Evidence map›Paper›PMID 35059918›Full record

ArticleCancer causes & control : CCC2022

Hormonal patterns in men with prediabetes and diabetes in NHANES III: possible links with prostate cancer.

Kerri Beckmann, Danielle Crawley, William G Nelson, Elizabeth A Platz, Elizabeth Selvin, Mieke Van Hemelrijck, Sabine Rohrmann

Abstract read
In one paragraph

Article in Cancer causes & control : CCC, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

3 citing papers in PubMed.

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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

7 authors.

Kerri BeckmannCancer Epidemiology and Population Health Research, University of South Australia, SAHMRI Building, North Terrace, Adelaide, SA, 5000, Australia. kerri.beckmann@unisa.edu.au.ORCID http://orcid.org/0000-0002-9798-1479
Danielle CrawleyTranslational Oncology and Urology Research, Kings College London, London, UK.
William G NelsonSydney Kimmel Comprehensive Cancer Centre, Johns Hopkins, Baltimore, MD, USA.
Elizabeth A PlatzSydney Kimmel Comprehensive Cancer Centre, Johns Hopkins, Baltimore, MD, USA.
Elizabeth SelvinDepartment of Epidemiology, Johns Hopkins Bloomsburg School of Public Health, Baltimore, MD, USA.
Mieke Van HemelrijckTranslational Oncology and Urology Research, Kings College London, London, UK.
Sabine RohrmannEpidemiology, Biostatistics and Prevention Institute, University of Zurich, Zurich, Switzerland.

Funding

Translational Research Central ServicesP30CA006973 · NCI · JOHNS HOPKINS UNIVERSITY · PI Rosalie Wollett · 1985 to 2026
$208.6M
National Health and Medical Research Council 1124210NCI NIH HHS P30 CA006973
6 · The paper itself

Abstract

purposePathways involving sex hormones and insulin-like growth factors (IGFs) have been proposed to explain, in part, the lower risk of prostate cancer among men with diabetes. To gain insights into potential biological mechanisms we explored differences in serum concentrations of sex hormones and IGFs across the trajectory from normoglycemia to prediabetes to poorly controlled diabetes.

methodsUsing cross-sectional data from the National Health and Nutrition Examination Survey III we examined differences in levels of circulating sex hormones, sex hormone-binding globulin (SHBG), IGF-1, and IFG-binding protein 3 (IGFBP-3), according to diabetes status: no diabetes [n = 648], prediabetes [n = 578], undiagnosed diabetes [n = 106], well-controlled diabetes [n = 42], and poorly controlled diabetes [n = 56]. Adjusted geometric mean concentrations were derived using multivariable linear regression, adjusted for age, race, and other lifestyle factors.

resultsTotal testosterone concentrations were lower among prediabetics (4.89 ng/mL, 95% confidence interval (CI) 4.95-5.21) than men without prediabetes/diabetes (5.29 ng/mL, 95% CI 5.06-5.53) but did not reduce further across diabetes groups. Concentrations of estradiol, estimated free testosterone, SHGB, IGF-1, and IGFBP-3 did not differ. While the ratio of IGF-1 to IGFBP-3 was lower among men with prediabetics and undiagnosed diabetes than men without prediabetes/diabetes, there was no trend across groups. A positive trend for the ratio of estradiol-to-testosterone levels was observed across groups (p trend = 0.045).

conclusionOur findings do not provide clear support for either an androgen driven or IGF-driven pathway for the inverse association between diabetes and prostate cancer risk.

Indexed as

Diabetes MellitusPrediabetic StateProstatic NeoplasmsCross-Sectional StudiesHumansInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor IMaleNutrition SurveysSex Hormone-Binding GlobulinTestosteroneInsulin-Like Growth Factor Binding Protein 3Insulin-Like Growth Factor ISex Hormone-Binding GlobulinTestosteroneC-peptideDiabetes mellitusInsulin growth factor-binding protein 3 (IGFBP-3)Insulin growth factor-I (IGF-I)Prostate cancerTestosterone, estradiol, and sex steroids

Identifiers

PMID35059918
PMCPMC9066414

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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.