Evidence map›Paper›PMID 16770611›Full record

ReviewIntensive care medicine2006

Acute lung injury and the coagulation pathway: Potential role of gene polymorphisms in the protein C and fibrinolytic pathways.

Anil Sapru, Joseph L Wiemels, John S Witte, Lorraine B Ware, Michael A Matthay

Open access · bronzeAbstract readReview
PubMed Publisher
In one paragraph

Review in Intensive care medicine, 2006. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 20 papers.

0numbers the graph read from it
0cells of the map it votes in
20citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

20 citing papers in PubMed, 39 citations in OpenAlex.

  1. Trial
  2. Review
  3. Observational
  4. Review
  5. Lung Epithelial Cell Transcriptional Regulation as a Factor in COVID-19-associated Coagulopathies.American journal of respiratory cell and molecular biology · 2021
    Article
  6. Histopathology features of the lung in COVID-19 patients.Diagnostic histopathology (Oxford, England) · 2021
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Article
  12. Article
  13. Anti-inflammatory and anticoagulative effects of paeonol on LPS-induced acute lung injury in rats.Evidence-based complementary and alternative medicine : eCAM · 2012
    Article
  14. Activated protein C inhalation: a novel therapeutic strategy for acute lung injury.Medical science monitor : international medical journal of experimental and clinical research · 2011
    Article
  15. Article
  16. Recent advances in genetic predisposition to clinical acute lung injury.American journal of physiology. Lung cellular and molecular physiology · 2009
    Review
  17. Review
  18. Making genomics functional: deciphering the genetics of acute lung injury.Proceedings of the American Thoracic Society · 2008
    Article
  19. Review
  20. 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

5 authors at 3 institutions in 1 country.

Anil SapruPediatric Critical Care Medicine, University of California, 505 Parnassus Avenue, Moffitt 680-B, San Francisco, CA 94143-0106, USA. anil@itsa.ucsf.edu
Joseph L Wiemels
John S Witte
Lorraine B Ware
Michael A Matthay
University of California, San Francisco · USUniversity of California San Francisco Medical Center · USVanderbilt University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is evidence that dysregulation of coagulation and fibrinolysis may participate in the pathogenesis of acute lung injury (ALI) and the acute respiratory distress syndrome (ARDS). Altered concentrations of several proteins of the coagulation and fibrinolytic pathways in plasma and pulmonary edema fluid from patients with acute lung injury have been related to the severity of lung injury and clinical outcomes. Polymorphisms in the genes encoding for proteins of the protein C and fibrinolysis pathways are known to regulate the production of the respective proteins. It is plausible that these polymorphisms may be associated with the susceptibility to and severity of illness in ALI and ARDS. Well-designed studies that examine the association of these polymorphisms with susceptibility and severity of ALI and ARDS are needed to test the influence of both genetic and environmental factors on the clinical outcomes in patients with ALI and ARDS. There are several important considerations in the design of these genetic association studies, including selection of candidate genes with the most biological plausibility, definition of the phenotype, selection of appropriate controls, determination of the appropriate sample size and assessment of Hardy-Weinberg equilibrium among controls as a measure of internal validity.

Indexed as

Polymorphism, GeneticBlood CoagulationFibrinolysisGenetic LinkageGenetic Predisposition to DiseaseHumansPhenotypeProtein CRespiratory Distress SyndromeProtein C

Identifiers

PMID16770611
OpenAlexW2007327258

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.