Evidence map›Paper›PMID 19531947›Full record

ReviewCritical care medicine2009

Diabetes, insulin, and development of acute lung injury.

Shyoko Honiden, Michelle N Gong

Open access · greenAbstract readReview
In one paragraph

Review in Critical care medicine, 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 63 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
63citing papers in PubMed, 1 pooled it
4.6field-weighted citation impact, top 5% 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

63 citing papers in PubMed, 1 synthesis or guideline pooled it, 126 citations in OpenAlex.

  1. Pooled it
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  13. In vivo molecular imaging stratifies rats with different susceptibilities to hyperoxic acute lung injury.American journal of physiology. Lung cellular and molecular physiology · 2022
    Article
  14. Observational
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  16. Review
  17. Review
  18. Review
  19. Article
  20. Management of diabetes in patients with COVID-19.The lancet. Diabetes & endocrinology · 2020
    Article

3 more citing papers are in PubMed but not listed here.

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.

Shyoko HonidenDepartment of Medicine, Section of Pulmonary and Critical Care Medicine, Yale University School of Medicine, New Haven, Connecticut, USA.
Michelle N Gong
Icahn School of Medicine at Mount Sinai · USYale University · US

Funding

MOLECULAR EPIDEMIOLOGY OF ARDSR01HL060710 · NHLBI · HARVARD UNIVERSITY (SCH OF PUBLIC HLTH) · PI CHRISTIANI, DAVID C · 2000 to 2015
$8.4M
Early Insulin Therapy and Development of ARDSR01HL086667 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GONG, MICHELLE NG · 2007 to 2011
$2.2M
Surrogate Consent in ResearchR01HL084060 · NHLBI · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GONG, MICHELLE NG · 2006 to 2010
$2.1M
NHLBI NIH HHS R01 HL060710NHLBI NIH HHS R01 HL084060NHLBI NIH HHS R01 HL086667NHLBI NIH HHS R01 HL60710
6 · The paper itself

Abstract

objectivesRecently, many studies have investigated the immunomodulatory effects of insulin and glucose control in critical illness. This review examines evidence regarding the relationship between diabetes and the development of acute lung injury/acute respiratory distress syndrome (ALI/ARDS), reviews studies of lung injury related to glycemic and nonglycemic metabolic features of diabetes, and examines the effect of diabetic therapies. DATA SOURCES AND STUDY SELECTION: A MEDLINE/PubMed search from inception to August 1, 2008, was conducted using the search terms acute lung injury, acute respiratory distress syndrome, hyperglycemia, diabetes mellitus, insulin, hydroxymethylglutaryl-CoA reductase inhibitors (statins), angiotensin-converting enzyme inhibitor, and peroxisome proliferator-activated receptors, including combinations of these terms. Bibliographies of retrieved articles were manually reviewed. DATA EXTRACTION AND SYNTHESIS: Available studies were critically reviewed, and data were extracted with special attention to the human and animal studies that explored a) diabetes and ALI; b) hyperglycemia and ALI; c) metabolic nonhyperglycemic features of diabetes and ALI; and d) diabetic therapies and ALI.

conclusionsClinical and experimental data indicate that diabetes is protective against the development of ALI/ARDS. The pathways involved are complex and likely include effects of hyperglycemia on the inflammatory response, metabolic abnormalities in diabetes, and the interactions of therapeutic agents given to diabetic patients. Multidisciplinary, multifaceted studies, involving both animal models and clinical and molecular epidemiology techniques, are essential.

Indexed as

Acute Lung InjuryAngiotensin-Converting Enzyme InhibitorsAnimalsDiabetes MellitusDisease SusceptibilityHumansHydroxymethylglutaryl-CoA Reductase InhibitorsHyperglycemiaHypoglycemic AgentsInsulinPeroxisome Proliferator-Activated ReceptorsRodentiaAngiotensin-Converting Enzyme InhibitorsHydroxymethylglutaryl-CoA Reductase InhibitorsHypoglycemic AgentsInsulinPeroxisome Proliferator-Activated Receptors

Identifiers

PMID19531947
PMCPMC3103784
OpenAlexW2040661588

What OpenQuestion holds

Texttitle and abstract
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.