Evidence map›Paper›PMID 36801984›Full record

ArticleDiabetes care2023

Effects of Semaglutide on Albuminuria and Kidney Function in People With Overweight or Obesity With or Without Type 2 Diabetes: Exploratory Analysis From the STEP 1, 2, and 3 Trials.

Hiddo J L Heerspink, Ellen Apperloo, Melanie Davies, Dror Dicker, Kristian Kandler, Julio Rosenstock, Rasmus Sørrig, Jack Lawson, Niels Zeuthen, David Cherney

3 registry-linked trialsOpen access · bronzeAbstract read
In one paragraph

Article in Diabetes care, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It reports registered trial NCT03548935. Cited by 48 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
48citing papers in PubMed, 3 pooled it
17.5field-weighted citation impact, top 1% 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.

NCT03548935 phase3completed

Effect and Safety of Semaglutide 2.4 mg Once-weekly in Subjects With Overweight or Obesity

Ran2018Enrolled1,961Registered outcomes42Posted comparisons4ConditionsMetabolism and Nutrition Disorder, Overweight or ObesityArmsPlacebo (semaglutide), semaglutide
PMID 33567185PMID 32441473other papers from this trial
Open the trial in the graph
NCT03552757 phase3completed

Effect and Safety of Semaglutide 2.4 mg Once-weekly in Subjects With Overweight or Obesity and Type 2 Diabetes

Ran2018Enrolled1,210Registered outcomes41Posted comparisons4ConditionsObesity, OverweightArmsPlacebo II (Semaglutide), Placebo I (Semaglutide), Semaglutide 1.0 mg, Semaglutide 2.4 mg
PMID 33667417PMID 32441473other papers from this trial
Open the trial in the graph
NCT03611582 phase3completed

Effect and Safety of Semaglutide 2.4 mg Once-weekly as Adjunct to Intensive Behavioural Therapy in Subjects With Overweight or Obesity

Ran2018Enrolled611Registered outcomes31Posted comparisons4ConditionsObesity, OverweightArmsPlacebo (semaglutide), semaglutide
PMID 33625476PMID 32441473other papers from this trial
Open the trial in the graph
3 · Its place in the literature

Who cites it

48 citing papers in PubMed, 3 syntheses or guidelines pooled it, 87 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. Effects of Semaglutide on Body Composition and GFR: A Prespecified Analysis of the SMART Trial.Clinical journal of the American Society of Nephrology : CJASN · 2026
    Trial
  5. Trial
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  8. GLP-1 receptor agonists-a potential therapy for chronic kidney disease?Clinical science (London, England : 1979) · 2026
    Review
  9. Article
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  12. Review
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  14. The Ethics of Ozempic and Wegovy.Journal of medical ethics · 2026
    Article
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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

10 authors at 6 institutions in 6 countries.

Hiddo J L HeerspinkDepartment of Clinical Pharmacy and Pharmacology, University of Groningen, Groningen, the Netherlands.ORCID 0000-0002-3126-3730
Ellen ApperlooDepartment of Clinical Pharmacy and Pharmacology, University of Groningen, Groningen, the Netherlands.
Melanie DaviesDiabetes Research Centre, University of Leicester, Leicester, U.K.
Dror DickerInternal Medicine D, Hasharon Hospital-Rabin Medical Center, Petach-Tikva, Israel.ORCID 0000-0001-8546-6245
Kristian KandlerMedical & Science, Novo Nordisk A/S, Søborg, Denmark.
Julio RosenstockVelocity Clinical Research at Medical City, Dallas, TX.ORCID 0000-0001-8324-3275
Rasmus SørrigGlobal Medical Affairs, Novo Nordisk A/S, Søborg, Denmark.
Jack LawsonGlobal Medical Affairs, Novo Nordisk A/S, Søborg, Denmark.
Niels ZeuthenBiostatistics Obesity & Metabolism, Novo Nordisk A/S, Søborg, Denmark.
David CherneyDivision of Nephrology, Department of Medicine, University Health Network and University of Toronto, Toronto, Ontario, Canada.ORCID 0000-0003-4164-0429
Novo Nordisk (Denmark) · DKUniversity of Groningen · NLTel Aviv University · ILUniversity Health Network · CAUniversity of Leicester · GBVelocity Clinical Research (United States) · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveThese post hoc analyses of the Semaglutide Treatment Effect in People with obesity (STEP) 1-3 trials (NCT03548935, NCT03552757, and NCT03611582) explored the effects of semaglutide (up to 2.4 mg) on kidney function. RESEARCH DESIGN AND

methodsSTEP 1-3 included adults with overweight/obesity; STEP 2 patients also had type 2 diabetes. Participants received once-weekly subcutaneous semaglutide 1.0 mg (STEP 2 only), 2.4 mg, or placebo for 68 weeks, plus lifestyle intervention (STEP 1 and 2) or intensive behavioral therapy (STEP 3). Changes in urine albumin-to-creatinine ratio (UACR) and UACR status from baseline to week 68 were assessed for STEP 2. Changes in estimated glomerular filtration rate (eGFR) were assessed from pooled STEP 1-3 data.

resultsIn STEP 2, 1,205 (99.6% total cohort) patients had UACR data; geometric mean baseline UACR was 13.7, 12.5, and 13.2 mg/g with semaglutide 1.0 mg, 2.4 mg, and placebo, respectively. At week 68, UACR changes were -14.8% and -20.6% with semaglutide 1.0 mg and 2.4 mg, respectively, and +18.3% with placebo (between-group differences [95% CI] vs. placebo: -28.0% [-37.3, -17.3], P < 0.0001 for semaglutide 1.0 mg; -32.9% [-41.6, -23.0], P = 0.003 for semaglutide 2.4 mg). UACR status improved in greater proportions of patients with semaglutide 1.0 mg and 2.4 mg versus placebo (P = 0.0004 and P = 0.0014, respectively). In the pooled STEP 1-3 analyses, 3,379 participants had eGFR data; there was no difference between semaglutide 2.4 mg and placebo in eGFR trajectories at week 68.

conclusionsSemaglutide improved UACR in adults with overweight/obesity and type 2 diabetes. In participants with normal kidney function, semaglutide did not have an effect on eGFR decline.

Indexed as

Diabetes Mellitus, Type 2AdultAlbuminuriaGlomerular Filtration RateHumansKidneyObesityOverweightSemaglutideTreatment OutcomeSemaglutide

Identifiers

PMID36801984
PMCPMC10090901
OpenAlexW4321182840

What OpenQuestion holds

Texttitle and abstract
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 OpenQuestion graph.