Evidence map›Paper›PMID 32329160›Full record

Trial reportDiabetes, obesity & metabolism2020

Exenatide once weekly decreases urinary albumin excretion in patients with type 2 diabetes and elevated albuminuria: Pooled analysis of randomized active controlled clinical trials.

Annemarie B van der Aart-van der Beek, Daniel H van Raalte, Cristian Guja, Klaas Hoogenberg, Lisa J Suchower, Elise Hardy, C David Sjöström, Hiddo J L Heerspink

Open access · hybridAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Diabetes, obesity & metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 3 pooled it
2.6field-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

17 citing papers in PubMed, 3 syntheses or guidelines pooled it, 26 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

8 authors at 7 institutions in 7 countries.

Annemarie B van der Aart-van der BeekClinical Pharmacy and Pharmacology, University of Groningen, Groningen, The Netherlands.ORCID 0000-0003-1473-3259
Daniel H van RaalteDiabetes Centre, Department of Internal Medicine, Amsterdam UMC location VUMC, Amsterdam, The Netherlands.
Cristian GujaCarol Davila University of Medicine and Pharmacy, Bucharest, Romania.ORCID 0000-0002-8703-0522
Klaas HoogenbergDepartment of Internal Medicine, Martini Hospital, Groningen, The Netherlands.
Lisa J SuchowerKelly Services, Gaithersburg, Maryland.
Elise HardyClinical Metabolism, Late-stage Development, Cardiovascular, Renal and Metabolism (CVRM), BioPharmaceuticals R&D, AstraZeneca, Gaithersburg, Maryland.
C David SjöströmClinical Metabolism, Late-stage Development, Cardiovascular, Renal and Metabolism (CVRM), BioPharmaceuticals R&D, AstraZeneca, Gothenburg, Sweden.ORCID 0000-0002-8380-9766
Hiddo J L HeerspinkClinical Pharmacy and Pharmacology, University of Groningen, Groningen, The Netherlands.ORCID 0000-0002-3126-3730
University Medical Center Groningen · NLAmsterdam Neuroscience · NLAstraZeneca (Finland) · FIAstraZeneca (Poland) · PLCarol Davila University of Medicine and Pharmacy · ROKelly Services (United States) · USMartini Ziekenhuis · NL

Funding

This study was funded by AstraZeneca Pharmaceuticals LP.
6 · The paper itself

Abstract

aimsTo examine the albuminuria-lowering effect of exenatide once weekly (EQW) compared with active glucose-lowering comparators in patients with type 2 diabetes and elevated urinary albumin-to-creatinine ratio (uACR).

methodsSix randomized double-blind and open-label phase III studies were pooled in a post hoc, exploratory analysis to evaluate the efficacy and safety of EQW versus non-glucagon-like peptide-1 receptor agonist comparators in patients with type 2 diabetes and baseline uACR ≥30 mg/g. Treatment groups were EQW versus all comparators pooled. Efficacy outcomes were percent change from baseline to week 26/28 in uACR and absolute change in glycated haemoglobin (HbA1c), systolic blood pressure (SBP), body weight and estimated glomerular filtration rate (eGFR).

resultsBaseline characteristics were generally similar between the two treatment groups (EQW: N = 194, all comparators: N = 274). Relative to the comparator group, EQW changed albuminuria by -26.2% (95% confidence interval [CI] -39.5 to -10). Similar improvements were observed with EQW versus oral glucose-lowering drugs (-29.6% [95% CI -47.6 to -5.3) or insulin (-23.8% [95% CI -41.8 to -0.2]). The effect of EQW on uACR was independent of baseline renin-angiotensin system inhibitor usage. Adjusted mean decreases in HbA1c, SBP and body weight were more pronounced in the EQW versus the comparator group. Adjustment for changes in HbA1c, eGFR and SBP did not substantially affect the uACR-lowering effect of EQW. When also adjusting for changes in body weight, the uACR-lowering effect was reduced to (-13.0% [95% CI -29.9 to 7.8]).

conclusionExenatide once weekly reduced uACR in patients with type 2 diabetes and elevated albuminuria compared to commonly used glucose-lowering drugs.

Indexed as

Diabetes Mellitus, Type 2Pharmaceutical PreparationsAlbuminsAlbuminuriaExenatideHumansHypoglycemic AgentsAlbuminsExenatideHypoglycemic AgentsPharmaceutical Preparationsdiabetic kidney diseaseexenatideGLP-1RAglucagon-like peptide-1 receptor agonistspooled analysis

Identifiers

PMID32329160
PMCPMC7496075
OpenAlexW3018599559

What OpenQuestion holds

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LicenceCC BY-NC
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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.