Evidence map›Paper›PMID 30972338›Full record

ArticleFrontiers in medicine2019

Stress Hyperglycemia in Critically Ill Patients: Insight Into Possible Molecular Pathways.

David Bar-Or, Leonard T Rael, Robert M Madayag, Kaysie L Banton, Allen Tanner, David L Acuna, Mark J Lieser, Gary T Marshall, Charles W Mains, Edward Brody

Open access · goldAbstract read
In one paragraph

Article in Frontiers in medicine, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 1 pooled it
7.3field-weighted citation impact, top 2% 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

42 citing papers in PubMed, 1 synthesis or guideline pooled it, 80 citations in OpenAlex.

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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 7 institutions in 1 country.

David Bar-OrTrauma Research Laboratory, Swedish Medical Center, Englewood, CO, United States.
Leonard T RaelTrauma Research Laboratory, Swedish Medical Center, Englewood, CO, United States.
Robert M MadayagSt. Anthony Hospital, Lakewood, CO, United States.
Kaysie L BantonTrauma Research Laboratory, Swedish Medical Center, Englewood, CO, United States.
Allen TannerPenrose Hospital, Colorado Springs, CO, United States.
David L AcunaWesley Medical Center, Wichita, KS, United States.
Mark J LieserResearch Medical Center, Kansas City, MO, United States.
Gary T MarshallMedical City Plano Hospital, Plano, TX, United States.
Charles W MainsSt. Anthony Hospital, Lakewood, CO, United States.
Edward BrodySomaLogic Inc., Boulder, CO, United States.
Research Medical Center · USSt. Anthony Hospital · USSwedish Medical Center · USPenrose Hospital · USPlano Cancer Institute · USSomaLogic (United States) · USWesley Medical Center · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Severe sepsis, systemic inflammatory response syndrome (SIRS), and traumatic brain injury are frequently associated with hyperglycemia in non-diabetic patients. In patients suffering from any of these conditions, hyperglycemia at admission to an intensive care unit (ICU) is directly correlated with increased mortality or morbidity. Although there was initial enthusiasm for insulin treatment to blood glucose levels below 110 mg/dL in these patients, recent understanding suggests that the potential for hypoglycemic complications make this approach potentially dangerous. More moderate glucose control seems to be more beneficial than the aggressive glucose lowering initially suggested. An important publication has shown that hyperlactatemia accompanying hyperglycemia could be the real culprit in bad outcomes. This suggests that coupling moderate glucose lowering with therapeutic agents which might treat the underlying metabolic disturbances in these conditions may be a better strategy. The key metabolic disturbance in these three conditions seems to be persistent glycolysis as an energy source even in the presence of adequate tissue oxygenation (the Warburg Effect). We look at recent advances in understanding aerobic glycolysis and possibly the action of DPP4 on incretins resulting in insulin dysregulation and suggest key metabolic pathways involved in hyperglycemia regulation.

Indexed as

dipeptidyl peptidase IVglycolysishyperglycemiaoxidative phosphorylationsepsisWarburg effect

Identifiers

PMID30972338
PMCPMC6445875
OpenAlexW2924371229

What OpenQuestion 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 OpenQuestion graph.