Evidence map›Paper›PMID 23437094›Full record

ArticlePloS one2013

Genetic susceptibility to non-necrotizing erysipelas/cellulitis.

Katariina Hannula-Jouppi, Satu Massinen, Tuula Siljander, Siru Mäkelä, Katja Kivinen, Rasko Leinonen, Hong Jiao, Päivi Aitos, Matti Karppelin, Jaana Vuopio and 2 more

Abstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing 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

8 citing papers in PubMed.

  1. Trial
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  3. Article
  4. Review
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  6. Article
  7. Correlations betweenBioscience reports · 2017
    Article
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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

12 authors.

Katariina Hannula-JouppiDepartment of Medical Genetics, University of Helsinki, and Folkhälsan Institute of Genetics, University of Helsinki, Helsinki, Finland. katariina.hannula@helsinki.fi
Satu Massinen
Tuula Siljander
Siru Mäkelä
Katja Kivinen
Rasko Leinonen
Hong Jiao
Päivi Aitos
Matti Karppelin
Jaana Vuopio
Jaana Syrjänen
Juha Kere

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundBacterial non-necrotizing erysipelas and cellulitis are often recurring, diffusely spreading infections of the skin and subcutaneous tissues caused most commonly by streptococci. Host genetic factors influence infection susceptibility but no extensive studies on the genetic determinants of human erysipelas exist.

methodsWe performed genome-wide linkage with the 10,000 variant Human Mapping Array (HMA10K) array on 52 Finnish families with multiple erysipelas cases followed by microsatellite fine mapping of suggestive linkage peaks. A scan with the HMA250K array was subsequently performed with a subset of cases and controls.

resultsSignificant linkage was found at 9q34 (nonparametric multipoint linkage score (NPL(all)) 3.84, p=0.026), which is syntenic to a quantitative trait locus for susceptibility to group A streptococci infections on chromosome 2 in mouse. Sequencing of candidate genes in the 9q34 region did not conclusively associate any to erysipelas/cellulitis susceptibility. Suggestive linkage (NPL(all)>3.0) was found at three loci: 3q22-24, 21q22, and 22q13. A subsequent denser genome scan with the HMA250K array supported the 3q22 locus, in which several SNPs in the promoter of AGTR1 (Angiotensin II receptor type I) suggestively associated with erysipelas/cellulitis susceptibility.

conclusionsSpecific host genetic factors may cause erysipelas/cellulitis susceptibility in humans.

Indexed as

Genetic Predisposition to DiseaseAnimalsCellulitisChromosomes, Human, Pair 9ErysipelasFamilyFemaleGenetic LinkageGenetic MarkersGenome, HumanGenotyping TechniquesHumansMaleMiceMicrosatellite RepeatsOligonucleotide Array Sequence AnalysisGenetic Markers

Identifiers

PMID23437094
PMCPMC3577772

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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.