Evidence map›Paper›PMID 34022121›Full record

Observational studyJournal of diabetes investigation2021

Effects of glucagon-like peptide-1 receptor agonists on secretions of insulin and glucagon and gastric emptying in Japanese individuals with type 2 diabetes: A prospective, observational study.

Hitoshi Kuwata, Daisuke Yabe, Kenta Murotani, Yuuka Fujiwara, Takuya Haraguchi, Sodai Kubota, Saki Kubota-Okamoto, Ryota Usui, Minori Ishitobi, Yuji Yamazaki and 5 more

Open access · goldAbstract readObservational Study
In one paragraph

Observational study in Journal of diabetes investigation, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed, 4 pooled it
4.1field-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

27 citing papers in PubMed, 4 syntheses or guidelines pooled it, 40 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

15 authors at 4 institutions in 1 country.

Hitoshi KuwataYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.
Daisuke YabeYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.ORCID https://orcid.org/0000-0002-5334-7687
Kenta MurotaniBiostatistics Center, Graduate School of Medicine, Kurume University, Kurume, Japan.ORCID https://orcid.org/0000-0003-0623-9365
Yuuka FujiwaraYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.
Takuya HaraguchiYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.
Sodai KubotaYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.ORCID https://orcid.org/0000-0002-6072-0080
Saki Kubota-OkamotoYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.
Ryota UsuiYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.ORCID https://orcid.org/0000-0002-4641-0158
Minori IshitobiCenter for Diabetes, Endocrinology and Metabolism, Kansai Electric Power Hospital, Osaka, Japan.
Yuji YamazakiYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.
Yoshiyuki HamamotoYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.ORCID https://orcid.org/0000-0002-1938-7394
Takeshi KuroseYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.ORCID https://orcid.org/0000-0003-3713-7919
Yusuke SeinoDepartment of Endocrinology and Metabolism, Fujita Health University, Toyoake, Japan.ORCID https://orcid.org/0000-0002-9099-3493
Yuichiro YamadaYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.
Yutaka SeinoYutaka Seino Distinguished Center for Diabetes Research, Kansai Electric Power Medical Research Institute, Kobe, Japan.ORCID https://orcid.org/0000-0002-1099-7989
Kansai Electric Power (Japan) · JPFujita Health University · JPKansai Electric Power Hospital · JPKurume University · JP

Funding

Japan Association for Diabetes Education and CareJapan Society for the Promotion of Science 17K09825Japan Society for the Promotion of Science 20K11619Japan Vascular Disease Research Foundation
6 · The paper itself

Abstract

AIMS/

introductionDifferences in the glucose-lowering mechanisms of glucagon-like peptide-1 receptor agonists (GLP-1RAs) have been noted. Clarifying these differences could facilitate the choice of optimal drugs for individuals with type 2 diabetes and requires investigation in a clinical setting. MATERIALS AND

methodsA single-arm, prospective, observational study was conducted to evaluate the effects of various GLP-1RAs on postprandial glucose excursion, secretions of insulin and glucagon as well as on the gastric emptying rate. Participants were subjected to meal tolerance tests before and 2 weeks and 12 weeks after GLP-1RA initiation. Effects on postprandial secretions of glucose-dependent insulinotropic polypeptide (GIP) and apolipoprotein B48 were also investigated.

resultsEighteen subjects with type 2 diabetes received one of three GLP-1RAs, i.e., lixisenatide, n = 7; liraglutide, n = 6; or dulaglutide, n = 5. While 12-week administration of all of the GLP-1RAs significantly reduced HbA1c, only lixisenatide and liraglutide, but not dulaglutide, significantly reduced body weight. Postprandial glucose elevation was improved by all of the GLP-1RAs. Postprandial insulin levels were suppressed by lixisenatide, while insulin levels were enhanced by liraglutide. Postprandial glucagon levels were suppressed by lixisenatide. The gastric emptying rate was significantly delayed by lixisenatide, while liraglutide and dulaglutide had limited effects on gastric emptying. GIP secretion was suppressed by lixisenatide and liraglutide. Apolipoprotein B48 secretion was suppressed by all of the GLP-1RAs.

conclusionsAll of the GLP-1RAs were found to improve HbA1c in a 12-week prospective observational study in Japanese individuals with type 2 diabetes. However, differences in the mechanisms of the glucose-lowering effects and body weight reduction were observed.

Indexed as

Glucagon-Like Peptide-1 Receptor AgonistsAdultApolipoprotein B-48Blood GlucoseDiabetes Mellitus, Type 2FemaleGastric EmptyingGastric Inhibitory PolypeptideGlucagonGlucagon-Like Peptide-2 ReceptorGlucagon-Like PeptidesHumansHypoglycemic AgentsImmunoglobulin Fc FragmentsInsulinJapanApolipoprotein B-48Blood GlucosedulaglutideGastric Inhibitory PolypeptideGlucagonGlucagon-Like Peptide-1 Receptor AgonistsGlucagon-Like Peptide-2 ReceptorGlucagon-Like PeptidesHypoglycemic AgentsImmunoglobulin Fc FragmentsInsulinLiraglutidelixisenatidePeptidesRecombinant Fusion ProteinsGastric emptyingGLP-1 receptor agonistislet hormones

Identifiers

PMID34022121
PMCPMC8668059
OpenAlexW3164830791

What OpenQuestion holds

Texttitle and abstract
LicenceCC BY-NC
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.