Evidence map›Paper›PMID 25203887›Full record

Observational studyAnnals of surgery2014

X chromosome-linked IRAK-1 polymorphism is a strong predictor of multiple organ failure and mortality postinjury.

Jason L Sperry, Samuel Zolin, Brian S Zuckerbraun, Yoram Vodovotz, Rami Namas, Matthew D Neal, Robert E Ferrell, Matthew R Rosengart, Andrew B Peitzman, Timothy R Billiar

Open access · greenAbstract readObservational Study
In one paragraph

Observational study in Annals of surgery, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed
2.8field-weighted citation impact, top 10% 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

17 citing papers in PubMed, 28 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. Journal of clinical medicine · 2019
    Article
  10. Frontiers in genetics · 2019
    Article
  11. Sex and bacterial infectious diseases.New microbes and new infections · 2018
    Review
  12. Article
  13. Observational
  14. Deletion of interleukin 1 receptor-associated kinase 1 (The Journal of biological chemistry · 2017
    Article
  15. Article
  16. Article
  17. 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

10 authors at 1 institution in 1 country.

Jason L SperryFrom the Division of Trauma and General Surgery, Department of Surgery, University of Pittsburgh, PA.
Samuel Zolin
Brian S Zuckerbraun
Yoram Vodovotz
Rami Namas
Matthew D Neal
Robert E Ferrell
Matthew R Rosengart
Andrew B Peitzman
Timothy R Billiar
University of Pittsburgh · US

Funding

Characterization of the Mechanisms Responsible for Sex Based Outcome Difference FK23GM093032 · NIGMS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI SPERRY, JASON LEE · 2010 to 2014
$597k
NIGMS NIH HHS K23 GM093032NIGMS NIH HHS K23GM093032
6 · The paper itself

Abstract

OBJECTIVE(S): Clinical research characterizing the mechanisms responsible for sex-based outcome differences postinjury remain conflicting. We sought to characterize an X chromosome-linked IRAK-1 (IL-1 receptor-associated kinase) polymorphism as an alternative mechanism responsible for sex differences postinjury. IRAK-1 is key intermediate in the toll-like receptor (TLR) pathway thought to drive inflammation postinjury.

methodsA prospective cohort study was performed over a 24-month period. Bluntly injured patients requiring intensive care unit admission were enrolled, whereas patients with isolated brain and spinal cord injuries were excluded. Outcomes of interest included multiple organ failure (MOF, Marshall MOD score > 5) and mortality. Logistic regression was utilized to determine the independent risk of poor outcome associated with the IRAK-1 variant after controlling for important differences.

resultsIn an enrolled cohort of 321 patients, the IRAK-1 variant was common (12.5%). Patients with and without the variant were similar in age, injury severity, and 24hr blood transfusion. After controlling for important confounders, the IRAK1 variant was independently associated with more than eightfold (OR = 8.4, P = 0.005, 95% CI: 1.9-37.1) and 11-fold (OR = 11.8, P = 0.037, 95% CI: 1.1-121) greater risk of MOF and mortality, respectively. These differences were most prominent in men, whereas women heterozygous for the variant demonstrated worse outcome in a dose-dependent fashion.

conclusionsThe IRAK1 polymorphism is a strong independent predictor of MOF and mortality postinjury and represents a common variant with prognostic potential. These data demonstrate the importance of TLR signaling postinjury and supports that a genetic mechanism may drive sex outcome differences postinjury.

Indexed as

Chromosomes, Human, XPolymorphism, Single NucleotideAdultAgedFemaleHumansImmunity, InnateInterleukin-1 Receptor-Associated KinasesMaleMiddle AgedMultiple Organ FailurePrognosisProspective StudiesRisk FactorsSepsisSex FactorsInterleukin-1 Receptor-Associated KinasesIRAK1 protein, humanToll-Like Receptors

Identifiers

PMID25203887
PMCPMC4159729
OpenAlexW2100115281

What OpenQuestion holds

Textmetadata
LicenceTDM
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.