Evidence map›Paper›PMID 41184627›Full record

ArticleBritish journal of cancer2026

Steroid hormone metabolites and mammographic breast density in premenopausal women.

Ghazaleh Pourali, Kayode A Matthew, Myung Sik Jeon, Chongliang Luo, Gary J Patti, Jingqin Luo, Adetunji T Toriola

Abstract read
In one paragraph

Article in British journal of cancer, 2026. 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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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

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5 · Who and what money

Authors and funding

7 authors.

Ghazaleh Pourali *Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0001-8981-0947
Kayode A Matthew *Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.
Myung Sik JeonDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.
Chongliang LuoDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.
Gary J PattiDepartments of Chemistry, Genetics, and Medicine, Siteman Cancer Center, Center for Mass Spectrometry and Metabolic Tracing, Washington University School of Medicine, St. Louis, MO, USA.
Jingqin LuoDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.ORCID http://orcid.org/0000-0003-2759-3072
Adetunji T ToriolaDivision of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA. a.toriola@wustl.edu.ORCID http://orcid.org/0000-0003-1079-2606

Funding

Metabolite Profiles and Mammographic Density in Premenopausal WomenR01CA246592 · NCI · WASHINGTON UNIVERSITY · PI TORIOLA, ADETUNJI T · 2020 to 2024
$1.8M
NCI NIH HHS R01 CA246592U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01CA246592
6 · The paper itself

Abstract

backgroundSteroid hormones influence breast morphology and cellular proliferation and are associated with breast carcinogenesis. However, their associations with mammographic breast density (MBD) are less studied, particularly in premenopausal women. We, therefore, investigated the associations of steroid hormone metabolites with MBD in premenopausal women.

methodsOur study included 700 premenopausal women scheduled for screening mammograms. We analyzed 54 steroid hormone metabolites (Metabolon®) and assessed volumetric measures of MBD including volumetric percent density (VPD), dense volume (DV), and non-dense volume (NDV) using Volpara. We investigated associations using linear regression modeling to estimate the covariate-adjusted means of VPD, NDV, and DV, corresponding to each steroid hormone metabolite tertile and on a continuous scale. Models were adjusted for age, body fat percentage, age at menarche, race, alcohol consumption, family history of breast cancer, oral contraceptive use, body shape at age 10, and parity/age at first birth. We applied false discovery rate (FDR) to control multiple testing and determined significance at FDR-adjusted p-value ≤ 0.05.

resultsOne corticosteroid (cortolone glucuronide (1)) and four androgenic steroid metabolites (androstenediol (3beta,17beta) monosulfate (2), androstenediol (3beta,17beta) disulfate (1), 5alpha-androstan-3alpha,17beta-diol monosulfate (2), and 5alpha-androstan-3alpha,17beta-diol disulfate) were inversely associated with VPD. For instance, VPD was lower monotonically across tertiles (T) of cortolone glucuronide (1) (T1 = 8.9%, T2 = 8.3%, and T3 = 7.3%; p-trend=7.55 × 10

conclusionWe identified novel inverse associations of cortolone glucuronide (1) and four androgenic steroid metabolites with VPD, underscoring the importance of steroid hormone metabolites in MBD and the potential for modulating these in reducing MBD.

Indexed as

BreastBreast DensityBreast NeoplasmsPremenopauseAdultFemaleHumansMammographyMiddle Aged

Identifiers

PMID41184627
PMCPMC12820243

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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.