Evidence map›Paper›PMID 15744536›Full record

ArticleImmunogenetics2005

Association between asthma-related phenotypes and the CC16 A38G polymorphism in an unselected population of young adult Danes.

Pierre V Candelaria, Vibeke Backer, Ingrid A Laing, Celeste Porsbjerg, Steen Nepper-Christensen, Nick de Klerk, Jack Goldblatt, Peter N Le Souëf

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Article in Immunogenetics, 2005. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing 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

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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

10 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. The Club Cell Marker SCGB1A1 Downstream of FOXA2 is Reduced in Asthma.American journal of respiratory cell and molecular biology · 2019
    Article
  5. Article
  6. Article
  7. Review
  8. Review
  9. The genetics of atopic dermatitis.Clinical reviews in allergy & immunology · 2007
    Review
  10. 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

8 authors.

Pierre V CandelariaSchool of Paediatrics and Child Health, University of Western Australia, GPO Box D184, Perth, Western Australia, Australia, 6840. pierrec@ichr.uwa.edu.au
Vibeke Backer
Ingrid A Laing
Celeste Porsbjerg
Steen Nepper-Christensen
Nick de Klerk
Jack Goldblatt
Peter N Le Souëf

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The gene for Clara cell 16-kDa (CC16) protein is a promising candidate for asthma susceptibility. The CC16 38A allele has been associated with decreased CC16 plasma levels and increased incidence of asthma in Australian children. To date these results have not been replicated in adults. Therefore, potential links between CC16 A38G, asthma and atopy were investigated in an unselected population of young adult Danes. Four hundred sixty-four Danes, aged 19-29 years, from Copenhagen participated in an asthma and allergy phenotype-genotype study. Genotyping was done by Sau96I restriction digestion of PCR products spanning the A38G polymorphism. Potential A38G genotype and asthma-related phenotype associations were investigated using regression analysis, adjusting for potential confounders where appropriate. Adults with the 38AA genotype had higher odds of current asthma (OR 3.2, P=0.013) and ever asthma (OR 2.2, P=0.045) compared with those with the 38GG genotype. Adjusting for atopy had minimal effect on this relationship. A positive linear trend was evident between the 38A allele and atopic dermatitis (OR 1.67, P=0.02). No associations were found between the A38G polymorphism and rhinitis, atopy, forced expiratory volume in 1 s (FEV(1)), forced vital capacity (FVC), airway responsiveness (AR) to histamine or peripheral blood eosinophil level (PBEL). An atopy-independent association between CC16 38AA and asthma prevalence was identified, suggesting the CC16 38A allele predisposes to adult asthma independent of Th1/Th2 processes. This finding is consistent with previous studies in children, but is the first reported association between CC16 A38G and asthma in adults. CC16 38A also displayed a positive linear trend with atopic dermatitis.

Indexed as

Genetic Predisposition to DiseasePolymorphism, Single NucleotideAdolescentAdultAsthmaChildDemographyDenmarkDermatitis, AtopicFemaleGenetics, PopulationHumansMalePhenotypeRhinitisUteroglobinSCGB1A1 protein, humanUteroglobin

Identifiers

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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 OpenQuestion graph.