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Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer

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...

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Autores principales: Glaser, Alexander, Shi, Zhuqing, Wei, Jun, Lanman, Nadia A., Ladson-Gary, Skylar, Vickman, Renee E., Franco, Omar E., Crawford, Susan E., Lilly Zheng, S., Hayward, Simon W., Isaacs, William B., Helfand, Brian T., Xu, Jianfeng
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638770/
https://www.ncbi.nlm.nih.gov/pubmed/36353071
http://dx.doi.org/10.1016/j.euros.2022.07.004
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author Glaser, Alexander
Shi, Zhuqing
Wei, Jun
Lanman, Nadia A.
Ladson-Gary, Skylar
Vickman, Renee E.
Franco, Omar E.
Crawford, Susan E.
Lilly Zheng, S.
Hayward, Simon W.
Isaacs, William B.
Helfand, Brian T.
Xu, Jianfeng
author_facet Glaser, Alexander
Shi, Zhuqing
Wei, Jun
Lanman, Nadia A.
Ladson-Gary, Skylar
Vickman, Renee E.
Franco, Omar E.
Crawford, Susan E.
Lilly Zheng, S.
Hayward, Simon W.
Isaacs, William B.
Helfand, Brian T.
Xu, Jianfeng
author_sort Glaser, Alexander
collection PubMed
description 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 (χ(2) = 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; χ(2) test). Furthermore, significant cross-disease GRS associations were also found; GRS(BPH) was significantly associated with PCa risk (odds ratio [OR] = 1.26 [1.18–1.36], p < 0.001), and GRS(PCa) was significantly associated with BPH risk (OR = 1.03 [1.02–1.04], p < 0.001). Moreover, GRS(BPH) 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.
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spelling pubmed-96387702022-11-08 Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer Glaser, Alexander Shi, Zhuqing Wei, Jun Lanman, Nadia A. Ladson-Gary, Skylar Vickman, Renee E. Franco, Omar E. Crawford, Susan E. Lilly Zheng, S. Hayward, Simon W. Isaacs, William B. Helfand, Brian T. Xu, Jianfeng Eur Urol Open Sci Benign Prostatic Hyperplasia 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 (χ(2) = 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; χ(2) test). Furthermore, significant cross-disease GRS associations were also found; GRS(BPH) was significantly associated with PCa risk (odds ratio [OR] = 1.26 [1.18–1.36], p < 0.001), and GRS(PCa) was significantly associated with BPH risk (OR = 1.03 [1.02–1.04], p < 0.001). Moreover, GRS(BPH) 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. Elsevier 2022-08-01 /pmc/articles/PMC9638770/ /pubmed/36353071 http://dx.doi.org/10.1016/j.euros.2022.07.004 Text en © 2022 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Benign Prostatic Hyperplasia
Glaser, Alexander
Shi, Zhuqing
Wei, Jun
Lanman, Nadia A.
Ladson-Gary, Skylar
Vickman, Renee E.
Franco, Omar E.
Crawford, Susan E.
Lilly Zheng, S.
Hayward, Simon W.
Isaacs, William B.
Helfand, Brian T.
Xu, Jianfeng
Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer
title Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer
title_full Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer
title_fullStr Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer
title_full_unstemmed Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer
title_short Shared Inherited Genetics of Benign Prostatic Hyperplasia and Prostate Cancer
title_sort shared inherited genetics of benign prostatic hyperplasia and prostate cancer
topic Benign Prostatic Hyperplasia
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9638770/
https://www.ncbi.nlm.nih.gov/pubmed/36353071
http://dx.doi.org/10.1016/j.euros.2022.07.004
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