDepartment of Medical Sciences, Respiratory-, Allergy- and Sleep Research, Uppsala University, Uppsala, Sweden.ORCID http://orcid.org/0000-0001-5093-6980

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionAsthma may increase the risk of comorbidities and systemic inflammation, but population data are scarce. This study aimed to compare comorbidities and systemic inflammation between those with and without current asthma and to identify characteristics linked to comorbidities and biomarkers.

methodsIn a cross-sectional analysis of 28 828 people aged 50-64 in the Swedish CArdioPulmonary bioImage Study, assessments included postbronchodilator forced expiratory volume in 1 s (FEV

resultsThe prevalence of current asthma was 6.3%. Current asthma was independently associated with a higher prevalence of hypertension (OR=1.30; 95% CI 1.16 to 1.46), hyperlipidaemia (OR=1.20; 95% CI 1.04 to 1.39), diabetes (OR=1.42; 95% CI 1.16 to 1.75), coeliac disease (OR=2.52; 95% CI 1.61 to 3.95) and rheumatic disease (OR=1.43; 95% CI 1.16 to 1.78). Asthma was also associated with higher levels of CRP (beta=0.25; 95% CI 0.06 to 0.44) and HbA1c (beta=0.47; 95% CI 0.18 to 0.77). In those with asthma, lower FVC % predicted was associated with a higher likelihood of hypertension (OR=1.10; 95% CI 1.01 to 1.19), diabetes (OR=1.47; 95% CI 1.26 to 1.71) and rheumatic disease (OR=1.22; 95% CI 1.05 to 1.42). Lower FEV

conclusionsOur findings suggest that in middle-aged people, asthma is independently associated with common comorbidities such as hypertension, diabetes and rheumatic disease, as well as elevated CRP and blood glucose. Our data suggest that some associations are connected with lung function impairment in those with asthma.

Indexed as

AsthmaHypertensionRheumatic DiseasesBiomarkersComorbidityC-Reactive ProteinCross-Sectional StudiesDiabetes MellitusFemaleForced Expiratory VolumeGlycated HemoglobinHumansHyperlipidemiasInflammationMaleMiddle AgedBiomarkersC-Reactive ProteinGlycated Hemoglobinhemoglobin A1c protein, humanAsthmaAsthma EpidemiologyAsthma MechanismsClinical EpidemiologySystemic disease and lungs

Identifiers

PMID40541274
PMCPMC12182154

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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.