Evidence mapPaperPMID 36894938Full record

SynthesisCardiovascular diabetology2023

Weight-dependent and weight-independent effects of dulaglutide on blood pressure in patients with type 2 diabetes.

Keith C Ferdinand, Julia Dunn, Claudia Nicolay, Flora Sam, Emily K Blue, Hui Wang

6 registry-linked trialsOpen access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Cardiovascular diabetology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT00734474. Cited by 9 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing 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.

NCT00734474 phase2 / phase3completed

A Phase 2/3, Placebo-Controlled, Efficacy and Safety Study of Once-Weekly, Subcutaneous LY2189265 Compared to Sitagliptin in Patients With Type 2 Diabetes Mellitus on Metformin

Ran2008Enrolled1,202Registered outcomes33Posted comparisons53ConditionsDiabetes Mellitus, Type 2ArmsLY2189265, Metformin, Placebo solution, Placebo tablet, Sitagliptin
Open the trial in the graph
NCT01064687 phase3completed

A Randomized, Placebo-Controlled Comparison of the Effects of Two Doses of LY2189265 or Exenatide on Glycemic Control in Patients With Type 2 Diabetes on Stable Doses of Metformin and Pioglitazone (AWARD-1: Assessment of Weekly Administration of LY2189265 in Diabetes-1)

Ran2010Enrolled978Registered outcomes47Posted comparisons59ConditionsDiabetes Mellitus, Type 2Armsexenatide, LY2189265, Metformin, Pioglitazone, Placebo
Open the trial in the graph
NCT01769378 phase3completed

A Randomized, Parallel-Arm, Double-Blinded Study Comparing the Effect of Once-Weekly Dulaglutide With Placebo in Patients With Type 2 Diabetes Mellitus on Sulfonylurea Therapy (AWARD-8: Assessment of Weekly AdministRation of LY2189265 in Diabetes - 8)

Ran2013Enrolled300Registered outcomes16Posted comparisons7ConditionsType 2 Diabetes MellitusArmsDulaglutide, Glimepiride, Placebo
Open the trial in the graph
NCT02597049 phase3completed

A Randomized, Parallel-Arm, Double-Blind Study of Efficacy and Safety of Dulaglutide When Added to SGLT2 Inhibitors in Patients With Type 2 Diabetes Mellitus

Ran2015Enrolled424Registered outcomes11Posted comparisons32ConditionsType 2 Diabetes MellitusArmsDulaglutide, Metformin, Placebo, SGLT2 inhibitor
Open the trial in the graph
NCT03495102 phase3completed

A Randomized, Double-Blind, Parallel Arm Study of the Efficacy and Safety of Investigational Dulaglutide Doses When Added to Metformin in Patients With Type 2 Diabetes Mellitus

Ran2018Enrolled1,842Registered outcomes7Posted comparisons8ConditionsDiabetes Mellitus, Type 2ArmsDulaglutide
Open the trial in the graph
NCT01149421 phase2completednot on this map

The Effect of LY2189265 on Blood Pressure and Heart Rate, as Assessed by Ambulatory Blood Pressure Monitoring, in Patients With Type 2 Diabetes Mellitus

TypeinterventionalSponsorEli Lilly and CompanyRan2010 to 2012Enrolled755ConditionsDiabetes Mellitus, Type 2ArmsLY2189265, Placebo
3 · Its place in the literature

Who cites it

9 citing papers in PubMed, 3 syntheses or guidelines pooled it, 13 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Possible mechanisms of action of glucagon-like peptide-1 receptor agonists on blood pressure beyond body weight.Hypertension research : official journal of the Japanese Society of Hypertension · 2025
    Review
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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

6 authors at 2 institutions in 1 country.

Keith C FerdinandTulane University School of Medicine, New Orleans, LA, USA. kferdina@tulane.edu.
Julia DunnEli Lilly and Company, Indianapolis, IN, USA.
Claudia NicolayEli Lilly and Company, Indianapolis, IN, USA.
Flora SamEli Lilly and Company, Indianapolis, IN, USA.
Emily K BlueEli Lilly and Company, Indianapolis, IN, USA.
Hui WangTechData Service Company, King of Prussia, PA, USA.
Eli Lilly (United States) · USTulane University · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with type 2 diabetes (T2D) treated with glucagon-like peptide-1 receptor agonists may experience reductions in weight and blood pressure. The primary objective of the current study was to determine the weight-dependent and weight-independent effects of ~ 6 months treatment with dulaglutide 1.5 mg treatment in participants with T2D.

methodsMediation analysis was conducted for five randomized, placebo-controlled trials of dulaglutide 1.5 mg to estimate the weight-dependent (i.e., mediated by weight) and weight-independent effects from dulaglutide vs. placebo on change from baseline for systolic blood pressure (SBP), diastolic blood pressure (DBP), and pulse pressure. A random-effects meta-analysis combined these results. To investigate a dose response between dulaglutide 4.5 mg and placebo, mediation analysis was first conducted in AWARD-11 to estimate the weight-dependent and weight-independent effects of dulaglutide 4.5 mg vs. 1.5 mg, followed by an indirect comparison with the mediation result for dulaglutide 1.5 mg vs. placebo.

resultsBaseline characteristics were largely similar across the trials. In the mediation meta-analysis of placebo-controlled trials, the total treatment effect of dulaglutide 1.5 mg after placebo-adjustment on SBP was - 2.6 mmHg (95% CI - 3.8, - 1.5; p < 0.001) and was attributed to both a weight-dependent effect (- 0.9 mmHg; 95% CI: - 1.4, - 0.5; p < 0.001) and a weight-independent effect (- 1.5 mmHg; 95% CI: - 2.6, - 0.3; p = 0.01), accounting for 36% and 64% of the total effect, respectively. For pulse pressure, the total treatment effect of dulaglutide (- 2.5 mmHg; 95% CI: - 3.5, - 1.5; p < 0.001) was 14% weight-dependent and 86% weight-independent. For DBP there was limited impact of dulaglutide treatment, with only a small weight-mediated effect. Dulaglutide 4.5 mg demonstrated an effect on reduction in SBP and pulse pressure beyond that of dulaglutide 1.5 mg which was primarily weight mediated.

conclusionsDulaglutide 1.5 mg reduced SBP and pulse pressure in people with T2D across the placebo-controlled trials in the AWARD program. While up to one third of the effect of dulaglutide 1.5 mg on SBP and pulse pressure was due to weight reduction, the majority was independent of weight. A greater understanding of the pleotropic effects of GLP-1 RA that contribute to reduction in blood pressure could support developing future approaches for treating hypertension. Trial registrations (clinicaltrials.gov) NCT01064687, NCT00734474, NCT01769378, NCT02597049, NCT01149421, NCT03495102.

Indexed as

Diabetes Mellitus, Type 2Blood PressureGlucagon-Like Peptide 1Glucagon-Like PeptidesHumansHypoglycemic AgentsImmunoglobulin Fc FragmentsRecombinant Fusion ProteinsdulaglutideGlucagon-Like Peptide 1Glucagon-Like PeptidesHypoglycemic AgentsImmunoglobulin Fc FragmentsRecombinant Fusion ProteinsBlood pressureDiabetesDulaglutideGlucagon-like peptide-1HypertensionWeight

Identifiers

PMID36894938
PMCPMC9999488
OpenAlexW4323659716

What Socratic holds

Textmetadata
LicenceCC BY
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 Socratic graph.