Evidence map›Paper›PMID 26831299›Full record

Trial reportDiabetologia2016

The insulinotropic effect of pulsatile compared with continuous intravenous delivery of GLP-1.

Mark P Plummer, Palash Kar, Caroline E Cousins, Kylie Lange, Marianne J Chapman, Michael A Nauck, Michael Horowitz, Juris J Meier, Adam M Deane

Open access · bronzeAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Diabetologia, 2016. 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
0.2field-weighted citation impact, top 37% 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, 2 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

9 authors at 3 institutions in 2 countries.

Mark P PlummerDiscipline of Acute Care Medicine, University of Adelaide, Adelaide, SA, Australia. mark.plummer@adelaide.edu.au.
Palash KarDiscipline of Acute Care Medicine, University of Adelaide, Adelaide, SA, Australia.
Caroline E CousinsIntensive Care Research Unit, Level 4 Emergency Block, Royal Adelaide Hospital, North Terrace, Adelaide, SA, 5000, Australia.
Kylie LangeDiscipline of Medicine, University of Adelaide, Adelaide, SA, Australia.
Marianne J ChapmanDiscipline of Acute Care Medicine, University of Adelaide, Adelaide, SA, Australia.
Michael A NauckDivision of Diabetes and GI Endocrinology, University Hospital St Josef-Hospital, Ruhr-University Bochum, Bochum, Germany.
Michael HorowitzDiscipline of Medicine, University of Adelaide, Adelaide, SA, Australia.
Juris J MeierDivision of Diabetes and GI Endocrinology, University Hospital St Josef-Hospital, Ruhr-University Bochum, Bochum, Germany.
Adam M DeaneDiscipline of Acute Care Medicine, University of Adelaide, Adelaide, SA, Australia.
University of Adelaide · AURoyal Adelaide Hospital · AURuhr University Bochum · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aims/hypothesisIn healthy individuals, both insulin and glucagon-like peptide 1 (GLP-1) are secreted in a pulsatile fashion. Insulin has greater glucose-lowering properties when administered in pulses compared with a constant i.v. infusion. The primary aim of this randomised double-dummy cross-over study was to compare the insulinotropic response to pulsatile and continuous i.v. infusions of equivalent doses of GLP-1.

methodsTwelve healthy participants aged 18-35 years were randomised to three different treatments on separate days: a continuous infusion day (GLP-1 at 0.6 pmol kg(-1) min(-1) [1 ml/min] and a 1 ml placebo bolus every 6 min); a pulsatile infusion day (placebo at 1 ml/min and a 3.6 pmol/kg GLP-1 bolus every 6 min); and a placebo day (placebo at 1 ml/min and a 1 ml placebo bolus every 6 min). Between 45 and 120 min, a hyperglycaemic clamp was used to maintain blood glucose at 9 mmol/l. Venous blood glucose and plasma insulin concentrations were measured every 5 min from 0 to 45 min and every 1 min from 45 to 120 min; plasma glucagon was measured every 15 min. The order of treatment was randomised by the Pharmacy Department and both study investigators and participants were blinded to the treatment arm. The dextrose requirement and glucagon data were analysed using repeated measures ANOVA and insulin data were analysed with a linear mixed effects maximum likelihood model.

resultsContinuous and pulsatile infusions of GLP-1 increased the dextrose requirement by ~threefold (p < 0.001) and increased insulin secretion by ~ninefold (p < 0.001). There was no difference in the effect of both treatments. Although hyperglycaemia reduced plasma glucagon concentrations, there was no difference between the treatment days. CONCLUSIONS/

interpretationIn healthy individuals, pulsatile and continuous administration of i.v. GLP-1 appears to have comparable insulinotropic effects.

trial registrationACTRN12612001040853

fundingThis study was supported by the National Health and Medical Research Council (NHMRC) of Australia.

Indexed as

AdolescentAdultCross-Over StudiesFemaleGlucagon-Like Peptide 1HumansHyperglycemiaInfusions, IntravenousInsulinMaleYoung AdultGlucagon-Like Peptide 1InsulinGlucagonGlucagon-like peptide 1InsulinPulsatile

Identifiers

PMID26831299
OpenAlexW2261590553

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.