Evidence map›Paper›PMID 26077880›Full record

ArticleCritical care (London, England)2015

Common variants of NFE2L2 gene predisposes to acute respiratory distress syndrome in patients with severe sepsis.

Marialbert Acosta-Herrera, Maria Pino-Yanes, Jesús Blanco, Juan Carlos Ballesteros, Alfonso Ambrós, Almudena Corrales, Francisco Gandía, Carlés Subirá, David Domínguez, Aurora Baluja and 6 more

Open access · goldAbstract read
In one paragraph

Article in Critical care (London, England), 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 20% 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

14 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Review
  6. Role of NRF2 and Sirtuin activators in COVID-19.Clinical immunology (Orlando, Fla.) · 2021
    Review
  7. Article
  8. Can Activation of NRF2 Be a Strategy against COVID-19?Trends in pharmacological sciences · 2020
    Review
  9. Review
  10. Review
  11. Clinical significance of Vδ1 T cell detection in sepsis patients.International journal of clinical and experimental pathology · 2017
    Article
  12. Percentage of Peripheral CD19+CD24hiCD38hi Regulatory B Cells in Neonatal Sepsis Patients and Its Functional Implication.Medical science monitor : international medical journal of experimental and clinical research · 2016
    Article
  13. Review
  14. 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

16 authors at 1 institution in 1 country.

Marialbert Acosta-HerreraCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain. m.acostaherrera@gmail.com.
Maria Pino-YanesCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain. mdelpino@ull.edu.es.
Jesús BlancoCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain. jblancov@saludcastillayleon.es.
Juan Carlos BallesterosIntensive Care Unit, Hospital Clínico Universitario de Salamanca, Salamanca, Spain. jcballes@ono.com.
Alfonso AmbrósIntensive Care Unit, Hospital General Universitario de Ciudad Real, Ciudad Real, Spain. alfonsoa@sescam.jccm.es.
Almudena CorralesCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain. acm4580@yahoo.es.
Francisco GandíaIntensive Care Unit, Hospital Clínico de Valladolid, Valladolid, Spain. fgandia@saludcastillayleon.es.
Carlés SubiráIntensive Care Unit, Fundació ALTHAIA, Manresa, Spain. csubira@althaia.cat.
David DomínguezDepartment Anesthesia, Hospital Universitario Nuestra Señora de Candelaria, Santa Cruz de Tenerife, Spain. daviddomgar@gmail.com.
Aurora BalujaDepartment Anesthesiology, Hospital Clínico Universitario, Santiago de Compostela, Spain. mariauror@gmail.com.
José Manuel AñónIntensive Care Unit, Hospital Virgen de La Luz, Cuenca, Spain. jmaelizalde@gmail.com.
Ramón AdaliaDepartment of Anesthesiology, Hospital Clinic de Barcelona, Barcelona, Spain. radalia@gmail.com.
Lina Pérez-MéndezCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain. cuidadospreventivos@hotmail.com.
Carlos FloresCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain. cflores@ull.edu.es.
Jesus VillarCIBER de Enfermedades Respiratorias, Instituto de Salud Carlos III, Madrid, Spain. jesus.villar54@gmail.com.
GRECIA and GEN-SEP networks
Instituto de Salud Carlos III · ES

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe purpose of this study was to investigate whether common variants across the nuclear factor erythroid 2-like 2 (NFE2L2) gene contribute to the development of the acute respiratory distress syndrome (ARDS) in patients with severe sepsis. NFE2L2 is involved in the response to oxidative stress, and it has been shown to be associated with the development of ARDS in trauma patients.

methodsWe performed a case-control study of 321 patients fulfilling international criteria for severe sepsis and ARDS who were admitted to a Spanish network of post-surgical and critical care units, as well as 871 population-based controls. Six tagging single-nucleotide polymorphisms (SNPs) of NFE2L2 were genotyped, and, after further imputation of additional 34 SNPs, association testing with ARDS susceptibility was conducted using logistic regression analysis.

resultsAfter multiple testing adjustments, our analysis revealed 10 non-coding SNPs in tight linkage disequilibrium (0.75 ≤ r (2)  ≤ 1) that were associated with ARDS susceptibility as a single association signal. One of those SNPs (rs672961) was previously associated with trauma-induced ARDS and modified the promoter activity of the NFE2L2 gene, showing an odds ratio of 1.93 per T allele (95 % confidence interval, 1.17-3.18; p = 0.0089).

conclusionsOur findings support the involvement of NFE2L2 gene variants in ARDS susceptibility and reinforce further exploration of the role of oxidant stress response as a risk factor for ARDS in critically ill patients.

Indexed as

AdultAgedCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenetic VariationHumansMaleMiddle AgedNF-E2-Related Factor 2Polymorphism, Single NucleotideRespiratory Distress SyndromeSepsisNFE2L2 protein, humanNF-E2-Related Factor 2

Identifiers

PMID26077880
PMCPMC4484894
OpenAlexW1888210466

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.