Evidence map›Paper›PMID 28851893›Full record

ArticleScientific reports2017

The FER rs4957796 TT genotype is associated with unfavorable 90-day survival in Caucasian patients with severe ARDS due to pneumonia.

José Hinz, Benedikt Büttner, Fabian Kriesel, Maximilian Steinau, Aron Frederik Popov, Michael Ghadimi, Tim Beissbarth, Mladen Tzvetkov, Ingo Bergmann, Ashham Mansur

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 1 pooled it
1.9field-weighted citation impact, top 14% 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, 1 synthesis or guideline pooled it, 22 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Article
  6. Article
  7. Review
  8. Article
  9. Article
  10. Article
  11. Article
  12. Review
  13. Review
  14. Article
  15. Article
  16. Observational
  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 2 institutions in 2 countries.

José HinzDepartment of Anaesthesiology, University Medical Centre, Georg August University, Robert-Koch-Str.40, D-37075, Goettingen, Germany.
Benedikt BüttnerDepartment of Anaesthesiology, University Medical Centre, Georg August University, Robert-Koch-Str.40, D-37075, Goettingen, Germany.
Fabian KrieselDepartment of Anaesthesiology, University Medical Centre, Georg August University, Robert-Koch-Str.40, D-37075, Goettingen, Germany.
Maximilian SteinauDepartment of Anaesthesiology, University Medical Centre, Georg August University, Robert-Koch-Str.40, D-37075, Goettingen, Germany.
Aron Frederik PopovDepartment of Cardiothoracic Transplantation & Mechanical Support, Royal Brompton and Harefield Hospital, Harefield, Hill End Road, UB9 6JH, London, United Kingdom.
Michael GhadimiDepartment of General and Visceral Surgery, University Medical Centre, Georg August University, D-37075, Goettingen, Germany.
Tim BeissbarthDepartment of Medical Statistics, University Medical Centre, Georg August University, Robert-Koch-Str.40, D-37075, Goettingen, Germany.
Mladen TzvetkovInstitute of Clinical Pharmacology, University Medical Center, Georg August University, Goettingen, Germany.
Ingo BergmannDepartment of Anaesthesiology, University Medical Centre, Georg August University, Robert-Koch-Str.40, D-37075, Goettingen, Germany.
Ashham MansurDepartment of Anaesthesiology, University Medical Centre, Georg August University, Robert-Koch-Str.40, D-37075, Goettingen, Germany. ashham.mansur@med.uni-goettingen.de.
University of Göttingen · DEHarefield Hospital · GB

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

A recent genome-wide association study showed that a genetic variant within the FER gene is associated with survival in patients with sepsis due to pneumonia. Because severe pneumonia is the main cause of acute respiratory distress syndrome (ARDS), we aimed to investigate the effect of the FER polymorphism rs4957796 on the 90-day survival in patients with ARDS due to pneumonia. An assessment of a prospectively collected cohort of 441 patients with ARDS admitted to three intensive care units at the University Medical Centre identified 274 patients with ARDS due to pneumonia. The 90-day mortality risk was recorded as the primary outcome parameter. Sepsis-related organ failure assessment (SOFA) scores and organ support-free days were used as the secondary variables. FER rs4957796 TT-homozygous patients were compared with C-allele carriers. The survival analysis revealed a higher 90-day mortality risk among T homozygotes than among C-allele carriers (p = 0.0144) exclusively in patients with severe ARDS due to pneumonia. The FER rs4957796 TT genotype remained a significant covariate for the 90-day mortality risk in the multivariate analysis (hazard ratio, 4.62; 95% CI, 1.58-13.50; p = 0.0050). In conclusion, FER rs4957796 might act as a prognostic variable for survival in patients with severe ARDS due to pneumonia.

Indexed as

AllelesGenotypeAdolescentAdultAgedAged, 80 and overComorbidityFemaleHumansMaleMiddle AgedPneumoniaPrognosisProportional Hazards ModelsProtein-Tyrosine KinasesRespiratory Distress SyndromeProtein-Tyrosine Kinasesproto-oncogene protein c-fes-fps

Identifiers

PMID28851893
PMCPMC5575093
OpenAlexW2746676612

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.