Evidence map›Paper›PMID 32374825›Full record

ArticleThe Journal of clinical endocrinology and metabolism2020

Novel Insights Into Effects of Cortisol and Glucagon on Nocturnal Glucose Production in Type 2 Diabetes.

Ananda Basu, Yogesh Yadav, Rickey E Carter, Rita Basu

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

0 citing papers in PubMed, 5 citations in OpenAlex.

No citing paper in PubMed yet.

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

4 authors at 2 institutions in 1 country.

Ananda BasuDivision of Endocrinology, University of Virginia School of Medicine, Charlottesville, VA, US.
Yogesh YadavDivision of Endocrinology, University of Virginia School of Medicine, Charlottesville, VA, US.
Rickey E CarterDepartment of Health Sciences Research, Mayo Clinic, Jacksonville, FL, US.
Rita BasuDivision of Endocrinology, University of Virginia School of Medicine, Charlottesville, VA, US.
University of Virginia · USMayo Clinic in Florida · US

Funding

Mayo Clinic Center for Translational Science ActivitiesUL1TR000135 · NCATS · MAYO CLINIC ROCHESTER · PI KHOSLA, SUNDEEP · 2012 to 2015
$41.2M
MECHANISMS OF INSULIN RESISTANCE IN MANR01DK029953 · NIDDK · UNIVERSITY OF VIRGINIA · PI BASU, RITA · 1986 to 2024
$11.5M
Integrated Approaches to Close the Loop in Type 1 DiabetesR01DK085516 · NIDDK · UNIVERSITY OF VIRGINIA · PI BASU, ANANDA · 2009 to 2021
$6.5M
Relative Efficacy of Single-, Bi-, and Tri-Hormonal Closed-Loop Control SystemsDP3DK106785 · NIDDK · UNIVERSITY OF VIRGINIA · PI BASU, ANANDA · 2015 to 2015
$3.5M
NCATS NIH HHS UL1 TR000135NIDDK NIH HHS R01 DK029953NIDDK NIH HHS R01 DK085516
6 · The paper itself

Abstract

contextThe effect of physiological changes in night-time cortisol and glucagon on endogenous glucose production (EGP) and nocturnal glycemia are unknown.

objectiveTo determine the effects of changes in cortisol and glucagon on EGP during the night.

designTwo overnight protocols were conducted. In Protocol 1, endogenous cortisol was blocked with metyrapone and hydrocortisone infused either at constant (constant) or increasing (variable) rates to mimic basal or physiological nocturnal cortisol concentrations. In Protocol 2, endogenous glucagon was blocked with somatostatin and exogenous glucagon was infused at either basal or elevated rates to mimic nocturnal glucagon concentrations observed in nondiabetic (ND) and type 2 diabetes (T2D) individuals. EGP was measured using [3-3H] glucose and gluconeogenesis estimated with 2H2O in all studies.

settingMayo Clinic Clinical Research Trials Unit, Rochester, MN, US.

participantsIn Protocol 1, 34 subjects (17 ND and 17 T2D) and in Protocol 2, 39 subjects (21 ND and 18 T2D) were studied.

main outcome measuresEndogenous glucose production.

resultsEGP, gluconeogenesis, and glycogenolysis were higher with variable than with constant cortisol at 7 am in T2D subjects. In contrast, nocturnal EGP did not differ in ND subjects between variable and constant cortisol. While elevated glucagon increased EGP, glycogenolysis, and gluconeogenesis in ND, the data in T2D subjects indicated that EGP and gluconeogenesis but not glycogenolysis were higher during the early part of the night.

conclusionNocturnal hyperglucagonemia, but not physiological rise in cortisol, contributes to nocturnal hyperglycemia in T2D due to increased gluconeogenesis.

Indexed as

AgedBlood GlucoseDiabetes Mellitus, Type 2FemaleGlucagonGluconeogenesisHumansHydrocortisoneHyperglycemiaMaleMiddle AgedTime FactorsBlood GlucoseGlucagonHydrocortisonecortisolendogenous glucose productionglucagongluconeogenesisglycogenolysistype 2 diabetes

Identifiers

PMID32374825
PMCPMC7274493
OpenAlexW3021372775

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.