Evidence map›Paper›PMID 41573197›Full record

ArticleFrontiers in endocrinology2025

Diabetes and tumor risk: a 23-year Danish national cohort study.

Katja F Skovbjerg, Julie C Antvorskov, Lonny M Stokholm, Tine D Bille, Nis Andersen, Jens Andresen, Toke Bek, Javad Hajar, Ryo Kawasaki, Caroline S Laugesen and 7 more

Abstract read
In one paragraph

Article in Frontiers in endocrinology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

17 authors.

Katja F Skovbjerg *Department of Clinical Research, Steno Diabetes Center Copenhagen, Herlev, Denmark.
Julie C Antvorskov *Department of Clinical Research, Steno Diabetes Center Copenhagen, Herlev, Denmark.
Lonny M StokholmDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Tine D BilleDepartment of Clinical Research, Steno Diabetes Center Copenhagen, Herlev, Denmark.
Nis AndersenOrganization of Danish Practicing Ophthalmologists, Copenhagen, Denmark.
Jens AndresenOrganization of Danish Practicing Ophthalmologists, Copenhagen, Denmark.
Toke BekDepartment of Ophthalmology, Aarhus University Hospital, Aarhus, Denmark.
Javad HajarDepartment of Ophthalmology, Rigshospitalet Glostrup, Glostrup, Denmark.
Ryo KawasakiDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Caroline S LaugesenDepartment of Ophthalmology, Zealand University Hospital Roskilde, Roskilde, Denmark.
Sören MöllerDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Frederik N PedersenDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Katja C SchielkeDepartment of Ophthalmology, Aalborg University Hospital, Aalborg, Denmark.
Anne S Thykjær PetersenDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Flemming PociotDepartment of Clinical Research, Steno Diabetes Center Copenhagen, Herlev, Denmark.
Jakob GrauslundDepartment of Clinical Research, University of Southern Denmark, Odense, Denmark.
Steffen HeegaardDepartment of Pathology, Rigshospitalet, Copenhagen, Denmark.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Diabetes mellitus is a recognized risk factor for cancer, yet the relationship between diabetes type and tumor risk remains unclear. This study aimed to estimate the overall tumor burden, including benign, premalignant, and malignant tumors, in individuals with type 1 and type 2 diabetes. Methods: In this nationwide cohort study spanning 23 years (1999-2022), data on diabetes diagnosis, tumor development, and potential confounding variables were retrieved from multiple Danish national health registries. The cohort included more than 6.5 million individuals and 128,647 tumor events among individuals with diabetes. Crude and adjusted hazard ratios (HRs) were estimated using Cox regression. Results: For individuals with type 1 diabetes, adjusted HRs indicated no association for overall tumor development compared to individuals without diabetes. For individuals with type 2 diabetes, adjusted HRs suggested a slightly decreased hazard for overall tumor development compared to individuals without diabetes. When excluding tumors in the skin, the association between type 1 and type 2 diabetes and overall tumor development, suggested an increased hazard compared with individuals without diabetes. Our exploratory sub-analyses were stratified by tumor topography based on Systematized Nomenclature of Medicine (SNOMED) codes. Among individuals with type 1 diabetes, eight of 28 tumor groups showed reduced hazard, including the pancreas, bile ducts, and kidney. For type 2 diabetes, one group showed reduced hazard, while 22 groups, including the heart, blood vessels, and liver, showed increased hazard. Estimates from exploratory analyses should be interpreted with caution. Discussion: Our findings provide population-level evidence that advances our understanding of the possible complex metabolic links between diabetes and tumor development. Further exploration of SNOMED-based tumor classifications in future studies may provide valuable knowledge on pathological differences and refine future tumor and cancer surveillance strategies in individuals with diabetes.

Indexed as

Diabetes Mellitus, Type 1Diabetes Mellitus, Type 2NeoplasmsAdolescentAdultAgedCohort StudiesDenmarkFemaleHumansMaleMiddle AgedRegistriesRisk FactorsYoung Adultcancerdiabetesdiabetes mellitusneoplasmpathologyT1DMT2DMtumor

Identifiers

PMID41573197
PMCPMC12819280

What Socratic holds

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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.