Evidence map›Paper›PMID 31178432›Full record

ReviewDiabetes2020

Repositioning Glucagon Action in the Physiology and Pharmacology of Diabetes.

Brian Finan, Megan E Capozzi, Jonathan E Campbell

Open access · bronzeAbstract readReview
In one paragraph

Review in Diabetes, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 73 papers.

0numbers the graph read from it
0cells of the map it votes in
73citing papers in PubMed
10.0field-weighted citation impact, top 1% 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

73 citing papers in PubMed, 116 citations in OpenAlex.

  1. Trial
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  9. Review
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  13. Article
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  16. Article
  17. Review
  18. Advances in clinical research on glucagon.Diabetology international · 2024
    Review
  19. Article
  20. Review

13 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

3 authors at 2 institutions in 1 country.

Brian FinanNovo Nordisk Research Center, Indianapolis, IN.
Megan E CapozziDuke Molecular Physiology Institute, Duke University, Durham, NC.
Jonathan E CampbellDuke Molecular Physiology Institute, Duke University, Durham, NC jonathan.campbell@duke.edu.ORCID 0000-0003-4358-6331
Duke University · USNovo Nordisk (United States) · US

Funding

Mechanisms of insulin secretion mediated by alpha cellsR01DK123075 · NIDDK · DUKE UNIVERSITY · PI CAMPBELL, JONATHAN E · 2019 to 2023
$1.9M
The Role of Islet DPP4 for Regulation of Glucose HomeostasisF32DK116542 · NIDDK · DUKE UNIVERSITY · PI CAPOZZI, MEGAN · 2018 to 2020
$188k
NIDDK NIH HHS F32 DK116542NIDDK NIH HHS R01 DK123075
6 · The paper itself

Abstract

Glucagon is historically described as the counterregulatory hormone to insulin, induced by fasting/hypoglycemia to raise blood glucose through action mediated in the liver. However, it is becoming clear that the biology of glucagon is much more complex and extends beyond hepatic actions to exert control on glucose metabolism. We discuss the inconsistencies with the canonical view that glucagon is primarily a hyperglycemic agent driven by fasting/hypoglycemia and highlight the recent advances that have reshaped the metabolic role of glucagon. These concepts are placed within the context of both normal physiology and the pathophysiology of disease and then extended to discuss emerging strategies that incorporate glucagon agonism in the pharmacology of treating diabetes.

Indexed as

Blood GlucoseDiabetes MellitusGlucagonHumansHypoglycemiaInsulinLiverBlood GlucoseGlucagonInsulin

Identifiers

PMID31178432
PMCPMC7085250
OpenAlexW2948394616

What Socratic 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 Socratic graph.