TY - JOUR
T1 - Association of type 2 diabetes susceptibility variants with advanced prostate cancer risk in the breast and prostate cancer cohort consortium
AU - MacHiela, Mitchell J.
AU - Lindström, Sara
AU - Allen, Naomi E.
AU - Haiman, Christopher A.
AU - Albanes, Demetrius
AU - Barricarte, Aurelio
AU - Berndt, Sonja I.
AU - Bas Bueno-De-Mesquita, H.
AU - Chanock, Stephen
AU - Michael Gaziano, J.
AU - Gapstur, Susan M.
AU - Giovannucci, Edward
AU - Henderson, Brian E.
AU - Jacobs, Eric J.
AU - Kolonel, Laurence N.
AU - Krogh, Vittorio
AU - Ma, Jing
AU - Stampfer, Meir J.
AU - Stevens, Victoria L.
AU - Stram, Daniel O.
AU - Tjønneland, Anne
AU - Travis, Ruth
AU - Willett, Walter C.
AU - Hunter, David J.
AU - Le Marchand, Loic
AU - Kraft, Peter
PY - 2012/12/15
Y1 - 2012/12/15
N2 - Observational studies have found an inverse association between type 2 diabetes (T2D) and prostate cancer (PCa), and genome-wide association studies have found common variants near 3 loci associated with both diseases. The authors examined whether a genetic background that favors T2D is associated with risk of advanced PCa. Data from the National Cancer Institute's Breast and Prostate Cancer Cohort Consortium, a genome-wide association study of 2,782 advanced PCa cases and 4,458 controls, were used to evaluate whether individual single nucleotide polymorphisms or aggregations of these 36 T2D susceptibility loci are associated with PCa. Ten T2D markers near 9 loci (NOTCH2, ADCY5, JAZF1, CDKN2A/B, TCF7L2, KCNQ1, MTNR1B, FTO, and HNF1B) were nominally associated with PCa (P < 0.05); the association for single nucleotide polymorphism rs757210 at the HNF1B locus was significant when multiple comparisons were accounted for (adjusted P = 0.001). Genetic risk scores weighted by the T2D log odds ratio and multilocus kernel tests also indicated a significant relation between T2D variants and PCa risk. A mediation analysis of 9,065 PCa cases and 9,526 controls failed to produce evidence that diabetes mediates the association of the HNF1B locus with PCa risk. These data suggest a shared genetic component between T2D and PCa and add to the evidence for an interrelation between these diseases.
AB - Observational studies have found an inverse association between type 2 diabetes (T2D) and prostate cancer (PCa), and genome-wide association studies have found common variants near 3 loci associated with both diseases. The authors examined whether a genetic background that favors T2D is associated with risk of advanced PCa. Data from the National Cancer Institute's Breast and Prostate Cancer Cohort Consortium, a genome-wide association study of 2,782 advanced PCa cases and 4,458 controls, were used to evaluate whether individual single nucleotide polymorphisms or aggregations of these 36 T2D susceptibility loci are associated with PCa. Ten T2D markers near 9 loci (NOTCH2, ADCY5, JAZF1, CDKN2A/B, TCF7L2, KCNQ1, MTNR1B, FTO, and HNF1B) were nominally associated with PCa (P < 0.05); the association for single nucleotide polymorphism rs757210 at the HNF1B locus was significant when multiple comparisons were accounted for (adjusted P = 0.001). Genetic risk scores weighted by the T2D log odds ratio and multilocus kernel tests also indicated a significant relation between T2D variants and PCa risk. A mediation analysis of 9,065 PCa cases and 9,526 controls failed to produce evidence that diabetes mediates the association of the HNF1B locus with PCa risk. These data suggest a shared genetic component between T2D and PCa and add to the evidence for an interrelation between these diseases.
KW - carcinoma
KW - diabetes mellitus, type 2
KW - genetic predisposition to disease
KW - genetics
KW - genome-wide association study
KW - humans
KW - polymorphism, single nucleotide
KW - prostatic neoplasms
UR - http://www.scopus.com/inward/record.url?scp=84871216134&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=84871216134&partnerID=8YFLogxK
U2 - 10.1093/aje/kws191
DO - 10.1093/aje/kws191
M3 - Article
C2 - 23193118
AN - SCOPUS:84871216134
SN - 0002-9262
VL - 176
SP - 1121
EP - 1129
JO - American journal of epidemiology
JF - American journal of epidemiology
IS - 12
ER -