Evidence map›Paper›PMID 39299705›Full record

ArticleThe Journal of infectious diseases2025

Genetic Susceptibility to Acute Viral Bronchiolitis.

Anu Pasanen, Minna K Karjalainen, Matti Korppi, Mikko Hallman, Mika Rämet, Research Project FinnGen

Abstract read
In one paragraph

Article in The Journal of infectious diseases, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
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

6 citing papers in PubMed.

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  5. Review
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Anu PasanenResearch Unit of Clinical Medicine, University of Oulu.ORCID 0000-0001-7460-5086
Minna K KarjalainenMedical Research Center Oulu, Oulu University Hospital and University of Oulu.
Matti KorppiChild Health Research Center, Tampere University and University Hospital.
Mikko HallmanResearch Unit of Clinical Medicine, University of Oulu.
Mika RämetResearch Unit of Clinical Medicine, University of Oulu.
Research Project FinnGen

Funding

AbbVie IncAstraZeneca UK LimitedBiogen MA IncBoehringer Ingelheim International GmbHBristol-Myers SquibbBusiness FinlandFoundation for Pediatric ResearchGenentech IncGlaxoSmithKline Intellectual Property Development LimitedJanssen Biotech IncMaze Therapeutics IncMerck Sharp and Dohme LLCNovartis AGPfizer IncSanofi US Services IncSigrid Jusélius FoundationStiftelsen Alma och K.A. Snellman Säätiö
6 · The paper itself

Abstract

backgroundAcute viral bronchiolitis is a major cause of infant hospitalizations worldwide. Childhood bronchiolitis is considered a risk factor for asthma, suggesting shared genetic factors and biological pathways. Genetic risk loci may provide new insights into disease pathogenesis.

methodsWe conducted a genome-wide association study to examine the genetic contributions to bronchiolitis susceptibility in the FinnGen project data. We analyzed 1465 infants hospitalized for bronchiolitis who were <2 years of age and 356 404 individuals without a history of acute lower respiratory infections.

resultsThe genome-wide association study identified associations (P < 5 × 10-8) for variants in gasdermin B (GSDMB) and a missense variant in cadherin-related family member 3 (CDHR3). Children with bronchiolitis in infancy were more likely to develop asthma later in life as compared with controls. The 2 associated loci were previously linked to asthma and susceptibility to wheezing illness by causative agents other than respiratory syncytial virus (RSV). The identified loci were associated with overall bronchiolitis, with larger effects in non-RSV than RSV-induced infection.

conclusionsOur results suggest that genetic variants in CDHR3 and GSDMB modulate susceptibility to bronchiolitis, especially when caused by viruses other than RSV. Severe bronchiolitis in infancy may trigger the development of asthma in genetically susceptible individuals, or it could be a marker of genetic predisposition to asthma.

Indexed as

Bronchiolitis, ViralCadherinsGenetic Predisposition to DiseaseAsthmaCadherin Related ProteinsChild, PreschoolFemaleGasderminsGenome-Wide Association StudyHumansInfantMaleMembrane ProteinsNeoplasm ProteinsPolymorphism, Single NucleotideCadherin Related ProteinsCadherinsCDHR3 protein, humanGasderminsGSDMB protein, humanMembrane ProteinsNeoplasm ProteinsasthmabronchiolitisCDHR3genetic risk factorsGSDMB

Identifiers

PMID39299705
PMCPMC12349955

What Socratic holds

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LicenceCC BY
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Registered trials

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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 Socratic graph.