Evidence map›Paper›PMID 39180769›Full record

ArticleInternational journal of epidemiology2024

Disentangling discordant vitamin D associations with prostate cancer incidence and fatality in a large, nested case-control study.

Lola Etiévant, Mitchell H Gail, Demetrius Albanes

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Article in International journal of epidemiology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

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2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Lola EtiévantDivision of Cancer Epidemiology and Genetics, Biostatistics Branch, National Cancer Institute, Rockville, MD, USA.
Mitchell H GailDivision of Cancer Epidemiology and Genetics, Biostatistics Branch, National Cancer Institute, Rockville, MD, USA.ORCID 0000-0002-3919-3263
Demetrius AlbanesDivision of Cancer Epidemiology and Genetics, Metabolic Epidemiology Branch, National Cancer Institute, Rockville, MD, USA.

Funding

National Institutes of Health, USANCI NIH HHS
6 · The paper itself

Abstract

backgroundPublished analyses of prostate cancer nested case-control and survival data in the Alpha-Tocopherol, Beta-Carotene Cancer Prevention (ATBC) Study cohort suggested that men with higher baseline vitamin D [25(OH)D] concentrations have both (i) increased prostate cancer risk and (ii) decreased prostate cancer-specific fatality.

methodsTo investigate possible factors responsible for a spurious association with prostate cancer fatality, we reanalysed baseline serum vitamin D associations with prostate cancer risk and prostate cancer-specific fatality in case-control data nested within the ATBC Study (1000 controls and 1000 incident prostate cancer cases). Conditional logistic regression and Cox proportion hazard models were used, respectively, to estimate odds ratios for risk and hazard ratios for prostate cancer-specific fatality, overall and by disease aggressiveness. We replicated these case-control analyses using baseline serum measurements of alpha-tocopherol (vitamin E), beta-carotene and retinol (vitamin A), and used the entire ATBC Study cohort (n = 29 085) to estimate marginal associations between these baseline vitamins and prostate cancer incidence and fatality following blood collection.

resultsVitamin D analyses agreed closely with those originally published, with opposite risk and fatality associations. By contrast, the analyses of alpha-tocopherol, beta-carotene and retinol yielded concordant associations for prostate cancer incidence and prostate cancer-specific fatality.

conclusionsWe found evidence of neither artefacts in the nested prostate cancer case-control data set nor detection or collider biases in the fatality analyses. The present findings therefore support a valid inverse (i.e. beneficial) association between vitamin D and prostate cancer-specific survival that warrants further evaluation, including possibly in controlled trials.

Indexed as

alpha-Tocopherolbeta CaroteneProstatic NeoplasmsVitamin DAgedCase-Control StudiesHumansIncidenceMaleMiddle AgedProportional Hazards ModelsRisk FactorsVitamin Aalpha-Tocopherolbeta CaroteneVitamin AVitamin DATBC Studybeta-carotenecollider biasprospective cohortprostate cancer fatalityprostate cancer riskrandomized–controlled trialvitamin Avitamin Dvitamin E

Identifiers

PMID39180769
PMCPMC12102485

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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.