Evidence mapPaperPMID 29341461Full record

Trial reportDiabetes, obesity & metabolism2018

Effect of immediate and prolonged GLP-1 receptor agonist administration on uric acid and kidney clearance: Post-hoc analyses of four clinical trials.

Lennart Tonneijck, Marcel H A Muskiet, Mark M Smits, Petter Bjornstad, Mark H H Kramer, Michaela Diamant, Ewout J Hoorn, Jaap A Joles, Daniël H van Raalte

Abstract readComparative StudyRandomized Controlled Trial
In one paragraph

Trial report in Diabetes, obesity & metabolism, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 19 papers.

0numbers the graph read from it
0cells of the map it votes in
19citing papers in PubMed
2.8field-weighted citation impact, top 9% 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

19 citing papers in PubMed, 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

9 authors at 4 institutions in 2 countries.

Lennart TonneijckDepartment of Internal Medicine, Diabetes Center, VU University Medical Center, Amsterdam, The Netherlands.ORCID 0000-0001-5637-910X
Marcel H A MuskietDepartment of Internal Medicine, Diabetes Center, VU University Medical Center, Amsterdam, The Netherlands.
Mark M SmitsDepartment of Internal Medicine, Diabetes Center, VU University Medical Center, Amsterdam, The Netherlands.
Petter BjornstadDepartment of Pediatric Endocrinology, University of Colorado School of Medicine and Barbara Davis Center for Diabetes, University of Colorado Denver, Aurora, Colorado.
Mark H H KramerDepartment of Internal Medicine, Diabetes Center, VU University Medical Center, Amsterdam, The Netherlands.
Michaela DiamantDepartment of Internal Medicine, Diabetes Center, VU University Medical Center, Amsterdam, The Netherlands.
Ewout J HoornDepartment of Internal Medicine, Division of Nephrology and Transplantation, Erasmus Medical Center, Rotterdam, The Netherlands.
Jaap A JolesDepartment of Nephrology and Hypertension, University Medical Center, Utrecht, The Netherlands.
Daniël H van RaalteDepartment of Internal Medicine, Diabetes Center, VU University Medical Center, Amsterdam, The Netherlands.ORCID 0000-0003-2894-6124
Amsterdam UMC Location Vrije Universiteit Amsterdam · NLErasmus MC · NLUniversity Medical Center Utrecht · NLUniversity of Colorado Denver · US

Funding

Training Program in Diabetes ResearchT32DK063687 · UNIVERSITY OF COLORADO DENVER · 2002 to 2025
$968k
NIDDK NIH HHS T32 DK063687
6 · The paper itself

Abstract

aimsTo determine the effects of glucagon-like peptide (GLP)-1 receptor agonists (RA) on uric acid (UA) levels and kidney UA clearance. MATERIAL AND

methodsThis study involved post-hoc analyses of 4 controlled clinical trials, which assessed actions of GLP-1RA administration on kidney physiology. The immediate effects of GLP-1RA exenatide infusion vs placebo were determined in 9 healthy overweight men (Study-A) and in 52 overweight T2DM patients (Study-B). The effects of 12 weeks of long-acting GLP-1RA liraglutide vs placebo in 36 overweight T2DM patients (Study-C) and of 8 weeks of short-acting GLP-1RA lixisenatide vs once-daily titrated insulin glulisine in 35 overweight T2DM patients (Study-D) were also examined. Plasma UA, fractional (inulin-corrected) and absolute urinary excretion of UA (UE

resultsMedian baseline plasma UA level was 5.39 to 6.33 mg/dL across all studies (17%-22% of subjects were hyperuricaemic). In Study-A, exenatide infusion slightly increased plasma UA (+0.07 ± 0.02 mg/dL, P = .04), and raised absolute-UE

conclusionImmediate exenatide infusion increases UE

Indexed as

Glucagon-Like Peptide-1 Receptor AgonistsAdultAgedAnti-Obesity AgentsBody Mass IndexDiabetes Mellitus, Type 2Diabetic NephropathiesFemaleGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-2 ReceptorHumansHypoglycemic AgentsInsulinKidneyMaleMiddle AgedAnti-Obesity AgentsGLP1R protein, humanGlucagon-Like Peptide-1 ReceptorGlucagon-Like Peptide-1 Receptor AgonistsGlucagon-Like Peptide-2 ReceptorHypoglycemic AgentsInsulininsulin glulisinelixisenatidePeptidesUric Aciddiabetic nephropathyexenatideGLP-1liraglutiderandomised trialtype 2 diabetes

Identifiers

PMID29341461
PMCPMC5899927
OpenAlexW2793719460

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.