Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer.

dc.contributor.author

Glaser, Alexander

dc.contributor.author

Shi, Zhuqing

dc.contributor.author

Wei, Jun

dc.contributor.author

Lanman, Nadia A

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Ladson-Gary, Skylar

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Vickman, Renee E

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Franco, Omar E

dc.contributor.author

Crawford, Susan E

dc.contributor.author

Lilly Zheng, S

dc.contributor.author

Hayward, Simon W

dc.contributor.author

Isaacs, William B

dc.contributor.author

Helfand, Brian T

dc.contributor.author

Xu, Jianfeng

dc.date.accessioned

2023-05-03T19:32:09Z

dc.date.available

2023-05-03T19:32:09Z

dc.date.issued

2022-09

dc.date.updated

2023-05-03T19:32:08Z

dc.description.abstract

Background

The association between benign prostatic hyperplasia (BPH) and prostate cancer (PCa) remains controversial, largely due to a detection bias in traditional observational studies.

Objective

To assess the association between BPH and PCa using inherited single nucleotide polymorphisms (SNPs).

Design setting and participants

The participants were White men from the population-based UK Biobank (UKB).

Outcome measurements and statistical analysis

The association between BPH and PCa was tested for (1) phenotypic correlation using chi-square, (2) genetic correlation (r g) based on genome-wide SNPs using linkage disequilibrium score regression, and (3) cross-disease genetic associations based on known risk-associated SNPs (15 for BPH and 239 for PCa), individually and cumulatively using genetic risk score (GRS).

Results and limitations

Among 214 717 White men in the UKB, 24 623 (11%) and 14 311 (6.7%) had a diagnosis of BPH and PCa, respectively. Diagnoses of these two diseases were significantly correlated (χ2 = 1862.80, p < 0.001). A significant genetic correlation was found (r g = 0.16; 95% confidence interval 0.03-0.28, p = 0.01). In addition, significant cross-disease genetic associations for established risk-associated SNPs were also found. Among the 250 established genome-wide association study-significant SNPs of PCa or BPH, 49 were significantly associated with the risk of the other disease at p < 0.05, significantly more than expected by chance (N = 12, p < 0.001; χ2 test). Furthermore, significant cross-disease GRS associations were also found; GRSBPH was significantly associated with PCa risk (odds ratio [OR] = 1.26 [1.18-1.36], p < 0.001), and GRSPCa was significantly associated with BPH risk (OR = 1.03 [1.02-1.04], p < 0.001). Moreover, GRSBPH was significantly and inversely associated with lethal PCa risk in a PCa case-case analysis (OR = 0.58 [0.41-0.81], p = 0.002). Only White men were studied.

Conclusions

BPH and PCa share common inherited genetics, which suggests that the phenotypic association of these two diseases in observational studies is not entirely caused by the detection bias.

Patient summary

For the first time, we found that benign prostatic hyperplasia and prostate cancer are genetically related. This finding may have implications in disease etiology and risk stratification.
dc.identifier

S2666-1683(22)00736-4

dc.identifier.issn

2666-1691

dc.identifier.issn

2666-1683

dc.identifier.uri

https://hdl.handle.net/10161/27333

dc.language

eng

dc.publisher

Elsevier BV

dc.relation.ispartof

European urology open science

dc.relation.isversionof

10.1016/j.euros.2022.07.004

dc.subject

Benign prostatic hyperplasia

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Genetic correlation

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Genetic risk score

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Heritability

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Lethal

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Prostate cancer

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Single nucleotide polymorphisms

dc.title

Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer.

dc.type

Journal article

pubs.begin-page

54

pubs.end-page

61

pubs.organisational-group

Duke

pubs.organisational-group

School of Medicine

pubs.organisational-group

Clinical Science Departments

pubs.organisational-group

Pathology

pubs.publication-status

Published

pubs.volume

43

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