Evidence map›Paper›PMID 41732754›Full record

ArticleKidney international reports2026

Dulaglutide Effect on Proteins Associated With CKD Progression.

Brandon E McFarlin, Sok Cin Tye, Eiichiro Satake, Zaipul I Md Dom, Afton Kechter, Jonathan M Wilson, Andrzej S Krolewski, Kevin L Duffin

Abstract read
In one paragraph

Article in Kidney international reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
–field-weighted citation impact
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

1 citing paper in PubMed.

  1. Article
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.

Brandon E McFarlinDiabetes, Obesity, and Complications Research Division, Eli Lilly and Company, Indianapolis, Indiana, USA.
Sok Cin TyeResearch Division, Joslin Diabetes Center, Boston, Massachusetts, USA.
Eiichiro SatakeResearch Division, Joslin Diabetes Center, Boston, Massachusetts, USA.
Zaipul I Md DomResearch Division, Joslin Diabetes Center, Boston, Massachusetts, USA.
Afton KechterDiabetes, Obesity, and Complications Research Division, Eli Lilly and Company, Indianapolis, Indiana, USA.
Jonathan M WilsonDiabetes, Obesity, and Complications Research Division, Eli Lilly and Company, Indianapolis, Indiana, USA.
Andrzej S KrolewskiResearch Division, Joslin Diabetes Center, Boston, Massachusetts, USA.
Kevin L DuffinDiabetes, Obesity, and Complications Research Division, Eli Lilly and Company, Indianapolis, Indiana, USA.

Funding

SPECIAL ASSAY COREP30DK036836 · NIDDK · JOSLIN DIABETES CENTER · PI JEAN E. SCHAFFER · 1986 to 2026
$50.5M
NIDDK NIH HHS P30 DK036836
6 · The paper itself

Abstract

Introduction: In the AWARD-7 clinical trial participants with type 2 diabetes mellitus (T2D) and moderate-to-severe chronic kidney disease (CKD), a once-weekly treatment with dulaglutide slowed kidney function decline compared with insulin glargine. This Methods: Plasma concentrations of JKP proteins in participants treated with dulaglutide ( Results: Baseline JKP protein concentrations were similar between groups. After 6 months, 14 JKP proteins increased in the insulin glargine group and decreased in the dulaglutide group with statistically significant between-group differences. The most significant differences were observed for 8 tumor necrosis factor (TNF)-receptors (TNF-R1, -R2, -R3, -R4, -R6B, -R7, -R19L, and -R27), key mediators of inflammatory and apoptotic pathways. In addition, CD160, WFDC2, DLL1, LAYN, SYND1, and EPHA2 were significantly different between treatments, although to a lesser degree, and 7 other proteins remained unaffected. Kidney injury molecule 1 (KIM1), a marker of proximal tubule stress, declined in both groups without significant differences. Treatment effects were more pronounced in participants with lower baseline estimated glomerular filtration rate or higher baseline urinary albumin-to-creatinine ratio, hemoglobin A1c, or body mass index. Conclusion: Six months of dulaglutide treatment significantly lowered concentrations of 14 JKP proteins, particularly those involved in inflammatory and fibrotic pathways. These findings provide insight into biological mechanisms that may underlie the reno-protective effects of dulaglutide.

Indexed as

biomarkerschronic kidney diseasediabetesdulaglutideglucagon-like peptide-1 (GLP-1) receptor agonists

Identifiers

PMID41732754
PMCPMC12925400

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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.