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Pleiotropy and pathway analyses of genetic variants associated with both type 2 diabetes and prostate cancer.

Authors :
Raynor LA
Pankow JS
Rasmussen-Torvik LJ
Tang W
Prizment A
Couper DJ
Source :
International journal of molecular epidemiology and genetics [Int J Mol Epidemiol Genet] 2013; Vol. 4 (1), pp. 49-60. Date of Electronic Publication: 2013 Mar 18.
Publication Year :
2013

Abstract

Aims: Epidemiological evidence shows that diabetes is associated with a reduced risk of prostate cancer. The objective of this study was to identify genes that may contribute to both type 2 diabetes and prostate cancer outcomes and the biological pathways these diseases may share.<br />Methods: The Atherosclerosis Risk in Communities (ARIC) Study is a population-based prospective cohort study in four U.S. communities that included a baseline examination in 1987-89 and three follow-up exams at three year intervals. Participants were 45-64 years old at baseline. We conducted a genomewide association (GWA) study of incident type 2 diabetes in males, summarized variation across genetic loci into a polygenic risk score, and determined if that diabetes risk score was also associated with incident prostate cancer in the same study population. Secondarily we conducted a separate GWA study of prostate cancer, performed a pathway analysis of both type 2 diabetes and prostate cancer, and qualitatively determined if any of the biochemical pathways identified were shared between the two outcomes.<br />Results: We found that the polygenic risk score for type 2 diabetes was not statistically significantly associated with prostate cancer. The pathway analysis also found no overlap between pathways associated with type 2 diabetes and prostate cancer. However, it did find that the growth hormone signaling pathway was statistically significantly associated with type 2 diabetes (p=0.0001).<br />Conclusion: The inability of this study to find an association between type 2 diabetes polygenic risk scores with prostate cancer or biological pathways in common suggests that shared genetic variants may not contribute significantly to explaining shared etiology.

Details

Language :
English
ISSN :
1948-1756
Volume :
4
Issue :
1
Database :
MEDLINE
Journal :
International journal of molecular epidemiology and genetics
Publication Type :
Academic Journal
Accession number :
23565322