» Articles » PMID: 23021708

A 2-stage Genome-wide Association Study to Identify Single Nucleotide Polymorphisms Associated with Development of Erectile Dysfunction Following Radiation Therapy for Prostate Cancer

Abstract

Purpose: To identify single nucleotide polymorphisms (SNPs) associated with development of erectile dysfunction (ED) among prostate cancer patients treated with radiation therapy.

Methods And Materials: A 2-stage genome-wide association study was performed. Patients were split randomly into a stage I discovery cohort (132 cases, 103 controls) and a stage II replication cohort (128 cases, 102 controls). The discovery cohort was genotyped using Affymetrix 6.0 genome-wide arrays. The 940 top ranking SNPs selected from the discovery cohort were genotyped in the replication cohort using Illumina iSelect custom SNP arrays.

Results: Twelve SNPs identified in the discovery cohort and validated in the replication cohort were associated with development of ED following radiation therapy (Fisher combined P values 2.1×10(-5) to 6.2×10(-4)). Notably, these 12 SNPs lie in or near genes involved in erectile function or other normal cellular functions (adhesion and signaling) rather than DNA damage repair. In a multivariable model including nongenetic risk factors, the odds ratios for these SNPs ranged from 1.6 to 5.6 in the pooled cohort. There was a striking relationship between the cumulative number of SNP risk alleles an individual possessed and ED status (Sommers' D P value=1.7×10(-29)). A 1-allele increase in cumulative SNP score increased the odds for developing ED by a factor of 2.2 (P value=2.1×10(-19)). The cumulative SNP score model had a sensitivity of 84% and specificity of 75% for prediction of developing ED at the radiation therapy planning stage.

Conclusions: This genome-wide association study identified a set of SNPs that are associated with development of ED following radiation therapy. These candidate genetic predictors warrant more definitive validation in an independent cohort.

Citing Articles

Towards Personalized Radiotherapy in Pelvic Cancer: Patient-Related Risk Factors for Late Radiation Toxicity.

Nuijens A, Oei A, Franken N, Rasch C, Stalpers L Curr Oncol. 2025; 32(1).

PMID: 39851963 PMC: 11763857. DOI: 10.3390/curroncol32010047.


Clinical and Preclinical Outcomes of Combining Targeted Therapy With Radiotherapy.

Elbanna M, Chowdhury N, Rhome R, Fishel M Front Oncol. 2021; 11:749496.

PMID: 34733787 PMC: 8558533. DOI: 10.3389/fonc.2021.749496.


Low dose ionizing radiation effects on the immune system.

Lumniczky K, Impens N, Armengol G, Candeias S, Georgakilas A, Hornhardt S Environ Int. 2020; 149:106212.

PMID: 33293042 PMC: 8784945. DOI: 10.1016/j.envint.2020.106212.


Harnessing genome-wide association studies to minimize adverse radiation-induced side effects.

Benitez C, Knox S Radiat Oncol J. 2020; 38(4):226-235.

PMID: 33233031 PMC: 7785837. DOI: 10.3857/roj.2020.00556.


Genetically-regulated transcriptomics & copy number variation of proctitis points to altered mitochondrial and DNA repair mechanisms in individuals of European ancestry.

Pathak G, Polimanti R, Silzer T, Wendt F, Chakraborty R, Phillips N BMC Cancer. 2020; 20(1):954.

PMID: 33008348 PMC: 7530964. DOI: 10.1186/s12885-020-07457-1.


References
1.
Merrick G, Butler W, Wallner K, Galbreath R, Anderson R, Kurko B . Erectile function after prostate brachytherapy. Int J Radiat Oncol Biol Phys. 2005; 62(2):437-47. DOI: 10.1016/j.ijrobp.2004.10.001. View

2.
Witte S, Villalba M, Bi K, Liu Y, Isakov N, Altman A . Inhibition of the c-Jun N-terminal kinase/AP-1 and NF-kappaB pathways by PICOT, a novel protein kinase C-interacting protein with a thioredoxin homology domain. J Biol Chem. 2000; 275(3):1902-9. DOI: 10.1074/jbc.275.3.1902. View

3.
Grimm P, Billiet I, Bostwick D, Dicker A, Frank S, Immerzeel J . Comparative analysis of prostate-specific antigen free survival outcomes for patients with low, intermediate and high risk prostate cancer treatment by radical therapy. Results from the Prostate Cancer Results Study Group. BJU Int. 2012; 109 Suppl 1:22-9. DOI: 10.1111/j.1464-410X.2011.10827.x. View

4.
Stock R, Stone N, Cesaretti J, Rosenstein B . Biologically effective dose values for prostate brachytherapy: effects on PSA failure and posttreatment biopsy results. Int J Radiat Oncol Biol Phys. 2005; 64(2):527-33. DOI: 10.1016/j.ijrobp.2005.07.981. View

5.
Zagar T, Stock R, Cesaretti J, Stone N . Assessment of postbrachytherapy sexual function: a comparison of the IIEF-5 and the MSEFS. Brachytherapy. 2007; 6(1):26-33. DOI: 10.1016/j.brachy.2006.11.003. View