Evidence map›Paper›PMID 41800807›Full record

ArticleEndocrine connections2026

Projected life-year gains with semaglutide in individuals with cardiovascular disease without type 2 diabetes in the UK.

Thomas Van Sloten, Steven H J Hageman, Jan Westerink, Silvia Capucci, João Diogo da Rocha Fernandes, Sara Holloway, Andrew Pijper, Natalie Tikhonovsky, Scott Emerson, A Michael Lincoff and 2 more

Abstract read
In one paragraph

Article in Endocrine connections, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Thomas Van SlotenDepartment of Vascular Medicine, Diabetology and Endocrinology, University Medical Center Utrecht, Utrecht, Netherlands.
Steven H J HagemanDepartment of Vascular Medicine, Diabetology and Endocrinology, University Medical Center Utrecht, Utrecht, Netherlands.
Jan WesterinkDepartment of Vascular Medicine, Diabetology and Endocrinology, University Medical Center Utrecht, Utrecht, Netherlands.
Silvia CapucciNovo Nordisk A/S, Søborg, Denmark.
João Diogo da Rocha FernandesNovo Nordisk A/S, Søborg, Denmark.
Sara HollowayLane Clark & Peacock LLP, London, UK.
Andrew PijperLane Clark & Peacock LLP, London, UK.
Natalie TikhonovskyLane Clark & Peacock LLP, London, UK.
Scott EmersonDepartment of Biostatistics, University of Washington, Seattle, Washington, USA.
A Michael LincoffDepartment of Cardiovascular Medicine, Cleveland Clinic, Cleveland Clinic Lerner College of Medicine, Case Western Reserve University, Cleveland, Ohio, USA.
Jorge PlutzkyDivision of Cardiovascular Medicine, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts, USA.
Ildiko LingvayDivision of Endocrinology, Department of Internal Medicine, University of Texas Southwestern Medical Center, Dallas, Texas, USA.ORCID https://orcid.org/0000-0001-7006-7401

Funding

UT Southwestern NORCP30DK127984 · NIDDK · UT SOUTHWESTERN MEDICAL CENTER · PI Jeffrey M Zigman · 2022 to 2026
$7.4M
NIDDK NIH HHS P30 DK127984
6 · The paper itself

Abstract

In the SELECT cardiovascular (CV) outcomes trial, semaglutide 2.4 mg significantly reduced all-cause mortality or non-fatal CV events versus placebo in patients with CV disease (CVD) and overweight/obesity, but without type 2 diabetes (T2D). By applying results from SELECT to a UK real-world population, this present cohort study evaluated the impact of semaglutide on life expectancy and CV event-free life-years. Included were individuals from the Discover electronic health record database who met SELECT eligibility criteria (≥45 years old; body mass index: ≥27 kg/m2; established CVD; no T2D). The Discover database comprises linked primary and secondary care data covering people residing in North West London, UK. Cohort entry was the first date between 2004 and 2019 when all inclusion criteria were met. Effect estimates from SELECT were applied using actuarial life tables, estimating the effect of semaglutide on life expectancy overall and by age group. Life expectancy gains and CV event-free life expectancy were estimated using the Arriaga and Sullivan methods, respectively. In total, 19,117 individuals aged ≥45 years were included in the main analysis (63% men; mean age: 65.4 years). The estimated gain in life expectancy with semaglutide treatment was 1.9 years. A CV event-free life-year gain of 2.0 years was predicted with semaglutide. Life-year gains were observed across all age groups but were higher for younger age groups. Based on SELECT data, semaglutide is predicted to increase life expectancy and CV event-free life-years in a real-world population with overweight/obesity and CVD, particularly in younger people.

Indexed as

cardiovascular diseaseglucagon-like peptide-1 receptor agonistoverweight/obesitySELECTsemaglutide

Identifiers

PMID41800807
PMCPMC13034523

What Socratic holds

Textmetadata
LicenceCC BY
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Registered trials

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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 Socratic graph.