Allostatic load and risk of prostate cancer in UK Biobank

Allostatic load (AL), a biomarker of chronic stress, has been implicated in the carcinogenesis of various types of cancers. However, its role in the etiology of prostate cancer is unclear. Utilizing valuable resources from the UK Biobank, we analyzed the association between AL and subsequent risk of prostate cancer in a total of 161,964 men. Levels of AL were higher in cases than in non-cancer controls (3.47 vs. 3.35, P < 0.001). In the univariate analysis, one unit increase in AL was associated with a 5% increased risk of prostate cancer (hazard ratio (HR) = 1.05, 95% Confidence Interval (CI) 1.03, 1.06). In the multivariate Cox regression analysis, the significant association was only observed among men younger than 58 years old. The significant association was further confirmed in the categorical analysis, and compared to men with AL of 0, those with AL of 1, 2, 3, 4, 5, and ≥ 6 had a statistically significantly increased risk of prostate cancer, respectively. Additionally, we observed a more than additive joint effect between AL and polygenic risk score (PRS) of prostate cancer among younger men (< 58 years old). In summary, those findings have shown that higher AL was associated with an increased prostate cancer risk in younger men.

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Publication Details

Journal
Scientific Reports
Published
2025-10-27
DOI
https://doi.org/10.1038/s41598-025-21510-8
Citations
1
Primary Topic
Sex and Gender in Healthcare
Type
article
Field-Weighted Citation Impact
1.88

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article

Allostatic load and risk of prostate cancer in UK Biobank

Bernard F. Fuemmeler, Lisa S. Shock, Hua Zhao, Yufan Guan et al.
1 citations
Scientific Reports
Sex and Gender in Healthcare
1.88
article

Allostatic load and risk of prostate cancer in UK Biobank

Bernard F. Fuemmeler, Lisa S. Shock, Hua Zhao, Yufan Guan, Jie Shen
article en
1 citations

Abstract

Allostatic load (AL), a biomarker of chronic stress, has been implicated in the carcinogenesis of various types of cancers. However, its role in the etiology of prostate cancer is unclear. Utilizing valuable resources from the UK Biobank, we analyzed the association between AL and subsequent risk of prostate cancer in a total of 161,964 men. Levels of AL were higher in cases than in non-cancer controls (3.47 vs. 3.35, P < 0.001). In the univariate analysis, one unit increase in AL was associated with a 5% increased risk of prostate cancer (hazard ratio (HR) = 1.05, 95% Confidence Interval (CI) 1.03, 1.06). In the multivariate Cox regression analysis, the significant association was only observed among men younger than 58 years old. The significant association was further confirmed in the categorical analysis, and compared to men with AL of 0, those with AL of 1, 2, 3, 4, 5, and ≥ 6 had a statistically significantly increased risk of prostate cancer, respectively. Additionally, we observed a more than additive joint effect between AL and polygenic risk score (PRS) of prostate cancer among younger men (< 58 years old). In summary, those findings have shown that higher AL was associated with an increased prostate cancer risk in younger men.

Scientific ReportsVol. 15(1)
Virginia Commonwealth University (US), University of Virginia (US)
Virginia Commonwealth University
Openalex Percentile: Top 11%
Sex and Gender in Healthcare
1.88
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