Evidence map›Paper›PMID 42711260›Full record

ArticleJNCI cancer spectrum2026

Genetic risk stratification of common diseases in breast cancer survivors: a population-based cohort study.

Annabelle Ashworth, Zhuqing Shi, Huy Tran, Jun Wei, Ashley J Mulford, Siqun Lilly Zheng, David Duggan, Brian T Helfand, Alan R Sanders, Tariq Azam and 5 more

Abstract read
In one paragraph

Article in JNCI cancer spectrum, 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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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

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

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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

15 authors.

Annabelle AshworthProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, United States.
Zhuqing ShiProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, United States.
Huy TranProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, United States.
Jun WeiProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, United States.
Ashley J MulfordGenomic Health Initiative, Endeavor Health, Evanston, IL, United States.
Siqun Lilly ZhengProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, United States.
David DugganTranslational Genomics Research Institute, Part of City of Hope, Phoenix, AZ, United States.
Brian T HelfandProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, United States.
Alan R SandersGenomic Health Initiative, Endeavor Health, Evanston, IL, United States.
Tariq AzamDepartment of Cardiology, Endeavor Health Cardiovascular Institute, Evanston, IL, United States.
Bruce BrocksteinKellogg Cancer Center, Endeavor Health, Evanston, IL, United States.
Allison DePersiaMark R. Neaman Center for Personalized Medicine, Endeavor Health, Evanston, IL, United States.
Poornima SahaKellogg Cancer Center, Endeavor Health, Evanston, IL, United States.
Jianfeng XuProgram for Genomic Translational Research, Endeavor Health, Evanston, IL, United States.ORCID 0000-0002-1343-8752
Ted A JamesKellogg Cancer Center, Endeavor Health, Evanston, IL, United States.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients diagnosed with breast cancer are at increased risk of multiple common diseases; however, the spectrum of these diseases and the contribution of inherited genetic susceptibility remain incompletely characterized.

methodsWe evaluated 15 common diseases and tested their associations with breast cancer exposure and disease-specific polygenic risk scores in the UK Biobank (n = 254 736). Analyses were performed using cause-specific Cox proportional hazards models within a full-cohort framework, with time-updated breast cancer status, delayed entry at study recruitment, and age as the underlying time scale.

resultsAfter recruitment, incident breast cancer was diagnosed in 11 386 women (4.47%), including 2742 (24.08%) with metastatic breast cancer. Patients with breast cancer had an increased risk of 9 diseases spanning cardiovascular, metabolic, and neuropsychiatric domains (P < .003, Bonferroni corrected). Elevated risks were generally observed among patients with both early-stage and advanced breast cancer. Inherited susceptibility further stratified disease risk, with the highest risks observed among patients with breast cancer and elevated disease-specific polygenic risk scores. For example, compared with women without breast cancer, the hazard ratio for osteoporosis was 2.33 (95% CI = 2.15 to 2.52) among women with any breast cancer, 2.38 (95% CI = 2.18 to 2.59) among women with nonmetastatic breast cancer, and 2.12 (95% CI = 1.78 to 2.54) among women with metastatic breast cancer; the hazard ratio was 4.48 (95% CI = 3.99 to 5.02) among patients with breast cancer in the highest quartile of osteoporosis-specific polygenic risk scores (all P < .001). In contrast, breast cancer was not statistically significantly associated with risk of coronary artery disease.

conclusionBreast cancer and inherited genetic susceptibility jointly contribute to increased risk of multiple common diseases, supporting the integration of genetic risk stratification into survivorship care.

Indexed as

Breast NeoplasmsCancer SurvivorsGenetic Predisposition to DiseaseAdultAgedCardiovascular DiseasesCohort StudiesFemaleGenetic Risk ScoreHumansMiddle AgedOsteoporosisProportional Hazards ModelsRisk AssessmentRisk FactorsUK Biobank

Identifiers

PMID42711260
PMCPMC13661004

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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.