Evidence map›Paper›PMID 30849212›Full record

ReviewJournal of neuroendocrinology2019

Ghrelin regulation of glucose metabolism.

Sarah M Gray, Laura C Page, Jenny Tong

Open access · greenAbstract readReview
In one paragraph

Review in Journal of neuroendocrinology, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
34citing papers in PubMed, 1 pooled it
3.9field-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

34 citing papers in PubMed, 1 synthesis or guideline pooled it, 68 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

3 authors at 1 institution in 1 country.

Sarah M GrayDuke Molecular Physiology Institute, Duke University, Durham, North Carolina.ORCID 0000-0003-2370-7968
Laura C PageDivision of Endocrinology, Department of Pediatrics, Duke University, Durham, North Carolina.
Jenny TongDuke Molecular Physiology Institute, Duke University, Durham, North Carolina.ORCID 0000-0002-5614-3671
Duke University · US

Funding

Endocrinology and Metabolism Training ProgramT32DK007012 · NIDDK · DUKE UNIVERSITY · PI DAVID A. D'ALESSIO · 1986 to 2026
$6.8M
The Role of Ghrelin to Regulate Insulin Secretion in Health and Diabetes.R01DK097550 · NIDDK · UNIVERSITY OF CINCINNATI · PI TONG, JENNY · 2013 to 2017
$1.7M
NIDDK NIH HHS R01 DK097550NIDDK NIH HHS T32 DK007012
6 · The paper itself

Abstract

Ghrelin and its receptor, the growth hormone secretagogue receptor 1a (GHSR1a), are implicated in the regulation of glucose metabolism via direct actions in the pancreatic islet, as well as peripheral insulin-sensitive tissues and the brain. Although many studies have explored the role of ghrelin in glucose tolerance and insulin secretion, a complete mechanistic understanding remains to be clarified. This review highlights the local expression and function of ghrelin and GHSR1a in pancreatic islets and how this axis may modulate insulin secretion from pancreatic β-cells. Additionally, we discuss the effect of ghrelin on in vivo glucose metabolism in rodents and humans, as well as the metabolic circumstances under which the action of ghrelin may predominate.

Indexed as

AnimalsBrainEnergy MetabolismGhrelinGlucoseHumansInsulinInsulin SecretionIslets of LangerhansReceptors, GhrelinGhrelinGHRL protein, humanGhsr1a protein, humanGlucoseInsulinReceptors, Ghrelinghrelinglucose toleranceinsulininsulin secretion

Identifiers

PMID30849212
PMCPMC6688917
OpenAlexW2921377118

What Socratic holds

Textmetadata
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 Socratic graph.