Evidence map›Paper›PMID 42634071›Full record

ArticleRespiratory research2026

Genome-wide association study of image-based emphysema scoring in the Swedish CArdioPulmonary bioImage Study (SCAPIS) suggests two new risk loci in smokers.

Fredrik Nyberg, Per Lundmark, Anders Blomberg, Koen Dekkers, Arne Egesten, Jonas Eriksson Ström, Bruna Gigante, Anders Gummesson, Cecilia Gunnarsson, Christer Janson and 10 more

Abstract read
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Article in Respiratory research, 2026. 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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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

20 authors.

Fredrik NybergSchool of Public Health and Community Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. Fredrik.Nyberg.2@gu.se.ORCID https://orcid.org/0000-0003-0892-5668
Per LundmarkDepartment of Medical Sciences, Molecular Epidemiology, Uppsala University, Uppsala, Sweden.
Anders BlombergDepartment of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Koen DekkersDepartment of Medical Sciences, Molecular Epidemiology, Uppsala University, Uppsala, Sweden.
Arne EgestenDepartment of Clinical Sciences Lund, Respiratory Medicine, Allergology, & Palliative Medicine, Lund University and Skåne University Hospital, Lund, Sweden.
Jonas Eriksson StrömDepartment of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Bruna GiganteDepartment of Medicine, Division of Cardiology, Karolinska Institutet, Stockholm, Sweden.
Anders GummessonDepartment of Molecular and Clinical Medicine, Institute of Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Cecilia GunnarssonDepartment of Clinical Genetics, and Department of Biomedical and Clinical Sciences, Linköping University, Linköping, Sweden.
Christer JansonDepartment of Medical Sciences, Respiratory, Allergy and Sleep Research, Uppsala University, Uppsala, Sweden.
Andrei MalinovschiDepartment of Medical Sciences, Clinical Physiology, Uppsala University, Uppsala, Sweden.
Anna-Carin OlinDepartment of Occupational and Environmental Medicine, School of Public Health and Community Medicine, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Marju Orho-MelanderDepartment of Clinical Sciences Malmö, Lund University, Malmö, Sweden.
Hans Lennart PerssonDepartment of Health, Medicine and Caring Sciences, Linköping University, Linköping, Sweden.
Ida PesonenDepartment of Respiratory Medicine and Allergy, Karolinska University Hospital, Stockholm, Sweden.
Magnus SköldDepartment of Respiratory Medicine and Allergy, Karolinska University Hospital, Stockholm, Sweden.
Stefan SöderbergDepartment of Public Health and Clinical Medicine, Umeå University, Umeå, Sweden.
Hanan TanashDepartment of Medicine, Skåne University Hospital, Lund University, Lund, Sweden.
Lowie E G W VanfleterenDepartment of Internal Medicine and Clinical Nutrition, COPD Center, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden.
Tove FallDepartment of Medical Sciences, Molecular Epidemiology, Uppsala University, Uppsala, Sweden.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDespite the high prevalence and clinical significance of emphysema, few genetic risk loci have been consistently replicated. We conducted a genome-wide association study (GWAS) of CT-based emphysema, with a particular focus on non-smoking-related genetic determinants.

methodsWe analyzed 25,639 individuals of European ancestry from the SCAPIS national cohort, aged 50-65 years, of which 51% were never-smokers. Emphysema was assessed through semi-quantitative visual scoring of CT scans. GWAS was performed in the whole sample and stratified on smoking status. We also examined the association of previously reported emphysema- and lung function-related variants with emphysema in our dataset.

resultsEmphysema criteria were fulfilled for 1,479 participants (5.6%), with higher prevalence among current (N = 576, 18.2%) and former smokers (N = 612, 6.5%) compared to never-smokers (N = 263, 2.0%). We identified three independent genetic loci for emphysema in smokers and no signals in never-smokers. The strongest signal was observed in the well-established nicotinic acetylcholine receptor cluster (CHRNA5-A3-B4) locus on chromosome 15. Additionally, we discovered novel associations near the dysferlin (DYSF) gene on chromosome 2 and in an intergenic region on chromosome 3. By assessing previously lung phenotype-associated variants we also found evidence supporting association with emphysema in smokers for variants in the EFEMP1/MIR217HG/PNPT1 locus on chromosome 2, previously linked to reduced FEV

conclusionThis study, based on the largest unselected population sample to date, provides novel insights into the genetic architecture of emphysema. However, no signals were detected in never-smokers despite the large sample-size, likely due to the low prevalence of emphysema in that group. The proposed genetic risk loci require external replication.

Indexed as

Genetic LociGenetic Predisposition to DiseaseGenome-Wide Association StudyPulmonary EmphysemaSmokersSmokingAgedCohort StudiesFemaleHumansMaleMiddle AgedRisk FactorsSwedenTomography, X-Ray ComputedComputed tomographyCOPDEmphysemaGeneticsPopulation-based

Identifiers

PMID42634071
PMCPMC13501701

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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.