Evidence map›Paper›PMID 28323959›Full record

ReviewEndocrinology2017

Insulin and Glucagon: Partners for Life.

Jens Juul Holst, William Holland, Jesper Gromada, Young Lee, Roger H Unger, Hai Yan, Kyle W Sloop, Timothy J Kieffer, Nicolas Damond, Pedro L Herrera

Open access · hybridAbstract readReview
In one paragraph

Review in Endocrinology, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 44 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
44citing papers in PubMed, 1 pooled it
8.4field-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

44 citing papers in PubMed, 1 synthesis or guideline pooled it, 88 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 6 institutions in 4 countries.

Jens Juul HolstNovo Nordisk Foundation Center for Basic Metabolic Research and Department of Biomedical Sciences, Faculty of Health Sciences, University of Copenhagen, DK-2200 Copenhagen, Denmark.
William HollandTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas 75390.
Jesper GromadaRegeneron Pharmaceuticals, Tarrytown, New York.
Young LeeTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas 75390.
Roger H UngerTouchstone Diabetes Center, Department of Internal Medicine, The University of Texas Southwestern Medical Center, Dallas, Texas 75390.
Hai YanREMD Biotherapeutics Inc., Camarillo, California.
Kyle W SloopEndocrine Discovery, Lilly Research Laboratories, Indianapolis, Indiana.
Timothy J KiefferDepartment of Cellular & Physiological Sciences, Life Sciences Institute, University of British Columbia, Vancouver, British Columbia, Canada.
Nicolas DamondDepartment of Genetic Medicine & Development, Faculty of Medicine, University of Geneva, CH-1211 Geneva 4, Switzerland.
Pedro L HerreraDepartment of Genetic Medicine & Development, Faculty of Medicine, University of Geneva, CH-1211 Geneva 4, Switzerland.
The University of Texas Southwestern Medical Center · USUniversity of Geneva · CHEli Lilly (United States) · USRegeneron (United States) · USUniversity of British Columbia · CAUniversity of Copenhagen · DK

Funding

Beta-cell Regeneration by Islet Cell Type Interconversion: Exploiting Islet Cell Plasticity for Diabetes RecoveryUC4DK104209 · NIDDK · UNIVERSITY OF GENEVA · PI HERRERA, PEDRO L · 2014 to 2014
$2.4M
NIDDK NIH HHS UC4 DK104209
6 · The paper itself

Abstract

In August 2016, several leaders in glucagon biology gathered for the European Association for the Study of Diabetes Hagedorn Workshop in Oxford, England. A key point of discussion focused on the need for basal insulin to allow for the therapeutic benefit of glucagon blockade in the treatment of diabetes. Among the most enlightening experimental results presented were findings from studies in which glucagon receptor-deficient mice were administered streptozotocin to destroy pancreatic β cells or had undergone diphtheria toxin-induced β cell ablation. This article summarizes key features of the discussion as a consensus was reached. Agents that antagonize glucagon may be of great benefit for the treatment of diabetes; however, sufficient levels of basal insulin are required for their therapeutic efficacy.

Indexed as

Blood GlucoseAnimalsDiabetes MellitusDiabetes Mellitus, ExperimentalGlucagonHumansHypoglycemic AgentsInsulinBlood GlucoseGlucagonHypoglycemic AgentsInsulin

Identifiers

PMID28323959
PMCPMC6061217
OpenAlexW2604759438

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.