Evidence map›Paper›PMID 15526005›Full record

ArticleGenes and immunity2004

TNF and TNFR polymorphisms in severe sepsis and septic shock: a prospective multicentre study.

A C Gordon, A L Lagan, E Aganna, L Cheung, C J Peters, M F McDermott, J L Millo, K I Welsh, P Holloway, G A Hitman and 3 more

Registry-linked trialAbstract readComparative StudyMulticenter Study
PubMed Publisher
In one paragraph

Article in Genes and immunity, 2004. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00131196 (Functional Genomic Influences on Disease Progression and Outcome in Sepsis Due to Pneumonia or Peritonitis), which is not on this map. Cited by 35 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
35citing papers in PubMed, 3 pooled it
4.1field-weighted citation impact, top 6% 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.

NCT00131196 unknown statusnot on this mapstarted 2005, after this paper: background citation

Functional Genomic Influences on Disease Progression and Outcome in Sepsis Due to Pneumonia or Peritonitis

TypeobservationalSponsorUniversity of OxfordRan2005 to 2017Enrolled4,000ConditionsPneumonia, Peritonitis
3 · Its place in the literature

Who cites it

35 citing papers in PubMed, 3 syntheses or guidelines pooled it, 112 citations in OpenAlex.

  1. Association between the Lymphotoxin-BioMed research international · 2020
    Pooled it
  2. Searching for genes that matter in acute kidney injury: a systematic review.Clinical journal of the American Society of Nephrology : CJASN · 2009
    Pooled it
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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

13 authors at 7 institutions in 2 countries.

A C GordonInstitute of Cell and Molecular Science & William Harvey Research Institute, Barts and The London Queen Mary's School of Medicine and Dentistry, University of London, London, UK.
A L Lagan
E Aganna
L Cheung
C J Peters
M F McDermott
J L Millo
K I Welsh
P Holloway
G A Hitman
R D Piper
C S Garrard
C J Hinds
University of London · GBJohn Radcliffe Hospital · GBGenomics (United Kingdom) · GBImperial College London · GBRoyal North Shore Hospital · AUUniversity of Sydney · AUWilliam Harvey Research Institute · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Tumour necrosis factor (TNF) is an important pro-inflammatory cytokine produced in sepsis. Studies examining the association of individual TNF single nucleotide polymorphisms with sepsis have produced conflicting results. This study investigated whether common polymorphisms of the TNF locus and the two receptor genes, TNFRSF1A and TNFRSF1B, influence circulating levels of encoded proteins, and whether individual polymorphisms or extended haplotypes of these genes are associated with susceptibility, severity of illness or outcome in adult patients with severe sepsis or septic shock. A total of 213 Caucasian patients were recruited from eight intensive care units (ICU) in the UK and Australia. Plasma levels of TNF (P = 0.02), sTNFRSF1A (P = 0.005) and sTNFRSF1B (P = 0.01) were significantly higher in those who died on ICU compared to those who survived. There was a positive correlation between increasing soluble receptor levels and organ dysfunction (increasing SOFA score) (sTNFRSF1A R = 0.51, P < 0.001; sTNFRSF1B R = 0.53, P < 0.001), and in particular with the degree of renal dysfunction. In this study, there were no significant associations between the selected candidate TNF or TNF receptor polymorphisms, or their haplotypes, and susceptibility to sepsis, illness severity or outcome. The influence of polymorphisms of the TNF locus on susceptibility to, and outcome from sepsis remains uncertain.

Indexed as

Genetic Predisposition to DiseasePolymorphism, GeneticAustraliaDNA PrimersEnglandFemaleGene FrequencyGenotypeHaplotypesHumansMaleProspective StudiesReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis Factor, Type IReceptors, Tumor Necrosis Factor, Type IISepsisDNA PrimersReceptors, Tumor Necrosis FactorReceptors, Tumor Necrosis Factor, Type IReceptors, Tumor Necrosis Factor, Type IIrecombinant human tumor necrosis factor-binding protein-1TNFRSF1B protein, humanTumor Necrosis Factor Decoy Receptors

Identifiers

PMID15526005
OpenAlexW2036169141

What OpenQuestion holds

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Registered trials

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.