Evidence map›Paper›PMID 24727586›Full record

ReviewAmerican journal of physiology. Lung cellular and molecular physiology2014

Applying metabolomics to uncover novel biology in ARDS.

Angela J Rogers, Michael A Matthay

Abstract readReview
In one paragraph

Review in American journal of physiology. Lung cellular and molecular physiology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 28 papers.

0numbers the graph read from it
0cells of the map it votes in
28citing papers in PubMed
3.6field-weighted citation impact, top 7% 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

28 citing papers in PubMed, 44 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Article
  6. Article
  7. Metabolomics of Respiratory Diseases.Handbook of experimental pharmacology · 2023
    Review
  8. Review
  9. ARDS in the time of corona: context and perspective.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  10. Review
  11. Review
  12. Therapeutic targeting of metabolic alterations in acute respiratory distress syndrome.European respiratory review : an official journal of the European Respiratory Society · 2020
    Review
  13. Review
  14. Article
  15. Review
  16. Review
  17. Evolution of ARDS biomarkers: Will metabolomics be the answer?American journal of physiology. Lung cellular and molecular physiology · 2018
    Review
  18. Article
  19. Article
  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

2 authors at 2 institutions in 1 country.

Angela J RogersDivision of Pulmonary and Critical Care Medicine, Stanford University, Stanford, California; and ajrogers@stanford.edu.
Michael A MatthayDepartment of Medicine and Anesthesia, University of California, San Francisco, California.
Stanford University · USUniversity of California, San Francisco · US

Funding

Resolution of Clinical Lung InjuryR37HL051856 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI MATTHAY, MICHAEL A. · 2006 to 2015
$3.9M
NHLBI NIH HHS R37 HL051856NHLBI NIH HHS R37HL51856
6 · The paper itself

Abstract

A better understanding of the pathogenesis and the resolution of the acute respiratory distress syndrome (ARDS) is needed. Although some progress has been made with the use of protein biomarkers and candidate gene studies in understanding the pathobiology of ARDS, we propose that new studies that measure the chemical breakdown products of cellular metabolism (metabolomics) may provide new insights into ARDS, in part because metabolomics targets a later point in the genomics cascade than is possible with studies of DNA, RNA, and protein biomarkers. Technological advances have made large-scale metabolomic profiling increasingly feasible. Metabolomic approaches have already achieved novel insights in nonpulmonary diseases such as diabetes mellitus and malignancy, as well as in sepsis, a major risk factor for developing ARDS. Metabolomic profiling is a promising approach to identify novel pathways in both patients at risk for developing ARDS as well as in the early phase of established ARDS.

Indexed as

AnimalsBiomarkersHumansMetabolomicsProteomeRespiratory Distress SyndromeSepsisBiomarkersProteomeacute lung injuryacute respiratory failuregenomicspulmonary edema

Identifiers

PMID24727586
PMCPMC4042190
OpenAlexW1977919262

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.