Evidence map›Paper›PMID 17443229›Full record

ArticleGenes and immunity2007

Common genetic variation in the gene encoding interleukin-1-receptor antagonist (IL-1RA) is associated with altered circulating IL-1RA levels.

S Rafiq, K Stevens, A J Hurst, A Murray, W Henley, M N Weedon, S Bandinelli, A M Corsi, J M Guralnik, L Ferruci and 2 more

Abstract read
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2007. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
2.9field-weighted citation impact, top 9% 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

42 citing papers in PubMed, 95 citations in OpenAlex.

  1. Trial
  2. Association of Interleukin 1 Receptor Antagonist (International journal of molecular sciences · 2026
    Article
  3. Review
  4. Article
  5. Review
  6. Article
  7. Review
  8. Article
  9. Interleukin 1 receptor antagonist (Annals of the rheumatic diseases · 2020
    Article
  10. Article
  11. Article
  12. Article
  13. Review
  14. Article
  15. Review
  16. Inflammation and the Silent Sequelae of Stroke.Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics · 2016
    Review
  17. Article
  18. Review
  19. Poststroke fatigue: hints to a biological mechanism.Journal of stroke and cerebrovascular diseases : the official journal of National Stroke Association · 2015
    Article
  20. The role of cytokines in breast cancer development and progression.Journal of interferon & cytokine research : the official journal of the International Society for Interferon and Cytokine Research · 2015
    Review
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 at 5 institutions in 3 countries.

S RafiqPeninsula College of Medicine and Dentistry, University of Exeter, Magdalen Road, Exeter, UK.
K Stevens
A J Hurst
A Murray
W Henley
M N Weedon
S Bandinelli
A M Corsi
J M Guralnik
L Ferruci
D Melzer
T M Frayling
Peninsula College of Medicine and Dentistry · GBNational Institute on Aging · USAgenzia Regionale di Sanità della Toscana · ITNational Research Council · ITUniversity of Plymouth · GB

Funding

Aging pathways polymorphisms in older personsR01AG024233 · NIA · UNIVERSITY OF CAMBRIDGE · PI MELZER, DAVID · 2004 to 2007
$1.2M
The InChianti StudyZ01AG001050 · NIA · NATIONAL INSTITUTE ON AGING · PI GURALNIK, JACK M · 2008 to 2008
$358k
Intramural NIH HHSNIA NIH HHS N01 AG 821336NIA NIH HHS N01 AG 916413NIA NIH HHS R01 AG 24233-01
6 · The paper itself

Abstract

Interleukin-1-receptor antagonist (IL-1RA) modulates the biological activity of the proinflammatory cytokine interleukin-1 (IL-1) and could play an important role in the pathophysiology of inflammatory and metabolic traits. We genotyped seven single nucleotide polymorphisms (SNPs) that capture a large proportion of common genetic variation in the IL-1RN gene in 1256 participants from the Invecchiare in Chianti study. We identified five SNPs associated with circulating IL-1RA levels with varying degrees of significance (P-value range=0.016-4.9 x 10(-5)). We showed that this association is likely to be driven by one haplotype, most strongly tagged by rs4251961. This variant is only in weak linkage disequilibrium (r(2)=0.25) with a previously reported variable number of tandem repeats polymorphism (VNTR) in intron-2 although a second variant, rs579543, that tags the VNTR (r(2)=0.91), may also be independently associated with IL-1RA levels (P=0.03). We found suggestive evidence that the C allele at rs4251961 that lowers IL-1RA levels is associated with an increased IL-1beta (P=0.03) level and may also be associated with interferon -gamma (P=0.03), alpha-2 macroglobulin (P=0.008) and adiponectin (P=0.007) serum levels. In conclusion, common variation across the IL-1RN gene is strongly associated with IL-1RA levels.

Indexed as

Polymorphism, Single NucleotideAgedAged, 80 and overCells, CulturedEnzyme-Linked Immunosorbent AssayGenetic VariationHumansInterleukin 1 Receptor Antagonist ProteinItalyMaleMiddle AgedMinisatellite RepeatsPolymerase Chain ReactionInterleukin 1 Receptor Antagonist Protein

Identifiers

PMID17443229
OpenAlexW2026094781

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.