Evidence map›Paper›PMID 39755867›Full record

ReviewClinical reviews in allergy & immunology2025

Copy Number Variation in Asthma: An Integrative Review.

Fernanda Mariano Garcia, Valdemir Pereira de Sousa, Priscila Pinto E Silva-Dos-Santos, Izadora Silveira Fernandes, Faradiba Sarquis Serpa, Flávia de Paula, José Geraldo Mill, Maria Rita Passos Bueno, Flávia Imbroisi Valle Errera

Abstract readReview
PubMed Publisher
In one paragraph

Review in Clinical reviews in allergy & immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Review
  2. Article
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.

Fernanda Mariano Garcia *Postgraduate Program in Biochemistry, Federal University of Espírito Santo (UFES), Vitória, Espírito Santo, Brazil. f.marianogarcia@gmail.com.
Valdemir Pereira de Sousa *Postgraduate Program in Biotechnology, Federal University of Espírito Santo (UFES), Vitória, Espírito Santo, Brazil.
Priscila Pinto E Silva-Dos-Santos *Department of Medicine, School of Sciences of Santa Casa de Misericórdia de Vitória (EMESCAM), Vitória, Espírito Santo, Brazil.
Izadora Silveira FernandesPostgraduate Program in Biochemistry, Federal University of Espírito Santo (UFES), Vitória, Espírito Santo, Brazil.
Faradiba Sarquis SerpaDepartment of Medicine, School of Sciences of Santa Casa de Misericórdia de Vitória (EMESCAM), Vitória, Espírito Santo, Brazil.
Flávia de PaulaPostgraduate Program in Biotechnology, Federal University of Espírito Santo (UFES), Vitória, Espírito Santo, Brazil.
José Geraldo MillDepartment of Physiological Sciences, Federal University of Espírito Santo (UFES), Vitória, Espírito Santo, Brazil.
Maria Rita Passos BuenoDepartment of Genetics and Evolutionary Biology, University of São Paulo (USP), São Paulo, São Paulo, Brazil.
Flávia Imbroisi Valle ErreraPostgraduate Program in Biochemistry, Federal University of Espírito Santo (UFES), Vitória, Espírito Santo, Brazil.

Funding

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior , Brasil 88887.839711/2023-00Fundação de Amparo à Pesquisa e Inovação do Espírito Santo SIAFEM: 2023-ZRJW
6 · The paper itself

Abstract

Asthma is a complex disease with varied clinical manifestations resulting from the interaction between environmental and genetic factors. While chronic airway inflammation and hyperresponsiveness are central features, the etiology of asthma is multifaceted, leading to a diversity of phenotypes and endotypes. Although most research into the genetics of asthma focused on the analysis of single nucleotide polymorphisms (SNPs), studies highlight the importance of structural variations, such as copy number variations (CNVs), in the inheritance of complex characteristics, but their role has not yet been fully elucidated in asthma. In this context, an integrative review was conducted to identify the genes and pathways involved, the location, size, and classes of CNVs, as well as their contribution to asthma risk, severity, control, and response to treatment. As a result of the review, 16 articles were analyzed, from different types of observational studies, such as case-control, cohort studies and genotyped-proband or trios design, that have been carried out in populations from different countries, ethnicities, and ages. Chromosomes 12 and 17 were the most studied in three publications each. CNVs located on 12 chromosomes were associated with asthma, the majority being found on chromosome 6p and 17q, of the deletion type, encompassing 30 different coding-protein genes and one pseudogene region. Six genes with CNVs were identified as significant expression quantitative locus (eQTLs) with mean expression in asthma-related tissues, such as the lung and whole blood. The phenotypic variability of asthma may hinder the clinical application of these findings, but the research shows the importance of investigating these genetic variations as possible biomarkers in asthma patients.

Indexed as

AsthmaDNA Copy Number VariationsGenetic Predisposition to DiseaseChromosomes, Human, Pair 12Chromosomes, Human, Pair 17Genetic Association StudiesHumansPhenotypePolymorphism, Single NucleotideBiological/genetic markersDeletionsEQTLInsertionsPhenotypes of asthmaPhenotypic variabilityPrecision medicineStructural variants

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.