Evidence map›Paper›PMID 40736377›Full record

ArticleCancer medicine2025

Use of Systemic Glucocorticoids and Risk of Prostate Adenocarcinoma: Evidence From a Danish Population-Based Case-Control Study.

Elea Olivier, Blánaid Hicks, Morten Olesen, Agnès Fournier, Gianluca Severi, Anton Pottegård, Manon Cairat

Abstract read
In one paragraph

Article in Cancer medicine, 2025. 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

7 authors.

Elea OlivierUniversité Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Villejuif, France.ORCID https://orcid.org/0000-0001-8065-5792
Blánaid HicksClinical Pharmacology and Pharmacy, Department of Public Health, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0002-5730-9469
Morten OlesenClinical Pharmacology and Pharmacy, Department of Public Health, University of Southern Denmark, Odense, Denmark.
Agnès FournierUniversité Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Villejuif, France.
Gianluca SeveriUniversité Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Villejuif, France.ORCID https://orcid.org/0000-0001-7157-419X
Anton PottegårdClinical Pharmacology and Pharmacy, Department of Public Health, University of Southern Denmark, Odense, Denmark.ORCID https://orcid.org/0000-0001-9314-5679
Manon CairatUniversité Paris-Saclay, UVSQ, Inserm, Gustave Roussy, CESP, Villejuif, France.

Funding

Doctoral funding from the University Paris-Saclay Doctoral School of Public Health EDSPLigue Contre le Cancer DOUBS - Montbéliard and JURA CommitteesUnion for International Cancer Control UICC Yamagiwa-Yoshida Memorial International Cancer
6 · The paper itself

Abstract

backgroundGlucocorticoids may promote prostate cancer by reducing apoptosis and the immune response, or prevent it by reducing inflammation, inhibiting androgens, and limiting cell proliferation. However, epidemiological evidence is limited. Thus, this study aimed to assess the association between systemic glucocorticoids and prostate cancer risk within the Danish registries.

methodsA nationwide case-control study was conducted using Danish healthcare registries. Men with a primary prostate adenocarcinoma diagnosis between 2001 and 2018 were identified as cases (n = 56,575). For each case, 10 controls were randomly selected from the general population, matched on age and calendar time. Exposure to systemic glucocorticoid was identified via the national prescription registry from 1995 onwards. Ever users of systemic glucocorticoids were defined as at least 2 filled prescriptions, and long-term use as filled prescriptions equivalent to ≥ 1000 defined daily doses (DDDs). Conditional logistic regressions were performed to calculate odds ratios (ORs) and 95% confidence intervals for the association between systemic glucocorticoid use and prostate cancer risk.

resultsTwelve percent of men had ever been exposed to systemic glucocorticoids. No association was observed between ever and long-term use of systemic glucocorticoids and prostate cancer risk [OR = 1.03 (1.00-1.06) and OR = 1.02 (0.92-1.14), respectively], compared with never use. However, an inverse association was observed with the highest use category (> 1500 DDDs) [OR = 0.86 (0.74-0.99)], though without evidence of a dose-response relationship [OR per 500 DDDs = 0.98 (0.95-1.01), p = 0.18]. Associations did not differ by prostate cancer stage.

conclusionThis large nationwide nested case-control study suggested no evidence of a higher risk of prostate adenocarcinoma associated with systemic glucocorticoid use.

Indexed as

AdenocarcinomaGlucocorticoidsProstatic NeoplasmsAdultAgedAged, 80 and overCase-Control StudiesDenmarkHumansMaleMiddle AgedRegistriesRisk FactorsGlucocorticoidsDanish registriesglucocorticoidspharmacoepidemiologyprostate cancer

Identifiers

PMID40736377
PMCPMC12308913

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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 OpenQuestion graph.