Evidence map›Paper›PMID 17003960›Full record

ArticleJournal of human genetics2006

Polymorphisms of the CD14 gene and atopic phenotypes in Czech patients with IgE-mediated allergy.

Dana Bučková, Lydie Izakovičová Hollá, Vladimír Znojil, Anna Vašků

Open access · bronzeAbstract read
PubMed Publisher
In one paragraph

Article in Journal of human genetics, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.7field-weighted citation impact, top 30% of its field
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

4 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. 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

4 authors at 1 institution in 1 country.

Dana BučkováInstitute of Pathological Physiology LF MU Medical Faculty, Masaryk University, Komenskeho nam. 2, Brno, 662 43, Czech Republic. dbuckova@med.muni.cz.
Lydie Izakovičová HolláInstitute of Pathological Physiology LF MU Medical Faculty, Masaryk University, Komenskeho nam. 2, Brno, 662 43, Czech Republic.
Vladimír ZnojilInstitute of Pathological Physiology LF MU Medical Faculty, Masaryk University, Komenskeho nam. 2, Brno, 662 43, Czech Republic.
Anna VaškůInstitute of Pathological Physiology LF MU Medical Faculty, Masaryk University, Komenskeho nam. 2, Brno, 662 43, Czech Republic.
Masaryk University · CZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

IgE-mediated allergy is a common chronic disorder resulting from interactions between genetic and environmental factors. The gene encoding CD14 is a positional candidate gene for allergic diseases as it is localised on chromosome 5q31.1, a region linked to asthma and bronchial hyperresponsiveness. We investigated the relationship among atopic phenotypes and six polymorphisms in the CD14 gene. Polymerase chain reaction with RFLP analyses was used to determine the CD14 genotypes in subjects with IgE-mediated allergic diseases (n=282) and random controls (n=187). No significant differences in allele or genotype frequencies for individual polymorphisms between patients and controls were found. However, when atopic patients were subdivided into subjects with positive and with negative skin prick tests for separate antigens, T allele of the 1341G/T polymorphism was significantly associated with positive reactivity to mites (P=0.007) and moulds (P=0.041). Similarly, the C allele frequency of the -159C/T variant was increased in patients with positive skin prick tests for mites (P=0.046) and moulds (P=0.056). In haplotype analysis, the common -1619A/-1359G/-550C/-159C/+1188G/+1341T haplotype was associated with positive reaction to these antigens (P values: 0.0008-0.0035). Our study supports the idea that CD14 plays a role in IgE-mediated allergic diseases, and its gene polymorphisms can be important for manifestation of these disorders.

Indexed as

Polymorphism, GeneticAdultChromosomes, Human, Pair 5Czech RepublicFemaleGene FrequencyGenetic LinkageGenotypeHumansHypersensitivityHypersensitivity, ImmediateImmunoglobulin ELipopolysaccharide ReceptorsMalePromoter Regions, GeneticImmunoglobulin ELipopolysaccharide Receptors

Identifiers

PMID17003960
OpenAlexW2081446519

What OpenQuestion 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 OpenQuestion graph.