Evidence map›Paper›PMID 24550190›Full record

Trial reportDiabetes2014

Acute administration of unacylated ghrelin has no effect on Basal or stimulated insulin secretion in healthy humans.

Jenny Tong, Harold W Davis, Suzanne Summer, Stephen C Benoit, Ahrar Haque, Martin Bidlingmaier, Matthias H Tschöp, David D'Alessio

Registry-linked trialOpen access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetes, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT02690987 (Do Appetitive Gut Hormones Reduce Addictive and Eating Behaviours in Obesity, and Nicotine and Alcohol Dependence?), which is not on this map. Cited by 25 papers.

0numbers the graph read from it
0cells of the map it votes in
25citing papers in PubMed
3.0field-weighted citation impact, top 8% 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.

NCT02690987 early_phase1unknown statusnot on this mapstarted 2015, after this paper: background citation

Do Appetitive Gut Hormones Reduce Addictive and Eating Behaviours in Obesity, and Nicotine and Alcohol Dependence?

TypeinterventionalSponsorImperial College LondonRan2015 to 2020Enrolled95ConditionsObesity, Smoking Cessation, AlcoholismArmsExenatide, Desacyl ghrelin, Saline
3 · Its place in the literature

Who cites it

25 citing papers in PubMed, 47 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Trial
  4. Trial
  5. Article
  6. Article
  7. Review
  8. Role of the Ghrelin System in Colorectal Cancer.International journal of molecular sciences · 2022
    Review
  9. Review
  10. Article
  11. Article
  12. Review
  13. Article
  14. Review
  15. Article
  16. Ghrelin regulation of glucose metabolism.Journal of neuroendocrinology · 2019
    Review
  17. Review
  18. Development and Characteristics of Pancreatic Epsilon Cells.International journal of molecular sciences · 2019
    Review
  19. Review
  20. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 2 countries.

Jenny TongDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Cincinnati, Cincinnati, OH jenny.tong@uc.edu.
Harold W DavisDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Cincinnati, Cincinnati, OH.
Suzanne SummerClinical Translational Research Center, Cincinnati Children's Hospital Medical Center, Cincinnati, OH.
Stephen C BenoitDepartment of Psychiatry, University of Cincinnati, Cincinnati, OH.
Ahrar HaqueDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Cincinnati, Cincinnati, OH.
Martin BidlingmaierMedizinische Klinik und Poliklinik IV, Ludwig-Maximilians-Universität, Munich, Germany.
Matthias H TschöpDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Cincinnati, Cincinnati, OHInstitute for Obesity and Diabetes, Helmholtz Center Munich and Division of Metabolic Diseases, Department of Medicine, Technical University, Munich, Germany.
David D'AlessioDivision of Endocrinology, Diabetes and Metabolism, Department of Medicine, University of Cincinnati, Cincinnati, OHCincinnati Veterans Affairs Medical Center, Cincinnati, OH.
University of Cincinnati · USCincinnati Children's Hospital Medical Center · USLudwig-Maximilians-Universität München · DEVeterans Health Administration · US

Funding

CTSA INFRASTRUCTURE FOR PEDIATRIC RESEARCHUL1RR026314 · NCRR · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2009 to 2011
$14.3M
LIPID, LIPOPROTEIN, AND GLUCOSE METABOLISM COREU24DK059630 · NIDDK · UNIVERSITY OF CINCINNATI · PI TSO, PATRICK · 2001 to 2015
$12.9M
Cincinnati Center for Clinical and Translational Sciences and TrainingUL1TR000077 · NCATS · UNIVERSITY OF CINCINNATI · PI HEUBI, JAMES E. · 2012 to 2014
$9.9M
The role of GLP-1 in normal and abnormal glucose toleranceR01DK057900 · NIDDK · UNIVERSITY OF CINCINNATI · PI D'ALESSIO, DAVID A. · 1999 to 2013
$3.4M
Impact of Ghrelin of Beta-cell Function and Insulin Sensitivity in HumansK23DK080081 · NIDDK · UNIVERSITY OF CINCINNATI · PI TONG, JENNY · 2007 to 2011
$865k
The Impact of Unacylated Ghrelin on Insulin Secretion and Glucose Tolerance in HuR03DK089090 · NIDDK · UNIVERSITY OF CINCINNATI · PI TONG, JENNY · 2010 to 2011
$156k
NCATS NIH HHS UL1 TR000077NCRR NIH HHS UL1 RR026314NCRR NIH HHS UL1-RR-026314NIDDK NIH HHS 1R03-DK-89090NIDDK NIH HHS 5K23-DK-80081NIDDK NIH HHS K23 DK080081NIDDK NIH HHS R01 DK057900NIDDK NIH HHS R01-DK-57900NIDDK NIH HHS R03 DK089090NIDDK NIH HHS U24 DK059630NIDDK NIH HHS U24-DK-059630
6 · The paper itself

Abstract

Unacylated ghrelin (UAG) is the predominant ghrelin isoform in the circulation. Despite its inability to activate the classical ghrelin receptor, preclinical studies suggest that UAG may promote β-cell function. We hypothesized that UAG would oppose the effects of acylated ghrelin (AG) on insulin secretion and glucose tolerance. AG (1 µg/kg/h), UAG (4 µg/kg/h), combined AG+UAG, or saline were infused to 17 healthy subjects (9 men and 8 women) on four occasions in randomized order. Ghrelin was infused for 30 min to achieve steady-state levels and continued through a 3-h intravenous glucose tolerance test. The acute insulin response to glucose (AIRg), insulin sensitivity index (SI), disposition index (DI), and intravenous glucose tolerance (kg) were compared for each subject during the four infusions. AG infusion raised fasting glucose levels but had no effect on fasting plasma insulin. Compared with the saline control, AG and AG+UAG both decreased AIRg, but UAG alone had no effect. SI did not differ among the treatments. AG, but not UAG, reduced DI and kg and increased plasma growth hormone. UAG did not alter growth hormone, cortisol, glucagon, or free fatty acid levels. UAG selectively decreased glucose and fructose consumption compared with the other treatments. In contrast to previous reports, acute administration of UAG does not have independent effects on glucose tolerance or β-cell function and neither augments nor antagonizes the effects of AG.

Indexed as

AdolescentAdultBasal MetabolismBlood GlucoseDrug Administration ScheduleFemaleGhrelinHealthHumansInsulinInsulin-Secreting CellsInsulin SecretionMaleMiddle AgedYoung AdultBlood GlucoseGhrelinInsulin

Identifiers

PMID24550190
PMCPMC4066344
OpenAlexW2097590409

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.